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| VAERS ID: | 271661 | Vaccinated: | 2007-01-29 | | Age: | 13.0 | Onset: | 2007-01-29, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-02-02, Days after onset: 26 | | Location: | California | Entered: | 2007-02-02, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: NO | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | FLU | AVENTIS PASTEUR | U2176FA | 0 | IM | RA | | HPV | UNKNOWN MANUFACTURER | 0954F | 0 | IM | RA | | TDAP | AVENTIS PASTEUR | C2638AA | 0 | IM | LA | | VARCEL | MERCK & CO. INC. | 1152F | 0 | SC | LA | |
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| VAERS ID: | 271956 | Vaccinated: | 2007-01-23 | | Age: | 23.0 | Onset: | 2007-01-24, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-02-08, Days after onset: 15 | | Location: | Massachusetts | Entered: | 2007-02-08, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Mircette, Claritin prn, Imitrex, Naprosyn, Valtrex | | Preexisting Conditions: migraines, eczema, condyloma, herpes simplex, lactose intolerance | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 1426F | 1 | IM | LA | |
| Administered by: Private Purchased by: Private | | Symptoms: Headache, Nausea | | Write-up: headache and nausea different than usual migraine for 2 wks beginning day after Gardasil vaccine administration |
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| VAERS ID: | 272358 | Vaccinated: | 2007-02-13 | | Age: | 14.0 | Onset: | 2007-02-13, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-02-15, Days after onset: 2 | | Location: | North Carolina | Entered: | 2007-02-15, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: ear infection | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | | R | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Loss of consciousness | | Write-up: Marlene passed out after having the Gardasil vaccine. |
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| VAERS ID: | 272861 | Vaccinated: | 2006-12-12 | | Age: | 19.0 | Onset: | 2007-01-30, Days after vaccination: 49 | | Gender: | Female | Submitted: | 2007-02-21, Days after onset: 8 | | Location: | California | Entered: | 2007-02-21, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: Scheduled appointment with Rhumatologist | | Previous Vaccinations: | | Other Medications: yasmin | | Preexisting Conditions: allgery to tylenol | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unkown | 0 | IM | GM | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Arthralgia, Fatigue, Gait disturbance, Influenza like illness, Muscular weakness | | Write-up: 3 weeks after injection, soreness in the left and right wrist, left ankle, and left knee. Pain has worsened and at times is hard to function. E.I- Fingers and wrist get too weak and painful to use, ankle pain increases making it hard to walk. Also, the feeling of having the flu, being constantly run-down and tired. This occured a month after recieving the vaccine. |
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| VAERS ID: | 272928 | Vaccinated: | 2007-02-22 | | Age: | 27.0 | Onset: | 2007-02-22, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-02-23, Days after onset: 1 | | Location: | California | Entered: | 2007-02-23, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: N/A | | Previous Vaccinations: | | Other Medications: Kariva, Nasonex | | Preexisting Conditions: None known | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 0011U | 0 | IM | RA | |
| Administered by: Private Purchased by: Private | | Symptoms: Pruritus, Swelling face | | Write-up: Pt. states he experienced mild itching last evening on upper part of body and leg. Also states that right side of face appears swollen |
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| VAERS ID: | 273127 | Vaccinated: | 2007-02-23 | | Age: | 13.0 | Onset: | 2007-02-24, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-02-27, Days after onset: 3 | | Location: | Washington | Entered: | 2007-02-27, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Lactaid 3000 unit tab take before eating dairy products | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 0961f | 0 | IM | RA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Fatigue, Malaise, Somnolence | | Write-up: Mother reports that the day after immunization the patient reported fatigue and was unable to get out of bed. No headache, no fever, and no other symptoms. Mother states that patient slept on and off for two days. No treatment required. Fatigue/malaise not listed on VIS as side effect. |
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| VAERS ID: | 273267 | Vaccinated: | 2007-03-01 | | Age: | 16.0 | Onset: | 2007-03-01, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-03-01, Days after onset: 0 | | Location: | Pennsylvania | Entered: | 2007-03-01, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: Dr. felt it was not a reaction to the injection or did she have a seizure. But it was a reaction of fear from having the injection. My dauther has never had a reaction to needle in this matter in her life time. Dr. said she may not have | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unknown | 0 | | | | TDAP | UNKNOWN MANUFACTURER | unknown | 0 | | | |
| Administered by: Private Purchased by: Private | | Symptoms: Convulsion, Dizziness, Dyskinesia, Injection site pain, Loss of consciousness, Musculoskeletal stiffness, Pain, Pallor | | Write-up: My daughter received 2 vaccines Tdap and HPV. The Tdap was injected in her right arm with no complaintsor event. Immediately after the Tdap injection she was injected with HPV vaccine in her left arm. She stated while the needle was still her arm that it hurt and she felt dizzy. As soon as she said she felt dizzy she passed out with her eyes closed. The nurse and I grap her to prevent her from falling off the exam table. Suddenly, she jerked back at the same time she jerked backwards her right arm jerked up over her head and her arm hit the window behind her then she became stiff and her whole body began to jerk. This appeared to me to look like she was having a seizure. The nusre also stated that she was having a seizure The nurse and I kept on calling her name and trying to stop her from banging into the window or to fall of the exam table. She came to in amount 30 seconds startled and wided eyed with her face pale and her lips white. The doctor came in after the entire event examined her said she was okay she laid down for about 15 mins and she was okay but still pale. Went home and my dauther slept for an hour. |
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| VAERS ID: | 273268 | Vaccinated: | 2007-02-28 | | Age: | 22.0 | Onset: | 2007-02-28, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-03-02, Days after onset: 25 | | Location: | Oregon | Entered: | 2007-03-02, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | DTAP | UNKNOWN MANUFACTURER | unknown | 0 | IM | LA | | HPV | UNKNOWN MANUFACTURER | unknown | 0 | IM | RA | |
| Administered by: Public Purchased by: Unknown | | Symptoms: Arthralgia, Asthenia, Discomfort, Erythema, Fatigue, Injection site pain, Insomnia, Pain, Pyrexia, Rash, Swelling, Urticaria | | Write-up: pain, redness & swelling, mild fever, tiredness, sore joints, rash, hives, severe pain at injections site, weakness, lost of sleep, discomfort. |
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| VAERS ID: | 273758 | Vaccinated: | 2007-03-07 | | Age: | 26.0 | Onset: | 2007-03-07, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-03-11, Days after onset: 4 | | Location: | Massachusetts | Entered: | 2007-03-11, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | | | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Nausea, Pyrexia | | Write-up: fever, nausea |
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| VAERS ID: | 273790 | Vaccinated: | 2007-03-09 | | Age: | 17.0 | Onset: | 2007-03-09, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-03-12, Days after onset: 3 | | Location: | Georga | Entered: | 2007-03-12, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: none | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: Allergic to Pertussis vaccine | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | SC | LA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Anxiety, Deafness, Fatigue, Flushing, Hypoaesthesia, Injected limb mobility decreased, Nausea, Pain in extremity, Syncope, Vertigo | | Write-up: 10:30am - Within 10 minutes of receiving vaccine, she fainted. She began to experience severe pain in her left arm with numbness in her hands and fingers. She had feelings of impending dome. 11:30am - She returned to school approximately 1 hour after the injection, but her symptoms did not improve and worsened. She was unable to use her left arm do to the pain and lack of feeling/strength in her hand. She then had periods of hearing loss. She experienced nausea, vertigo, facial flushing, upper chest flushing, and profound fatigue. 12:30pm - I returned her back to the MD office. There they did vital signs and administered Bendaryl by mouth. Her symptoms lasted 12 hours. By the next morning, she back to normal. |
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| VAERS ID: | 274170 | Vaccinated: | 0000-00-00 | | Age: | 23.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 0000-00-00 | | Location: | New York | Entered: | 2007-03-19 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: Hay fever | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | FLU | UNKNOWN MANUFACTURER | | | | | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Public Purchased by: Unknown | | Symptoms: Rash erythematous, Rash maculo-papular, Urticaria | | Write-up: On day 6th after 1st dose of HPV and Influenza vaccine given at health center, forearms, hands, palms maculopapular erythematous rash that became heavy and spread to entire body. Patient had been seen by 2 dermatologist, patches/hives last for 1 1/2 weeks. Required treatment with oral steroids (Medrol pack). No other current illness such as fever, headache, arthralgia, arthritis or myalgia. Reaction developed despite oral Claritin daily. |
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| VAERS ID: | 274430 | Vaccinated: | 2007-03-20 | | Age: | 22.0 | Onset: | 2007-03-21, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-03-21, Days after onset: 0 | | Location: | Minnesota | Entered: | 2007-03-21, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 0688F | 0 | IM | RA | | TDAP | AVENTIS PASTEUR | C2688AA | 0 | IM | LL | |
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| VAERS ID: | 274432 | Vaccinated: | 2007-03-08 | | Age: | 4.0 | Onset: | 2007-03-09, Days after vaccination: 1 | | Gender: | Male | Submitted: | 2007-03-21, Days after onset: 12 | | Location: | North Dakota | Entered: | 2007-03-21, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: Child brought in to physician 3/12/07 after calling in to report cellulitis to clinic. s (occured on weekend.) Parent asked for Hep A for child (NOT HPV!!!)will have lot# soon from Public Health as they are the ones who notified me of the | | Previous Vaccinations: none~~~0~In Patient | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | DTAP | UNKNOWN MANUFACTURER | | | | LL | | HPV | UNKNOWN MANUFACTURER | | | | LL | | MMRV | UNKNOWN MANUFACTURER | | | | LL | | OPV | UNKNOWN MANUFACTURER | | | | RL | |
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| VAERS ID: | 274662 | Vaccinated: | 2007-02-09 | | Age: | 27.0 | Onset: | 2007-02-10, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-03-03, Days after onset: 6 | | Location: | Florida | Entered: | 2007-03-23, Days after submission: 20 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: NONE | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Loestrin FE | | Preexisting Conditions: Allergies: Ceclor; no conditions | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 1163F | 0 | | | |
| Administered by: Private Purchased by: Other | | Symptoms: Dyspnoea, Tachycardia | | Write-up: Patient experienced rapid heart rate and shortness of breath. Patient went to ER. |
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| VAERS ID: | 275186 | Vaccinated: | 2007-03-22 | | Age: | 13.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2007-03-29 | | Location: | California | Entered: | 2007-03-29, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: none | | Previous Vaccinations: none~~NULL~~In Patient | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 0245U | 2 | IM | UN | |
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| VAERS ID: | 276172 | Vaccinated: | 2007-03-23 | | Age: | 16.0 | Onset: | 2007-03-28, Days after vaccination: 5 | | Gender: | Female | Submitted: | 2007-04-12, Days after onset: 15 | | Location: | Missouri | Entered: | 2007-04-12, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: none | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | GM | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Erythema, Rash | | Write-up: Developlep red lesion on left breast about 1 week after injection then next week developed red raised bumps with white centers all over abdomen progressively spread to back breasts and neck. |
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| VAERS ID: | 276186 | Vaccinated: | 2007-04-10 | | Age: | 13.0 | Onset: | 2007-04-12, Days after vaccination: 2 | | Gender: | Female | Submitted: | 2007-04-12, Days after onset: 0 | | Location: | Oklahoma | Entered: | 2007-04-12, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 1208f | 0 | IM | RA | | MNQ | AVENTIS PASTEUR | 42142AA | 0 | IM | RA | | PPV | MERCK & CO. INC. | 0866f | 0 | IM | LA | |
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| VAERS ID: | 276289 | Vaccinated: | 2007-04-11 | | Age: | 17.0 | Onset: | 2007-04-11, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-04-14, Days after onset: 3 | | Location: | Colorado | Entered: | 2007-04-14, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: Acid Reflux | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Nexium | | Preexisting Conditions: Migrains | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | LA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Muscle spasms, Pain, Pelvic pain | | Write-up: 4/11/07 @3:10pm - patient went to the doctor for pain in stomache, diagnosed as Acid Reflux. We were given a flyer fo HPV, and we all agreed that patient needed to recieve the vaccine. Approximately 3 hours after that, patient complained of cramping in her pelvic area (right, left, and middle of her pany-line area). She took 1-600mg Ibuprophin, which eased the pain. She still complains of pain in that area today. I called the nurse who gave the vaccine, and she said this was not a symptom. Just thought I'd write what we have experienced after recieving the HPV vaccine. |
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| VAERS ID: | 276422 | Vaccinated: | 2007-04-13 | | Age: | 17.0 | Onset: | 2007-04-13, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-04-16, Days after onset: 3 | | Location: | North Carolina | Entered: | 2007-04-16, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: None but she has fainted before while receiving vaccines but had never had a convulsion. The same thing happenned to her friend | | Diagnostic Lab Data: Doctor recommended and EKG. We are still pending on this. | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | | | | MMR | MERCK & CO. INC. | | 2 | | | | MNQ | AVENTIS PASTEUR | | 0 | | | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Convulsion, Eye rolling, Musculoskeletal stiffness, Screaming, Syncope | | Write-up: Sindy fainted and had a convulsion/seizure immediately after receiving the first HPV shot. While she was out, she suddenly lifted her upper body, rolled her eyes, made a screeching noise (like scared) and stiffed her hands. |
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| VAERS ID: | 277232 | Vaccinated: | 2007-03-27 | | Age: | 17.0 | Onset: | 2007-04-02, Days after vaccination: 6 | | Gender: | Female | Submitted: | 2007-04-05, Days after onset: 3 | | Location: | South Dakota | Entered: | 2007-04-23, Days after submission: 18 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 1425F | 1 | IM | LA | |
| Administered by: Private Purchased by: Public | | Symptoms: Arthralgia, Joint swelling | | Write-up: 6 days after Gardasil dose #2, she developed swollen, painful joints in the elbows, wrists, ankles and knees bilaterally. Has taken Ibuprofen with little relief. Pain and swelling persists for 3 days now. Will monitor, no fever. |
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| VAERS ID: | 277639 | Vaccinated: | 2007-04-24 | | Age: | 12.0 | Onset: | 2007-04-25, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-04-30, Days after onset: 5 | | Location: | Pennsylvania | Entered: | 2007-04-30, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: Apparently healthy | | Diagnostic Lab Data: Strep test was negative. Afternoon temperature tests by Dr. office on 4/27 and 4/30 showed no fever. AM temperature at home on 4/30 showed no fever. | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: None -- she does have a bit of hayfever | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | HPV | 0 | | RA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Body temperature, Cough, Dizziness, Headache, Pharyngolaryngeal pain, Pyrexia, Streptococcus identification test negative, Viral infection | | Write-up: Within 12 hours of vaccine, patient had 102 degree fever. First day symptoms were also headache, dizzy, sore throat. Morning fever last multiple days. Today, 6 days later, fever is gone, throat is raw with cough, strep test is negative, patient is ill. Dr. believes it is a viral infection, but cannot determine if related to vaccine or independent cause. |
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| VAERS ID: | 281968 | Vaccinated: | 2007-06-13 | | Age: | 12.0 | Onset: | 2007-06-13, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-06-15, Days after onset: 2 | | Location: | Colorado | Entered: | 2007-06-15, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Strattera 25mg | | Preexisting Conditions: ADHD inattentive type | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | | RA | | MNQ | SANOFI PASTEUR | | 0 | | LA | | VARCEL | UNKNOWN MANUFACTURER | | 1 | | LA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Convulsion, Dizziness, Fatigue, Headache, Pain in extremity, Pruritus, Syncope, Urticaria | | Write-up: She fainted after the administration of the last of three vaccines administered that day. The third was the HPV Vaccine. She had on convulsion as she came to. 36 hours after the vaccine she started having intense itching which broke in to hives after about 48 hours. She was very tired, dizzy, and had a bad headache and sore arms for the 24 hours following the vaccines. |
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| VAERS ID: | 282414 | Vaccinated: | 2007-06-19 | | Age: | 11.0 | Onset: | 2007-06-19, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-06-20, Days after onset: 1 | | Location: | Florida | Entered: | 2007-06-20, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: CBC BLOOD TEST, RESULTS- WBC-6.6;LY-21.8;MO-27.1;GR-51.1;LY-1.4;MO-1.8 & 2 PHYSICIANS CHECKING HER OUT AFTER SHOTS WERE ADMINISTERED | | Previous Vaccinations: Christina Aponte~ ()~~11~In Patient | | Other Medications: | | Preexisting Conditions: Environmental allergies, Chronic asthma, has sensitivity to prlone, & albuterol & allergic to Loribid | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | UN | RA | | MNQ | SANOFI PASTEUR | O2351AA | 0 | UN | RA | | TD | UNKNOWN MANUFACTURER | | 0 | UN | LA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Asthenia, Dizziness, Full blood count, Granulocyte count increased, Headache, Monocyte count increased, Pain, Pyrexia, White blood cell count | | Write-up: 102 fever, headache, dizziness, weak, body aches.Given Motin 200mg(1) for fever & aches |
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| VAERS ID: | 282608 | Vaccinated: | 2006-11-29 | | Age: | 16.0 | Onset: | 2006-11-29, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-06-21, Days after onset: 356 | | Location: | | Entered: | 2007-06-21, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: Unknown | | Diagnostic Lab Data: UNK | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': B0475795A | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEP | GLAXOSMITHKLINE BIOLOGICALS | ABVB221BA | | | | | HPV | UNKNOWN MANUFACTURER | | | UN | UN | |
| Administered by: Other Purchased by: Other | | Symptoms: Crying, Dyspnoea, Swollen tongue | | Write-up: This case was reported by a regulatory authority and described the occurrence of difficulty breathing in a 16-year-old female subject who was vaccinated with Engerix B and HPV vaccine. On 29 November 2006, the subject received a single dose of Engerix B (intravenous) a single dose of HPV vaccine. Thirty minutes after vaccination with Engerix B and HPV vaccine, the subject experienced crying difficulty breathing and swollen tongue. The regulatory authority reported that the events were clinically significant (or requiring intervention). The subject was treated with Piriton. At the time of reporting the outcome of the events were unspecified. |
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| VAERS ID: | 283673 | Vaccinated: | 2007-07-03 | | Age: | 13.0 | Onset: | 2007-07-03, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-07-04, Days after onset: 1 | | Location: | South Carolina | Entered: | 2007-07-04, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: stye on right eye | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Malarone 250-100 mg tablet GSK | | Preexisting Conditions: allergies to turkey, lamb, lobster | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unknown | 0 | UN | RA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Pruritus, Rash, Urticaria | | Write-up: Broke out in hives and large patchy spots over her body with sever itching. She was take to the hospital where they gave her a eppy pin injection and benedryl. |
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| VAERS ID: | 285001 | Vaccinated: | 2007-07-17 | | Age: | 13.0 | Onset: | 2007-07-18, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-07-18, Days after onset: 0 | | Location: | Pennsylvania | Entered: | 2007-07-18, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: EKG - normal, tachy; RA Po2 was 94% | | Previous Vaccinations: | | Other Medications: loratadine 10 mg. daily | | Preexisting Conditions: seasonal allergies | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | | VARCEL | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Body temperature increased, Chest pain, Cough, Dyspnoea, Electrocardiogram normal, Headache, Heart rate increased, Myalgia, PO2 normal, Tachycardia | | Write-up: Came to ER at 10:09 7/18/07 with complaints of chest pain of severity of 5 on a scale of 0-5 (5 being worst pain) Stated it started at 9 a.m. 7/18/07. VS 100.9 - 111-18 109/73 room air sat was 94%. Other complaints were cough, headache, and trouble breathing. EKG was normal - tachy. Diagnosis by ER physician - mylagia, possible reaction to vaccine. Given 1 gram tylenol. Instructed to return if wheezing or rash. |
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| VAERS ID: | 286082 | Vaccinated: | 2007-07-26 | | Age: | 16.0 | Onset: | 2007-07-26, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-07-26, Days after onset: 0 | | Location: | Kentucky | Entered: | 2007-07-26, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: syncope~Hep A (no brand name)~1~16.20~In Patient | | Other Medications: none | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unk | 0 | IM | LA | |
| Administered by: Military Purchased by: Unknown | | Symptoms: Eye rolling, Grunting, Loss of consciousness | | Write-up: Received a Gardasil shot. Was talking for about 20 secs, said she was going down and she was out. Nurse ran to get ammonia capsule. Eyes rolled back in her head, arms drew up, making grunting sounds, was out around 45 secs. Took about 20 secs to get her back with the ammonia. |
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| VAERS ID: | 286575 | Vaccinated: | 2007-07-23 | | Age: | 12.0 | Onset: | 2007-07-24, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-08-02, Days after onset: 21 | | Location: | Florida | Entered: | 2007-08-02, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: normal | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | DTAP | SANOFI PASTEUR | ac52b0012aa | 5 | IM | RA | | HEPA | UNKNOWN MANUFACTURER | | 0 | IM | LA | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | LA | | MNQ | SANOFI PASTEUR | u2172aa | 0 | IM | RA | | VARCEL | UNKNOWN MANUFACTURER | | 1 | IM | LA | |
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| VAERS ID: | 287579 | Vaccinated: | 2007-07-17 | | Age: | 12.0 | Onset: | 2007-07-17, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-07-18, Days after onset: 1 | | Location: | Pennsylvania | Entered: | 2007-08-09, Days after submission: 8 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Tylenol 1000mg | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | | | | MNQ | SANOFI PASTEUR | | 0 | | | | TD | UNKNOWN MANUFACTURER | | 0 | | | | VARCEL | UNKNOWN MANUFACTURER | | 0 | | | |
| Administered by: Public Purchased by: Unknown | | Symptoms: Hyperhidrosis, Nausea, Pallor, Presyncope | | Write-up: Patient turned pale. felt nauseous, and broke out in a sweat for approximately 5 minutes. Patient almost passed out. *As her mother, I believe the long-term benefits of this drug far outweigh the risks. |
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| VAERS ID: | 287841 | Vaccinated: | 0000-00-00 | | Age: | 9.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2007-08-12 | | Location: | Virginia | Entered: | 2007-08-12, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: Patient has had blood work done and other tests with no help | | Previous Vaccinations: | | Other Medications: at this time she is on no other medications only over the counter flinstone vitimans with iron | | Preexisting Conditions: Truncusaterious Type 1 1/2 with complications & Antiphosphilipid Syndrom ( wich in in remission at the moment ) | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | UN | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Blood test, Erythema, Pruritus, Rash | | Write-up: Patient has developed spots on her legs that are bothering her , itching and red and not clearing up since she has recieved the Gardasil shots , she is also a heart patient with Truncusaterious Aterious type 1 1/2 with complications & also in remission for Antiphospholipid syndrom.. i dont know if any of these mixed with the Gardasil has made it possible for her to have a reaction but i would appricatiate if you could look into this matter , she does not have the spots anywhere but on her legs and they are getting worse , her doctor as listed above does not seem to be able to find solution to this |
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| VAERS ID: | 288595 | Vaccinated: | 2007-08-20 | | Age: | 17.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2007-08-21 | | Location: | North Carolina | Entered: | 2007-08-21, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: pain at the injection site. | | Diagnostic Lab Data: none | | Previous Vaccinations: | | Other Medications: seroquel, 50mg | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | RA | | MNQ | SANOFI PASTEUR | u2578aa | | IM | RA | | TDAP | UNKNOWN MANUFACTURER | | 0 | IM | LA | |
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| VAERS ID: | 288637 | Vaccinated: | 0000-00-00 | | Age: | 19.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2007-08-21 | | Location: | Pennsylvania | Entered: | 2007-08-22, Days after submission: 1 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: CBC; HIV | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | SC | UN | |
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| VAERS ID: | 288992 | Vaccinated: | 2007-08-23 | | Age: | 17.0 | Onset: | 2007-08-24, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-08-25, Days after onset: 1 | | Location: | Washington | Entered: | 2007-08-25, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | | 0 | | UN | | HPV | UNKNOWN MANUFACTURER | | 0 | | UN | | MEN | UNKNOWN MANUFACTURER | | 0 | | UN | | TDAP | UNKNOWN MANUFACTURER | | 0 | | UN | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Chills, Dizziness, Dyspnoea, Fatigue, Headache, Hypoaesthesia, Malaise, Pain, Pyrexia | | Write-up: The day after receiving the meningococcal vaccine (she also received HPV,Hep A & Tdap at the same time)she woke up not feeling well. As the day progressed she got a 102.5 fever, chills, headache, whole body ache, difficulty breathing and her hands felt numb at times. This lasted until the next day. She felt better the next day but still felt tired, some what achy and dizzy at times. By the next day she felt normal again. I gave her ibuprofen, which brought the fever down some and somewhat helped with the aches. I did not take her in to the doctors office. She received two shots in the left arm and two in the right (which ones in each, I do not know). I clicked unkown manufacturer below, because I do not know what was used. |
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| VAERS ID: | 289333 | Vaccinated: | 2007-08-27 | | Age: | 15.0 | Onset: | 2007-08-27, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-08-29, Days after onset: 2 | | Location: | Michigan | Entered: | 2007-08-29, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: N/A | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: IBD | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | unknown | 0 | IM | UN | | HPV | UNKNOWN MANUFACTURER | unknown | 0 | IM | UN | | MNQ | SANOFI PASTEUR | unknown | 0 | IM | UN | | VARCEL | UNKNOWN MANUFACTURER | unknown | 1 | IM | RA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Headache, Injection site erythema, Injection site swelling, Injection site warmth, Malaise, Pain in extremity | | Write-up: At injection site there was immediate swelling, redness and skin/muscle was hot to touch. Patient experienced a fairly intense headache, her entire arm was quite painful and she was not feeling well ingeneral. This lasted for several days. PLEASE NOTE: HEP A IMMUNIZATION WAS ADMINISTERED ON THE SAME DATE AT A DIFFERENT LOCATION (PUBLIC HEALTH CLINIC). |
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| VAERS ID: | 290155 | Vaccinated: | 2007-09-07 | | Age: | 13.0 | Onset: | 2007-09-07, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-09-09, Days after onset: 2 | | Location: | Pennsylvania | Entered: | 2007-09-09, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: allergic to penicillin | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | | 0 | IM | RA | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | LA | |
| Administered by: Private Purchased by: Private | | Symptoms: Urticaria | | Write-up: Developed hives all over neck and arms approximately 4 hours after the shot. Benadryl was administered and the hives subsided. They returned the next day and were treated again with Benadryl |
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| VAERS ID: | 290653 | Vaccinated: | 2007-09-07 | | Age: | 11.0 | Onset: | 2007-09-07, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-09-15, Days after onset: 8 | | Location: | Minnesota | Entered: | 2007-09-15, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | | TDAP | UNKNOWN MANUFACTURER | | | | | | VARCEL | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Asthenia, Dyskinesia, Dysphonia, Fall, Headache, Pallor, Speech disorder, Syncope | | Write-up: Nurse had my daughter sitting on the edge of the exam table. She administered HPV and my daughter fainted, fell off exam table head first and had a mild jerking episode. She was pale and had a headache when she woke up. She was hoarse and weak and couldn't speak easily. |
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| VAERS ID: | 290915 | Vaccinated: | 2007-09-19 | | Age: | 17.0 | Onset: | 2007-09-19, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-09-19, Days after onset: 0 | | Location: | Pennsylvania | Entered: | 2007-09-19, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 0927U | 1 | IM | UN | | VARCEL | UNKNOWN MANUFACTURER | 0722U | | | | |
| Administered by: Private Purchased by: Public | | Symptoms: Anaphylactic reaction, Chest discomfort, Throat tightness, Wheezing | | Write-up: Patient had anaphylaxis. About 20 to 30 minutes after her immunizations, patient complained of her 'throat closing' and chest tightness. EMS arrived and felt the patient was wheezing, so gave an Albuterol treatment and a dose of Benadryl. When the patient arrived in the ED about 20 minutes later, she no longer had chest pain or difficulty breathing. Her vitals signs were stable, on exam she was not wheezing nor had any rash. We gave her a dose of steriod and H2 blocker and observed her for 6 hours after the event. No further events occured. Patient was discharged on steroids and benadryl. |
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| VAERS ID: | 291644 | Vaccinated: | 2007-09-20 | | Age: | 17.0 | Onset: | 2007-09-21, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-09-28, Days after onset: 7 | | Location: | New Jersey | Entered: | 2007-09-28, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: TAKES PAXIL 10 MG DAILY | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Dizziness | | Write-up: PATIENT WAS DIZZY FOR 3 DAYS AFTER SHE RECEIVED 2ND HPV VACCINE |
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| VAERS ID: | 292439 | Vaccinated: | 2007-10-02 | | Age: | 14.0 | Onset: | 2007-10-03, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-10-08, Days after onset: 5 | | Location: | Washington | Entered: | 2007-10-08, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: sulfa drugs | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | UN | LA | | VARCEL | UNKNOWN MANUFACTURER | | 1 | UN | LA | |
| Administered by: Private Purchased by: Private | | Symptoms: Injection site nodule, Pruritus, Skin warm | | Write-up: Resulted in approx 2"X3" bump at injection site on left arm. Very itchy, hot to the touch. Lasted 2.5-3 days. |
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| VAERS ID: | 292485 | Vaccinated: | 2007-09-21 | | Age: | 13.0 | Onset: | 2007-09-21, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-10-05, Days after onset: 15 | | Location: | North Carolina | Entered: | 2007-10-09, Days after submission: 4 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: Asthma, Hypothyroidism, sleep apnea, bipolar disorder | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 1060U | 0 | | LA | | MEN | UNKNOWN MANUFACTURER | U2329AA | 0 | | LA | | TDAP | UNKNOWN MANUFACTURER | AC52BB13AA | 0 | | RA | | VARCEL | MERCK & CO. INC. | 0854U | 1 | | RA | |
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| VAERS ID: | 293872 | Vaccinated: | 2007-10-18 | | Age: | 12.0 | Onset: | 2007-10-19, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-10-21, Days after onset: 2 | | Location: | Washington | Entered: | 2007-10-22, Days after submission: 1 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: Monica was in good health at the time of the vaccination. | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | | | | | | HPV | UNKNOWN MANUFACTURER | | | | | | MEN | UNKNOWN MANUFACTURER | | | | | | TDAP | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Asthenia, Crying, Headache, Nausea, No reaction on previous exposure to drug, Urticaria | | Write-up: Patient has felt weak, nauseated and has broken out in hives repeatedly since she received her immunizations 3 days ago. She was given 4 shots in the same day, TDAP, HEP A, HPV, and Meningococcal. She has not had an allergic reaction to any previous immunizations, nor has she had hives or rashes as reactions to any substance in the past. At the outbreak of the hives we have treated her with the maximum dose of Benadryl which has controlled the rash temporarily, however, it has returned twice. On the third day she began complaining of a severe headache, so bad she began to cry uncontrollably. We gave her ibuprofen and within an hour her headache had improved. |
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| VAERS ID: | 296323 | Vaccinated: | 2007-11-20 | | Age: | 17.0 | Onset: | 2007-11-20, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-11-10, Days after onset: 10 | | Location: | Georga | Entered: | 2007-11-10, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: ongoing sinus infection - no fever | | Diagnostic Lab Data: xrays, haven't received results yet (11/10/07); | | Previous Vaccinations: | | Other Medications: Unknown | | Preexisting Conditions: none | | CDC 'Split Type': WAES0801USA01707 | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | FLU | UNKNOWN MANUFACTURER | | 5 | UN | RA | | HPV | UNKNOWN MANUFACTURER | 1287U | 2 | IM | RA | |
| Administered by: Private Purchased by: Private | | Symptoms: Cold sweat, Dyspnoea, Injection site pain, Loss of consciousness, Pain in extremity, Sleep disorder, Syncope, X-ray | | Write-up: Patient received 3rd HPV vaccine and flu shot in right upper arm on 10/19/07. At time vaccine (HPV first) was given she experienced extreme pain described as a line down her arm into her thumb. Patient asked Kaiser employee to wait until the pain subsided some before giving the flu shot. Flu shot was then given in same arm a couple of minutes later. Over the course of the next few weeks, the pain somewhat subsided in the whole arm and was more above the elbow to the injection site. The pain has been so extreme that it has woken the patient from sleep on 3 occasions. Returned to Dr on November 7, 2007 for an evaluation. Dr. ordered shoulder xrays, physical therepy, 600 MG ibuprofin 3X a day until further notice and would consult with another doctor and be in touch about recommendations for further assessment. NOTE:parent observation of injection was that the injection was given in a manner of puncture/poke like compared to more of a pushing the injection into the arm. There was no 'squeezing' of the muscle/arm prior to injection. This is in follow-up to report(s) previously submitted on 2/14/2008. Information has been received from a physician concerning a 17 year old female who on 20-NOV-2007 was vaccinated IM into his left deltoid with a first dose of GARDASIL (lot#655327/1287U). Within 15 minutes, the patient fainted and stopped breathing for a moment. It was reported that the patient sat for 15 minutes and when she walked into the waiting room she passed out for about a minute. The patient was conscious but not talking and clammy. After 10 minutes (approximately) of being monitored the patient became talkative and laughd about what happened with her mother. An ambulance was called but the patient was not admitted to the hospital. Unspecified medical attention was sought. On 20-NOV-2007, the patient recovered. No product quality complaint was involved. Additional information is not expected. |
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| VAERS ID: | 297362 | Vaccinated: | 2007-11-19 | | Age: | 19.0 | Onset: | 2007-11-19, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2007-11-20, Days after onset: 1 | | Location: | Colorado | Entered: | 2007-11-20, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | FLU | UNKNOWN MANUFACTURER | | | | | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Blood pressure decreased, Dizziness, Dysarthria, Hypoaesthesia, Hypokinesia, Nausea, Pallor, Peripheral coldness, Posture abnormal, Visual disturbance | | Write-up: Minutes after receiving the HPV, patient beacme pale and dizzy. She then felt like her head was on fire, vision went black,couldn't hold up her head, couldn't move her body, speech slurred, felt like fainting, head kept dropping, left arm "asleep" and fingers cold, nauseus, blood pressure drop. |
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| VAERS ID: | 297670 | Vaccinated: | 0000-00-00 | | Age: | | Onset: | 0000-00-00 | | Gender: | | Submitted: | 2007-11-21 | | Location: | Unknown | Entered: | 2007-11-21, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | | | | | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Rash | | Write-up: rash |
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| VAERS ID: | 298886 | Vaccinated: | 2007-11-14 | | Age: | 13.0 | Onset: | 2007-11-25, Days after vaccination: 11 | | Gender: | Female | Submitted: | 2007-12-06, Days after onset: 18 | | Location: | Unknown | Entered: | 2007-12-06, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? Yes, 3 days | | Extended hospital stay? No |
| Current Illness: Unknown | | Diagnostic Lab Data: Body temperature 27Nov2007 39.4C, Body temperature 27Nov2007 38.6C, White blood cells 27Nov2007 17.1 Rash diagnosed as macropapular with hives. | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': B0497683A | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 2 | IM | LA | |
| Administered by: Other Purchased by: Other | | Symptoms: Asthenia, Body temperature increased, Headache, Malaise, Myalgia, Rash, Rash papular, Serum sickness, Urticaria, White blood cell count increased | | Write-up: This female subject was enrolled in the prophylactic open study 107682 (HPV-018). On 02 April 2007, the subject received the 1st dose of HPV 16 and 18 (IM left upper deltoid), the dose of Aventis Pasteur's Menactra (IM, right lower deltoid) and the dose of Boostrix (IM right upper deltoid). On 08 May 2007 and 14 November 2007, the subject received the 2nd and 3rd dose of HPV (IM left upper deltoid). On 25 November 2007, 11 days after the 3rd of HPV 16-18, seven months after the 1st dose of Boostrix and seven months after the 1st dose of Menactra, this 13-year-old subject developed febrile rash. The subject was hospitalised. The subject was treated with adrenaline, diphenhydramine hydrochloride and corticosteroid. The event was unresolved at time of reporting. The investigator considered there was no reasonable possibility that the febrile rash may have been caused by Boostrix or Menactra but the investigator considered that there was a reasonable possibility that the febrile rash may have been caused by HPV 16-18. Investigator Comments: On 21 November 2007, the subject stated she had headache, muscle pain and weakness. On 25 November 2007, the rash started on legs during the evening. On 26 November 2007, the subject came to clinic with a rash covering most of her body. Given Epinephrine and told to take Benadryl. Return to clinic on 27 November 2007 in AM. On 27 November 2007, the rash was worse, subject had temperature of 39.4 C and general malaise. She was sent to hospital ER for evaluation where she was admitted. Per mother, the subject was given a steroids IV and discharged with Prednisone and Motrin. Information received on 28 November 2007 following a phone call with her grandmother; the subject had a temperature of 38.6 C yesterday afternoon. She stated that she was admitted for 3 days of treatment. The doctors there felt it was related to the HPV vaccine. The subject was feeling better and the rash has decreased. On 28 November 2007, the subject was going to be discharged in this afternoon. She stated th |
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| VAERS ID: | 299071 | Vaccinated: | 2007-12-06 | | Age: | 16.0 | Onset: | 2007-12-07, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2007-12-08, Days after onset: 1 | | Location: | New Jersey | Entered: | 2007-12-08, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 1 | IM | LA | | TDAP | UNKNOWN MANUFACTURER | | | IM | RA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Crying, Headache, Pain in extremity, Pyrexia | | Write-up: C/O pain in both arms and legs, severe headache and fever....crying...gave tylenol and slept for 16 hours |
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| VAERS ID: | 300558 | Vaccinated: | 2007-09-11 | | Age: | 10.0 | Onset: | 2007-09-27, Days after vaccination: 16 | | Gender: | Female | Submitted: | 2007-12-20, Days after onset: 6 | | Location: | Ohio | Entered: | 2007-12-20, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | RA | |
| Administered by: Private Purchased by: Private | | Symptoms: Biopsy skin, Blood test normal, Eczema, Pityriasis rosea, Rash, Skin depigmentation, Swelling | | Write-up: Daughter received HPV on 09/11/2007. 2 weeks after receiving the vaccine she started breaking out in a rash on her chest. It rapidly spread to her back, up her neck, her face and covered her entire trunk within a few days. It continued to spread into her groin area, her arms, and her legs down to her ankles. This all took place starting 09/27/2007. I had to to her PCP, whom she received the shot and to a dermatologist, who first diagnosed her with Pitariosis Rosea. The dermatologist did a biopsy and came back with "eczema". The rash continued to break out until there was barely any skin NOT covered with this rash. My daughter started swelling. I immediately demanded full blood work up. All of the counts came back as normal. I scheduled an appointment with an allergist, thinking that maybe she was allergic to something. All tests were negative. The only way we got her cleared up was with Prednisone. After she did her round with Prednisone, she broke out again, but not as extreme. My daughter had this rash for 2 months. She is now scared from the biopsy and during all of this she has "white spots" where the pigment in her skin is gone. She is possibly scared for life. |
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| VAERS ID: | 301402 | Vaccinated: | 2007-12-27 | | Age: | 1.5 | Onset: | 0000-00-00 | | Gender: | Male | Submitted: | 2008-01-02 | | Location: | South Dakota | Entered: | 2008-01-02, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: None | | Previous Vaccinations: None noted~HPV (no brand name)~1~~In Patient | | Other Medications: None | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | DTAP | UNKNOWN MANUFACTURER | | | | | | HPV | UNKNOWN MANUFACTURER | | | | | |
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| VAERS ID: | 302664 | Vaccinated: | 2007-10-05 | | Age: | 17.0 | Onset: | 2007-11-15, Days after vaccination: 41 | | Gender: | Female | Submitted: | 2008-01-10, Days after onset: 359 | | Location: | Michigan | Entered: | 2008-01-14, Days after submission: 4 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? Yes, 1 days | | Extended hospital stay? No |
| Current Illness: | | Diagnostic Lab Data: platelet count dropped to 8000; lab results avail. if necessary 1/16/08-records received-CT brain normal. 4/28/08-Pathology Report for DOS 1/2/08-Peripheral Blood Smear: Red Blood Cells normochromic and normocytic in appearance. White bl | | Previous Vaccinations: | | Other Medications: birth control pills | | Preexisting Conditions: 1/16/08-records received-HX of heavy periods for past 1 1/2 years treated with hormone medication. HX of recent dental cleaning with gums bleeding 'too much'. | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | UN | UN | |
| Administered by: Public Purchased by: Public | | Symptoms: Blood product transfusion, Computerised tomogram normal, Contusion, Headache, Lymphocyte count decreased, Musculoskeletal discomfort, Nausea, Neutrophil count increased, Photophobia, Platelet count decreased, Platelet transfusion, Thrombocytopenia, White blood cell count normal | | Write-up: 1-2-08-Diag. with thrombocytopenia, platelet count dropped to 8000. Plt transfusion x2. Easy bruising began Nov. 07. 1/16/08-records received for DOS 1/4/08-consultation for C/O headache since 1/3/08 now improved-admitted on 1/3/08-with easy bruising and platelet count of 7000. No other systemic symptoms. While receiving treatment with IV gamma globulin, C/O severe headache, throbbing with sensitive to bright lights and some nausea. Saw spots in her eyes. Denies neck stiffness, but has some mild neck discomfort. |
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| VAERS ID: | 303366 | Vaccinated: | 2008-01-04 | | Age: | 14.0 | Onset: | 2008-01-05, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2008-01-16, Days after onset: 11 | | Location: | California | Entered: | 2008-01-23, Days after submission: 7 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: None known | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 2 | UN | LA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Hypoaesthesia, Injection site pain | | Write-up: Pt received HPV #3 on 1/4/08, has had continued pain at inj site since day after vaccine. On approx 1/9/08 developed "numbness" in hand (small & ring finger) which has persisted. On 1/16/08 reports spreading "numbness" to middle finger. Injection & numbness both on pts left upper extremity. |
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| VAERS ID: | 304343 | Vaccinated: | 2007-12-19 | | Age: | 24.0 | Onset: | 2008-01-17, Days after vaccination: 29 | | Gender: | Female | Submitted: | 2008-02-05, Days after onset: 11 | | Location: | Kentucky | Entered: | 2008-02-05, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Yasmin | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Injection site mass | | Write-up: One month after having the HPV (Gardisal) vaccine administered at her doctor's office at home she developed a raised mass at the site (Left upper arm)2.5 cm in diameter round. She was treated with warm compresses and Keflex 500 mg 4 times daily for 10 days |
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| VAERS ID: | 305428 | Vaccinated: | 0000-00-00 | | Age: | 18.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2008-02-14 | | Location: | Texas | Entered: | 2008-02-19, Days after submission: 5 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: None | | Previous Vaccinations: | | Other Medications: DEPAKOTE; SEASONALE; LAMICTAL | | Preexisting Conditions: Convulsion | | CDC 'Split Type': WAES0801USA00892 | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 1 | UN | UN | | HPV4 | MERCK & CO. INC. | 0523U | 0 | IM | UN | |
| Administered by: Other Purchased by: Other | | Symptoms: Pharyngeal oedema, Urticaria, Vaccine positive rechallenge | | Write-up: Information has been received from a licensed practical nurse concerning an 18 year old female with seizure disorder who on 16-JUL-2007 was vaccinated IM with a 0.5 ml first dose of GARDASIL (lot #657868/0523U). Concomitant therapy included DEPAKOTE, SEASONALE and LAMICTAL. Subsequently the patient experienced hives and "throat swelling." Subsequently, the patient recovered. On an unspecified date, the patient was vaccinated with a second dose of GARDASIL. Subsequently the patient experienced hives and "throat swelling." Subsequently, the patient recovered. The patient reported the event at an unrelated office visit. Additional information has been requested. |
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| VAERS ID: | 306054 | Vaccinated: | 2008-02-27 | | Age: | 17.0 | Onset: | 2008-02-27, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-02-28, Days after onset: 1 | | Location: | New Mexico | Entered: | 2008-02-28, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: Penicillin | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | Unknown | 0 | UN | LA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Headache, Loss of consciousness, Mydriasis, Pallor, Tinnitus, Visual disturbance | | Write-up: 20 minutes after receiving the injection, my child told me that she couldn't see and that her ears were ringing. She was extremely pale and her pupils were fully dialated. She passed out and was assisted by a nurse at the doctor's office. No further treatment was administered. My child complained of an moderate headache that evening. All symptoms were resolved by this morning. |
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| VAERS ID: | 306680 | Vaccinated: | 2007-11-01 | | Age: | 19.0 | Onset: | 2007-12-01, Days after vaccination: 30 | | Gender: | Female | Submitted: | 2008-03-07, Days after onset: 370 | | Location: | Colorado | Entered: | 2008-03-07, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: Several diagnostic labs including internal and external cultures / smears | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: asthma | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Culture, Fungal infection, Injection site pain, Laboratory test, Smear test | | Write-up: At the time of the injection (date is uncertain) and soon afterward only pain at site were a problem. Within a week or so, a stubborn yeast infection started that is still recurring and never quite clears up even today, 4 months later, with agressive physician care and prolonged internal and external medical treatment. As the HPV vaccine is yeast based, I believe there is a definite correlation. There is no history previously of recurrent yeast infections in her. |
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| VAERS ID: | 308432 | Vaccinated: | 2008-03-27 | | Age: | 15.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2008-03-27 | | Location: | California | Entered: | 2008-03-27, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Convulsion, Gaze palsy, Mydriasis, Syncope | | Write-up: Within a minute of Gardisil Vaccine she fainted with eyes open and dilated at full extend, started comvulsing for 5 seconds, eyes started to shake also |
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| VAERS ID: | 308712 | Vaccinated: | 2008-03-31 | | Age: | 18.0 | Onset: | 2008-03-31, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-04-01, Days after onset: 29 | | Location: | Illinois | Entered: | 2008-04-01, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: none~ ()~NULL~~In Patient | | Other Medications: none | | Preexisting Conditions: none but her father's sister had guimome/barre syndrome | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | IM | LA | | MEN | UNKNOWN MANUFACTURER | | | IM | RA | |
| Administered by: Private Purchased by: Private | | Symptoms: Cold sweat, Convulsion, Dyskinesia, Feeling hot, Gaze palsy, Hyperhidrosis, Malaise, Musculoskeletal stiffness, Pallor, Peripheral coldness, Pyrexia | | Write-up: Within 5 minutes of the shots, my daughter walked out to the waiting room, sat next to me, told me what shots she had, said she needed some water, looked like not feeling well, I fanned her with the papers,her eyes rolled back, she stiffened, her body jerked, looked like a convulsion, it lasted less than a minute, as nurses and doctor came out to check her, her body relaxed, eyes were still closed, she said she had a dream. Her head was very hot, her hair got wet with sweat, hands were cold and clammy. Nurse said she fainted but I disagreed. In fainting, the body goes limp and drops. She went stiff and stayed above the chair, never fell. We gave her water, waited for about 15 minutes, nurse checked her blood pressure and let us go. When she came home she slept soundly for 1 hour. Later in the evening, she still had a low fever. The next day her coloring is still pale. |
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| VAERS ID: | 308719 | Vaccinated: | 2007-11-21 | | Age: | 19.0 | Onset: | 2007-11-20, Days after vaccination: -1 | | Gender: | Female | Submitted: | 2008-04-01, Days after onset: 345 | | Location: | Wisconsin | Entered: | 2008-04-01, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: Pneumonia - cough - chest x-ray effusion +/- sm. right pleural right lower lobe pneumonia. | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | UN | UN | |
| Administered by: Public Purchased by: Other | | Symptoms: Chest X-ray abnormal, Cough, Dysphonia, Dyspnoea, Lobar pneumonia, Musculoskeletal stiffness, Pharyngolaryngeal pain, Pleural effusion, Pyrexia | | Write-up: HPV given 11/20/07 - In UC 11/25/07 with 5 days of cough, hoarseness, fever. Non-productive cough - sore throat, stiff neck - hurting to take deep breath. |
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| VAERS ID: | 308909 | Vaccinated: | 2008-04-04 | | Age: | 13.0 | Onset: | 2008-04-04, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-04-04, Days after onset: 0 | | Location: | Pennsylvania | Entered: | 2008-04-04, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | | 1 | UN | RA | | HPV | UNKNOWN MANUFACTURER | | 2 | UN | LA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Back pain, Vomiting | | Write-up: Amanda received the third dose of HPV and her second dose of Hepatitis A yesterday, April 3, 2008, around 3:30 p.m. She was feeling totally fine, no problems. On Friday, April 4, 2008, I received a call from her school to pick her up due to vomiting and lower back pain. She left for school feeling fine and I received the call about one hour later-8:45a.m. |
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| VAERS ID: | 309244 | Vaccinated: | 2007-04-30 | | Age: | 33.0 | Onset: | 2007-04-30, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-04-10, Days after onset: 345 | | Location: | Unknown | Entered: | 2008-04-10, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? Yes, 3 days | | Extended hospital stay? No |
| Current Illness: | | Diagnostic Lab Data: A MRI of the brain performed the same day was suspicious for an early demyelinating process. The cervical spine MRI was within normal limits, as were the visual evoked potentials and the brainstem evoked potentials. On 01 May 2007, the MR | | Previous Vaccinations: | | Other Medications: Since 2000, the subject was taking bupropion hydrochloride (for depression), was taking omeprazole since 01 April 2007 (for gastroesophageal reflux disease), and used baclofen and Vicodin for chronic pain control. | | Preexisting Conditions: The subject has a medical history of tension headaches, anxiety-depressionbipolar disorder, reflux esophagitis and gastroeseophageal reflux disease. In 2005, she was diagnosed with chronic lower back pain associated with disc disease. In November 2006, the subject developed migrainous headache for which a CAT scan of the head without contrast was unremarkable on 01 March 2007. | | CDC 'Split Type': B0470726A | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 1 | UN | UN | |
| Administered by: Other Purchased by: Other | | Symptoms: Back pain, Brain stem auditory evoked response normal, Demyelination, Intervertebral disc disorder, Migraine, Nuclear magnetic resonance imaging brain abnormal, Nuclear magnetic resonance imaging normal, Spinal X-ray normal, Vision blurred, Visual evoked potentials normal | | Write-up: This 33-year old female subject was enrolled in the prophylactic observer blind study 108933 (HPV-010) which compares GSK's Human Papillomavirus type 16 and 18 vaccine to Merck's GARDASIL. She received three doses of blinded vaccine on 21 February 2007, 28 March 2007 and 30 April 2007. The subject has a medical history of tension headaches, anxiety-depression bipolar disorder, reflux esophagitis and gastrooesophageal reflux disease. In 2005, she was diagnosed with chronic lower back pain associated with a disc disease. In November 2006, the subject developed migrainous headache for which a CAT scan of the head without contrast was unremarkable on 01 March 2007. Since 2000, the subject was taking bupropion hydrochloride (for depression), was taking Omeprazole since 01 April 2007 (for gastrooesophageal reflux disease), and used baclofen and vicodin for chronic pain control. On 30 April 2007, 33 days after the second of vaccine and on the same day as the third dose of vaccine, the subject went to the emergency room because of blurred vision. A MRI of the brain performed the same day was suspicious for an early demyelinating process. The cervical spine MRI was within normal limits, as were the visual evoked potentials and brainstem evoked potentials. She was treated with sodium chloride, prednisone and methylpredisolone sodium succinate for treatment of multiple sclerosis. Following this treatment, the double vision resolved. On 01 May 2007, the MRI of the cervical spine with and without contrast was negative. She was discharged from the hospital on 02 May 2007. At the time of reporting, the event was unresolved. The subject is being followed by a neurologist. The investigator considered there was no reasonable possibility that the multiple sclerosis may have been caused by the administration of the investigational product. Expert review: A blinded review of the case by an independent expert did not support the diagnosis of multiple sclerosis as this diagnosis required a dissemination of lesions in space and time. Th |
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| VAERS ID: | 309381 | Vaccinated: | 2008-04-11 | | Age: | 18.0 | Onset: | 2008-04-11, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-04-13, Days after onset: 2 | | Location: | Texas | Entered: | 2008-04-13, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unknown | 2 | IM | LA | |
| Administered by: Public Purchased by: Unknown | | Symptoms: Headache, Pyrexia, Vomiting | | Write-up: Vomiting, headache, fever of 102' Lasted fro 24 hrs |
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| VAERS ID: | 310289 | Vaccinated: | 2003-01-10 | | Age: | 19.0 | Onset: | 2003-05-27, Days after vaccination: 137 | | Gender: | Female | Submitted: | 2008-04-18, Days after onset: 1816 | | Location: | | Entered: | 2008-04-21, Days after submission: 3 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: chest computed axial tomography, 16May03, mediastinal tumor; biopsy, 27May03, morbus Hodgkin nodula sclerose stadium 11A; chest computed axial tomography, 04Aug03, strong decrease of the glandules on neck and the mediastinal tumor | | Previous Vaccinations: | | Other Medications: Unknown | | Preexisting Conditions: None | | CDC 'Split Type': WAES0804USA03544 | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Computerised tomogram abnormal, Hodgkin's disease, Lymphadenopathy, Lymphatic system neoplasm, Malignant mediastinal neoplasm, Mediastinal mass, Nasopharyngitis, Radiotherapy | | Write-up: This report is being submitted in response to an FDA request for information. A 19 year old female entered a study, and reported Hodgkin's lymphoma as new medical history at Month 6. On 10-JAN-2003 and 14-MAR-2003, the patient was vaccinated intramuscularly with a 0.5 mL first and second dose of Gardasil. She did not receive a third dose of vaccine, but did remain in the study (discontinued vaccination due to Hodgkin's disease but remained in the study for follow-up). The condition was reported as active, diagnosed in 2003 (27-MAY-2003). Annotations indicate the following: On 26-MAY-2003, CT thorax: mediastinal tumor 8.3 x4cm + lymphatic nodes. On 27-MAY-2003, a biopsy: Morbus Hodgkin nodula sclerose stadium IIA (Her father: 1995: lymphogranulomadosis). Stage IIIA. She caught a cold in May 2003 and discovered lymphatic nodes on the right side of her neck. Beyond that, no other symptoms. She was asymptomatic before entering the trial and until May 2003. It was felt that this diagnosis was probably not vaccine related. She had received cytostatica and radiation therapy. 04-AUG CT thorax: strong decrease of the glandules on the neck and the mediastinal tumor. No other medical history was reported for this subject. No serious clinical adverse experiences were reported. No additional information is available regarding the Hodgkin's disease. The subject entered the study extension (Protocol 015-10): study extension which offered vaccine to subject who received placebo or received incomplete vaccination regimens of HPV vaccine and received her third dose of vaccine on 05-MAY-2007. The patient completed the study extension on 19-JUN-2007. No serious adverse experiences were reported in the study extension. Per protocol, because the episode of Hodgkin's disease was not vaccine related and reported beyond the follow-up period for adverse experiences, the Hodgkin's disease was not reported as an Adverse Experience, but was reported as medical history in the protocol study data base. No further informati |
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| VAERS ID: | 310290 | Vaccinated: | 2003-02-13 | | Age: | 17.0 | Onset: | 2003-02-13, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-04-18, Days after onset: 1831 | | Location: | | Entered: | 2008-04-21, Days after submission: 3 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? Yes, 0 days | | Extended hospital stay? No |
| Current Illness: | | Diagnostic Lab Data: Unknown | | Previous Vaccinations: | | Other Medications: Unknown | | Preexisting Conditions: Unknown | | CDC 'Split Type': WAES0804USA03545 | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Hodgkin's disease | | Write-up: This report is being submitted in response to an request for information. Information has been received from an investigator concerning a 17 year old white female who entered a study title as stated above. On 13-FEB-2003, 31-MAR-2008 and 25-AUG-2003 the patient was vaccinated IM with a first, second and third dose of GARDASIL, respectively. The first report of Hodgkin's disease was at the month 12 visit, which occurred on 16-FEB-2004. At that time, the disease was reported to be active with a start date in 2003. The patient was hospitalized. An annotation related to this event reported the subject no longer received treatment (stopped August 2004). The subject received "cytotoxin" and radiation therapy. No other medical history was reported on this patient. No serious clinical adverse experiences were reported for this patient. There was no additional information regarding Hodgkin's disease. On 05-OCT-2006 the patient completed the study. It was reported that per protocol because the episode of Hodgkin's disease was not vaccine related and reported beyond the follow-up period for adverse experiences, the Hodgkin's disease was not reported as an adverse experience but is reported as medical history in the protocol study base. The reporting investigator felt that Hodgkin's disease were not related to study therapy. Additional information has been requested. |
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| VAERS ID: | 312503 | Vaccinated: | 2007-09-12 | | Age: | 13.0 | Onset: | 2008-02-19, Days after vaccination: 160 | | Gender: | Female | Submitted: | 2008-05-16, Days after onset: 2 | | Location: | Unknown | Entered: | 2008-05-16, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? Yes |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: Unknown | | Diagnostic Lab Data: On 20 February 2008: Exam in clinic- findings: left eyelid cannot be approximated, numbness left cheek. Exam reveals facial asymmetry left facial palsy. Patient never seen by neurologist-referral by neurologist office for physical therapy. | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': B0519583A | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | IM | UN | |
| Administered by: Other Purchased by: Other | | Symptoms: Blepharospasm, Dyskinesia, Eyelid disorder, Facial palsy, Hypoaesthesia facial | | Write-up: This female subject was enrolled in the prophylactic open study 107682 (HPV-018). On 03 April 2007, the subject received the 1st dose of Gardasil (IM left upper deltoid) and the dose of Boostrix (IM right upper deltoid). On 14 May 2007, the subject received the 2nd dose of Gardasil (IM left upper deltoid) and the dose of Aventis Pasteur's (Menactra, IM right upper deltoid) On 12 September 2007, the subject received the 3rd dose of Gardasil (IM left upper deltoid). On 19 February 2008, five months after the 3rd dose of Gardasil, nine months after the 1st dose of Menactra, 10 months after the 1st dose of Boostrix, this 13-year-old subject developed Bell's palsy. The event was disabling. The subject was treated with acyclovir and prednisolone. The event was unresolved at time of reporting. The investigator considered that there was a reasonable possibility that the Bell's palsy may have been caused by Gardasil 16-18, Menactra and Boostrix. Investigator's comments: On 19 February 2008, left eyelid starting twitching. The eyelid felt numb + left side of face was numb. She could not close her eyes, mouth angle twists to right when smiling. Continues to worsen. On 20 February 2008, patient given Zovirax and prednisolone. On 28 February 2008, patient returned to clinic for recheck-no improvement-referred for a neurology consult- patient did not get a neuro consult. On 09 April 2008, recheck in clinic- Bell's Palsy worsening. On 25 April 2008, patient not improved, worsened. Patient is receiving physical therapy. On 01 May 2008, no improvement. On 08 May 2008, the Bell's Palsy is probably related to the study. |
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| VAERS ID: | 312974 | Vaccinated: | 2008-05-21 | | Age: | 19.0 | Onset: | 2008-05-21, Days after vaccination: 0 | | Gender: | Male | Submitted: | 2008-05-22, Days after onset: 1 | | Location: | California | Entered: | 2008-05-22, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: Normal | | Previous Vaccinations: | | Other Medications: Loratidine | | Preexisting Conditions: Allergy to cats | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unknown | 4 | ID | RA | | TYP | UNKNOWN MANUFACTURER | unknown | 0 | IM | RA | | YF | UNKNOWN MANUFACTURER | unknown | 0 | ID | LA | |
| Administered by: Public Purchased by: Private | | Symptoms: Dysphagia, Throat tightness | | Write-up: Mild difficulty swallowing 15 minutes after shot administered. Mild muscle tension in the throat as well. Went to the ER, was given adrenaline, benadryl, and pregnazone. Symptoms went away after these treatments. |
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| VAERS ID: | 313360 | Vaccinated: | 2007-05-14 | | Age: | 13.0 | Onset: | 2008-02-19, Days after vaccination: 281 | | Gender: | Female | Submitted: | 2008-05-22, Days after onset: 3 | | Location: | Unknown | Entered: | 2008-05-27, Days after submission: 5 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? Yes |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: Not reported | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: Not reported | | CDC 'Split Type': 200801581 | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 2 | IM | LA | | MNQ | SANOFI PASTEUR | | 0 | IM | RA | | TDAP | GLAXOSMITHKLINE BIOLOGICALS | | 0 | IM | RA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Blepharospasm, Facial palsy, Hypoaesthesia facial | | Write-up: Initial report was received from another manufacturer (ID# B0519583A), who received the report from an investigator participating in their clinical trial. Verbatim from the report: "This female subject was enrolled an a prophylactic open study. On 03 April 2007, the subject received the 1st dose of HPV (IM, left upper deltoid) and the dose of BOOSTRIX (IM, right upper deltoid). On 14 May 2007, the subject received the 2nd dose of HPV (IM, left upper deltoid) and the dose of MENACTRA (IM, right upper deltoid). On 12 September 2007, the subject received the 3rd dose of HPV (IM, left upper deltoid). On 19 February 2008, five months after the 3rd dose of HPV 16-18, nine months after the 1st dose of MENACTRA, 10 months after the 1st dose of BOOSTRIX, this 13-year-old subject developed bell's palsy. the event was disabling. The subject was treated with ACYCLOVIR and PREDNISOLONE. The event was unresolved at the time of reporting. The investigator considered that there was a reasonable possibility that the bell's palsy may have been caused by HPV 16-18, MENACTRA and BOOSTRIX. Investigator comments: On 19 February 2008, left eyelid started twitching. The eyelid felt numb + left side of face was numb. she could not close her eyes, mouth angle twists to right when smiling. Continues to worsen. On 20 February 2008, patient given ZOVIRAX and PREDNISOLONE. On 28 February 2008, patient returned to clinic for recheck - no improvement - referred for a neurology consult - patient did not get a neuro consult. On 09 April 2008, recheck in clinic - Bell's Palsy worsening. On 25 April 2008, patient had not improved, worsened. Patient is receiving physical therapy. On 01 May 2008, no improvement. On 08 May 2008, the Bell's Palsy is probably related to the study. On 20 February 2008: Exam in clinic - findings: left eyelid cannot be approximated, numbness left cheek. Exam reveals facial asymmetry left facial palsy. Patient never seen by neurologist - referral by neurologist office for physical therapy." No further information was provid |
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| VAERS ID: | 314390 | Vaccinated: | 2008-04-30 | | Age: | 15.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2008-05-30 | | Location: | Arkansas | Entered: | 2008-05-30, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: none | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | msd1758y | 0 | IM | RA | | TDAP | UNKNOWN MANUFACTURER | pmcc2899aa | 0 | IM | LA | |
| Administered by: Public Purchased by: Public | | Symptoms: Unevaluable event | | Write-up: none |
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| VAERS ID: | 316429 | Vaccinated: | 2007-03-20 | | Age: | 13.0 | Onset: | 2007-04-06, Days after vaccination: 17 | | Gender: | Female | Submitted: | 2008-06-16, Days after onset: 375 | | Location: | Texas | Entered: | 2008-06-17, Days after submission: 1 | |
| Life Threatening Illness? Yes |
| Died? No |
| Disability? Yes |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: 6/26/08-records received-EEG abnormal due to bifrontal spike and wave activity. CT brain unremarkable. MRI no abnormalities. | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: 6/26/08-records received-/11/07-Over past year and half has had events characterized by right foot tingling, sometimes shaking, head turning to right. | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | UN | UN | | MEN | UNKNOWN MANUFACTURER | | | UN | UN | | TDAP | UNKNOWN MANUFACTURER | | | UN | UN | | VARCEL | UNKNOWN MANUFACTURER | | | UN | UN | |
| Administered by: Public Purchased by: Other | | Symptoms: Complex partial seizures, Electroencephalogram abnormal, Gaze palsy, Nuclear magnetic resonance imaging normal, Paraesthesia, Posture abnormal, Scan brain, Tremor | | Write-up: 1st HPV series done on 3/20/07. First grand mal seizure on 04/16/07; Has been diagnosed epileptic on 5/3/07 6/26/08-records received-seen in ED 4/9/07-C/Ogeneralized shaking, confused after event. Impression new onset of seizure. Seen on 5/11/07-Over past year and half has had events characterized by right foot tingling, sometimes shaking, head turning to right. These spells have increased over past 1-2 months, especially tingling sensation. Seizure event eyes rolled back, jerking and limp. Impression:complex partial seizures with secondary generalization except EEG is showing tendencies towards generalized epilepsy. |
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| VAERS ID: | 316520 | Vaccinated: | 2008-05-23 | | Age: | 16.0 | Onset: | 2008-05-23, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-06-18, Days after onset: 4 | | Location: | Virginia | Entered: | 2008-06-18, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: n/a | | Previous Vaccinations: | | Other Medications: n/a | | Preexisting Conditions: allergic to nickel | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | RA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Convulsion, Dizziness, Feeling abnormal, Immediate post-injection reaction, Musculoskeletal stiffness, Pain in extremity | | Write-up: Immediately following the shot, while walking to a chair in the doctors office my daughter said her arm really hurt and she could feel the medicine running through her body. SHe then said she felt dizzy. Before I could get to the nurse, her head dropped and she stiffened up and had a seizure. She was out for about 3-5 minutes. When she awoke, she didn't remember anything but feeling dizzy. |
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| VAERS ID: | 318396 | Vaccinated: | 2008-05-02 | | Age: | 18.0 | Onset: | 2008-05-02, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-07-07, Days after onset: 5 | | Location: | North Carolina | Entered: | 2008-07-07, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: Failed PFT's X 2, Elevated serum IGE levels, Negative CXR. | | Previous Vaccinations: none~ ()~NULL~~In Patient|none~ ()~NULL~~In Sibling1|none~ ()~NULL~~In Sibling2 | | Other Medications: PRN Albuterol rescue inhaler | | Preexisting Conditions: Asthma, chronic nosebleeds - Allergic to Codiene | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unknown | 0 | IM | LA | | TDAP | UNKNOWN MANUFACTURER | unknown | | IM | RA | |
| Administered by: Private Purchased by: Private | | Symptoms: Asthma, Blood immunoglobulin E increased, Chest X-ray normal, Myalgia, Pulmonary function test abnormal, Pyrexia, Upper respiratory tract infection | | Write-up: After recieving the 1st injection at approximately 0900 on 5/2/08 patient had low grade fever of 100.6, myalgias, upper respiratory system symptoms that rapidly progressed to exacerbation of asthma by 4pm which required being evaluated by pulmonologist within 24 hours of injection. Patient received antibiotics, initiation of Advair Diskus prescription, burst of steroids, Veramist, change of nebulizer meds to Xopenex and increase in frequency of inhaled nebs. Patient had to be re-treated less than 3 weeks later after relapse after completing antibiotic and steroid therapy. Patient is now on maintenance doses of Advair diskus, Veramist and back to using Albuterol for rescue inhaler use. |
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| VAERS ID: | 324866 | Vaccinated: | 2008-09-10 | | Age: | 15.0 | Onset: | 2008-09-10, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-09-11, Days after onset: 1 | | Location: | Oregon | Entered: | 2008-09-11, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: | | Previous Vaccinations: high fever, aches and pains, fainting~HPV (no brand name)~3~16~In Patient|fever, vaccinated site has pain~HPV (no brand name)~3~ | | Other Medications: none | | Preexisting Conditions: asthma, seafood allergies | | CDC 'Split Type': asthma, seafood allergies | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 2 | IM | LA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Arthralgia, Dizziness, Eye irritation, Myalgia, Pain in extremity, Pyrexia, Respiratory disorder, Syncope, Thirst | | Write-up: High fever up to 103, fainted, dizziness, respiratory problem, muscles and joints hurting, eyes burning,thirsty and injected arm was hurting. |
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| VAERS ID: | 326582 | Vaccinated: | 2008-09-30 | | Age: | 13.0 | Onset: | 2008-09-30, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-09-30, Days after onset: 0 | | Location: | Maryland | Entered: | 2008-09-30, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Convulsion, Syncope | | Write-up: Fainting and Seizure after injection |
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| VAERS ID: | 326913 | Vaccinated: | 0000-00-00 | | Age: | | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2008-09-15 | | Location: | Ohio | Entered: | 2008-09-17, Days after submission: 2 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: Unknown | | Previous Vaccinations: | | Other Medications: Unknown | | Preexisting Conditions: Unknown | | CDC 'Split Type': WAES0808USA02088 | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | UN | UN | |
| Administered by: Other Purchased by: Other | | Symptoms: Rash macular | | Write-up: Information has been received from a physician concerning a female who was vaccinated with GARDASIL injection. The physician reported that a patient received GARDASIL and five days later developed blotches on her back. Patient was referred to dermatologist. The outcome was not reported. There was no product quality complaint. Additional information has been requested. |
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| VAERS ID: | 326968 | Vaccinated: | 2008-09-22 | | Age: | 12.0 | Onset: | 2008-09-22, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-09-29, Days after onset: 7 | | Location: | Pennsylvania | Entered: | 2008-10-03, Days after submission: 25 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: None | | Previous Vaccinations: | | Other Medications: None | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | | 0 | UN | LA | | HPV | UNKNOWN MANUFACTURER | | 0 | UN | LA | | TD | UNKNOWN MANUFACTURER | | | UN | LA | |
| Administered by: Private Purchased by: Other | | Symptoms: Immediate post-injection reaction, Pallor, Presyncope | | Write-up: Daughter seen for a routine well checkup. Dr. administered vaccines GARDASIL, Hep A and TD. A few minutes after injections daughter became very pale. She was standing - almost fainted. she was placed on exam table - laid flat for 5 minutes. Did not return to school that day. remained pale for about 30 mins. |
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| VAERS ID: | 328345 | Vaccinated: | 2007-01-02 | | Age: | 12.0 | Onset: | 2007-01-02, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-10-13, Days after onset: 376 | | Location: | Michigan | Entered: | 2008-10-13, Days after submission: 0 | |
| Life Threatening Illness? Yes |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? Yes, 21 days | | Extended hospital stay? Yes |
| Current Illness: cold | | Diagnostic Lab Data: Labs and Diagnsotics: HSV PCR (-). Mycoplasma IgG and IgM (+). HSV cx (+). HSV IgG (+). Alk Phos 83-111 (L). IgA 80 (L). Pre-albumin 9-18 (L). CRP 175 on 1/21/07 down to 14 by 2/4/07. EBV IgG, IgM (+). VZV IgG (+), IgM (-). Blood cx (-), | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: PMH: none. NKDA | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | DHPVB017A | 0 | UN | UN | | MNQ | SANOFI PASTEUR | U2094AA | 0 | IM | RA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Amenorrhoea, Atelectasis, Blood alkaline phosphatase normal, Blood culture negative, Blood immunoglobulin A decreased, Blood product transfusion, C-reactive protein increased, Catheter placement, Chest X-ray abnormal, Cough, Culture positive, Diet refusal, Dysmenorrhoea, Dysuria, Emotional distress, Epstein-Barr virus antibody positive, Eye pain, Furuncle, Gastrointestinal tube insertion, Glossodynia, Herpes simplex, Herpes simplex serology positive, Hypophagia, Immune system disorder, Influenza, Influenza serology positive, Lip haemorrhage, Menorrhagia, Menstruation irregular, Mycoplasma serology positive, Oral disorder, Pain, Photophobia, Polymerase chain reaction, Prealbumin decreased, Pyrexia, Rash generalised, Speech disorder, Stevens-Johnson syndrome, Tongue disorder, Tongue exfoliation, Vaginal lesion, Varicella zoster virus serology positive, Weight decreased, X-ray abnormal | | Write-up: Fever, legions growing in mouth and vaginal area, and pain on mucous membranes, including eyes. Onset on early Tuesday morning with these symptoms waking the patient. By the the next evening spots were breaking out all over. Took child to emergency room. Attending Dr. diagnosed her with SJS(Stevens Johnson Syndrome). She had just had started a clinical trial by her prior pediatrician. It included Menactra and the HPV vaccine. He refused to believe anything was really wrong with her when we took her on that Tuesday morning. Thus, we took her to the E.R. During the stay in the PICU, the dermitologist changed diagnosis to a variation to varicella, because SJS is so rare. By Friday afternoon it was very apparent it was incorrect and she went back to the first diagnosis of SJS and told us to choose another hospital. We chose. They transported her soon after, and hospital knew what to do. By this time the spots, which had turned to boils at the first hospital were everywhere. She had not ate in over a week and was in severe pain when urinating from the open boils in her vaginal area. She was put in the ICU Burn Unit. They first gave her a catheter and treated her body like a burn patient, morphine, and continued with many eye drops to save her eyesight. She had dermatologists, infectious disease doctors, opthamologists, and others I cannot be sure of. She was given a feeding tube the next day. After running their battery of tests, they started the IVIG treatments on Monday. It was a very stressful, long, and scary two more weeks to see if her body would respond well, or if it had been to late. Finally, she went to the hospital, for she looked to be recovering. It took another week or so for her body to be weaned and accept supplement shakes. Her tongue was disformed and painful from the skin sloghing off. Plus the muscles had not been used, so talking was difficult. She lost 20 pounds, but her lips, which had continued to bleed during the time, started to heal, along with her eyes and boils on bod |
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| VAERS ID: | 328536 | Vaccinated: | 2008-09-11 | | Age: | 26.0 | Onset: | 2008-09-11, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-09-15, Days after onset: 4 | | Location: | Washington | Entered: | 2008-10-15, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | | TDAP | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Private Purchased by: Private | | Symptoms: Local reaction | | Write-up: Large, local reaction left upper arm. |
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| VAERS ID: | 329013 | Vaccinated: | 2008-10-08 | | Age: | 12.0 | Onset: | 0000-00-00 | | Gender: | Female | Submitted: | 2008-10-17 | | Location: | Texas | Entered: | 2008-10-17, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: no | | Diagnostic Lab Data: CT scan done by doctor. | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: none | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 1446u | | IM | | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Computerised tomogram, Crying, Dizziness, Headache, Vomiting | | Write-up: Vaccine administered at approximately 2:00 P.M. Child awoke at 1:30 AM complaining of severe headache stated pounding and throbbing. Child crying. Thirty minutes later, she vomited. Also complained of dizziness. Headache unrelieved by Tylenol. Headache intermittently comes back, but not as bad. Exactly one week later, headache came back (severe headache). |
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| VAERS ID: | 330380 | Vaccinated: | 2008-10-20 | | Age: | 24.0 | Onset: | 2008-10-20, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-10-28, Days after onset: 8 | | Location: | Michigan | Entered: | 2008-10-28, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Birth Control & Valtrex | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Private Purchased by: Private | | Symptoms: Activities of daily living impaired, Crying, Injected limb mobility decreased, Pain in extremity, Sleep disorder | | Write-up: It's been 1 week and 1 day since my vaccination and i'm experiencing extreme arm pain. To the point where i cannot lift my arm and when getting dressed i'm in so much pain that I'm crying because it hurts so much. If take motrin all the time to make the pain bareable, however when I sleep i wake up as soon as the pain medicine wears off and I wake up in extreme pain and agony. |
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| VAERS ID: | 331877 | Vaccinated: | 2008-09-05 | | Age: | 12.0 | Onset: | 2008-09-05, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-11-10, Days after onset: 5 | | Location: | Wisconsin | Entered: | 2008-11-10, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: Dx with ear infection | | Diagnostic Lab Data: NO testing with 9/12/08 visit Dx ear infection issue with ATBX changed her ATBX NO testing with 9/23/08 visit stomache issue was ATBX changed ATBX even though stomache issue was before the ATBX started NO testing 10/18/08 D | | Previous Vaccinations: | | Other Medications: None at the time of injection | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unk | 0 | IM | LA | | MEN | UNKNOWN MANUFACTURER | unk | 0 | IM | LA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Adenoidal disorder, Condition aggravated, Diarrhoea, Ear infection, Headache, Mononucleosis heterophile test, Sinusitis, Stomach discomfort, Urinary tract infection, Urine analysis abnormal, X-ray | | Write-up: Ashli started with ear issues was given AMOXI/CLAV same day as injection then after the injection it was stomache, headaches, diarrhea, then and now they claim an adenoid issue. Was seen by MD 9/12/08, 10/18/08, and 10/22/08. DX with ear infection still then stated stomach issues were the ATBX. Next was DX: without Xray it was a sinus infect was given Zithromax then it was a UTI was given Sulfa. I was one thing after another and she has never been sick like this before. She still doen't "feel herself" yet. |
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| VAERS ID: | 332181 | Vaccinated: | 2008-10-16 | | Age: | | Onset: | 2008-10-29, Days after vaccination: 13 | | Gender: | Male | Submitted: | 2008-10-31, Days after onset: 2 | | Location: | Unknown | Entered: | 2008-11-12, Days after submission: 18 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? Yes, days | | Extended hospital stay? No |
| Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Lipitor; Paxil; Nitroglycerin patch | | Preexisting Conditions: Myocardial infarction; Coronary artery disease; Premature ventricular contractions; Hypercholesterolemia; Seizures | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | AC0544 | 1 | SC | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Chest pain, Troponin | | Write-up: Admitted to hospital telemetry unit via ambulance late in the evening of 10/29/08. Patients chief complaint: chest pain. Troponin levels normal. No further information is available at this time. |
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| VAERS ID: | 335221 | Vaccinated: | 2008-02-20 | | Age: | 21.0 | Onset: | 2008-05-07, Days after vaccination: 77 | | Gender: | Female | Submitted: | 2008-12-12, Days after onset: 5 | | Location: | Massachusetts | Entered: | 2008-12-12, Days after submission: 0 | |
| Life Threatening Illness? Yes |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? Yes, 3 days | | Extended hospital stay? No |
| Current Illness: no | | Diagnostic Lab Data: 2/19/09-records received-Echocardiogram T wave anormality consider anterior ischemia. Abnormal ECG. | | Previous Vaccinations: | | Other Medications: oral birth control | | Preexisting Conditions: oral contraceptives | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | 2 | IM | UN | |
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| VAERS ID: | 336094 | Vaccinated: | 2008-11-15 | | Age: | 16.0 | Onset: | 2008-11-15, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2008-12-28, Days after onset: 13 | | Location: | Arizona | Entered: | 2008-12-28, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: Xrays, MRI, Dr. visits | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: Ashma | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPAB | UNKNOWN MANUFACTURER | | | | RA | | HPV | UNKNOWN MANUFACTURER | | | | LA | | MMR | UNKNOWN MANUFACTURER | | | | LA | |
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| VAERS ID: | 339564 | Vaccinated: | 2009-01-09 | | Age: | 17.0 | Onset: | 2009-01-09, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2009-02-12, Days after onset: 3 | | Location: | | Entered: | 2009-02-13, Days after submission: 1 | |
| Life Threatening Illness? Yes |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: Nausea | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: Dicyclomine hydrochloride | | Preexisting Conditions: Latex allergy | | CDC 'Split Type': B0557758A | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | AHPVA043AA | | IM | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Anaphylactic reaction | | Write-up: This case was reported by the Medicines and Healthcare products Regulatory Agency (GB-MHRA-ADR 20375770) and described the occurrence of anaphylactic reaction in a 17-year-old female subject who was vaccinated with CERVARIX. Previous vaccination included CERVARIX. The subject's medical history included latex allergy. Concurrent medications included MERBENTYL. Concurrent medical conditions included nausea. On 9 January 2009 the subject received unspecified dose of CERVARIX (.5 ml, intramuscular). On 9 January 2009, at an unspecified time after vaccination with CERVARIX, the subject experienced anaphylactic reaction. The regulatory authority reported that the event was life threatening. The patient was treated with chlorphenamine, prednisolone and oxygen. On 9 January 2009, the event was resolved. MHRA Verbatim Text: Patient had anaphylactic reaction. Treated with chlorphenamine, prednisolone and oxygen. Licenses: IND BB-7,920 |
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| VAERS ID: | 339565 | Vaccinated: | 2009-01-15 | | Age: | | Onset: | 2009-01-15, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2009-02-12, Days after onset: 2 | | Location: | | Entered: | 2009-02-13, Days after submission: 1 | |
| Life Threatening Illness? Yes |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': B0557755A | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | AHPVA043AA | | SC | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Influenza like illness, Loss of consciousness, Musculoskeletal stiffness, Tremor, Vomiting | | Write-up: This case was reported by the Agency (GB-MHRA-ADR 20375835) and described the occurrence of vomiting in a female subject of unspecified age who was vaccinated with CERVARIX. On 15 January 2009 the subject received unspecified dose of CERVARIX (1, subcutaneous). On 15 January 2009, at an unspecified time after vaccination with CERVARIX, the subject experienced vomiting, flu-like symptoms, tremor and stiffness for 20 minutes and became unconscious. The regulatory authority reported that the events were life threatening. At the time of reporting the events were improved. Patient had flu-like symptoms, vomiting. Patient had 20 minute episode with stiffness, shaking and became unconscious-possible fit. Licenses: IND BB-7,920. |
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| VAERS ID: | 341167 | Vaccinated: | 2009-03-04 | | Age: | 12.0 | Onset: | 2009-03-05, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2009-03-05, Days after onset: 0 | | Location: | California | Entered: | 2009-03-05, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: N/A | | Previous Vaccinations: | | Other Medications: Children's Motrin | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HEPA | UNKNOWN MANUFACTURER | unknown | | UN | UN | | HPV | UNKNOWN MANUFACTURER | unknown | | UN | UN | | MEN | UNKNOWN MANUFACTURER | unknown | | UN | UN | | TDAP | UNKNOWN MANUFACTURER | unknown | | UN | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Disorientation, Dizziness, Dysarthria, Fall, Fatigue, Heart rate increased, Immediate post-injection reaction, Nausea, Paraesthesia, Paraesthesia oral, Sensation of heaviness, Somnolence | | Write-up: Within 5 minutes of injection, arms felt heavy and tingly, tongue was tingling, felt nautious and felt dizzy, collapsed in waiting area but did not loose conciousness. Was disoriented and was slurring while trying to talk, and pulse was 98. Nurses arrived promptly and gave her orange juice and rested for 15 minutes. Blood pressure was taken after the rest and pulse returned to normal 72. Was released to go home. Felt very tired and sleepy the rest of the evening. |
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| VAERS ID: | 341500 | Vaccinated: | 2009-02-10 | | Age: | | Onset: | 2009-02-11, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2009-03-11, Days after onset: 0 | | Location: | | Entered: | 2009-03-11, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: Unknown | | Diagnostic Lab Data: UNK | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': B0562800A | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | AHPVA020BE | | IM | UN | | TD | UNKNOWN MANUFACTURER | B5210 | | IM | UN | |
| Administered by: Other Purchased by: Other | | Symptoms: Syncope | | Write-up: This case was reported by a regulatory authority (# ES-AGEMED-014206343) and described the occurrence of syncope in a female subject of unspecified age who was vaccinated with CERVARIX (GlaxoSmithKline), Td. On 10 February 2009, the subject received unspecified dose of CERVARIX (intramuscular, unknown injection site), unspecified dose of Td (intramuscular, unknown injection site). On 11 February 2009, 1 day after vaccination with CERVARIX and Td, the subject experienced syncope. The regulatory authority reported that the event was clinically significant (or requiring intervention). On 11 February 2009, the event was resolved. The regulatory authority reported that the event was possibly related to vaccination with CERVARIX and Td. Further information is not expected as the regulatory authority has provided all the available information. This case has therefore been closed. |
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| VAERS ID: | 341635 | Vaccinated: | 2009-03-11 | | Age: | 11.0 | Onset: | 2009-03-11, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2009-03-12, Days after onset: 1 | | Location: | Texas | Entered: | 2009-03-12, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? Yes, 1 days | | Extended hospital stay? No |
| Current Illness: COUGH 3/18/09-records received-Mild upper respiratory symptoms and cough for 3 days prior. | | Diagnostic Lab Data: 3/18/09-records received- BUN/creat ratio increased 28.0. | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: 3/18/09-records received-PMH:abdominal pain, H. pylori, lactose intolerance. Allergic rhinitis. | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | DTAP | UNKNOWN MANUFACTURER | | | IM | UN | | HPV | UNKNOWN MANUFACTURER | | | IM | UN | | MEN | UNKNOWN MANUFACTURER | | | IM | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Abasia, Arthralgia, Back pain, Pain in extremity | | Write-up: MOM STATE FEW MINUTES AFTER VACCINE PT COMPLAIN OF PAIN LOWER BACK RADIATING TO BOTH HIP AND LEGS THEN GOT WORST UNABLE TO WALK AND ADMITTED FOR EVALUATION 3/18/09-records received for DOS 3/12-3/13/09-DC DX Acute myalgia post vaccination. Bronchitis. Presented with bilateral hip pain and upper legs and associated heaviness feeling and weakness of legs. Symptoms began 30 minutes after vaccinations. Unable to walk due to pain in legs. |
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| VAERS ID: | 342311 | Vaccinated: | 2009-03-19 | | Age: | 12.0 | Onset: | 2009-03-20, Days after vaccination: 1 | | Gender: | Female | Submitted: | 2009-03-20, Days after onset: 0 | | Location: | Minnesota | Entered: | 2009-03-20, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: uri | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: none | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | DTAP | UNKNOWN MANUFACTURER | | 4 | IM | UN | | HPV | UNKNOWN MANUFACTURER | | 0 | IM | UN | | MEN | UNKNOWN MANUFACTURER | | 0 | IM | UN | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Muscle spasms, Pyrexia | | Write-up: fever to 103.4, muscle spasm, r thumb-treated with anti-pyretics, time |
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| VAERS ID: | 342313 | Vaccinated: | 2009-03-12 | | Age: | 25.0 | Onset: | 2009-03-12, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2009-03-20, Days after onset: 8 | | Location: | Pennsylvania | Entered: | 2009-03-20, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: penicillin allergy | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | unknown | 1 | IM | LA | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Injection site mass, Injection site pain | | Write-up: After receiving the second dose of the Gardasil vaccine, I had a large lump under the skin at the injection site that felt almost like a marble. The skin was not hotter than usual or red, it was just a lump. It does not hurt all the time, only when bumped or touched. The bump decreases in size, but it is 8 days after the injection and it is still present. |
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| VAERS ID: | 342483 | Vaccinated: | 2009-02-06 | | Age: | 23.0 | Onset: | 2009-02-06, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2009-03-19, Days after onset: 13 | | Location: | Montana | Entered: | 2009-03-23, Days after submission: 4 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: None | | Diagnostic Lab Data: MRI - Pending. | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: None | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | FLU | UNKNOWN MANUFACTURER | | | UN | UN | | HPV | UNKNOWN MANUFACTURER | | | UN | UN | |
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| VAERS ID: | 343368 | Vaccinated: | 2007-08-29 | | Age: | 11.0 | Onset: | 2007-09-19, Days after vaccination: 21 | | Gender: | Female | Submitted: | 2009-04-02, Days after onset: 713 | | Location: | Nebraska | Entered: | 2009-04-02, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? Yes, 1 days | | Extended hospital stay? No |
| Current Illness: None | | Diagnostic Lab Data: Normal upper GI, normal colonscopy, normal upper endoscopy, negative red blood count, normal blood work. 5/26/09 Hospital records received ED and inpatient DOS 9/18/07 to 11/19/08. LABS and DIAGNOSTICS: CBC - Platelet Count 157 thous (L | | Previous Vaccinations: high fever, abdominal pain, dizziness, pale~HPV (no brand name)~3~12.10~Patient|none~ ()~~0.00~Sibling|none~ ()~~0.00~Sibling | | Other Medications: None. 5/26/09 Hospital records received ED and inpatient DOS 9/18/07 to 11/19/08. Tylenol, ibuprofen, Prevacid | | Preexisting Conditions: None. 5/26/09 Hospital records received ED and inpatient DOS 9/18/07 to 11/19/08. Adhesive tape allergy, asthma | | CDC 'Split Type': None. 5/26/09 Hospital records received ED and inpatient DOS 9/18/07 to 11/19/08. Adhesive tape allergy, asthma | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | 1 | 1 | IM | LA | |
| Administered by: Unknown Purchased by: Unknown | | Symptoms: Abdominal pain lower, Abdominal pain upper, Alanine aminotransferase decreased, Biopsy intestine abnormal, Blood alkaline phosphatase increased, Blood amylase decreased, Blood test normal, Blood urine present, C-reactive protein increased, Colitis, Colonoscopy abnormal, Cough, Culture throat negative, Cytomegalovirus antibody positive, Endoscopy normal, Epstein-Barr virus antibody negative, Haematocrit increased, Haemoglobin increased, Headache, Hepatitis A virus test, Hepatitis B virus test, Hepatitis C virus test, Hepatosplenomegaly, Ketonuria, Lymphocyte count increased, Lymphocyte percentage increased, Nasal congestion, Nausea, Neutrophil percentage decreased, Oesophagogastroduodenoscopy, Oropharyngeal pain, Platelet count decreased, Polydipsia, Polyuria, Protein urine present, Pyrexia, Red blood cell count increased, Red blood cell count normal, Rhinorrhoea, Streptococcus identification test negative, Ultrasound abdomen abnormal, Wheezing, X-ray with contrast upper gastrointestinal tract, pH urine increased | | Write-up: High fever of 106F, wheezing, upper right quadrant pain and lower right quadrant pain. It lasted for 8 months. Treatments were antibioctics. 5/26/09 Hospital records received ED and inpatient DOS 9/18/07 to 11/19/08. FINAL DIAGNOSIS: Focal acute colitis. Post vaccination presented with abdominal pain all quadrants, fever, headache, nausea, hepatosplenomegaly, polyuria, polydipsia. Additional visits for sore throat, congestion, runny nose and cough. 8/7/09 ICD-9 Codes: 789.00 abdominal pain unspecified, 789.01 Right upper quadrant abdominal pain, 793.6 Nonspecific radiologic abnormality of the abdomen or retroperitoneum, 309.24 Adjustment disorder with anxiety, V15.09 Other allergy other than to medicinal agents, 462 Acute pharyngitis, 465.9 Acute upper respiratory infection unspecified sites, 079.99 Viral infection unspecified in condition classified elsewhere, 571.8 Other non-alcoholic chronic liver disease. |
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| VAERS ID: | 343499 | Vaccinated: | 2009-04-03 | | Age: | 16.0 | Onset: | 2009-04-03, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2009-04-03, Days after onset: 0 | | Location: | Oklahoma | Entered: | 2009-04-03, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? Yes | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | | TDAP | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Private Purchased by: Unknown | | Symptoms: Flushing, Headache, Musculoskeletal stiffness, Staring, Vision blurred | | Write-up: Within 5-10 minutes of patient receiving TdaP and gardasil, pt had a 30 second episode of stiffening and blank staring. Since that time she has had a headache and blurry vision. Had some flushing as well. |
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| VAERS ID: | 346326 | Vaccinated: | 2009-05-01 | | Age: | 5.0 | Onset: | 2009-05-03, Days after vaccination: 2 | | Gender: | Female | Submitted: | 2009-05-14, Days after onset: 11 | | Location: | California | Entered: | 2009-05-14, Days after submission: 0 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? Yes |
| Hospitalized? No | | Current Illness: none | | Diagnostic Lab Data: none ordered by hospital | | Previous Vaccinations: | | Other Medications: | | Preexisting Conditions: Cerebal palsy | | CDC 'Split Type': | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | | | | MEA | UNKNOWN MANUFACTURER | | | | | | SMALL | UNKNOWN MANUFACTURER | | | | | |
| Administered by: Public Purchased by: Public | | Symptoms: Injection site rash, Injection site swelling, Rash | | Write-up: Received vaccination on Friday, by Saturday evening developed rash at site of injection. Two days later reaction (rash, swelling) was appro 2" x 2". At day four rash disappeared. On day 11 another rash at the site of the injection developed. Upon awakening on day 13, the rash had spread to be approx 4" x4" and red "dots" had appeared on entire body. At this point uncertain to outcome of reaction! |
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| VAERS ID: | 347601 | Vaccinated: | 2008-07-03 | | Age: | 18.0 | Onset: | 2008-07-03, Days after vaccination: 0 | | Gender: | Female | Submitted: | 2009-05-15, Days after onset: 377 | | Location: | Nebraska | Entered: | 2009-05-21, Days after submission: 6 | |
| Life Threatening Illness? No |
| Died? No |
| Disability? No |
| Recovered? No | | ER or Doctor Visit? No |
| Hospitalized? No | | Current Illness: | | Diagnostic Lab Data: None | | Previous Vaccinations: | | Other Medications: MIRALAX | | Preexisting Conditions: Unknown | | CDC 'Split Type': WAES0807USA04575 | |
| Vaccination | Manufacturer | Lot | Dose | Route | Site | | HPV | UNKNOWN MANUFACTURER | | | UN | UN | | MNQ | SANOFI PASTEUR | | | UN | UN | | TDAP | UNKNOWN MANUFACTURER | | | UN | UN | | VARCEL | MERCK & CO. INC. | 1900U | 1 | SC | RA | |
| Administered by: Private Purchased by: Other | | Symptoms: Inappropriate schedule of drug administration, Pruritus, Rash papular | | Write-up: Information has been received from a physician concerning an 18 year old female who on 19-JAN-1998 was vaccinated with the first dose of VARIVAX (Merck). On 03-JUL-2008 at 11:00 AM the patient was vaccinated subcutaneously with the second dose of VARIVAX (Merck) (lot no. 659935/1900U) into the right arm. At the same time the patient was vaccinated with HPV (MSD), MENACTRA and Tdap. Concomitant therapy included MIRALAX. On 18-JUL-2008 the patient experienced rash. On 21-JUL-2008 the patient was examined in clinic. The patient had no fever. The patient had vesicular and papulovesicular lesions everywhere on scalp, face, trunk and extremities and pruritus. The patient was treated with VALTREX and antihistamines for for pruritus. On 25-JUL-2008 the patient was followed up by phone. The lesions were crusted. No new lesions and no fever. Additional information is not expected. |
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| VAERS ID: | 348449 | Vaccinated: | 2009-06-03 | | Age: | |