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Found 580 cases where Location is Texas and Vaccine is HPV or HPV2 or HPV4 and ER Visit

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VAERS ID: 276670 (history)  
Form: Version 1.0  
Age: 16.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-03-02
Onset:2007-03-02
   Days after vaccination:0
Submitted: 2007-04-13
   Days after onset:41
Entered: 2007-04-16
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0188U / 1 LA / IM

Administered by: Private       Purchased by: Private
Symptoms: Fall, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0703USA02372

Write-up: Information has been received from a nurse concerning a 16 year old female (ptreviously reported as 15 year old) with no illness at the time of vaccination and no pre-existing illness or allergies who on 02-MAR-2007 (previously reported as 09-MAR-2007) was vaccinated with first dose of Gardasil (lot# 657006/0188U). 0.5 ml once IM in the left deltoid at 5:15 PM. On 02-MAR-2007, after receiving the injection, the patient fainted and fell from the chair where she was sitting. Medical attention was sought. However, she regained consciousness after five minutes. She went home after the recovery. No further information was available at the time of reporting. Additional information has been requested. Additional infromation was received from a licensed vocational nurse. On 02-MAR-2007, at 5:15 PM after receiving the vaccination the patient stated that she felt lightheaded and fell forward and laid her head on the nurses shoulder. The patient then briefly had a "seizure like" motion of her head. The nurse laid her back on the table. The patient quickly resumed normal fucntion and stated she felt fine. The physician stated vasovagal episode. No additional information is expected.


VAERS ID: 276683 (history)  
Form: Version 1.0  
Age: 25.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-03-12
Onset:2007-03-12
   Days after vaccination:0
Submitted: 2007-04-13
   Days after onset:32
Entered: 2007-04-16
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0187U / 1 UN / UN

Administered by: Private       Purchased by: Other
Symptoms: Pruritus
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: hormonal contraceptives; YAZ; vitamins (unspecified)
Current Illness: Contraception
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: None
CDC Split Type: WAES0703USA02911

Write-up: This is in follow-up to report(s) previously submitted on 4/13/2007. Information has been received from a registered nurse concerning a 25 year old female police officer (151 lb, 62 inches), with no pertinent medical history, who on 12-MAR-2007 was vaccinated with a dose of GARDASIL (lot # 656049/0187U), left upper arm, in the morning. Concomitant therapy included hormonal contraceptives (YAZ). On 12-MAR-2007, in the afternoon or evening, the patient experienced severe itching in legs, feet, calves and hands. Unspecified medical attention was sought. After four days, on 15-MAR-2007, the patient recovered from the severe itching in calves, feet and hands. No product quality complaint was involved. Additional information is not expected.


VAERS ID: 276758 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-04-09
Onset:2007-04-10
   Days after vaccination:1
Submitted: 2007-04-18
   Days after onset:8
Entered: 2007-04-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (VAQTA) / MERCK & CO. INC. 1213F / 1 LA / IM
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1424F / 1 RA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR 42158CA / 1 RA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. 0150F / 1 LA / SC

Administered by: Private       Purchased by: Private
Symptoms: Culture throat positive, Guttate psoriasis, Rash macular, Rash maculo-papular, Streptococcus identification test positive
SMQs:, Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: fever~Vaccine not specified (no brand name)~~0.00~Patient
Other Medications: Unknown
Current Illness: Acne
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Throat culture, 04/10/07, +, strep
CDC Split Type: WAES0704USA04271

Write-up: Patient returned to clinic within 24 hours of vaccination for macular rash on trunk. Macules approx 1-2 cm, annular. Pt did test (+) for strep and was diagnosed with gutate psoriasis vs vaccine rxn. This is in follow-up to report(s) previously submitted on 5/14/2007. Initial and follow up information has been received from a physician concerning a 15 year old female with acne, who on 09-APR-2007 at 1:00 pm was vaccinated with a first dose of GARDASIL (lot #654895/1424F) into the right arm IM. Concomitant therapy included VAQTA (lot # 656497/1213F) into the left arm IM, VARIVAX (lot # "0150F) into the left arm SC, and MENACTRA (lot # 42158CA) into the right arm IM. Within 24 hours, the patient experienced a diffuse maculopapular rash. On 10-APR-2007, the patient returned to the office and a strep test was positive for strep throat. The patient subsequently recovered from the strep throat and the maculopapular rash. Additional information has been requested.


VAERS ID: 277140 (history)  
Form: Version 1.0  
Age: 26.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-04-02
Onset:2007-04-09
   Days after vaccination:7
Submitted: 2007-04-20
   Days after onset:11
Entered: 2007-04-20
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 00914 / 2 LA / -

Administered by: Private       Purchased by: Private
Symptoms: Oedema peripheral, Pain in extremity
SMQs:, Cardiac failure (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: swelling, painful arm (L)


VAERS ID: 277262 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: Texas  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 2007-04-23
Entered: 2007-04-24
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 2 UN / SC

Administered by: Other       Purchased by: Other
Symptoms: Adverse event, Incorrect route of drug administration, Unevaluable event
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0704USA02388

Write-up: Information has been received from a physician concerning a female (age not reported) who on an unspecified date, the patient was vaccinated with second dose of Gardasil (lot # not reported) SQ. Subsequently, the patient experienced an unspecified adverse event after the second dose of Gardasil was given. The patient sought medical attention and was hospitalized. The reporting physician did not administer the vaccine and was requesting follow-up from a medical team member. No further information was available at the time of reporting. Additional information has been requested. 4/26/07 CDC spoke with a nurse at the reporters office (the reporter for 277262). "While rounding in the hospital he was asked for advice about a patient (not his patient) who received her second HPV vaccine SQ instead of IM. They wanted to know if they should repeat the dose or not. He contacted Merck who responded with a letter saying they had not looked at this in the trials, etc. The patient did not have any problems.....the vaccine was administered incorrectly. " 4/27/07 Per email from CDC, "the report says the patient was hospitalized. According to your note, the pt. was NOT hospitalized. Correct? If so, we will have this corrected in VAERS." 4/27/07 Per email from CDC, "according to the nurse the patient was NOT hospitalized" 4/27/07 Per email from CDC, "Please change this in the VAERS database." Database change completed.


VAERS ID: 277273 (history)  
Form: Version 1.0  
Age: 15.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-04-10
Onset:2007-04-13
   Days after vaccination:3
Submitted: 2007-04-19
   Days after onset:6
Entered: 2007-04-24
   Days after submission:5
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0187U / 2 RA / IM

Administered by: Private       Purchased by: Private
Symptoms: Burning sensation, Haematoma, Injection site swelling, Skin reaction
SMQs:, Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Skin reaction w/cresent shaped burn like reaction one week after 2nd dose of Gardasil. Swollen below injection site, probable hematoma.


VAERS ID: 278026 (history)  
Form: Version 1.0  
Age: 11.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-02-15
Onset:2007-04-05
   Days after vaccination:49
Submitted: 2007-04-30
   Days after onset:25
Entered: 2007-05-07
   Days after submission:7
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR - / UNK UN / IM
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0014U / UNK UN / UN
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1922A / UNK UN / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR C2631A / UNK UN / IM

Administered by: Private       Purchased by: Private
Symptoms: Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: History of no known allergies. She has the Fluzone vaccine annually.
Allergies:
Diagnostic Lab Data:
CDC Split Type: 200701400

Write-up: Hives, cluster of 2 patients (patient identification provided) with generalized hives throughout the entire body, after receiving Adacel (lot number C2631AA); Fluzone (lot number unknown), and Menactra (lot number U1922AB), received from a health care professional in the USA on 24 April 2007. Case 1: An 11 year old, female patient ( with a history of no known allergies) developed generalized hives throughout the entire body, 1.1/2 months after she received Adacel (lot number C2631AA); Fluzone (lot number unknown), and Menactra (lot number U1922AB) and Gardasil (Merck, lot number 0014U ) on the 15 February 2007. She has the Fluzone vaccine annually. The patient denies any illness or medications at the time of the vaccinations. She was treated with Cortisone, Singulair and Atarax. It was reported the hives resolved and the patient recovered. The second case (the patient ''s brother ) is detailed in case 2007-01399.


VAERS ID: 278183 (history)  
Form: Version 1.0  
Age: 13.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-04-30
Onset:2007-05-01
   Days after vaccination:1
Submitted: 2007-05-08
   Days after onset:7
Entered: 2007-05-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1424F / 1 RA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. 1504F / 2 LA / SC

Administered by: Private       Purchased by: Public
Symptoms: Injection site erythema, Injection site swelling, Injection site warmth, Throat irritation
SMQs:, Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Astelin, Zyrtec D
Current Illness: None
Preexisting Conditions: None
Allergies:
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Swelling of injection site, red and hot to touch, later that evening throat "felt swollen itchy" went to ER prednisolone 10 mg x 5 days.


VAERS ID: 278268 (history)  
Form: Version 1.0  
Age: 12.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-04-24
Onset:2007-04-25
   Days after vaccination:1
Submitted: 2007-05-08
   Days after onset:13
Entered: 2007-05-09
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (VAQTA) / MERCK & CO. INC. - / UNK UN / UN
HIBV: HIB (PEDVAXHIB) / MERCK & CO. INC. - / UNK UN / UN
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 1 UN / UN
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Groin pain, Headache, Herpes zoster, Laboratory test normal, Meningitis viral, Rash
SMQs:, Anaphylactic reaction (broad), Osteonecrosis (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
   Extended hospital stay? Yes
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Unknown PMH: hemolytic uremic syndrome requiring hospitalization & blood transfusions out of country, shingles 4/24/07. right wrist tendon injury & fracture of growth plate.
Allergies:
Diagnostic Lab Data: diagnostic laboratory 04/25/07 - negative LABS: WBC 4.4, AST 43, Mag 2.5. CK 292, MBs neg. CSF WBC 55, RBC 10, lymphs 86, monos 14, protein 28, glucose 44, pleocytosis of CSF. CSF herpes & VZ was neg. Blood & urine c/s neg. CT of head was WNL.
CDC Split Type: WAES0705USA00797

Write-up: Information has been received from a physician, via a company representative, concerning a 12 year old female patient who on 24-APR-2007 was vaccinated with the first dose of Gardasil. Concomitant therapy included hepatitis A virus vaccine (manufacturer unspecified), PedvaxHib and Menactra. On 25-APR-2007, the day following the vaccinations, the patient returned to the office with complaints of groin pain; blood work (unspecified) testing was performed, and was negative. On 30-APR-2007 the patient experienced a headache and a rash on her leg, and again returned to the physician''s office; the patient was diagnosed with zoster, and was given Tylenol and codeine for treatment of the symptoms. On 03-MAY-2007, the patient presented that the patient may have viral meningitis. At the time of this report, the physician reported that the patient may have viral meningitis. At the time of this report, the patient had not recovered from the events. Additional information has been requested. 5/18/2007 Received medical records from hospital which reveal patient experienced shingles, severe HA which continued to worsen, photosensitivity, nausea. Opthal exam prior to admit was WNL. Admitted 5/3-5/6/07. ID consult obtained. Treated w/IV antibiotics & antivirals. Symptoms resolved day after treatment started & patient continued to progress well. D/C home on no meds w/close outpatient PCP f/u. FINAL DX: meninigitis, presumed viral (aseptic), final c/s pending; HA, resolved; herpes zoster right leg suspected. 6/8/07 Received note from PCP stating CSF PCRs for HSV & entervirus were neg. Also included name of admitting physician at hospital where PCP does not have privileges.


VAERS ID: 278697 (history)  
Form: Version 1.0  
Age: 18.0  
Sex: Female  
Location: Texas  
Vaccinated:2007-04-23
Onset:2007-04-24
   Days after vaccination:1
Submitted: 2007-04-25
   Days after onset:1
Entered: 2007-05-16
   Days after submission:21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0387U / 1 RA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR U1920AA / 1 LA / IM

Administered by: Private       Purchased by: Private
Symptoms: Axillary pain, Fatigue, Injection site erythema, Injection site pain, Malaise, Pain, Pyrexia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: None
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Fever up to 103 F, fatigue, malaise, body aches, redness and pain at Menactra site and pain in L axillary area for 26 hours. 2 cm area of erythema at vaccine site.


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