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Found 41672 cases where Vaccine is HPV4

Case Details

This is page 1806 out of 4168

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VAERS ID: 413259 (history)  
Age: 24.0  
Gender: Female  
Location: New York  
Vaccinated:2009-09-01
Onset:2010-04-19
   Days after vaccination:230
Submitted: 2010-12-17
   Days after onset:242
Entered: 2010-12-20
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Abortion induced, Blood human chorionic gonadotropin positive, Drug exposure during pregnancy, Pregnancy test positive
SMQs:, Tumour markers (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SUBOXONE
Current Illness:
Preexisting Conditions: Caesarean section
Diagnostic Lab Data: beta-human chorionic, positive
CDC Split Type: WAES1003USA00488

Write-up: Information has been received from a 25 year old female with no known drug reactions/allergies and with a history of caesarean section for first pregnancy who in approximately September 2009, "about six months ago" was vaccinated with the first dose of GARDASIL. Concomitant therapy included SUBOXONE. The patient reported that she received the third dose of GARDASIL the same day she had a positive pregnancy test. The patient reported to be about 1 month pregnant. The last menstrual period was estimated happened in January 2010 and the estimated delivery date is 08-OCT-2010. The patient sought medical attention visiting the physician. Follow up information has been received from a physician from a pregnancy questionnaire who reported that the patient had an elective termination of pregnancy on 19-APR-2010, 11 weeks from last menstrual period. It was unknown if the products of conception were examined. It was unknown if the fetus was normal. The patient''s last menstrual period was on 01-JAN-2010. Upon internal review elective termination was considered to be an other important medical event. No further information is available.


VAERS ID: 413260 (history)  
Age: 15.0  
Gender: Male  
Location: New Mexico  
Vaccinated:2010-11-20
Onset:2010-12-04
   Days after vaccination:14
Submitted: 2010-12-17
   Days after onset:13
Entered: 2010-12-20
   Days after submission:3
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. 801047A / - UN / UN
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0768Z / 0 RA / IM

Administered by: Other       Purchased by: Other
Symptoms: Arrhythmia, Bacterial infection, Cardiac enzymes, Cardiac monitoring, Condition aggravated, Genital lesion, Lip blister, Oropharyngeal blistering, Pyrexia, Stevens-Johnson syndrome, White blood cell count increased
SMQs:, Severe cutaneous adverse reactions (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow)

Life Threatening? Yes
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness: Stevens-Johnson syndrome
Preexisting Conditions:
Diagnostic Lab Data: WBC count, high
CDC Split Type: WAES1012USA01611

Write-up: Information has been received from a nurse practitioner concerning a 15 year old male patient with Stevens-Johnson syndrome and no drug reaction/allergies, who on approximately on 17-NOV-2010 was vaccinated with a first dose of GARDASIL (Lot # not reported) (4 days ago, reported date as 08-DEC-2010). The nurse reported that on 04-DEC-2010 about three weeks after vaccination, the patient had a flare up of Stevens-Johnson syndrome. The patient had a fever, high white cell count, blisters on his mouth, lips and genitals and was diagnosed with a bacterial infection. He also had cardiac arrhythmias and required a cardiac monitor and evaluation of his cardiac enzymes. He was hospitalized on 05-DEC-2010 and released on 07-DEC-2010. He was prescribed with antibiotics and steroids for 6 months. At the time of the report, the patient was recovering. Flare up of Stevens-Johnson syndrome, cardiac arrhythmia and bacterial infection were considered to be immediately life-threatening by the reporter. Upon internal review flare up of Stevens-Johnson syndrome and hospitalization were considered to be an other important medical events. Additional information has been requested.


VAERS ID: 413320 (history)  
Age: 17.0  
Gender: Female  
Location: Virginia  
Vaccinated:2010-12-21
Onset:2010-12-21
   Days after vaccination:0
Submitted: 2010-12-21
   Days after onset:0
Entered: 2010-12-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0766Z / 1 - / IM

Administered by: Public       Purchased by: Public
Symptoms: Presyncope, Unresponsive to stimuli
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: none
Preexisting Conditions: none
Diagnostic Lab Data:
CDC Split Type: VA10021

Write-up: Vasovagal event after receiving HPV vaccine - nonresponsive 5 seconds. No fall, no injury.


VAERS ID: 413335 (history)  
Age: 23.0  
Gender: Female  
Location: Virginia  
Vaccinated:2010-11-30
Onset:0000-00-00
Submitted: 2010-12-21
Entered: 2010-12-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR U3777BA / - RA / IM
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1778Y / - RA / IM
TDAP: TDAP (ADACEL) / SANOFI PASTEUR C3448AA / - LA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. 0720Z / - LA / SC

Administered by: Public       Purchased by: Public
Symptoms: Drug exposure during pregnancy, Pregnancy test urine positive
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Normal pregnancy conditions and outcomes (narrow)

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None reported
Preexisting Conditions: None reported
Diagnostic Lab Data: Urine pregnancy test completed on 11-30-10, results negative; - urine pregnancy test completed on 12-17-10, results positive
CDC Split Type:

Write-up: Client received vaccines on 11-30-10; pregnancy test performed 11-30-10 was negative; on 12-17-10 pregnancy test performed during a physical exam - result was positive. Possibility of being pregnant at the time she received vaccines (1st trimester?).


VAERS ID: 413350 (history)  
Age: 19.0  
Gender: Female  
Location: Tennessee  
Vaccinated:2010-12-20
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2010-12-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR U3787AA / - RA / IM
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 1317Y / 0 LA / IM

Administered by: Private       Purchased by: Private
Symptoms: Headache, Pain
SMQs:

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? Yes
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: SEASONIQUE; ZOFRAN
Current Illness: None
Preexisting Conditions: Abdominal pain; post gastrectomy syndrome
Diagnostic Lab Data:
CDC Split Type:

Write-up: HA started 5-6 hours after injections - worsened over next 4 hours (at worst 9/10 on pain scale). Pt took Ibuprofen at that time then was able to sleep. At worst point, pt unable to turn head secondary pain. ER visit strongly recommended but pt declined. When seen in office next day pain 3/10.


VAERS ID: 413382 (history)  
Age: 25.0  
Gender: Female  
Location: Colorado  
Vaccinated:2008-06-12
Onset:2010-06-17
   Days after vaccination:735
Submitted: 2010-12-22
   Days after onset:188
Entered: 2010-12-22
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 2 RA / IJ

Administered by: Unknown       Purchased by: Private
Symptoms: Abortion spontaneous, Antepartum haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

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

Write-up: Vaginal bleeding


VAERS ID: 413440 (history)  
Age: 17.0  
Gender: Female  
Location: Texas  
Vaccinated:2010-11-08
Onset:2010-11-08
   Days after vaccination:0
Submitted: 2010-12-20
   Days after onset:42
Entered: 2010-12-22
   Days after submission:2
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0768Z / 0 UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Asthenia, Bone scan abnormal, Complex regional pain syndrome, Computerised tomogram abnormal, Dysphagia, Dyspnoea, Joint effusion, Muscle atrophy, Nuclear magnetic resonance imaging abnormal, Pain in extremity, Streptococcal infection, Streptococcus test positive, Walking aid user, White blood cell count increased
SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Osteonecrosis (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Died? No
Permanent Disability? Yes
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: NECON
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: magnetic resonance, 11/09?/10, Fluid on the patient''s hip; computed axial, 11/09?/10, Fluid on the patient''s hip; bone scan, 11/09?/10, Fluid on the patient''s hip; diagnostic laboratory, 11/08?/10, Positive for a strep infection; WBC count, 11/08?/10, Elevated
CDC Split Type: WAES1012USA01863

Write-up: Information has been received from a physician and from a licensed practical nurse concerning a 17 year old female patient with no pertinent medical history and no drug reactions or allergies who on 08-NOV-2010, was vaccinated IM with the first 0.5 ml dose of GARDASIL (Lot# 666597/0768Z, expire date 17-OCT-2012). Concomitant medication included NECON. The patient did not receive any concomitant vaccination at that time. The nurse stated that on 08-NOV-2010, sometime after the patient had received the GARDASIL, the patient complained of difficulty breathing and was unable to swallow. The patient was seen in the emergency room. It was reported that the patient was positive for a strep infection (not specified). The patient''s white blood cell (WBC) count was elevated. The patient was treated with a penicillin shot and was sent home and was not admitted to the hospital. Approximately twelve hours later on 09-NOV-2010, the patient experienced left leg pain (also reported as bilateral lower extremity pain) and weakness on. The patient was seen in the hospital and was admitted. The patient was hospitalized on 09-NOV-2010. The patient had a magnetic resonance imaging (MRI), computed axial tomography (CT) scan and a bone scan. The tests revealed fluid on the patient''s hip. The patient was diagnosed with chronic regional pain syndrome. The patient was treated with extensive physical therapy. The patient was discharged on 14-NOV-2010 on NEURONTIN, amitriptyline hydrochloride and hydrocodone. The patient was now recovering but still had persistent pain and required a walker for ambulate due to muscular atrophy. The GARDASIL series had been discontinued. Chronic regional pain syndrome and the patient require a walker to ambulate due to muscular was considered by a physician to be disabling. Additional information has been requested.


VAERS ID: 413508 (history)  
Age: 18.0  
Gender: Female  
Location: Florida  
Vaccinated:2010-12-23
Onset:2010-12-23
   Days after vaccination:0
Submitted: 2010-12-23
   Days after onset:0
Entered: 2010-12-27
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0546X / 0 RA / UN

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

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

Write-up: Patient fainted about 2 minutes after receiving vaccine. Pt immediately regained consciousness (in about 1 min) - 911 was called. Pt was not taken to the hospital. Pt was able to walk out of clinic.


VAERS ID: 413515 (history)  
Age: 12.0  
Gender: Male  
Location: Kansas  
Vaccinated:2010-12-20
Onset:2010-12-20
   Days after vaccination:0
Submitted: 2010-12-23
   Days after onset:3
Entered: 2010-12-23
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS AHAVB446AA / 0 RA / IM
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0664Z / 0 RA / IM
MNQ: MENINGOCOCCAL CONJUGATE (MENVEO) / NOVARTIS VACCINES AND DIAGNOSTICS 100005 / 0 LA / IM
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. 1594Y / 1 LA / SC

Administered by: Private       Purchased by: Private
Symptoms: Injection site erythema, Injection site swelling, Injection site warmth
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: ADDERALL XR 15mg qd
Current Illness: None
Preexisting Conditions: Allergies - PCN; AUGMENTIN; no defects; ADHD
Diagnostic Lab Data: Not done
CDC Split Type:

Write-up: Patient first noticed arm red and swollen 12/20/10 in the evening after inj. given the next day 12/21/10 pt mom - noticed and stated entire back of pt (L) upper arm red, swollen and warm to touch on 12/22/10 pt mom contacted clinic arm assessed and red, swollen, warm to touch area approx 3" long and 1" wide mom instructed to give pt BENADRYL & monitor 12/23/10 pt mom contacted she stated area cont. to decrease in size. No SOB or other adverse reactions ever noticed on pt. No fever noted either.


VAERS ID: 413570 (history)  
Age: 15.0  
Gender: Female  
Location: Unknown  
Vaccinated:2010-10-13
Onset:2010-10-19
   Days after vaccination:6
Submitted: 2010-12-23
   Days after onset:65
Entered: 2010-12-27
   Days after submission:4
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED - / 0 UN / UN
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. - / 2 UN / UN
HPV4: HPV (GARDASIL) / MERCK & CO. INC. 0766Z / 2 UN / IM

Administered by: Other       Purchased by: Other
Symptoms: Drug exposure during pregnancy, Neonatal disorder
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Neonatal disorders (narrow)

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? Yes
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: Unknown
CDC Split Type: WAES1012USA02470B1

Write-up: Information has been received from a Registered Nurse concerning a 0 day male baby patient. On 13-OCT-2010 the patient''s mother was vaccinated IM with the third dose of GARDASIL (Lot# 666596/0766Z) (Expiration date: 15-OCT-2012). The patient''s mother also received on the same day a third dose of RECOMBIVAX HB (Lot# unknown) (manufacturer unknown) and a first dose of AFLURIA (Lot# unknown) (manufacturer unknown). The nurse reported that the patient was born at gestation age of 36 weeks and 5 days. The baby boy was admitted to neonatal intensive care unit (NICU) for oxygen desaturation and was diagnosed with severe laryngomalacia. Epiglottis prolapsed was present as well. At the time of the report, the patient''s outcome was unknown. The mother''s experience has been captured in WAES# 1012USA02470. Additional information has been requested.


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