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Found 584 cases where Vaccine is HPV4 and Life Threatening

Case Details

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VAERS ID:295876 (history)  Vaccinated:2007-08-28
Age:16.0  Onset:2007-08-29, Days after vaccination: 1
Gender:Female  Submitted:2007-11-07, Days after onset: 70
Location:Texas  Entered:2007-11-07
Life Threatening? Yes
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: No
Preexisting Conditions: No 1/3/08-records received-PMH: Seizures during phlebotomy and hair salon.
Diagnostic Lab Data: MRI; EEG; Lead testing 1/3/08-records received-EEG normal. Echocardiogram normal. 24 hour Holter monitor normal.MRI brain normal.CT normal.
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC.0929U0UNUN
Administered by: Private     Purchased by: Public
Symptoms: Blood lead, Bradycardia, Computerised tomogram normal, Confusional state, Convulsion, Dizziness, Echocardiogram normal, Electrocardiogram ambulatory normal, Electroencephalogram normal, Fatigue, Headache, Loss of consciousness, Migraine, Nuclear magnetic resonance imaging brain normal, Pallor, Tremor
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Convulsions (narrow), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow)
Write-up: During a blood test patient went pale and had a seizure. First had them 2 or 3 a day or more than 3 times per week during period of 8/29 to 10/11. Went to ER for testing on 9/11. Started taking Topamax on 10/18. Doctor described them as migraine induced seizures. 1/3/08-records received-clinic visit 11/20/07-seen in follow up of seizures, headache and dizziness without seizure risk factors. Bradycardia. First episode was approximately 4 years ago and next was approximately 18 months ago. Starting on 8/29/07-began having frequent spells and LOC, shaking of left leg and upper extremity. All other seizures are staring lasting 1-2 minutes with LOC. Fatigued. confused afterwards. Previously had daily headache now less frequent. 1/15/2010 She still has seizures 1 to 3 a month. She is on Topamax 25mg in am and 50 mg at night. This has helped control them to 1 upt to 3 a month.

VAERS ID:297034 (history)  Vaccinated:2007-08-01
Age:15.0  Onset:2007-10-01, Days after vaccination: 61
Gender:Female  Submitted:2007-11-15, Days after onset: 45
Location:California  Entered:2007-11-16, Days after submission: 1
Life Threatening? Yes
Died? No
Permanent Disability? Yes
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness:
Preexisting Conditions: None
Diagnostic Lab Data: diagnostic laboratory - Positive antibodies to Mycoplasma; hemoglobin - 5; Epstein-Barr virus - Positive (IgM); serum ANA - Positive; cold agglutinin test - Positive
CDC 'Split Type': WAES0711USA01791
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC. 0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Anaemia haemolytic autoimmune, Antibody test positive, Antinuclear antibody positive, Cold agglutinins positive, Epstein-Barr virus antibody positive, Fatigue, Haemoglobin decreased, Jaundice, Mycoplasma serology positive, Transfusion
SMQs:, Cholestasis and jaundice of hepatic origin (narrow), Haemolytic disorders (narrow), Acute pancreatitis (broad), Haematopoietic erythropenia (broad), Haemorrhage laboratory terms (broad), Systemic lupus erythematosus (narrow), Biliary system related investigations, signs and symptoms (narrow), Biliary tract disorders (narrow), Vasculitis (broad), Hypersensitivity (broad)
Write-up: Information has been received from a physician concerning a 15 year old female with no known medical history, drug reactions/allergies or concomitant medication use who at the end of August 2007 (exact date unknown), was vaccinated (site and route not reported) with the 1st dose of Gardasil (dose and lot# not reported). In the beginning of October 2007, the patient became very tired and later jaundiced with a low hemoglobin at 5. Laboratory evaluations revealed IgM positive to Epstein Barr virus, positive cold agglutinins, positive antibodies to mycoplasma and positive antinuclear antibodies (ANA). The patient was admitted to the hospital with Autoimmune Hemolytic Anemia for 2.5 weeks with blood transfusions given. The patient was discharged from the hospital (exact date not reported). The patient had been receiving steroids for approximately one week and was undergoing a steroid taper. The physician felt that the patient''s tiredness, jaundice and Hemolytic Anemia were considered disabling and life threatening and other important medical events. No ongoing hemolysis at the time. At the time of this report the patient was recovering. Additional information has been requested.

VAERS ID:297035 (history)  Vaccinated:2007-01-08
Age:16.0  Onset:2007-03-11, Days after vaccination: 62
Gender:Female  Submitted:2007-11-15, Days after onset: 249
Location:New York  Entered:2007-11-16, Days after submission: 1
Life Threatening? Yes
Died? No
Permanent Disability? Yes
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: hormonal contraceptives 7/7/08-records received-Medications include birth control pills and Effexor.
Current Illness: Oral contraceptives
Preexisting Conditions: Smoker 7/7/08-records received-PMH:extensive cardiac problems in which multiple Holter moniors and echos for chest pain and palpitations was carried out;however, there was no pathyology identified and no known other medical history. Depression. Allergic to Sulfa results in rash. Smokes and drinks alcohol. 7/9/08-records received-PMH: Hypertension untreated. HX of alcohol overdose
Diagnostic Lab Data: Unknown 7/7/08-records received-CT head dense left MCA sign, evidence of left MCA distribution ischemia, 7mm left-to-right shift of midline sutures, left lateral ventricle effacement. Cisterns mildly effaced. TEE shows no patent foramen ov
CDC 'Split Type': WAES0711USA02177
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC.0688F1IMUN
Administered by: Other     Purchased by: Other
Symptoms: Brain herniation, Cerebral ischaemia, Cerebrovascular accident, Computerised tomogram abnormal, Craniectomy, Culture negative, Depressed level of consciousness, Dyskinesia, Echocardiogram, Electroencephalogram abnormal, Encephalomalacia, Fall, Headache, Hemiparesis, Hyperreflexia, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Ischaemic cerebrovascular conditions (narrow), Haemorrhagic cerebrovascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Dyskinesia (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad)
Write-up: Information has been received from a Registered Nurse (R.N.) concerning a 16 year old female with a history of smoking and use of oral contraception who was vaccinated IM with a second dose of Gardasil. Concomitant therapy included hormonal oral contraceptives (unspecified). The nurse reported that after 2 months getting her second vaccination the patient had a stroke and she was hospitalized. The patient continued to have weakness on one side of her body. The patient was recovering. The reporter considered the event stroke as disabling and life threatening. Additional information has been requested. 7/4/08-records received for DOS 3/12-3/21/07-DC DX: Left-sided middle cerebral artery stroke with subfalcine herniation status post left-sided craniectomy for decompression. Presented with left-sided MCA stroke. Witnessed collapse to the ground had been exerting herself physically lately. PE: reflexes increased on right side, awakens to voice but does not follow commands, semipurposeful movement in left upper extremity. Consensus cause of stroke was postulated to be a combination of smoking and birth control pill use. Discharged to rehab. 7/9/08-ER report for DOS 3/11/07-non-responsive- 7/9/08-records received for DOS 4/6-4/9/08-DC DX: Encephalomalacia. During rehab hospitalization developed worsening headache and swelling in area of craniectomy flap, new baseline right-sided weakness secondary to stroke. Questionable LSD use. Readmitted to rehab.

VAERS ID:297062 (history)  Vaccinated:0000-00-00
Age:14.0  Onset:0000-00-00
Gender:Female  Submitted:2007-11-15
Location:New York  Entered:2007-11-16, Days after submission: 1
Life Threatening? Yes
Died? No
Permanent Disability? Yes
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: magnetic resonance - Result not available
CDC 'Split Type': WAES0711USA02181
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC. 2IMUN
Administered by: Other     Purchased by: Other
Symptoms: Craniotomy, Haemorrhagic arteriovenous malformation, Nuclear magnetic resonance imaging
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Congenital, familial and genetic disorders (narrow)
Write-up: Information has been received from a Registered Nurse concerning a 14 year old female patient who was vaccinated IM with a third dose of Gardasil. The nurse reported that 2 months after the vaccination patient was diagnosed with a bleeding arteriovenous malformation. It was reported that patient was hospitalized (date and duration not reported) and had a craniotomy. The patient had a magnetic resonance imaging (MRI) diagnostic test done but no result was available. No other information was available. The outcome was unknown. The reporter considered the event as disabling and life threatening. The reporter felt that patient having arteriovenous malformation was a serious other medical event because it required craniotomy. Additional information has been requested.

VAERS ID:297528 (history)  Vaccinated:2007-09-15
Age:12.0  Onset:2007-10-06, Days after vaccination: 21
Gender:Female  Submitted:2007-11-20, Days after onset: 45
Location:Unknown  Entered:2007-11-23, Days after submission: 3
Life Threatening? Yes
Died? Yes
   Date died: 2007-10-06
   Days after onset: 0
Permanent Disability? No
Recovered? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0711USA02619
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC.  UNUN
Administered by: Unknown     Purchased by: Unknown
Symptoms: Death
SMQs:
Write-up: Information has been received from a physician''s assistant concerning a 12 year old female with no reported medical history who on approximately 15-SEP-2007 was vaccinated with Gardasil. It was noted that this was not where the vaccine was administered, rather they were the patient''s family physician. On 06-OCT-2007 the patient died in her sleep. No further information was provided. No lot number was given. Additional information has been requested.

VAERS ID:297899 (history)  Vaccinated:2006-12-06
Age:20.0  Onset:2007-01-01, Days after vaccination: 26
Gender:Female  Submitted:2007-11-20, Days after onset: 323
Location:Florida  Entered:2007-11-27, Days after submission: 7
Life Threatening? Yes
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Bacterial Vaginosis
Preexisting Conditions: Cervical dysplasia (treated 2002), Depression, Drug abuse. PMH: Cervical Dysplasia (CIN I) in 2002, High Risk HPV (+), Cryosurgery. Chlamydia and venereal warts.
Diagnostic Lab Data: Not available. Labs and Diagnostics: PAP 12/06/2006 (-). PAP 9/26/07 (-), HPV (+).
CDC 'Split Type':
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC.0688F0IMRA
Administered by: Private     Purchased by: Private
Symptoms: Abdominal distension, Blood pressure increased, Human papilloma virus test positive, Hypertension, Oedema peripheral, Proteinuria, Smear cervix normal
SMQs:, Acute renal failure (broad), Cardiac failure (broad), Acute pancreatitis (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypertension (narrow), Chronic kidney disease (broad)
Write-up: 4-6 weeks after receiving Gardasil, patient developed severe pedal edema and abdominal swelling. She went to the E.R. She was found to be hypertensive with proteinuria. She was diagnosed with SLE by Nephrologist. Currently on Prednisone, Plaquenil, Lisinopril, Procardia, Celicept and Boniva. 01/03/2008 MR received for multiple OVs. AE onset date received as early January 2007. Updated in database OV 12/06/06 requesting Gardasil. OV 2/8/07 in F/U to ER visit for pedal edema, abd swelling, (+) proteinuria, and increased BP. DX: SLE. Per 60 day follow up: The patient is still being treated for SLE with several medications including CELLCEPT, prednisone, PLAQUENIL, lisinopril and PROCARDIA. She is under the care of a nephrologist. 1/15/2010 She is still undergoing treatmen for S.L.E. Her current medications include Prednisone, Plaquenil, Cellcept, Lisinopril, Procardia and Boniva.

VAERS ID:297983 (history)  Vaccinated:2007-11-12
Age:15.0  Onset:2007-11-12, Days after vaccination: 0
Gender:Female  Submitted:2007-11-27, Days after onset: 15
Location:New Jersey  Entered:2007-11-28, Days after submission: 1
Life Threatening? Yes
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Zyrtec
Current Illness: Drug hypersensitivity; Environmental allergy
Preexisting Conditions: Hypersensitivity symptom; Rash; Swollen mouth; Chest tightness; No reaction on previous exposure to vaccine; cough
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0711USA04199
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC.1425F1IMUN
Administered by: Other     Purchased by: Other
Symptoms: Chest discomfort, Cough, Oedema mouth, Rash generalised
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Oropharyngeal allergic conditions (narrow), Hypersensitivity (narrow)
Write-up: Information has been received from a physician, concerning a 15 year old female patient with drug hypersensitivity to methylphenidate (RITALIN) (involved rash, swollen mouth, chest tightness and cough), allergies (not specified), who on 11-SEP-2007 was vaccinated IM with the first dose of Gardasil (lot # invalid) with no reaction reported, and on approximately 12-NOV-2007, was vaccinated with the second dose of Gardasil (lot # 655165/1425F). Concomitant therapy included cetirizine hydrochloride (ZYRTEC). Following the second dose on 12-NOV-2007 the patient developed a rash all over her body, swelling of the mouth, tightness of her chest and coughing (treatment not specified). At the time of this report, the patient was recovering from the events. The reporting physician felt that rash all over body, swelling of the mouth, tightness of chest and coughing were considered to be immediately life-threatening. She noted that the patient had a "similar reaction" to methylphenidate (RITALIN). Additional information has been requested.

VAERS ID:298170 (history)  Vaccinated:2007-10-01
Age:16.0  Onset:2007-10-01, Days after vaccination: 0
Gender:Female  Submitted:2007-11-28, Days after onset: 58
Location:Kansas  Entered:2007-11-29, Days after submission: 1
Life Threatening? Yes
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Unknown
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0711USA03656
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC. 0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Cardiac disorder, Loss of consciousness
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad)
Write-up: Information has been received from a physician concerning a 16 year old female who in October 2007 (exact date unknown), was vaccinated (route and site not reported) with the 1st dose of Gardasil (lot # not reported). Three hours post vaccination, the patient passed out and was hospitalized. At the time of this report the patient was still in the hospital based on a cardiac related issue. The cardiologist states that the cardiac issue has nothing to do with the Gardasil the patient received. The physician felt that the patient''s passing out and cardiac related issue were considered to be immediately life-threatening. Additional information has been requested.

VAERS ID:299032 (history)  Vaccinated:2007-06-19
Age:15.0  Onset:2007-10-07, Days after vaccination: 110
Gender:Female  Submitted:2007-12-06, Days after onset: 60
Location:New Hampshire  Entered:2007-12-07, Days after submission: 1
Life Threatening? Yes
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Mircette
Current Illness: Contraception; Hay fever
Preexisting Conditions:
Diagnostic Lab Data: diagnostic laboratory 10/10/07 - pulmonary embolism; chest computed axial 10/10/07 - pulmonary embolism 12/13/07-records received- Diagnosed with positive D-Dimer 1574 and a CAT scan to have a pulmonary embolism. CT demonstrated multiple m
CDC 'Split Type': WAES0712USA01135
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC.0388U1IMUN
Administered by: Other     Purchased by: Other
Symptoms: Activated partial thromboplastin time prolonged, Antiphospholipid antibodies negative, Antithrombin III, Beta-2 glycoprotein antibody, Blood homocysteine, Cardiolipin antibody, Chest discomfort, Coagulation factor VIII level normal, Dyspnoea, Dyspnoea exertional, Factor V Leiden mutation, Fibrin D dimer normal, International normalised ratio increased, Protein C increased, Prothrombin time prolonged, Pulmonary embolism, Seasonal allergy
SMQs:, Liver-related coagulation and bleeding disturbances (narrow), Anaphylactic reaction (broad), Haemorrhage laboratory terms (broad), Congenital, familial and genetic disorders (narrow), Embolic and thrombotic events, venous (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Conjunctival disorders (narrow), Hypersensitivity (broad)
Write-up: Information has been received from a registered nurse, concerning a 16 year old female patient with hay fever and no other pertinent medical history, who was vaccinated IM with the first and second dose, 0.5 ml, of Gardasil as follows: on 03-APR-2007 with the first dose (lot #654702/0011U), and on 19-JUN-2007 and the second dose (lot # 657622/0388U). Concomitant therapy on 03-APR-2007 included diphtheria toxoid (+) pertussis acellular vaccine (unspecified) (+) tetanus toxoid (manufacturer not specified). Noted therapy initiated on approximately 07-SEP0-2007 ("one month prior" to the event), included MIRCETTE (dose not reported). On 07-OCT-2007, approximately 4 months after the second vaccination, the patient experienced shortness of breath and chest discomfort. On 10-OCT-2007, she presented to a walk-in clinic and a diagnostic "blood test" and CAT scan of tee lungs revealed a pulmonary embolus. She was hospitalized and treated with oxygen and IV heparin LOVENOX. On 15-OCT-2007, she was discharged from the hospital. On an unknown date, enoxaparin sodium was discontinued and COUMADIN was initiated, and continued. A consultation was planned with a hematologist or oncologist to rule out any blood dyscrasia. At the time of this report, the patient was recovering. The nurse considered pulmonary embolus to be immediately life-threatening and serious as an other important medical event. Additional information has been requested. 12/13/07-records received for DOS 10/10-10/15/07-DC DX: Pulmonary embolism. Presented to ED with shortness of breath.Exertional dyspnea began last Sunday, three days ago.

VAERS ID:299724 (history)  Vaccinated:2007-09-27
Age:14.0  Onset:2007-09-27, Days after vaccination: 0
Gender:Female  Submitted:2007-11-14, Days after onset: 48
Location:Tennessee  Entered:2007-11-15, Days after submission: 1
Life Threatening? Yes
Died? No
Permanent Disability? Yes
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness:
Preexisting Conditions: None
Diagnostic Lab Data: Unknown
CDC 'Split Type': WAES0710USA05575
Vaccination
Manufacturer
Lot
Dose
Route
Site
HPV4: HPV (GARDASIL)MERCK & CO. INC.UNK0UNUN
Administered by: Other     Purchased by: Other
Symptoms: Guillain-Barre syndrome
SMQs:, Peripheral neuropathy (narrow), Guillain-Barre syndrome (narrow), Demyelination (narrow)
Write-up: Information has been received from a physician concerning a 14 year old female with no pertinent medical history or drug reaction/allergies, who on 27-SEP-2007 was vaccinated with the first dose of Gardasil vaccine (0.5 mL). There was no concomitant medication. On 27-SEP-2007 the patient experienced Guillain-Barre Syndrome and was hospitalized. Hospitalization time was unknown. No further details were provided. The Guillain-Barre Syndrome was considered to be immediately life-threatening and disabling. At the time of this report, the patient was recovering.

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