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This is VAERS ID 618773

(NOTE: This result is from the 2/14/2018 version of the VAERS database)

Case Details

VAERS ID: 618773 (history)  
Form: Version 1.0  
Sex: Female  
Location: Foreign  
Submitted: 2015-11-18
Entered: 2015-11-18
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Other       Purchased by: Other
Symptoms: Abasia, Autonomic nervous system imbalance, Bed rest, Cardiac disorder, Dizziness, Dyspnoea, Fatigue, Food allergy, Gait disturbance, Herpes zoster, Loss of consciousness, Paraesthesia, Rash macular, Visual impairment
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dystonia (broad), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Glaucoma (broad), Optic nerve disorders (broad), Cardiomyopathy (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: No other medications
Current Illness: Not known
Preexisting Conditions:
Diagnostic Lab Data:
CDC Split Type: WAES1511NZL008873

Write-up: Information has been received from an unspecified reporter via webpage article and refers to unspecified number of female patients. No information about the patients'' medical history, concurrent conditions or concomitant medications was provided. On an unknown dates, the patients were vaccinated with GARDASIL (dose, frequency, route of administration, lot # and expiration date were not reported). On an unknown dates. those patients experienced fatigue, breathing difficulties, poor vision, the patient struggling to walk the stairs, bed rest, constant tingling of legs and legs being all purple and blotchy-looking, cardiac disorder, blacking out, autonomic nervous disorder, abasia, shingles, dizziness and food allergy (reported as "girls around the world displaying the same or similar symptoms"). Outcomes of all the events were not reported. The related between the events and GARDASIL was not specified by the reporter (reported as "Whether the vaccine triggered the problems or caused them is not proven.") The Company considered all the events to be serious. This is one of several reports from the same source. Additional information is expected.

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