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This is VAERS ID 618773

History of Changes from the VAERS Wayback Machine

First Appeared on 6/14/2017

VAERS ID: 618773
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Other      Purchased by: Other
Symptoms: Autonomic nervous system imbalance, Dizziness, Dyspnoea, Fatigue, Food allergy, Gait disturbance, Herpes zoster, Loss of consciousness, Paraesthesia, Rash macular, Visual impairment, Abasia, Bed rest, Cardiac disorder

Life Threatening? No
Died? No
Permanent Disability? Yes
Recovered? No
ER or Doctor Visit? Yes
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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