Your Health. Your Family. Your Choice.
|History of Changes from the VAERS Wayback Machine|
First Appeared on 5/14/2017
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|HPV4: HPV (GARDASIL) / MERCK & CO. INC.||H013055 / -||UN / UN|
Administered by: Other Purchased by: Other
Symptoms: Malaise, Pain, Rheumatoid factor positive, Post viral fatigue syndrome, Loss of personal independence in daily activities
Life Threatening? Yes
Permanent Disability? Yes
ER or Doctor Visit? Yes
Hospitalized? Yes, days:
Write-up:This spontaneous report as received from a patient''s mother via Agency (ADR 23256758) refers to a 14 year old female patient. The patient''s medical history included hypersensitivity and rheumatoid factor positive. On 26-NOV-2014, the patient was vaccinated with a dose of quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine (manufacturer unknown) lot # H013055 (expiration date and dose were not reported), parenteral for human papilloma virus immunization. Concomitant therapies included CIRCADIN, gabapentin, melatonin, acetaminophen, co-codamol, amitriptyline hydrochloride (manufacturer unknown) and ibuprofen. On an unknown date, the patient experience myalgic encephalomyelitis, chronic pain and generalized illness. The patient was unable to get of bed, she stopped school, learning and everyday activities. On an unknown date, the patient was hospitalized (reported as "is no in full-time hospital"). Lab diagnostic studies showed persistence presence of a positive high rheumatoid factor in recent blood tests. The outcome of adverse events was reported as not recovered. The relatedness between adverse events and quadrivalent human papillomavirus (types 6,11,16,18) recomb. vaccine)manufacturer unknown) was not reported. The reported considered events of myalgic encephalomyelitis, chronic pain and generalized illness as medically significant, life threatening and disability. Additional information is not expected since no further follow up information can be obtained from Local Health Authority. Agency narrative: My daughter had no experienced myalgic encephalomyelitis after taking the vaccination, she is very ill and is now in full-time hospital. My daughter had hypersensitivity and was at a weight which was under 6.5 stone, which seems dangerous to give the vaccine. She is unable to get of bed, stopped school and learning, everyday activities have stopped. Her body is now at the age of an old woman. Chronic pain.
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