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This is VAERS ID 618554

History of Changes from the VAERS Wayback Machine

First Appeared on 6/14/2017

VAERS ID: 618554
Age:13.0
Gender:Female
Location:Foreign
Vaccinated:2010-12-15
Onset:2011-01-15
Submitted:2015-11-17
Entered:2015-11-17
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. NL48770 / 0 UN / IM

Administered by: Other      Purchased by: Other
Symptoms: Chest discomfort, Malaise, Nausea, Restlessness, Tremor, Blood test normal, Pulmonary function test abnormal

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: Immunisation; Asthma
Preexisting Conditions:
Diagnostic Lab Data: Blood test (date unspecified): normal; Pulmonary function test, peak flow variation gives suspicion of asthma.
CDC 'Split Type': WAES1511DNK008358

Write-up:Information has been received via Sanofi Pasteur MSD (Manufacturer control # E2015-12802) on 13-NOV-2015, as a part of business agreement. Case received from Health Care Professional via Health Authorities on 11-Nov-2015, under the reference number DK-DKMA-ADR 23224114 and DK-DKMA-WBS-0001611. The case is medically confirmed. The primary reporter was a physician. A 13 years-old female patient (weight: 54: kg; height: 174 cm) with a medical history of suspected asthma, had received the first primary dose of GARDASIL, lot/batch number reported as NL48770 via intramuscular route of administration in unspecified site of administration on 15-Dec-2010, and later on 15-Jan-2011, she developed chest pressure at physical activity, shaking, inner restlessness. On 15-Feb-2011, the patient developed malaise and nausea. The patient has been under investigation by physician several times. No reasons found. It is a bit unclear to the reporter exactly when the problems started, but the family remembers it being after the first GARDASIL vaccination (approximately as stated). The case is serious due to seriousness criterion disability. The patient had received concomitant injection of PRIORIX via unspecified route of administration in unspecified site of administration on 20-DEC-2010. No other medication. Patient has undergone blood tests and lung function. Blood tests were normal. Lung function (peakflow variation gives suspicion of asthma). At the time of reporting, the patient had not recovered.


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