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This is VAERS ID 271126

Case Details

VAERS ID: 271126 (history)  
Age: 20.0  
Gender: Female  
Location: New York  
Vaccinated:2006-11-16
Onset:2006-11-17
   Days after vaccination:1
Submitted: 2007-04-06
   Days after onset:139
Entered: 2007-01-22
   Days after submission:73
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HPV4: HPV (GARDASIL) / MERCK & CO. INC. - / 0 UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Arthralgia, Full blood count normal, Injection site pain, Red blood cell sedimentation rate normal
SMQs:, Extravasation events (injections, infusions and implants) (broad), Arthritis (broad)

Life Threatening? No
Died? No
Permanent Disability? No
Recovered? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: UNK
Current Illness:
Preexisting Conditions: Allergic reaction to antibiotics
Diagnostic Lab Data: complete blood cell 11?/??/06 - normal erythrocyte 11?/??/06 - normal
CDC Split Type: WAES0612USA02899

Write-up: Information has been received from a physician concerning a 20 year old female with an allergy to antibiotics who on 16-Nov-2006 was vaccinated with a first dose of Gardasil vaccine (yeast). On 17-Nov-2006 the patient developed pain at the injection site. The patient began to have joint pain throughout her body. The location of the joint rotated and was in her right knee at the time of this report. Laboratory evaluations revealed that erythrocyte sedimentation rate and complete blood count were normal. The patient was to be seen by a neurologist. The physician reported that she would most likely hold off on the second dose of Gardasil vaccine (yeast). At the time of this report, the patient''s joint pain persisted. Additional information has been requested. This is in follow-up to report (s) previously submitted on 1/16/2007. Information has been received from a physician concerning a 20 year old female with an allergy to antibiotics who on 16-NOV-2006 was vaccinated with a first dose of GARDASIL. On 17-NOV-2006 the patient developed pain at the injection site. The patient then began to have joint pain throughout her body. The location of the joint rotated and was in her right knee at the time of this report. Laboratory evaluations revealed that erythrocyte sedimentation rate and complete blood count were normal. The physician reported that the patient was seen by a rheumatologist, but she did not have the details of the visit. The physician reported that the patient cancelled her appointment to received her second dose of GARDASIL. At the time of this report, the patient''s joint pain persisted. Additional information has been requested.


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