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From the 1/14/2022 release of VAERS data:

This is VAERS ID 261581

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Case Details

VAERS ID: 261581 (history)  
Form: Version 1.0  
Age: 75.0  
Sex: Male  
Location: California  
Vaccinated:2006-06-20
Onset:2006-07-18
   Days after vaccination:28
Submitted: 2006-08-10
   Days after onset:23
Entered: 2006-08-15
   Days after submission:5
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. - / UNK - / -

Administered by: Other       Purchased by: Other
Symptoms: Influenza like illness, Pulmonary congestion, Pyrexia
SMQs:, Cardiac failure (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: PROSCAR, SYNTHROID, PRAVACHOL, BENEMID
Current Illness:
Preexisting Conditions: Medical history: Shingles
Allergies:
Diagnostic Lab Data: NONE
CDC Split Type: WAES0607USA05370

Write-up: Information has been received from a 75 year old male consumer with a history of shingles "once or twice many years ago" and no other reported allergies or history who approximately 20-JUN-2006 was vaccinated with a dose of varicella-zoster virus vaccine live. Concomitant therapy included finasteride (MSD), pravastatin Na (PRAVACHOL), levothyroxine Na (SYNTHROID) and probenecid (BENEMID). About 4 weeks after vaccination, on approximately 18-JUL-2006, the patient developed a high fever and felt very sick with chest congestion and flu-like symptoms. He said was seen by his doctor and the doctor''s diagnosis was that he had a bacterial infection. Subsequently, the patient recovered. There was no product quality complaint involved. Additional information has been requested.


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