Vaccine Adverse Event Reporting System Browser
Easily Browse through the VAERS adverse event reports for any year by by type of vaccine, manufacturer.
The following is all the information available on report# VAERS_ID: 739019
Vaccine(s) were received on 07/15/2016
Patient sex : U
Reaction was life threatening?: N
Patient eventually recovered from reaction ?: U
Patient eventually died?: N

The following Data for this patients ALLERGIES is available: [ ]

Description of adverse reaction: This spontaneous report was received from a nurse concerning a patient of unknown age and gender. There was no information about the patient's concurrent conditions, medical history or concomitant medication. On 15-JUL-2016, the patient was vaccinated with a dose of M-M-R II lot # L049316 with expiration date of 03-DEC-2017, subcutaneously (dose was not reported) and with a dose of PROQUAD lot # M012986 with expiration date of 12-SEP-2017 (dose and route of administration were not reported) for prophylaxis.


Vaccine(s) associated with report# 739019

TypeNameManufacturerVaccine LOT #Dose SeriesROUTESite
MMRMEASLES + MUMPS + RUBELLA (MMR II) MERCK & CO. INC.L0493160SCUN
MMRVMEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) MERCK & CO. INC.M0129860UNUN

Symptoms(s) associated with report# 739019

Extra dose administered