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Reactogenecity of indigenously produced measles vaccine.
Indian Pediatr ; 1996 Oct; 33(10): 827-31
Article in English | IMSEAR | ID: sea-9758
ABSTRACT

OBJECTIVE:

To assess the safety and reactogenecity of indigenously produced measles vaccine derived from EZ strain.

DESIGN:

A longitudinal clinical follow up after vaccination.

SETTING:

Hospital based and home follow up, as required.

SUBJECTS:

12,470 children, 9 to 15 months old, immunized with measles vaccine of EZ strain, in accordance with the National Immunization Schedule, at five centers.

METHODS:

A clinical follow up of children at 1 day, 1 week, 2 weeks, 3 weeks and 6 weeks after measles vaccination. A detailed clinical neurological examination in children showing side effects.

RESULTS:

Mild side effects were documented in 31%. Of these, 90% were seen in the first two weeks, out of which two thirds were seen during the first week. Commonest side effects were coryza (10%), fever (9.8%), cough (3.2%) and diarrhea (3.2%). Convulsions, with no later sequelae were documented in 2 cases only.

CONCLUSIONS:

Measles vaccine manufactured in India, using EZ strain is a safe vaccine. It has a level of reactogenecity including neurological aspects, lower than that reported in India with the Schwarz strain vaccine.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Measles Vaccine / Longitudinal Studies / India / Infant Type of study: Observational study Country/Region as subject: Asia Language: English Journal: Indian Pediatr Year: 1996 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Measles Vaccine / Longitudinal Studies / India / Infant Type of study: Observational study Country/Region as subject: Asia Language: English Journal: Indian Pediatr Year: 1996 Type: Article