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Title
Adverse events associated with childhood vaccines other than pertussis and rubella. Summary of
a report from the Institute of Medicine.
AuthorStratton KR; Howe CJ; Johnston RB Jr
AddressInstitute of Medicine, National Academy of Sciences, Washington, DC.
Source
JAMA,
271:
20, 1994 May 25,
1602-5
AbstractIn September 1993, the Institute of Medicine released a report entitled Adverse Events Associated
With Childhood Vaccines: Evidence Bearing on Causality. The report examined putative serious adverse
consequences
associated with administration of diphtheria and tetanus toxoids; measles, mumps, and measles-mumps-rubella
vaccines; oral polio vaccine and inactivated polio vaccine; hepatitis B vaccines; and Haemophilus
influenzae type b (Hib) vaccines. The committee spent 18 months reviewing all available scientific and
medical data, from individual case reports (published and unpublished) to controlled clinical trials.
The committee found that the evidence favored the rejection of a causal relation between diphtheria and
tetanus toxoids and encephalopathy, infantile spasms, and sudden infant death syndrome, and between
conjugate Hib vaccines and susceptibility to Hib disease. The committee found that the evidence favored
acceptance of a causal relation between diphtheria and tetanus toxoids and Guillain-Barré syndrome
and brachial neuritis, between measles vaccine and anaphylaxis, between oral polio vaccine and Guillain-Barré
syndrome, and between unconjugated Hib vaccine and susceptibility to Hib disease. The committee
found that the evidence established causality between diphtheria and tetanus toxoids and anaphylaxis,
between measles vaccine and death from measles vaccine-strain viral infection, between measles-mumps-rubella
vaccine and thrombocytopenia and anaphylaxis, between oral polio vaccine and poliomyelitis and death
from polio vaccine-strain viral infection, and between hepatitis B vaccine and anaphylaxis. For five
vaccine-related adverse events, there was no evidence identified. For the remaining 33 vaccine-related
adverse events, the evidence was inadequate to accept or reject a causal relation.