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Recent reports (see References) documented seven patients between 1996 and 2001 who developed severe illness following receipt of yellow fever vaccine (17D-204 or 17DD strains). Although reported in a very small proportion of approximately 300 million worldwide yellow fever vaccine recipients, this association warrants further investigation. The Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA) are enhancing preexisting surveillance for yellow fever vaccine adverse events with special laboratory support. Healthcare providers are encouraged to report cases of febrile illness potentially caused by yellow fever vaccination to the CDC/FDA Vaccine Adverse Events Reporting System (VAERS) by one of the following methods:
Persons who develop a fever
will be prioritized by VAERS for further evaluation. Note: Because local healthcare providers need to be involved in the evaluation, reports cannot be accepted directly from individual patients.
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