Menomune
PATIENT INFORMATION
Patients, parents or guardians should be fully informed of the benefits and risks of immunization with Menomune™ A/C/Y/W-135.
Patients, parents or guardians should be instructed to report any serious adverse reactions to their health-care provider.
As part of the patient's immunization record, the date, lot number and manufacturer of the vaccine administered should be recorded.22, 23, 24
REFERENCES
22. CDC. National Childhood Vaccine Injury Act: requirements for permanent vaccination records and for reporting of selected events after vaccination. MMWR 37: 197-200, 1988
23. Food and Drug Administration. New reporting requirements for vaccine adverse events. FDA Drug Bull 18 (2), 16-18, 1988
24. CDC. Vaccine Adverse Event Reporting System — United States. MMWR 39: 730-733, 1990
Generic Name: Meningococcal Polysaccharide Vaccine
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