HIGHLIGHTS OF PRESCRIBING INFORMATIONThese highlights do not include all the information needed to use North American Coral Snake Antivenin (Equine) safely and effectively. See full prescribing information for North American Coral Snake Antivenin (Equine). North American Coral Snake Antivenin (Equine) Lyophilized Powder for Solution for Intravenous Injection Initial U.S. Approval: 1967 INDICATIONS AND USAGENorth American Coral Snake Antivenin (Equine) is a horse-derived antivenin indicated for the treatment of envenomation caused by North American coral snakes - Micrurus. (1) DOSAGE AND ADMINISTRATIONFor intravenous use only.
DOSAGE FORMS AND STRENGTHSLyophilized powder in single use vial for reconstitution for injection. (3) CONTRAINDICATIONS
WARNINGS AND PRECAUTIONSPatients sensitive to North American Coral Snake Antivenin (Equine) or horse serum may develop anaphylaxis. Prior to intravenous North American Coral Snake Antivenin (Equine) administration consider performing a proper skin test and modify therapy if indicated. (5.1) ADVERSE REACTIONSAdverse reactions may include anaphylaxis and serum sickness, vomiting, and abdominal pain. (6) To report SUSPECTED ADVERSE REACTIONS, contact Pfizer, Inc. at 1-800-438-1985 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. See 17 for PATIENT COUNSELING INFORMATION. Revised: 7/2019 |

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ANTIVENIN® Highlights (micrurus fulvius)
To report an adverse event related to a Pfizer product and you are not part of a clinical trial* for this product, click the link below to submit your information: Pfizer Safety Reporting Site
*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.
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