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BENZA‑PEN

FDA Application Number: 065-488

Based on the FDA Center for Veterinary Medicine data from February 1989 to June 1992: Of 5 reported animal deaths involving BENZA‑PEN, 3 occurred when BENZA‑PEN was the only drug administered - representing 60% of all fatalities.

60%
SINGLE-DRUG FATALITIES
BENZA‑PEN ONLY
13
TOTAL ANIMALS REPORTED
5
TOTAL FATALITIES
3
SINGLE-DRUG FATALITIES

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Top 3 Reported Reactions

Restlessness
Hypersalivation
Death

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SafeVetMeds equips users with the intelligence tools to ask better questions about veterinary drug safety. Powered by 100 million FDA adverse event data points, it delivers advanced safety insights, cross-drug comparisons, and real-world FDA data that is easy to search and simple to understand. The first platform of its kind now available to protect animals.

All data is sourced from the FDA Center for Veterinary Medicine adverse event reports submitted voluntarily by veterinarians, pet owners, and drug manufacturers. This information has not been independently verified and does not establish that any drug caused the reported outcomes. These reports reflect what was submitted to the FDA, not confirmed cause-and-effect relationships or actual risk rates. Reporting rates may vary by drug, manufacturer, and time period, and may be delayed up to 6 months. The percentage shown represents proportions within the reported dataset and does not indicate risk probability or safety ratings. SafeVetMeds is a 501(c)(3) nonprofit providing data transparency infrastructure and does not provide veterinary medical advice, diagnostic services, or legal counsel. For medical decisions regarding your animal, consult a licensed veterinarian. For legal questions, consult an attorney. This data should be considered as one factor among many in medical decision-making, not as definitive evidence of drug safety or danger.