PENICILLIN G POTASSIUM

Generic: PENICILLIN G

Baxter Healthcare CorporationManufacturer
INTRAVENOUSRoute
PENICILLIN G POTASSIUMActive Substance
1990-06-25Original Approval

PENICILLIN G POTASSIUM is FDA application NDA050638, sponsored by BAXTER HLTHCARE. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.

Recalls

Class I2025-06-27
Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Ma

Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled a

Top Reported Reactions

1
DRUG HYPERSENSITIVITY
670 reports
2
DRUG INEFFECTIVE
337 reports
3
DYSPNOEA
241 reports
4
RASH
241 reports
5
DIARRHOEA
233 reports
6
NAUSEA
211 reports
7
OFF LABEL USE
206 reports
8
MALAISE
198 reports
9
DRUG INTOLERANCE
192 reports
10
ABDOMINAL PAIN UPPER
180 reports