CEFOXITIN

Generic: CEFOXITIN

SAMSON MEDICAL TECHNOLOGIES LLCManufacturer
INTRAVENOUSRoute
CEFOXITIN SODIUMActive Substance
2015-11-16Original Approval

CEFOXITIN is FDA application ANDA200938, sponsored by SAMSON MEDCL. 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 I2013-11-21
Cefoxitin for Injection and Dextrose Injection, 1 g in Duplex, 50 mL Container, Catalog No. 3123-11, For IV Use Only, Si

Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due t

Top Reported Reactions

1
OFF LABEL USE
93 reports
2
DRUG RESISTANCE
90 reports
3
NAUSEA
80 reports
4
DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS
79 reports
5
RASH
77 reports
6
DRUG INEFFECTIVE
63 reports
7
PRODUCT USE IN UNAPPROVED INDICATION
63 reports
8
THROMBOCYTOPENIA
62 reports
9
CONDITION AGGRAVATED
56 reports
10
DYSPNOEA
51 reports