CEFTRIAXONE SODIUM

Generic: CEFTRIAXONE SODIUM

Apotex Corp.Manufacturer
INTRAVENOUSRoute
CEFTRIAXONE SODIUMActive Substance
2018-10-17Original Approval

CEFTRIAXONE SODIUM is FDA application ANDA209218, sponsored by QILU ANTIBIOTICS. 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 III2016-10-19
Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH f

Labeling: Missing Label

Top Reported Reactions

1
DYSPNOEA
521 reports
2
OFF LABEL USE
426 reports
3
DRUG INEFFECTIVE
392 reports
4
DRUG HYPERSENSITIVITY
346 reports
5
NAUSEA
342 reports
6
PYREXIA
333 reports
7
VOMITING
313 reports
8
SEPSIS
284 reports
9
ABDOMINAL PAIN
280 reports
10
COUGH
277 reports