CEFTRIAXONE SODIUM

Generic: CEFTRIAXONE SODIUM

Qilu Pharmaceutical Co.Manufacturer
INTRAMUSCULAR, INTRAVENOUSRoute
CEFTRIAXONE SODIUMActive Substance
2016-06-29Original Approval

CEFTRIAXONE SODIUM is FDA application ANDA203702, 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
OFF LABEL USE
3,898 reports
2
DRUG INEFFECTIVE
3,554 reports
3
PYREXIA
2,055 reports
4
ACUTE KIDNEY INJURY
1,826 reports
5
DYSPNOEA
1,592 reports
6
CONDITION AGGRAVATED
1,585 reports
7
PNEUMONIA
1,337 reports
8
VOMITING
1,266 reports
9
NAUSEA
1,253 reports
10
DRUG INTERACTION
1,155 reports