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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CEFOXITIN Cause Condition aggravated? 38 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Condition aggravated have been filed in association with CEFOXITIN (Cefoxitin and Dextrose). This represents 5.1% of all adverse event reports for CEFOXITIN.

38
Reports of Condition aggravated with CEFOXITIN
5.1%
of all CEFOXITIN reports
0
Deaths
10
Hospitalizations

How Dangerous Is Condition aggravated From CEFOXITIN?

Of the 38 reports, 10 (26.3%) required hospitalization, and 9 (23.7%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CEFOXITIN. However, 38 reports have been filed with the FAERS database.

What Other Side Effects Does CEFOXITIN Cause?

Drug reaction with eosinophilia and systemic symptoms (78) Drug resistance (63) Rash (47) Off label use (46) Nausea (44) Drug ineffective (39) Thrombocytopenia (35) Rash maculo-papular (34) Treatment failure (33) Anaphylactic reaction (27)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which CEFOXITIN Alternatives Have Lower Condition aggravated Risk?

CEFOXITIN vs CEFPODOXIME CEFOXITIN vs CEFPODOXIME PROXETIL CEFOXITIN vs CEFPROZIL CEFOXITIN vs CEFTAROLINE CEFOXITIN vs CEFTAROLINE FOSAMIL

Related Pages

CEFOXITIN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated CEFOXITIN Demographics