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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 CEFDINIR Cause Product use issue? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product use issue have been filed in association with CEFDINIR (Cefdinir). This represents 0.8% of all adverse event reports for CEFDINIR.

13
Reports of Product use issue with CEFDINIR
0.8%
of all CEFDINIR reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product use issue From CEFDINIR?

Of the 13 reports, 1 (7.7%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CEFDINIR. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does CEFDINIR Cause?

Drug hypersensitivity (244) Diarrhoea (177) No adverse event (124) Rash (117) Product storage error (115) Drug ineffective (111) Urticaria (94) Nausea (83) Vomiting (76) Hypersensitivity (73)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which CEFDINIR Alternatives Have Lower Product use issue Risk?

CEFDINIR vs CEFEPIME CEFDINIR vs CEFEPIME\CEFEPIME CEFDINIR vs CEFIDEROCOL CEFDINIR vs CEFIXIME CEFDINIR vs CEFMETAZOLE

Related Pages

CEFDINIR Full Profile All Product use issue Reports All Drugs Causing Product use issue CEFDINIR Demographics