Does CEFDINIR Cause Incorrect product storage? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Incorrect product storage have been filed in association with CEFDINIR (Cefdinir). This represents 0.3% of all adverse event reports for CEFDINIR.
5
Reports of Incorrect product storage with CEFDINIR
0.3%
of all CEFDINIR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From CEFDINIR?
Of the 5 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFDINIR. However, 5 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which CEFDINIR Alternatives Have Lower Incorrect product storage Risk?
CEFDINIR vs CEFEPIME
CEFDINIR vs CEFEPIME\CEFEPIME
CEFDINIR vs CEFIDEROCOL
CEFDINIR vs CEFIXIME
CEFDINIR vs CEFMETAZOLE