Does CEFDINIR Cause Poor quality product administered? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Poor quality product administered have been filed in association with CEFDINIR (Cefdinir). This represents 0.5% of all adverse event reports for CEFDINIR.
8
Reports of Poor quality product administered with CEFDINIR
0.5%
of all CEFDINIR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Poor quality product administered From CEFDINIR?
Of the 8 reports.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFDINIR. However, 8 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which CEFDINIR Alternatives Have Lower Poor quality product administered Risk?
CEFDINIR vs CEFEPIME
CEFDINIR vs CEFEPIME\CEFEPIME
CEFDINIR vs CEFIDEROCOL
CEFDINIR vs CEFIXIME
CEFDINIR vs CEFMETAZOLE