Does CEFDINIR Cause Recalled product administered? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Recalled product administered have been filed in association with CEFDINIR (Cefdinir). This represents 2.8% of all adverse event reports for CEFDINIR.
46
Reports of Recalled product administered with CEFDINIR
2.8%
of all CEFDINIR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Recalled product administered From CEFDINIR?
Of the 46 reports.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFDINIR. However, 46 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which CEFDINIR Alternatives Have Lower Recalled product administered Risk?
CEFDINIR vs CEFEPIME
CEFDINIR vs CEFEPIME\CEFEPIME
CEFDINIR vs CEFIDEROCOL
CEFDINIR vs CEFIXIME
CEFDINIR vs CEFMETAZOLE