Does CEFDINIR Cause Product administration error? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Product administration error have been filed in association with CEFDINIR (Cefdinir). This represents 1.4% of all adverse event reports for CEFDINIR.
23
Reports of Product administration error with CEFDINIR
1.4%
of all CEFDINIR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From CEFDINIR?
Of the 23 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFDINIR. However, 23 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which CEFDINIR Alternatives Have Lower Product administration error Risk?
CEFDINIR vs CEFEPIME
CEFDINIR vs CEFEPIME\CEFEPIME
CEFDINIR vs CEFIDEROCOL
CEFDINIR vs CEFIXIME
CEFDINIR vs CEFMETAZOLE