Does CEFDINIR Cause Condition aggravated? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Condition aggravated have been filed in association with CEFDINIR (Cefdinir). This represents 2.2% of all adverse event reports for CEFDINIR.
35
Reports of Condition aggravated with CEFDINIR
2.2%
of all CEFDINIR reports
2
Deaths
8
Hospitalizations
How Dangerous Is Condition aggravated From CEFDINIR?
Of the 35 reports, 2 (5.7%) resulted in death, 8 (22.9%) required hospitalization, and 1 (2.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFDINIR. However, 35 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CEFDINIR Alternatives Have Lower Condition aggravated Risk?
CEFDINIR vs CEFEPIME
CEFDINIR vs CEFEPIME\CEFEPIME
CEFDINIR vs CEFIDEROCOL
CEFDINIR vs CEFIXIME
CEFDINIR vs CEFMETAZOLE