Does NIFUROXAZIDE Cause Product prescribing issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product prescribing issue have been filed in association with NIFUROXAZIDE. This represents 11.3% of all adverse event reports for NIFUROXAZIDE.
8
Reports of Product prescribing issue with NIFUROXAZIDE
11.3%
of all NIFUROXAZIDE reports
8
Deaths
7
Hospitalizations
How Dangerous Is Product prescribing issue From NIFUROXAZIDE?
Of the 8 reports, 8 (100.0%) resulted in death, 7 (87.5%) required hospitalization, and 6 (75.0%) were considered life-threatening.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NIFUROXAZIDE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does NIFUROXAZIDE Cause?
Coma (18)
Toxicity to various agents (18)
Cardiomyopathy (12)
Confusional state (11)
Coronary artery stenosis (11)
Drug interaction (11)
Encephalopathy (11)
Hepatic enzyme increased (11)
Hyperglycaemia (11)
Jaundice (11)
What Other Drugs Cause Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)