Does FIDAXOMICIN Cause Incorrect product administration duration? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Incorrect product administration duration have been filed in association with FIDAXOMICIN (Dificid). This represents 1.5% of all adverse event reports for FIDAXOMICIN.
23
Reports of Incorrect product administration duration with FIDAXOMICIN
1.5%
of all FIDAXOMICIN reports
0
Deaths
12
Hospitalizations
How Dangerous Is Incorrect product administration duration From FIDAXOMICIN?
Of the 23 reports, 12 (52.2%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIDAXOMICIN. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does FIDAXOMICIN Cause?
Clostridium difficile infection (309)
Drug ineffective (302)
Diarrhoea (144)
Treatment failure (95)
No adverse event (75)
Clostridium difficile colitis (54)
Off label use (51)
Death (50)
Nausea (49)
Pyrexia (43)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which FIDAXOMICIN Alternatives Have Lower Incorrect product administration duration Risk?
FIDAXOMICIN vs FILGOTINIB
FIDAXOMICIN vs FILGRASTIM
FIDAXOMICIN vs FILGRASTIM-AAFI
FIDAXOMICIN vs FILGRASTIM-SNDZ
FIDAXOMICIN vs FINASTERIDE