Does FIDAXOMICIN Cause Product dose omission issue? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product dose omission issue have been filed in association with FIDAXOMICIN (Dificid). This represents 2.4% of all adverse event reports for FIDAXOMICIN.
35
Reports of Product dose omission issue with FIDAXOMICIN
2.4%
of all FIDAXOMICIN reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission issue From FIDAXOMICIN?
Of the 35 reports, 4 (11.4%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FIDAXOMICIN. However, 35 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which FIDAXOMICIN Alternatives Have Lower Product dose omission issue Risk?
FIDAXOMICIN vs FILGOTINIB
FIDAXOMICIN vs FILGRASTIM
FIDAXOMICIN vs FILGRASTIM-AAFI
FIDAXOMICIN vs FILGRASTIM-SNDZ
FIDAXOMICIN vs FINASTERIDE