Does CLOFAZIMINE Cause Incorrect product administration duration? 73 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 73 reports of Incorrect product administration duration have been filed in association with CLOFAZIMINE. This represents 1.7% of all adverse event reports for CLOFAZIMINE.
73
Reports of Incorrect product administration duration with CLOFAZIMINE
1.7%
of all CLOFAZIMINE reports
26
Deaths
27
Hospitalizations
How Dangerous Is Incorrect product administration duration From CLOFAZIMINE?
Of the 73 reports, 26 (35.6%) resulted in death, 27 (37.0%) required hospitalization, and 1 (1.4%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOFAZIMINE. However, 73 reports have been filed with the FAERS database.
What Other Side Effects Does CLOFAZIMINE Cause?
Electrocardiogram qt prolonged (629)
Nausea (403)
Vomiting (399)
Off label use (389)
Anaemia (353)
Dyspnoea (313)
Neuropathy peripheral (238)
Diarrhoea (213)
Drug resistance (196)
Drug ineffective (191)
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 CLOFAZIMINE Alternatives Have Lower Incorrect product administration duration Risk?
CLOFAZIMINE vs CLOMETHIAZOLE
CLOFAZIMINE vs CLOMIPHENE
CLOFAZIMINE vs CLOMIPRAMINE
CLOFAZIMINE vs CLONAZEPAM
CLOFAZIMINE vs CLONIDINE