Does CLOFAZIMINE Cause Intentional product use issue? 135 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 135 reports of Intentional product use issue have been filed in association with CLOFAZIMINE. This represents 3.1% of all adverse event reports for CLOFAZIMINE.
135
Reports of Intentional product use issue with CLOFAZIMINE
3.1%
of all CLOFAZIMINE reports
56
Deaths
65
Hospitalizations
How Dangerous Is Intentional product use issue From CLOFAZIMINE?
Of the 135 reports, 56 (41.5%) resulted in death, 65 (48.1%) required hospitalization, and 16 (11.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOFAZIMINE. However, 135 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which CLOFAZIMINE Alternatives Have Lower Intentional product use issue Risk?
CLOFAZIMINE vs CLOMETHIAZOLE
CLOFAZIMINE vs CLOMIPHENE
CLOFAZIMINE vs CLOMIPRAMINE
CLOFAZIMINE vs CLONAZEPAM
CLOFAZIMINE vs CLONIDINE