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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CLOFAZIMINE Cause Hyperuricaemia? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Hyperuricaemia have been filed in association with CLOFAZIMINE. This represents 0.3% of all adverse event reports for CLOFAZIMINE.

13
Reports of Hyperuricaemia with CLOFAZIMINE
0.3%
of all CLOFAZIMINE reports
1
Deaths
3
Hospitalizations

How Dangerous Is Hyperuricaemia From CLOFAZIMINE?

Of the 13 reports, 1 (7.7%) resulted in death, 3 (23.1%) required hospitalization, and 2 (15.4%) were considered life-threatening.

Is Hyperuricaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CLOFAZIMINE. However, 13 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 Hyperuricaemia?

RITUXIMAB (130) PREDNISONE (118) RIBAVIRIN (116) TACROLIMUS (116) VENETOCLAX (115) FUROSEMIDE (100) ALLOPURINOL (94) RUXOLITINIB (92) CYCLOPHOSPHAMIDE (91) DEXAMETHASONE (87)

Which CLOFAZIMINE Alternatives Have Lower Hyperuricaemia Risk?

CLOFAZIMINE vs CLOMETHIAZOLE CLOFAZIMINE vs CLOMIPHENE CLOFAZIMINE vs CLOMIPRAMINE CLOFAZIMINE vs CLONAZEPAM CLOFAZIMINE vs CLONIDINE

Related Pages

CLOFAZIMINE Full Profile All Hyperuricaemia Reports All Drugs Causing Hyperuricaemia CLOFAZIMINE Demographics