- Lepromatous Leprosy (including Dapsone resistant)
- Must be used as part of multi-drug regimen (high risk of developed Antibiotic Resistance)
- Lepromatous Leprosy Type 2 Reaction (Erythema Nodosum)
- Rimino-phenazine dye (red color) synthetically derived from lichen extracts (Buellia canescens)
- Anti-inflammatory properties (used in treatment of Leprosy type 2 reaction)
- Anti-Mycobacterial
- Preferentially binds Mycobacterial DNA, inhibiting DNA Replication and cell growth
- Activity against Mycobacterium leprae (as well as other Mycobacteria)
- Slowly bactericidal
- Clofazimine (Lamprene) soft gel capsules: 50 mg
- Precautions
- Clofazimine must be used in combination with other agents (risk of resistance)
- Decrease dose for significant gastrointestinal adverse effects
- Discontinue for significant QTc Prolongation
- Lepromatous Leprosy (in combination with other agents)
- Clofazimine 50 mg orally daily for 2 years
- FDA label dosing is 100 mg daily for 2 years (3 years if Dapsone resistance)
- Lepromatous Leprosy Type 2 Reaction (Erythema Nodosum)
- Other treatment regimens are preferred (e.g. Corticosteroids, Methotrexate)
- Clofazimine 100 to 200 mg orally daily for up to 3 months (taper to 100 mg as soon as possible)
- Skin and body fluid reddish discoloration (40-50% of patients)
- Deposits in skin, mucosa and Conjunctiva
- Leprosy lesions treated with Clofazimine will appear tan or black
- Gastrointestinal (related to drug deposits in intestinal mucosa)
- Small Bowel Obstruction
- Gastrointestinal Hemorrhage
- Splenic infarction
- Cardiovascular
- QTc Prolongation (esp. dose >100 mg/day)
- Unknown safety in Lactation
- Unknown safety in pregnancy
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