Lamprene Side Effects
Generic name: clofazimine
Note: This document contains side effect information about clofazimine. Some of the dosage forms listed on this page may not apply to the brand name Lamprene.
Some side effects of Lamprene may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA.
For the Consumer
Applies to clofazimine: oral capsule
Along with its needed effects, clofazimine (the active ingredient contained in Lamprene) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor immediately if any of the following side effects occur while taking clofazimine:Rare
- Bloody or black, tarry stools
- colicky or burning abdominal or stomach pain
- mental depression
- yellow eyes or skin—may be an orange color if already have a pink to brownish-black skin or eye discoloration
Some side effects of clofazimine may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:More common
- dry, rough, or scaly skin
- loss of appetite
- nausea or vomiting
- pink or red to brownish-black discoloration of skin and eyes
- skin rash and itching
- Changes in taste
- dryness, burning, itching, or irritation of the eyes
- increased sensitivity of skin to sunlight
Clofazimine commonly causes discoloration of the feces, lining of the eyelids, sputum, sweat, tears, and urine. Usually this side effect does not require medical attention, but the discoloration may not go away. However, clofazimine may also cause bloody or black, tarry stools. This side effect may be a symptom of serious bleeding problems that do require medical attention.
For Healthcare Professionals
Applies to clofazimine: oral capsule
Clofazimine (the active ingredient contained in Lamprene) enteropathy may manifest as colicky abdominal pain, nausea, vomiting, diarrhea, and weight loss. In some cases these side effects have prompted unnecessary discontinuation or exploratory laparotomy. Exploratory laparotomy findings in some patients with clofazimine-associated severe abdominal pain have often shown diffuse visceral hyperpigmentation, lymphadenopathy, eosinophilic mucosal and submucosal infiltration. Clofazimine crystalline infiltration in the intestinal and gall bladder mucosa, and in the bile, liver, and spleen have been documented.
Gastrointestinal (GI) side effects have included clofazimine enteropathy. Abdominal and epigastric pain, diarrhea, nausea, vomiting, and GI intolerance have been reported in 40% to 50% of patients. Rare reports of GI bleeding, bowel obstruction, anorexia, constipation, weight loss, and eosinophilic enteritis have been reported in less than 1% of patients.
The reddish-brown rash may become generalized, but typically involves only lepromatous lesions in patients with leprosy. The discoloration is reversible upon drug discontinuation, may be seen for up to 5 years, and may also involve the tears, saliva, feces, and sputum.
Dermatologic side effects have been commonly reported. These have included pigmentation from pink to brownish-black in 75% to 100% of the patients within a few weeks of treatment. Ichthyosis and dryness have been reported in 8% to 28% of patients. Rash and pruritus have been reported in 1% to 5% of patients. Erythroderma, acneiform eruptions, monilial cheilosis have been reported in less than 1% of patients. Phototoxicity and erythroderma have been reported rarely. Melanosis has also been observed, which resolved at a slower rate after the drug was discontinued.
Rare cases of "bull's eye" retinopathy due to annular macular pigmentary abnormalities have been reported, but may have been associated with CMV retinitis in some of the patients since they also had AIDS and, in some cases, evidence of CMV infection.
Ocular side effects have included corneal and conjunctival pigmentation and decreased visual acuity. Diminished vision and ocular dryness, burning, itching, and irritation have been reported in greater than 1% of patients. Macular pigmentary abnormalities have also been reported.
Metabolic side effects have been unusually reported. These have included significant increases in the fasting serum glucose and hypokalemia.
Hypersensitivity side effects have rarely included exfoliative dermatitis.
Rare cases of exfoliative dermatitis have been believed to be due to hypersensitivity since rechallenge with even small doses reproduced the signs and symptoms.
Cardiovascular side effects including thromboembolism have been reported.
Genitourinary side effects including cystitis have been reported in less than 1% of patients.
Musculoskeletal side effects including bone pain have been reported in less than 1% of patients.
Nervous system side effects including dizziness, drowsiness, fatigue, headache, giddiness, neuralgia, taste disorder, and vascular pain have been reported in less than 1% of patients.
Psychiatric side effects including depression secondary to skin discoloration have been reported. At least two cases of suicides have also been reported.
Hematologic side effects including elevated erythrocyte sedimentation rate (ESR) have been reported in greater than 1% of patients. Eosinophilia, splenic infarction, anemia, and lymphadenopathy have been reported in less than 1% of patients.
Hepatic side effects including hepatitis, jaundice, enlarged liver, elevated AST (SGOT), and elevated total bilirubin have been reported in less than 1% of patients.
Other side effects including elevated albumin, fever, and edema have been reported in less than 1% of patients.
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