First approved in Germany |
1992 (Psoriasis vulgaris) |
Recommended control parameters |
Erythrocyte sedimentation rate (ESR), complete blood count, liver values, renal values, blood lipid values, pregnancy test, x-ray control of the bones in case of long-term therapy |
Recommended initial dosage |
0.3–0.5 mg/kg BW per day for approximately 4 weeks, then 0.5–0.8 mg/kg BW |
Recommended maintenance dosage |
Individual dosaging dependent on the results and tolerance |
Expected beginning of clinical effect |
After 4–8 weeks |
Response rate |
Widely variable and dose-dependent, no definite statement possible, partial remission (PASI 75) in 25–75% of the patients (30–40 mg per day) (LE 3) in studies |
Important contraindications (limited selection) |
Renal and liver damage, desire to have children in female patients of child-bearing age, pregnancy, nursing, alcohol abuse, manifest diabetes mellitus, wearing of contact lenses, history of pancreatitis, hyperlipidemia requiring drug treatment |
Important ADRs (limited selection) |
Hypervitaminosis A (e.g., cheilitis, xerosis, nose-bleeding, alopecia, increased skin fragility) |
Important drug interactions (limited selection) |
Phenytoin, tetracyclines, methotrexate, alcohol, mini-pill |
Other |
Contraception up to 2 years after discontinuation in female patients of child-bearing age |