First approved in Germany |
1995 (Psoriasis vulgaris) |
Recommended control parameters |
Serum creatinine, transaminases/γGT, complete blood count including differential blood count, urinanalysis |
Recommended initial dosage |
According to recommended dosage regimen see Table 17
|
Recommended maintenance dosage |
Individually adapted dosage |
Expected beginning of clinical effect |
After approximately 6 weeks |
Response rate |
PASI 75 in 50–70% of the patients at the end of the induction phase after 16 weeks (LE 2) |
Important contraindications (limited selection) |
Chronic diseases of the gastrointestinal tract and/or the kidneys and chronic diseases, which are accompanied by an impairment of the leukocyte count or functions, malignant diseases, pregnancy and nursing |
Important ADRs (limited selection) |
Gastrointestinal complaints, flush, lymphopenia, eosinophilia |
Important drug interactions |
None known |
Other |
– |