Citaat | Gerechtshof Den Haag 27 februari 2018

Onder 2.8.4. Gerechtshof Den Haag 27 februari 2018

Een alinea uit Gerechtshof Den Haag 27 februari 2018, ECLI:NL:GHDHA:2018:4021.

average of 51 (range: 8-104) weeks (…). Eight patients (40%) (5 with systemic and 3 with polyarthritis) experienced some form of toxicity; the most common was transient raised liver enzymes (SOOT and SGPT), which occurred in 5 patients. There were 9 episodes of increased plasmatic levels; in 7 these were more than twice the upper normal limit. In all cases, liver enzyme levels returned to normal after the drug was withheld for 2 weeks. Four patients reported pain at the site of the injection; loss of appetite and stomach discomfort occurred in 2 patients; 1 patient each experienced abdominal pain, vomiting, headaches, and sleepiness. No patient needed to permanently discontinue the drug due to side effects. The time between the treatment onset and the occurrence of toxicity was 31 (range 4-60) weeks.”

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