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BNF for Children 2011-2012

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<strong>BNF</strong>C <strong>2011</strong>–<strong>2012</strong> 8.2.4 Other immunomodulating drugs 441required during treatment and <strong>for</strong> up to 3 months afterlast doseBreast-feeding consider if benefit outweighs risk—not known if present in human milkSide-effects vertigo, increased susceptibility to infection,injection-site reactionsIndication and doseCryopyrin-associated periodic syndromes. By subcutaneous injectionChild 4–18 yearsBody-weight 15–40 kg 2 mg/kg every 8 weeks. Ifclinical response not achieved 7 days after startingtreatment, a repeat dose of 2 mg/kg can be considered;if a full response is then achieved, subsequentdosing should be 4 mg/kg every 8 weeksBody-weight over 40 kg 150 mg every 8 weeks. Ifclinical response not achieved 7 days after startingtreatment, a repeat dose of 150 mg can be considered;if a full response is then achieved, subsequentdosing should be 300 mg every 8 weeksIlaris c (Novartis) TAInjection, powder <strong>for</strong> reconstitution, canakinumab,net price 150-mg vial = £9927.80Indication and doseSee notes above. By intravenous infusion (over 1 hour)Consult local treatment protocols <strong>for</strong> detailsMepact c (Takeda) TAIntravenous infusion, powder <strong>for</strong> reconstitution,mifamurtide, net price 4-mg vial = £2375.008.3 Sex hormones andhormone antagonists inmalignant diseaseClassification not used in <strong>BNF</strong> <strong>for</strong> <strong>Children</strong>.MifamurtideMifamurtide is licensed in children and adolescents <strong>for</strong>the treatment of high-grade, resectable, non-metastaticosteosarcoma after complete surgical resection. It isused in combination with chemotherapy.MIFAMURTIDECautions asthma and chronic obstructive pulmonarydisease—consider prophylactic bronchodilator therapy;history of autoimmune, inflammatory, or collagendisease; monitor renal function, hepatic functionand clotting parameters; monitor patients withhistory of venous thrombosis, vasculitis, or unstablecardiovascular disorders <strong>for</strong> persistent or worseningsymptoms during administration—consult productliterature interactions: Appendix 1 (mifamurtide)Hepatic impairment use with caution—no in<strong>for</strong>mationavailableRenal impairment use with caution—no in<strong>for</strong>mationavailablePregnancy avoid; effective contraception requiredBreast-feeding avoid—no in<strong>for</strong>mation availableSide-effects gastro-intestinal disturbances (includinganorexia, nausea, vomiting, diarrhoea, constipation,abdominal pain, dyspepsia); tachycardia, hypertension,palpitations, hypotension, phlebitis; oedema,respiratory disorders (including dyspnoea, epistaxis,cough, tachypnoea, haemoptysis, pleural effusion);confusion, depression, insomnia, headache, dizziness,paraesthesia, hypoaesthesia, tremor, drowsiness,anxiety; hypokalaemia, anaemia, leucopenia, thrombocytopenia,granulocytopenia; haematuria, dysuria,pollakiuria; musculoskeletal pain; blurred vision;vertigo, tinnitus, hearing loss; sweating, alopecia, rash,dry skin, flushing8 Malignant disease and immunosuppression

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