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BNF for Children 2011-2012

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222 4.8.1 Control of the epilepsies <strong>BNF</strong>C <strong>2011</strong>–<strong>2012</strong>4 Central nervous systemChild 12–18 years initially 25 mg on alternatedays <strong>for</strong> 14 days then 25 mg daily <strong>for</strong> further 14days, thereafter increased by max. 50 mg every 7–14 days; usual maintenance 100–200 mg daily in1–2 divided dosesAdjunctive therapy of seizures (with enzymeinducing drugs) without valproateChild 2–12 years initially 300 micrograms/kgtwice daily <strong>for</strong> 14 days then 600 micrograms/kgtwice daily <strong>for</strong> further 14 days, thereafter increasedby max. 1.2 mg/kg every 7–14 days; usual maintenance2.5–7.5 mg/kg (max. single dose 200 mg)twice dailyChild 12–18 years initially 50 mg daily <strong>for</strong> 14days then 50 mg twice daily <strong>for</strong> further 14 days,thereafter increased by max. 100 mg every 7–14days; usual maintenance 100–200 mg twice daily(up to 700 mg daily has been required)Adjunctive therapy of seizures (withoutenzyme inducing drugs) without valproateChild 2–12 years initially 300 micrograms/kgdaily in 1–2 divided doses <strong>for</strong> 14 days then600 micrograms/kg daily in 1–2 divided doses <strong>for</strong>further 14 days, thereafter increased by max.600 micrograms/kg every 7–14 days; usual maintenance1–10 mg/kg daily in 1–2 divided doses;max. 200 mg dailyChild 12–18 years initially 25 mg daily <strong>for</strong> 14days, increased to 50 mg daily <strong>for</strong> further 14 days,then increased by max. 100 mg every 7–14 days;usual maintenance 100–200 mg daily in 1–2divided dosesMonotherapy of seizuresChild 12–18 years initially 25 mg daily <strong>for</strong> 14days, increased to 50 mg daily <strong>for</strong> further 14 days,then increased by max. 100 mg every 7–14 days;usual maintenance as monotherapy, 100–200 mgdaily in 1–2 divided doses (up to 500 mg daily hasbeen required)Monotherapy of typical absence seizures. By mouthChild 2–12 years initially 300 micrograms/kgdaily in 1–2 divided doses <strong>for</strong> 14 days, then600 micrograms/kg daily in 1–2 divided doses <strong>for</strong>further 14 days, thereafter increased by max.600 micrograms/kg every 7–14 days; usual maintenance1–10 mg/kg daily in 1–2 divided doses (upto 15 mg/kg daily has been required)Note Dose titration should be repeated if restarting afterinterval of more than 5 daysSafe PracticeDo not confuse the different combinations; see alsonotes aboveLamotrigine (Non-proprietary) TATablets, lamotrigine 25 mg, net price 56-tab pack =£2.25; 50 mg, 56-tab pack = £3.07; 100 mg, 56-tabpack = £4.53; 200 mg, 30-tab pack = £27.53, 56-tabpack = £7.51. Label: 8, counselling, driving (see notesabove), skin reactions (see above)Dispersible tablets, lamotrigine 5 mg, net price 28-tab pack = £2.27; 25 mg, 56-tab pack = £2.91; 100 mg,56-tab pack = £5.86. Label: 8, 13, counselling, driving(see notes above), skin reactions (see above)Lamictal c (GSK) TATablets, yellow, lamotrigine 25 mg, net price 56-tabpack = £19.61; 50 mg, 56-tab pack = £33.35; 100 mg,56-tab pack = £57.53; 200 mg, 56-tab pack = £97.79.Label: 8, counselling, driving (see notes above), skinreactions (see above)Dispersible tablets, chewable, lamotrigine 2 mg, netprice 30-tab pack = £10.45; 5 mg, 28-tab pack = £7.82;25 mg, 56-tab pack = £19.61; 100 mg, 56-tab pack =£57.53. Label: 8, 13, counselling, driving (see notesabove), skin reactions (see above)LevetiracetamLevetiracetam is used <strong>for</strong> monotherapy and adjunctivetreatment of focal seizures with or without secondarygeneralisation, and <strong>for</strong> adjunctive treatment of myoclonicseizures in children with juvenile myoclonic epilepsy,and primary generalised tonic-clonic seizures.LEVETIRACETAMCautions avoid abrupt withdrawal; interactions:Appendix 1 (levetiracetam)Hepatic impairment halve dose in severe hepaticimpairment if estimated glomerular filtration rate lessthan 60 mL/minute/1.73 m 2Renal impairment reduce dose if estimated glomerularfiltration rate less than 80 mL/minute/1.73 m 2(consult product literature)Pregnancy see Pregnancy, p. 216Breast-feeding present in milk—manufactureradvises avoid; see also Breast-feeding, p. 217Side-effects anorexia, weight changes, abdominalpain, nausea, vomiting, dyspepsia, diarrhoea, cough,drowsiness, amnesia, ataxia, convulsion, dizziness,headache, tremor, hyperkinesia, malaise, impairedattention, aggression, agitation, depression, insomnia,anxiety, irritability, personality disorder, thrombocytopenia,myalgia, diplopia, blurred vision, rash; alsoreported pancreatitis, hepatic failure, paraesthesia,confusion, hallucinations, psychosis, suicidal ideation,leucopenia, neutropenia, pancytopenia, alopecia,toxic epidermal necrolysis, Stevens-JohnsonsyndromeIndication and doseMonotherapy of focal seizures with or withoutsecondary generalisation. By mouth or by intravenous infusionNote If switching between oral therapy and intravenoustherapy (<strong>for</strong> those temporarily unable to take oral medication),the intravenous dose should be the same as theestablished oral doseChild 16–18 years initially 250 mg once dailyincreased after 1 week to 250 mg twice daily;thereafter, increased according to response insteps of 250 mg twice daily every 2 weeks; max.1.5 g twice dailyAdjunctive therapy of focal seizures with orwithout secondary generalisation. By mouthChild 1–6 months initially 7 mg/kg once daily,increased gradually by max. 7 mg/kg twice dailyevery 2 weeks; max. 21 mg/kg twice daily

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