Land: Singapore
Språk: engelska
Källa: HSA (Health Sciences Authority)
BUPROPION HCl
GLAXOSMITHKLINE PTE LTD
N06AX12
150 mg
TABLET, FILM COATED
BUPROPION HCl 150 mg
ORAL
Prescription Only
GlaxoSmithKline LLC d/b/a GlaxoSmithKline
ACTIVE
1999-06-16
WELLBUTRIN SR TM BUPROPION HYDROCHLORIDE QUALITATIVE AND QUANTITATIVE COMPOSITION _WELLBUTRIN SR_ is available as sustained-release, film-coated tablet each containing 150 mg of bupropion hydrochloride. INDICATIONS _WELLBUTRIN_ _SR _is indicated for the treatment of depressive illnesses. DOSAGE AND ADMINISTRATION _ _ _WELLBUTRIN SR _tablets should be swallowed whole. The tablets should not be cut, crushed or chewed as this may lead to an increased risk of adverse effects including seizures. Studies suggest that exposure to bupropion may be increased when sustained release bupropion tablets are taken with food (see _Pharmacokinetics_). USE IN ADULTS The maximum single dose of _WELLBUTRIN SR _is 150 mg. _ _ _WELLBUTRIN SR_ tablets should be taken twice daily with an interval of at least 8 hours between successive doses. Insomnia is a very common adverse event which is often transient. Insomnia may be reduced by avoiding dosing at bedtime (provided there is at least 8 hours between doses) or, if clinically indicated, dose reduction may be considered. Initial Treatment Dosing with _WELLBUTRIN SR_ Tablets should begin at 150 mg/day given as a single daily dose in the morning. If the 150 mg initial dose is adequately tolerated, patients who are not responding adequately may benefit from an increase to 300 mg/day, given as 150 mg twice daily, after an interval of at least one week. There should be an interval of at least 8 hours between successive doses. The maximum daily dose should not exceed 300 mg/day. Maintenance therapy It is generally agreed that acute episodes of depression require 6 months or longer of antidepressant drug treatment. USE IN CHILDREN AND ADOLESCENTS _ _ _WELLBUTRIN SR_ is not indicated for use in children or adolescents aged less than 18 years (see _Warnings and Precautions_). The safety and efficacy of _WELLBUTRIN_ _SR _ tablets in patients unde Läs hela dokumentet
WELLBUTRIN SR BUPROPION HYDROCHLORIDE QUALITATIVE AND QUANTITATIVE COMPOSITION _WELLBUTRIN SR_ is available as sustained-release, film-coated tablet each containing 150 mg of bupropion hydrochloride. CLINICAL INFORMATION INDICATIONS _WELLBUTRIN_ _SR _is indicated for the treatment of major depressive episodes. DOSAGE AND ADMINISTRATION _ _ Pharmaceutical form: Sustained-release (SR) film-coated tablet. _ _ _WELLBUTRIN SR _tablets should be swallowed whole. The tablets should not be cut, crushed or chewed as this may lead to an increased risk of adverse effects including seizures. Studies suggest that exposure to bupropion may be increased when sustained-release bupropion tablets are taken with food (see _Pharmacokinetics_). USE IN ADULTS The maximum single dose of _WELLBUTRIN SR _is 150 mg. _ _ _WELLBUTRIN SR_ tablets should be taken twice daily with an interval of at least eight hours between successive doses. Insomnia is a very common adverse event which is often transient. Insomnia may be reduced by avoiding dosing at bedtime (provided there is at least eight hours between doses) or, if clinically indicated, dose reduction may be considered . Initial treatment Dosing with _WELLBUTRIN SR_ tablets should begin at 150 mg/day given as a single daily dose in the morning. If the 150 mg initial dose is adequately tolerated, patients who are not responding adequately may benefit from an increase to 300 mg/day, given as 150 mg twice daily, after an interval of at least one week. There should be an interval of at least eight hours between successive doses. The maximum daily dose should not exceed 300 mg/day. Maintenance therapy It is generally agreed that acute episodes of depression require 6 months or longer of antidepressant drug treatment. USE IN CHILDREN AND ADOLESCENTS _ _ _WELLBUTRIN SR_ is not indicated for use in children or adolescents aged less than 18 years (see _Warnings and Precautions_). The safety and efficacy of _WELLBUTRIN_ _SR _ tablets in patients under 18 years of age have not been established. USE Läs hela dokumentet