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Indication & Dosage
 
 
Oral
SMOKING CESSATION
Adult: Modified-release preparation: Initially, 150 mg once daily increased to 150 mg bid after 3 days. Period of treatment: 7-12 wk. To discontinue treatment if abstinence is not achieved by 7th wk. Max: 300 mg/day.
Elderly: 150 mg/day.
 
Oral
TREATMENT OF DEPRESSION
Adult:
   
Administration May be taken with or without food.
   
Precautions History of seizure disorders, bipolar disorders; MI or unstable heart disease; pregnancy; renal or hepatic impairment. Monitor BP before and after treatment; monitor wkly if used with nicotine products. May impair ability to drive and operate machinery. Avoid use within 2 wk of MAO inhibitor withdrawal.
   
Potentially Life-threatening 
Adverse Drug Reactions
Facial oedema; nausea, dry mouth, constipation, diarrhoea, anorexia; mouth ulcer; thirst; myalgia, arthralgia; insomnia, dream, abnormality, anxiety, disturbed concentration, dizziness, nervousness, tremor, dysphoria; rhinitis, increased cough, pharyngitis, sinusitis; dyspnoea, epistaxis, agitation, insomnia, tremor, headache, weight loss, vomiting, skin rash.
   
Adverse Drug Reactions Stevens-Johnson syndrome.
   
Interactions

Concurrent use with MAO inhibitors may cause acute toxicity symptoms and increased risk of fatality.

Neuroleptics, lithium and TCAs, benzodiazepine, alcohol, drugs that lower seizure threshold. Increased risk of side effects when co-admin with levodopa. Reduced hepatic clearance with fluoxetine. Caution when administering with agents that will affect hepatic drug metabolizing enzymes. Increased risk of toxicity when used with ritonavir.

   
   
 

 

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