Monotherapy in Parkinson's disease
Adult: As hydrochloride: Initially, 2.5 mg tid; increase gradually depending on clinical response to a total of 15-60 mg daily in divided doses.
Indications and Dosage
Oral
Monotherapy in Parkinson's disease Adult: As hydrochloride: Initially, 2.5 mg tid; increase gradually depending on clinical response to a total of 15-60 mg daily in divided doses.
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Contraindications
Closed-angle glaucoma, myasthenia gravis; paralytic ileus; pyloric stenosis and prostatic hyperplasia; hyperthyroidism; tachycardia.
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Special Precautions
Down's syndrome. Child. Acute MI; cardiac insufficiency; pyrexia. Severe hepatic impairment and renal failure. Pregnancy and lactation.
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Adverse Reactions
Dryness of the mouth, constipation, nausea, asthenia, vertigo, blurred vision, ataxia, fever, headache, rash, acute glaucoma.
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Overdosage
Symptoms: Dilated and sluggish pupils, warm and dry skin, facial flushing, dryness of mouth, pharynx, nose and bronchi, foul-smelling breath, elevated temperature, tachycardia, cardiac arrhythmias, decreased bowel sounds, urinary retention, delirium, disorientation, anxiety, hallucinations, illusions, confusion, incoherence, agitation, hyperactivity, ataxia, loss of memory, paranoia, combativeness, seizures.
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Drug Interactions
Effects may be enhanced by other drugs with antimuscarinic properties e.g. amantadine, antihistamines, phenothiazine antipsychotics and TCAs. MAOIs may possibly enhance antimuscarinic effects. May affect the absorption of other drugs. Antimuscarinics and parasympathomimetics may counteract each other's effects.
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Action
Description: Metixene is a tertiary antimuscarinic with both central and peripheral actions. It also has antihistaminic and direct antispasmodic effects.
Pharmacokinetics: Absorption: Absorbed from the GI tract. Metabolism: Hepatic via sulfoxydation and N-demethylation. Excretion: Via urine. |
MIMS Class
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