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Indication & Dosage
 
 
Oral
TREATMENT OF PSYCHOSES
Adult: Initially, 20-60 mg weekly, increased up to 250 mg once a wk in severe or resistant conditions.
   
Precautions Pregnancy and lactation; elderly; epilepsy; preexisting cardiac conduction problems; hypokalaemia, hypomagnesemia; hypothyroidism.
   
Potentially Life-threatening 
Adverse Drug Reactions
Lower threshold for seizures, blurring of vision, dry mouth, retention of urine, constipation, orthostatic hypotension, weight gain, impaired glucose tolerance, allergic skin rashes, cholestatic jaundice; extrapyramidal effects; delirium; agitation, anxiety, depression, euphoria; anorexia, constipation, diarrhoea; alopecia; amenorrhoea, hypoglycaemia; hyponatraemia; hypersalivation, nausea, vomiting; bronchospasm; reported increased risk of breast cancer.
   
Adverse Drug Reactions Blood dyscrasias; neuroleptic malignant syndrome; alteration of heart conduction leading to QT prolongation and life threatening arrhythmias.
   
Interactions

May produce neurotoxicity with lithium.

Orthostatic hypotension with MAOIs; may increase sedation with alcohol, hypnotics, antihistamines, opiates; antacids containing aluminum salts may decrease absorption; additive antimuscarinic effects with TCAs; may reduce bromocriptine's ability to reduce serum prolactin; amphetamines may increase phycosis; may inihibit antiparkinsonian effects of levodopa; may increase risk of extrapyrimidal symptoms with metoclopramide; may increase phenytoin levels (phenytoin may reduce penfluridol levels); possible additive effects on QT interval with type 1a antiarrhythmics, TCAs, some quinolone antibiotics (eg moxifloxacin), may have additive hypotensive effects with trazodone; may increase levels of valproic acid.

Avoid valerian, st john's wort, kava kava, gotta kola; increased risk of CNS depression.

   
   
 

 

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