Suplac

Suplac

bromocriptine

Manufacturer:

Biolab

Distributor:

Biopharm
Concise Prescribing Info
Contents
Bromocriptine mesylate
Indications/Uses
Adult: Monotherapy or in combination w/ other antiparkinsonian drugs for all stages of idiopathic & postencephalitic Parkinson's disease. Hyperprolactinaemia in men. Adult & ped 7-17 yr: Prolactinomas: Conservative treatment of prolactin-secreting pituitary micro- or macro-adenomas; reduce tumour size & facilitate removal prior to surgery; after surgery if prolactin level is still elevated. Adjunct in acromegaly or alternative to surgery or RT.
Dosage/Direction for Use
Adult Parkinson's disease Monotherapy or combined therapy: 10-40 mg daily. Starting dose: 1.25 mg (½ tab) daily preferably in the evening. Gradually increase dose by 1.25 mg daily each wk in 2-3 divided doses. May further increase by 2.5 mg daily each wk if therapeutic response is not reached w/in 6-8 wk. Prolactinomas 1.25 mg (½ tab) bid or tid, gradually increased to several tab daily. Acromegaly Initially 1.25 mg (½ tab) bid or tid, gradually increasing to 10-20 mg daily. Hyperprolactinaemia in men 1.25 mg (½ tab) bid or tid, gradually increased to 5-10 mg daily. Paed (7-17 yr) Prolactinomas 1.25 mg (½ tab) bid or tid, gradually increased to several tab daily. Max daily dose: 20 mg in adolescent 13-17 yr, 5 mg in childn 7-12 yr. Acromegaly Initially 1.25 mg (½ tab) bid or tid, gradually increased to several tab daily. Max daily dose: 20 mg in adolescent 13-17 yr, 10 mg in childn 7-12 yr.
Administration
Should be taken with food.
Contraindications
Hypersensitivity to bromocriptine or ergot alkaloids. Patient w/ uncontrolled HTN; pre-existing valve problems. Toxaemia of pregnancy.
Special Precautions
Not to be used postpartum or in the puerperium in women w/ HTN, CAD, or symptoms or history of serious psychiatric disorders. Patients w/ hyperprolactinaemia (possible pituitary tumour). Carefully monitor BP, especially during 1st few days in postpartum women. Monitor signs of progressive fibrotic disorders eg, retroperitoneal fibrosis in patients on long-term, high dose therapy. Hypotensive reactions; may affect ability to drive or operate machinery. May result in ovulation; use contraceptive measures in patients not wishing to conceive; avoid oral contraceptives. Not to be used during pregnancy & lactation.
Adverse Reactions
Headache, migraine, dizziness, drowsiness, fatigue, insomnia, lightheadedness, faintness, fainting, sedation; nausea, vomiting, anorexia, abdominal cramps, epigastric pain, dyspepsia, constipation, diarrhea, dry mouth; postural hypotension, syncope, severe prolonged hypotension, shock, angina, palpitation, arrhythmia, ventricular tachycardia, bradycardia, edema, cold-induced vasospasm w/ pallor of fingers & toes, exacerbation of Raynaud's syndrome; nasal congestion, pulmonary infiltrates, pleural effusion; leg cramps, muscle cramps; rash, mottling skin, facial pallor, urticaria, hair loss; blurred vision, diplopia.
Drug Interactions
Enhanced adverse/toxic effect w/ ethyl alcohol. May enhance adverse/toxic effect of ethyl alcohol; bupropion. Enhanced vasoconstricting effect w/ β-blockers. Enhanced serotonergic effect w/ anti-parkinson's agents (MAOIs). Increased serum conc w/ CYP 3A4 inhibitors; macrolides. Enhanced hypotensive effect w/ barbiturates; levodopa. Enhanced hypertensive & vasoconstricting effect of α-/β-agonists. Diminished effects w/ metoclopramide; antipsychotics.
MIMS Class
Trophic Hormones & Related Synthetic Drugs
ATC Classification
G02CB01 - bromocriptine ; Belongs to the class of prolactine inhibitors. Used to suppress lactation.
Presentation/Packing
Form
Suplac tab 2.5 mg
Packing/Price
10 × 10's
Register or sign in to continue
Asia's one-stop resource for medical news, clinical reference and education
Already a member? Sign in
Register or sign in to continue
Asia's one-stop resource for medical news, clinical reference and education
Already a member? Sign in