Labegest 200 mg is a dual-action alpha- and beta-adrenoceptor blocker used to manage various forms of hypertension and related cardiovascular conditions. It effectively lowers blood pressure without causing reflex tachycardia, making it suitable for chronic hypertension, pregnancy-induced hypertension, and situations where rapid or controlled blood pressure reduction is required. Labegest also plays a role in managing angina in hypertensive patients, catecholamine excess, and pheochromocytoma.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Alpha- and Beta-Adrenoceptor Blocking Drugs
Labegest 200 mg is indicated for:
Hypertension
All grades of essential hypertension
Pregnancy-induced hypertension
Cardiovascular Conditions
Angina in hypertensive patients
Hypertensive episodes during anesthesia
Hypertension related to catecholamine excess or pheochromocytoma
Labegest 200 mg works by competitively blocking β-receptors in the myocardium, bronchial and vascular smooth muscle, and α1-receptors in vascular smooth muscle. This dual blockade reduces blood pressure without reflex tachycardia. Labegest also exhibits mild β2-agonist and membrane-stabilizing activity.
Alpha-blockade: Attenuates pressor responses to stimuli such as phenylephrine or cold exposure.
Beta1-blockade: Lowers resting heart rate and blunts exercise-induced tachycardia.
Beta2-blockade: Inhibits isoproterenol-induced decrease in diastolic blood pressure.
Labetalol reduces cardiac output slightly, decreases total peripheral resistance, and lowers plasma renin activity, contributing to overall antihypertensive effects.
Oral (Adults):
Initial dose: 100 mg twice daily, alone or with diuretics
Titration: Increase in 100 mg increments every 2–3 days as needed
Maintenance: 200–400 mg twice daily
Severe hypertension: 1,200–2,400 mg per day (split doses or thrice daily for tolerability)
Intravenous (Adults):
Bolus injection: 50 mg IV over ≥1 minute, repeat every 5 minutes if needed (max 200 mg)
IV infusion: 1 mg/ml diluted in compatible fluids (5% dextrose, 0.9% saline)
Pregnancy-induced hypertension: Start at 20 mg/hr, double every 30 minutes up to 160 mg/hr
Acute myocardial infarction: Start at 15 mg/hr, increase gradually to max 120 mg/hr
Hypotensive anesthesia:
IV induction: 10–30 mg depending on patient condition
Incremental doses: 5–10 mg until desired blood pressure achieved
Halothane concentration: ≤1–1.5% due to synergistic effects
Pediatric Use:
Safety and efficacy not established
Elderly:
Initiate at 100 mg twice daily; lower maintenance doses may be sufficient due to slower drug elimination
Synergistic hypotension: With halothane, nitroglycerin
Bioavailability changes: Increased with cimetidine; decreased with glutethimide
Other interactions: Tremor with tricyclic antidepressants; bradycardia/heart block with calcium channel blockers (e.g., verapamil, diltiazem)
Obstructive airway disease (e.g., asthma)
Second or third-degree heart block
Cardiogenic shock, severe/prolonged hypotension
Uncompensated heart failure
Severe bradycardia
Common and serious side effects may include:
Postural hypotension, dizziness, lightheadedness
Fatigue, weakness, headache
Rash, scalp tingling
Gastrointestinal symptoms: nausea, vomiting, epigastric pain
Liver injury in rare cases
Difficulty in urination
Pregnancy Category C: Use only if benefits outweigh risks
Teratogenic studies in animals showed no consistent fetal malformations, though increased fetal resorption was observed at high doses
Neonates of treated mothers may experience hypotension, bradycardia, hypoglycemia, and respiratory depression
Small amounts excreted in breast milk; caution advised
Patients with pheochromocytoma, DM, non-allergic bronchospasm, or compromised cardiac function
May mask hypoglycemia symptoms in diabetics
Avoid abrupt withdrawal to prevent angina exacerbation
Monitor closely in hepatic impairment, elderly, pregnant, or lactating patients
Store in a cool, dry place, protected from light
Keep out of reach of children.
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