Metoprolol and labetalol are beta-blockers (beta-adrenergic blocking agents) used to treat high blood pressure (hypertension). Metoprolol is also used to treat heart pain (angina), congestive heart failure, hyperthyroidism, abnormal heart rhythms, and some neurologic conditions, and to prevent migraine headaches.

Labetalol may prove useful in preventing rebound hypertension following clonidine withdrawal. Because of negative inotropic effects, care is required when prescribing a beta-adrenoceptor blocking drug with class 1 antidysrhythmic agents such as disopyramide.

In contrast to metoprolol and esmolol (β 1 -selective antagonists), labetalol acts as competitive antagonist at α 1 and β receptors. Se hela listan på drugs.com Labetalol is a secondary amino compound formally derived from ammonia by replacing two of the hydrogens by 2- (3-carbamoyl-4-hydroxyphenyl)-2-hydroxyethyl and 4-phenylbutan-2-yl groups. It is an adrenergic antagonist used to treat high blood pressure. 2013-12-10 · Labetalol . DRUG CLASS AND MECHANISM: Labetalol is Alpha- and beta-adrenergic blocker drug that is used for treating high blood pressure.Nerves from the adrenergic nervous system travel from the spinal cord to arteries where they release norepinephrine. Labetalol Drug Class. Adrenergic antagonist.

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What is the drug class of labetalol? 5-10 mg bolus or 0.1-0.5 mg/kg. What is the adult dose of labetalol?

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Labetalol was found to be unequivocally a high-solubility compound.

These work by relaxing blood vessels and slowing the heart rate to improve blood flow and decrease blood pressure. Avexa(labetalol): Control of BP in severe HTN including severe HTN of pregnancy. Drug Interactions .
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LABETALOL: Normodyne, Various. Class: α/β-Adrenergic Blocker. Dosage Forms. Tablet: 100 mg, 200 mg, 300 mg. Image. Common FDA

Brand names: Normodyne, Trandate. Drug class (es): non-cardioselective beta blockers. Labetalol systemic is used in the treatment of: High Blood Pressure. Hypertensive Emergency. Labetalol belongs to the class of drugs that serve as competitive antagonists at both the α1 -adrenergic and β-adrenergic receptors (see Table 11.3).