Beta Blockers
Atenolol (tenormin ® )
Receptor(s) affected: ß1 Selective.
Dosing (Adults): Angina: Oral: 50 mg once daily; may increase to 100 mg/day. Some patients may require 200 mg/day. Post MI: I.V.: Early treatment: 5 mg slow I.V. over 5 minutes; may repeat in 10 minutes. If both doses are tolerated, may start oral atenolol 50 mg every 12 hours or 100 mg/day for 6-9 days postmyocardial infarction. Oral: Follow I.V. dose with 100 mg/day or 50 mg twice daily for 6 to 9 days postmyocardial infarction. [Supplied: 25, 50, 100mg tablets. Injection: 10ml (0.5mg/ml) ] |
Betaxolol (kerlone ®)
Receptor(s) affected: ß1
Dosing (Adults): [Supplied: 10, 20mg tablet] |
Bisoprolol (zebeta ®)
Receptor(s) affected:: ß1 [Selective inhibitor of beta1-adrenergic receptors; competitively blocks beta1-receptors, with little or no effect on beta2-receptors at doses <10 mg] Dosing (Adults): Hypertension (JNC 7): 2.5-10 mg once daily Elderly: Initial dose: 2.5 mg/day; may be increased by 2.5-5 mg/day; maximum recommended dose: 20 mg/day Dosing adjustment in renal/hepatic impairment: Clcr<40 mL/minute: Initial: 2.5 mg/day; increase cautiously. [Supplied: 5, 10 mg tablets] |
Carvedilol (coreg ®, coreg cr™)
Receptor(s) affected: ß1,ß2, alpha. Admin: Administer with food. Extended release capsules should not be crushed or chewed. Capsules may be opened and sprinkled on applesauce for immediate use.
Dosing (Adults): Hypertension:: Immediate release: 6.25 mg twice daily; if tolerated, dose should be maintained for 1-2 weeks, then increased to 12.5 mg twice daily. Dosage may be increased to a maximum of 25 mg twice daily after 1-2 weeks. Maximum dose: 50 mg/day. Extended release: Initial: 20 mg once daily, if tolerated, dose should be maintained for 1-2 weeks then increased to 40 mg once daily if necessary; maximum dose: 80 mg once daily. Left ventricular dysfunction following MI:: Oral: Note: Should be initiated only after patient is hemodynamically stable and fluid retention has been minimized. Immediate release: Initial 3.125 to 6.25 mg twice daily; increase dosage incrementally (ie, from 6.25-12.5 mg twice daily) at intervals of 3-10 days, based on tolerance, to a target dose of 25 mg twice daily. Extended release: Initial: 20 mg once daily; increase dosage incrementally at intervals of 3-10 days. Target dose: 80 mg once daily. Conversion from immediate release to extended release: [Supplied: 3.125 mg, 6.25 mg, 12.5 mg, 25 mg tablets. Extended release capsule: 10 mg, 20 mg, 40 mg, 80 mg ] |
Esmolol (brevibloc ®)
Receptor(s) affected: ß1
Dosing (Adults): Supraventricular tachycardia or gradual control of postoperative tachycardia/hypertension:: IV: Loading dose: 500 mcg/kg over 1 minute; follow with a 50 mcg/kg/minute infusion for 4 minutes; response to this initial infusion rate may be a rough indication of the responsiveness of the ventricular rate. Infusion may be continued at 50 mcg/kg/minute or, if the response is inadequate, titrated upward in 50 mcg/kg/minute increments (increased no more frequently than every 4 minutes) to a maximum of 200 mcg/kg/minute. Note: To achieve more rapid response, following the initial loading dose and 50 mcg/kg/minute infusion, rebolus with a second 500 mcg/kg loading dose over 1 minute, and increase the maintenance infusion to 100 mcg/kg/minute for 4 minutes. If necessary, a third (and final) 500 mcg/kg loading dose may be administered, prior to increasing to an infusion rate of 150 mcg/minute. After 4 minutes of the 150 mcg/kg/minute infusion, the infusion rate may be increased to a maximum rate of 200 mcg/kg/minute (without a bolus dose). Supraventricular tachycardias (SVT); usual dose range: Usual dosage range: 50-200 mcg/kg/minute with average dose of 100 mcg/kg/minute.
Supplied: Injection, solution, as hydrochloride: 10 mg/mL (10 mL) [premixed in sodium chloride] Brevibloc®: 10 mg/mL (10 mL) [premixed in sodium chloride]; 20 mg/mL (5 mL) [double strength; premixed in sodium chloride]; 250 mg/mL (10 mL) |
Labetalol (normodyne ®)
Receptor(s) affected: ß1,ß2, alpha
Dosing (Adults): [Supplied: 100, 200, 300mg tablets; 5 mg/ml--20ml vial] |
Metoprolol (lopressor ®)
Receptor(s) affected: ß1 Dosing (Adults): Hypertension: Oral: 100-450 mg/day in 2-3 divided doses, begin with 50 mg twice daily and increase doses at weekly intervals to desired effect; usual dosage range (JNC 7): 50-100 mg/day Extended release: Same daily dose administered as a single dose . Angina, SVT, MI prophylaxis: Oral: 100-450 mg/day in 2-3 divided doses, begin with 50 mg twice daily and increase doses at weekly intervals to desired effect. Extended release: Same daily dose administered as a single dose. Hypertension/ventricular rate control: I.V. (in patients having nonfunctioning GI tract): Initial: 1.25-5 mg every 6-12 hours; titrate initial dose to response. Initially, low doses may be appropriate to establish response; however, up to 15 mg every 3-6 hours has been employed. Congestive heart failure: Oral (extended release): Initial: 25 mg once daily (reduce to 12.5 mg once daily in NYHA class higher than class II); may double dosage every 2 weeks as tolerated, up to 200 mg/day Myocardial infarction (acute): I.V.: 5 mg every 2 minutes for 3 doses in early treatment of myocardial infarction; thereafter give 50 mg orally every 6 hours 15 minutes after last I.V. dose and continue for 48 hours; then administer a maintenance dose of 100 mg twice daily. Elderly: Oral: Initial: 25 mg/day; usual range: 25-300 mg/day. Extended release: 25-50 mg/day initially as a single dose; increase at 1- to 2-week intervals. --------------------------------------------------------- |
Nadolol (corgard ®)
Receptor(s) affected: ß1,ß2
Dosing (Adults): [Supplied: 20, 40, 80, 120, 160mg tablets] |
Nebivolol -bystolic®
DESCRIPTION The chemical name for the active ingredient in BYSTOLIC (nebivolol) tablets is (1RS,1'RS)-1,1'-[(2RS,2'SR)-bis(6-fluoro-3,4-dihydro-2H-1-benzopyran-2-yl)]- 2,2'-iminodiethanol hydrochloride. Nebivolol is a racemate composed of d-Nebivolol and l-Nebivolol with the stereochemical designations of [SRRR]-nebivolol and [RSSS]-nebivolol, respectively. INDICATIONS AND USAGE DOSAGE AND ADMINISTRATION Renal Impairment Hepatic Impairment HOW SUPPLIED |
Pindolol (visken ®)
Receptor(s) affected: ß1,ß2, ISA
Dosing (Adults): [Supplied: 5, 10mg tablet] |
Propranolol (inderal ®)
Receptor(s) affected: ß1,ß2
Dosing (Adults): Essential tremor: Oral: Adults: 20-40 mg twice daily initially; maintenance doses: usually 120-320 mg/day. Hypertension: Initial: 40 mg twice daily; increase dosage every 3-7 days; usual dose: 320 mg divided in 2-3 doses/day; maximum daily dose: 640 mg; usual dosage range (JNC 7): 40-160 mg/day in 2 divided doses. Long-acting formulation: Initial: 80 mg once daily; usual maintenance: 120-160 mg once daily; maximum daily dose: 640 mg; usual dosage range (JNC 7): 60-180 mg/day once daily Hypertrophic subaortic stenosis: Oral: Adults: 20-40 mg 3-4 times/day. Long-acting formulation: 80-160 mg once daily. Migraine headache prophylaxis: Initial: 80 mg/day divided every 6-8 hours; increase by 20-40 mg/dose every 3-4 weeks to a maximum of 160-240 mg/day given in divided doses every 6-8 hours; if satisfactory response not achieved within 6 weeks of starting therapy, drug should be withdrawn gradually over several weeks. Long-acting formulation: Initial: 80 mg once daily; effective dose range: 160-240 mg once daily. Myocardial infarction prophylaxis: Oral: Adults: 180-240 mg/day in 3-4 divided doses. Pheochromocytoma: Oral: Adults: 30-60 mg/day in divided doses Tachyarrhythmias: Thyrotoxicosis: Oral: Adults: Oral: 10-40 mg/dose every 6 hours. I.V.: Adults: 1-3 mg/dose slow IVP as a single dose. SUPPLIED: |
Sotalol (betapace ®)
Receptor(s) affected: ß1,ß2
Dosing (Adults):
Ventricular arrhythmias (Betapace®, Sorine®): Atrial fibrillation or atrial flutter (Betapace AF®): Initial: 80 mg twice daily. If the initial dose does not reduce the frequency of relapses of atrial fibrillation/flutter and is tolerated without excessive QT prolongation (not >520 msec) after 3 days, the dose may be increased to 120 mg twice daily. This may be further increased to 160 mg twice daily if response is inadequate and QT prolongation is not excessive. Elderly: Age does not significantly alter the pharmacokinetics of sotalol, but impaired renal function in elderly patients can increase the terminal half-life, resulting in increased drug accumulation Dosage adjustment in renal impairment: Adults: Impaired renal function can increase the terminal half-life, resulting in increased drug accumulation. Sotalol (Betapace AF®) is contraindicated per the manufacturer for treatment of atrial fibrillation/flutter in patients with a Clcr<40 mL/minute. Ventricular arrhythmias (Betapace®, Sorine®): Atrial fibrillation/flutter (Betapace AF®): SUPPLIED: |
Timolol (blocadren ®)
Receptor(s) affected: ß1,ß2 Treatment of hypertension and angina, to reduce mortality following myocardial infarction, and for prophylaxis of migraine. Dosing (Adults): Start 10 mg orally twice a day. Hypertension: Initial: 10 mg twice daily, increase gradually every 7 days, usual dosage: 20-40 mg/day in 2 divided doses; maximum: 60 mg/day Prevention of myocardial infarction: 10 mg twice daily initiated within 1-4 weeks after infarction Migraine headache: Initial: 10 mg twice daily, increase to maximum of 30 mg/day [Supplied: 5, 10, 20mg tablet] |
Reference(s)
National Institutes of Health, U.S. National Library of Medicine, DailyMed Database.
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