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BYSTOLIC (nebivolol) tablets
2016-02-16 13:55:05 来源: 作者: 【 】 浏览:371次 评论:0
  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use BYSTOLIC safely and effectively. See full prescribing information for BYSTOLIC.
    BYSTOLIC ® (nebivolol) tablets, for oral use
    Initial U.S. Approval: 2007
     INDICATIONS AND USAGE

    BYSTOLIC is a beta-adrenergic blocking agent indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. (1.1)DOSAGE AND ADMINISTRATION

    Can be taken with and without food. Individualize to the needs of the patient and monitor during up-titration. (2)

    • Hypertension: Most patients start at 5 mg once daily. Dose can be increased at 2-week intervals up to 40 mg. (2.1)
    DOSAGE FORMS AND STRENGTHS

    Tablets: 2.5, 5, 10, 20 mg (3)

    CONTRAINDICATIONS

    • Severe bradycardia (4)
    • Heart block greater than first degree (4)
    • Patients with cardiogenic shock (4)
    • Decompensated cardiac failure (4)
    • Sick sinus syndrome (unless a permanent pacemaker is in place) (4)
    • Patients with severe hepatic impairment (Child-Pugh >B) (4)
    • Hypersensitive to any component of this product (4)

    WARNINGS AND PRECAUTIONS

    • Acute exacerbation of coronary artery disease upon cessation of therapy: Do not abruptly discontinue (5.1)
    • Diabetes: Monitor glucose as β-blockers may mask symptoms of hypoglycemia (5.5)
    ADVERSE REACTIONS

    Most common adverse reactions (6.1):

    • Headache, fatigue

    To report SUSPECTED ADVERSE REACTIONS, Contact Forest Laboratories, Inc. at 1-800-678-1605 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    DRUG INTERACTIONS
    • CYP2D6 enzyme inhibitors may increase nebivolol levels (7.1)
    • Reserpine or clonidine may produce excessive reduction of sympathetic activity. (7.2)
    • Both digitalis glycosides and β-blockers slow atrioventricular conduction and decrease heart rate. Concomitant use can increase the risk of bradycardia. (7.3)
    • Verapamil- or diltiazem-type calcium channel blockers may cause excessive reductions in heart rate, blood pressure, and cardiac contractility. (7.4)
    See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.

    Revised: 1/2014

  • FULL PRESCRIBING INFORMATION: CONTENTS*
  • 1. INDICATIONS AND USAGE

     

     

    1.1 Hypertension

    BYSTOLIC is indicated for the treatment of hypertension, to lower blood pressure [see Clinical Studies (14.1)]. BYSTOLIC may be used alone or in combination with other antihypertensive agents [see Drug Interactions (7)].

    Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes, including the class to which this drug principally belongs. There are no controlled trials demonstrating risk reduction with BYSTOLIC.

    Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program's Joint National Committee on Prevention, Detection, eva luation, and Treatment of High Blood Pressure (JNC).

    Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly.

    Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal.

    Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy.

  • 2. DOSAGE AND ADMINISTRATION

     

     

    2.1 Hypertension

    The dose of BYSTOLIC must be individualized to the needs of the patient. For most patients, the recommended starting dose is 5 mg once daily, with or without food, as monotherapy or in combination with other agents. For patients requiring further reduction in blood pressure, the dose can be increased at 2-week intervals up to 40 mg. A more frequent dosing regimen is unlikely to be beneficial.

     

    Renal Impairment

    In patients with severe renal impairment (ClCr less than 30 mL/min) the recommended initial dose is 2.5 mg once daily; titrate up slowly if needed. BYSTOLIC has not been studied in patients receiving dialysis [see Clinical Pharmacology (12.4)].

     

    Hepatic Impairment

    In patients with moderate hepatic impairment, the recommended initial dose is 2.5 mg once daily; titrate up slowly if needed. BYSTOLIC has not been studied in patients with severe hepatic impairment and therefore it is not recommended in that population [see Clinical Pharmacology (12.4)].

     

    2.2 Subpopulations

    Geriatric Patients

    It is not necessary to adjust the dose in the elderly [see use in Specific Populations (8.5)].

    CYP2D6 Polymorphism

    No dose adjustments are necessary for patients who are CYP2D6 poor metabolizers. The clinical effect and safety profile observed in poor metabolizers were similar to those of extensive metabolizers [see Clinical Pharmacology (12.3)].

  • 3. DOSAGE FORMS AND STRENGTHS

    BYSTOLIC is available as tablets for oral administration containing nebivolol hydrochloride equivalent to 2.5, 5, 10, and 20 mg of nebivolol.

    BYSTOLIC tablets are triangular-shaped, biconvex, unscored, differentiated by color and are engraved with “FL” on one side and the number of mg (2 ½, 5, 10, or 20) on the other side.

  • 4. CONTRAINDICATIONS

    BYSTOLIC is contraindicated in the following conditions:

    • Severe bradycardia
    • Heart block greater than first degree
    • Patients with cardiogenic shock
    • Decompensated cardiac failure
    • Sick sinus syndrome (unless a permanent pacemaker
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