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Atenolol/Chlorthalidone

    DEA Class;  Rx

    Common Brand Names; Tenoretic

    • Thiazide Combos

    Oral beta-blocker and long-acting thiazide diuretic; additive hypotensive activity; used qd for HTN; long-acting; beta-1-specific; hydrophilic, renally eliminated; lacks membrane-stabilizing activity (MSA) or intrinsic sympathomimetic properties (ISA).

    Indicated for the treatment of hypertension in patients who do not respond to monotherapy.
    NOTE: Individualize the dosage by titration of the separate components. If the optimal dose corresponds to the ratio contained in the combination formulation, this product can be used for convenient dosing.

    Anuria

    Cardiogenic shock

    Heart block 2°/3°

    Hypersensitivity to either component or sulfonamides

    Overt cardiac failure

    Sinus bradycardia

    Untreated pheochromocytoma

    No adverse effects specific to the combination have been observed; adverse effects limited to those previously reported with atenolol and chlorthalidone

    Atenolol

    • 2/3° AV block
    • Bradycardia
    • Cold extremities
    • Diarrhea
    • Drowsiness
    • Hypotension
    • Leg pain
    • Lethargy
    • Lightheadedness
    • Nausea
    • Postural hypotension
    • Unusual dreams
    • Vertigo

    Chlorthalidone

    • Blurred vision, xanthopsia
    • Constipation
    • Diarrhea
    • Dizziness
    • Electrolyte abnormalities
    • Headache, vasculitis
    • Hyperglycemia
    • Hyperuricemia
    • Hypotension
    • Impotence
    • Loss of appetite
    • Muscular spasticity, restlessness
    • Nausea/vomiting
    • Paresthesia
    • Photosensitivity, phototoxicity

    Surgery/Anesthesia: Chronically administered beta-blockers should not be routinely withdrawn prior to major surgery; however, impaired ability of the heart to respond to reflex adrenergic stimuli may augment the risks of general anesthesia and surgical procedures

    Bronchospastic disease

    Cerebrovascular insufficiency

    Correct hypokalemia before initiating therapy

    CHF, beta blockade carries the potential hazard of further depressing myocardial contractility and precipitating more severe failure

    Use caution in diabetes mellitus, fluid or electrolyte imbalance (hypochloremic alkalosis, hypercalcemia, hyponatremia), moderate or high cholesterol concentrations, history of asthma, hyperuricemia or gout, hypotension, SLE

    Hyperthyroidism/thyrotoxicosis, liver disease

    May aggravate digitalis toxicity

    Peripheral vascular disease

    Renal impairment

    Risk of male sexual dysfunction

    Sensitivity reactions may occur with or without history of allergy or asthma

    Compromised left ventricular function

    Patients receiving clonidine – discontinue atenolol several days prior to withdrawal of clonidine

    Pregnancy Category: D

    Lactation: excreted in breast milk, use caution

    Adults

    100 mg/day PO atenolol and 25 mg/day PO chlorthalidone.

    Geriatric

    100 mg/day PO atenolol and 25 mg/day PO chlorthalidone.

    Adolescents

    Safety and efficacy have not been established.

    Children

    Safety and efficacy have not been established.

    Infants

    Safety and efficacy have not been established.

    Neonates

    Safety and efficacy have not been established.

    Atenolol/Chlorthalidone

    tablet

    • 50mg/25mg
    • 100mg/25mg