Drug Guide
Bisoprolol fumarate and hydrochlorothiazide
Classification
Therapeutic: Antihypertensive, combination
Pharmacological: Beta-adrenergic blocker (bisoprolol), Thiazide diuretic (hydrochlorothiazide)
FDA Approved Indications
- Hypertension
Mechanism of Action
Bisoprolol reduces heart rate and cardiac output by selective beta1-adrenergic blockade. Hydrochlorothiazide decreases blood volume and peripheral vascular resistance by promoting diuresis and salt excretion, leading to lowered blood pressure.
Dosage and Administration
Adult: Typically 1 tablet once daily. Dose may be adjusted based on response.
Pediatric: Not indicated for pediatric use.
Geriatric: Start at lower doses due to increased sensitivity and comorbidities.
Renal Impairment: Use caution; dose adjustments may be necessary.
Hepatic Impairment: Use with caution; monitor liver function.
Pharmacokinetics
Absorption: Well absorbed after oral administration.
Distribution: Bisoprolol is highly protein-bound (~30%).
Metabolism: Minimal hepatic metabolism; primarily excreted unchanged.
Excretion: Renally excreted; dose adjustment may be needed in renal impairment.
Half Life: Approximately 10-12 hours for bisoprolol.
Contraindications
- Known hypersensitivity to bisoprolol, hydrochlorothiazide, or other sulfonamide derivatives.
- Severe bradycardia, sinus node failure, or second- or third-degree AV block without a pacemaker.
- Uncompensated heart failure.
- Pulmonary edema.
Precautions
- Use cautiously in asthma or obstructive airway disease.
- Monitor for signs of hypotension or worsening heart failure.
- Pregnancy category C; use only if clearly needed during pregnancy. Breastfeeding: Use with caution; consult healthcare provider.
Adverse Reactions - Common
- Dizziness (Common)
- Fatigue (Common)
- Headache (Common)
- Gastrointestinal disturbances (Common)
Adverse Reactions - Serious
- Bradycardia (Serious)
- Hypotension (Serious)
- Electrolyte imbalance (hypokalemia, hyponatremia) (Serious)
- Bronchospasm (rare) (Serious)
Drug-Drug Interactions
- Other antihypertensives, digoxin, antiarrhythmics.
- NSAIDs may reduce diuretic effectiveness.
- Calcium channel blockers, especially non-dihydropyridines (verapamil, diltiazem).
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood pressure, heart rate, serum electrolytes, renal function.
Diagnoses:
- Risk for electrolyte imbalance
- Potential for decreased cardiac output
Implementation: Administer as directed, preferably in the morning. Monitor for side effects.
Evaluation: Assess blood pressure and heart rate regularly to ensure therapeutic effect and adjust dose accordingly.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Do not stop abruptly; consult provider before discontinuing.
- Report signs of dizziness, fatigue, or irregular heartbeat.
- Limit use of alcohol and avoid hot environments to prevent hypotension.
Special Considerations
Black Box Warnings:
- Use with caution in patients with bronchospastic conditions.
- Potential for masking hypoglycemia symptoms in diabetics.
Genetic Factors: Pharmacogenomic differences may influence drug metabolism and response.
Lab Test Interference: Hct and serum electrolyte levels may be altered.
Overdose Management
Signs/Symptoms: Severe bradycardia, hypotension, bronchospasm, cardiogenic shock.
Treatment: Supportive care, atropine for bradycardia, vasopressors for hypotension, mechanical ventilation if needed. Consider activated charcoal if ingestion recent.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F).
Stability: Stable under recommended storage conditions until expiration date.