Drug Guide
Levobunolol Hydrochloride
Classification
Therapeutic: Beta-adrenergic blocker, ophthalmic agent
Pharmacological: Non-selective beta-adrenergic antagonist
FDA Approved Indications
- Ocular hypertension
- Open-angle glaucoma
Mechanism of Action
Levobunolol reduces intraocular pressure by decreasing aqueous humor formation through non-selective beta-adrenergic blockade in the ciliary body.
Dosage and Administration
Adult: Typically, one drop in affected eye(s) twice daily.
Pediatric: Use not well established; consult specialized references.
Geriatric: Start with lower frequency or concentration; monitor appropriately.
Renal Impairment: Use with caution; adjust dosing if necessary based on renal function.
Hepatic Impairment: Use caution; no specific dose adjustment established.
Pharmacokinetics
Absorption: Minimal systemic absorption when used ocularly.
Distribution: Widely distributed; primarily local action.
Metabolism: Metabolized minimally systemically; hepatic metabolism is limited.
Excretion: Primarily eliminated via urine.
Half Life: Approximately 4-6 hours, but ocular half-life may vary.
Contraindications
- Bronchial asthma or related bronchospastic conditions
- Sinus bradycardia
- AV block (second or third degree)
- Uncompensated heart failure
Precautions
- Use with caution in patients with cardiovascular diseases, diabetes, or thyroid disorders; ocular surface disease; systemic absorption risk.
Adverse Reactions - Common
- Ocular irritation, including subconjunctival hemorrhage (Common)
- Blurred vision (Common)
Adverse Reactions - Serious
- Systemic beta-blockade effects, such as bradycardia, hypotension, bronchospasm (Rare)
- Corneal anesthesia, keratopathy (Rare)
Drug-Drug Interactions
- Other systemic beta-blockers; calcium channel blockers (e.g., verapamil, diltiazem); digitalis glycosides
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor intraocular pressure pre- and post-treatment; assess for systemic beta-blocker effects; check for contraindications.
Diagnoses:
- Risk for systemic side effects such as bradycardia or bronchospasm
- Risk for ocular surface irritation
Implementation: Administer as prescribed; educate patient on proper instillation technique; counsel on warning signs of systemic effects.
Evaluation: Evaluate reduction in intraocular pressure and monitor for adverse effects.
Patient/Family Teaching
- Use drops exactly as prescribed.
- Inform about potential systemic side effects, including symptoms of bradycardia or breathing difficulties.
- Report any vision changes, eye irritation, or systemic symptoms promptly.
- Do not discontinue abruptly without consulting healthcare provider.
Special Considerations
Black Box Warnings:
- None specific for levobunolol.
Genetic Factors: Genetic variations in drug metabolism may influence individual response, but specific guidance is limited.
Lab Test Interference: May affect serum glucose levels in diabetic patients or thyroid function tests due to systemic absorption.
Overdose Management
Signs/Symptoms: Bradycardia, hypotension, bronchospasm, dizziness, fainting.
Treatment: Supportive care; administer atropine for bradycardia; avoid beta-agonists unless indicated; monitor cardiovascular status.
Storage and Handling
Storage: Store at room temperature, away from light and moisture.
Stability: Stable until the expiration date on the container.