Drug Guide
Dorzolamide Hydrochloride; Timolol Maleate
Classification
Therapeutic: Glaucoma agent
Pharmacological: Combination carbonic anhydrase inhibitor and beta blocker
FDA Approved Indications
- Open-angle glaucoma
- Ocular hypertension
Mechanism of Action
Dorzolamide inhibits carbonic anhydrase in the ciliary processes of the eye, reducing aqueous humor production, while Timolol is a non-selective beta-adrenergic receptor blocker that decreases aqueous humor formation, leading to lowered intraocular pressure.
Dosage and Administration
Adult: One drop in affected eye(s) twice daily.
Pediatric: Use not established; consult a pediatric ophthalmologist.
Geriatric: No specific dosage adjustment, but consider renal and hepatic function.
Renal Impairment: Use with caution; monitor intraocular pressure.
Hepatic Impairment: Use with caution; no specific dose adjustment.
Pharmacokinetics
Absorption: Absorbed through the eye tissues after topical administration.
Distribution: Minimal systemic absorption; some may enter systemic circulation.
Metabolism: Dorzolamide undergoes partial systemic hydrolysis; timolol undergoes hepatic metabolism.
Excretion: Renal and hepatic routes, depending on the component.
Half Life: Approximately 4-9 hours for timolol; not well-defined for dorzolamide, but generally in a similar range.
Contraindications
- Hypersensitivity to any component
- Reactive airway disease (asthma)
- Sinus bradycardia
- Second- or third-degree AV block
- Cardiac failure
Precautions
- Use with caution in patients with COPD, bronchospasm, or hypotension.
- Monitor intraocular pressure regularly.
- Use during pregnancy only if clearly needed.
Adverse Reactions - Common
- Ocular burning, stinging, or discomfort (Common)
- Blurred vision (Common)
- bitter taste in the mouth (Common)
Adverse Reactions - Serious
- Systemic effects of timolol (e.g., bradycardia, hypotension, bronchospasm) (Serious but less common)
- Allergic conjunctivitis or keratitis (Rare)
Drug-Drug Interactions
- Systemic beta-blockers (additive effects)
- Calcium channel blockers (bradycardia, hypotension)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor intraocular pressure, visual acuity, and for signs of ocular irritation.
Diagnoses:
- Risk for increased intraocular pressure
- Ineffective tissue perfusion
Implementation: Administer eye drops as prescribed; instruct on proper instillation technique; monitor for systemic side effects.
Evaluation: Assess intraocular pressure regularly; evaluate symptom relief.
Patient/Family Teaching
- Wash hands before and after use.
- Avoid touching the dropper tip to the eye or other surfaces.
- Report any signs of allergic reactions, eye irritation, or systemic side effects.
- Carry medical ID indicating use of beta-blocker if appropriate.
Special Considerations
Black Box Warnings:
- No known black box warnings.
- Systemic absorption of timolol may cause systemic adverse effects, especially in patients with cardiovascular or respiratory diseases.
Genetic Factors: No specific genetic factors impacting use.
Lab Test Interference: May interfere with serum potassium and blood glucose readings due to systemic absorption.
Overdose Management
Signs/Symptoms: Systemic absorption may cause bradycardia, hypotension, bronchospasm, hypoglycemia.
Treatment: Supportive care; monitor vital signs; administer atropine or vasoconstrictors if indicated; hemodialysis not effective for timolol.
Storage and Handling
Storage: Store at room temperature, 59°F to 86°F (15°C to 30°C).
Stability: Stable until expiration date if unopened; once opened, use within 6 weeks.