Timoptic Ocudose

— THERAPEUTIC CATEGORIES —
  • Glaucoma

Timoptic Ocudose Generic Name & Formulations

General Description

Timolol (as maleate) 0.25%, 0.5%; (0.2mL/dose); oph soln; preservative-free.

Pharmacological Class

Noncardioselective beta-blocker.

See Also

How Supplied

Soln, gel—contact supplier; Ocudose—60

Generic Availability

YES

Mechanism of Action

Timolol maleate is a beta1 and beta2 (non-selective) adrenergic receptor blocking agent that does not have significant intrinsic sympathomimetic, direct myocardial depressant, or local anesthetic (membrane-stabilizing) activity. When applied topically on the eye, it has the action of reducing elevated, as well as normal intraocular pressure, whether or not accompanied by glaucoma. The precise mechanism of the ocular hypotensive action is not clearly established at this time. Tonography and fluorophotometry studies in man suggest that its predominant action may be related to reduced aqueous formation.

Timoptic Ocudose Indications

Indications

Elevated intraocular pressure in ocular hypertension or open-angle glaucoma.

Timoptic Ocudose Dosage and Administration

Adults and Children

<2yrs: not established. ≥2yrs: Initially 1 drop of 0.25% twice daily; max 1 drop of 0.5% twice daily. Transfer from other drugs, see full labeling.

Timoptic Ocudose Contraindications

Contraindications

Greater than 1st-degree AV block. Uncompensated cardiac failure. Cardiogenic shock. Sinus bradycardia. History of bronchospasm. Bronchial asthma. Severe COPD.

Timoptic Ocudose Boxed Warnings

Not Applicable

Timoptic Ocudose Warnings/Precautions

Warnings/Precautions

Not for use as sole agent in angle-closure glaucoma. Poor cardiac reserve should be controlled with digitalis and diuretics. Diabetes. Presbyopia. May mask hypoglycemia or thyrotoxicosis. Myasthenia gravis. Cerebrovascular insufficiency. Measure intraocular pressure after 4 weeks of treatment. Avoid abrupt cessation. Discontinue at 1st sign of cardiac failure and before surgery. Pregnancy. Nursing mothers: not recommended.

Timoptic Ocudose Pharmacokinetics

Metabolism

Hepatic.

Elimination

Renal. Half-life: ~2.9 hours.

Timoptic Ocudose Interactions

Interactions

May potentiate systemic β-blockers, reserpine, hypoglycemics and mydriatic effect of topical epinephrine. Additive cardiac and pulmonary effects with anticholinesterase miotics. May antagonize bronchodilation from β-adrenergic agonists. May cause conduction defects with calcium channel blockers, digoxin. May be potentiated by CYP2D6 inhibitors (eg, quinidine, SSRIs).

Timoptic Ocudose Adverse Reactions

Adverse Reactions

Ocular irritation, sensitization, rash, dizziness, blurred vision, corneal anesthesia, headache, GI upset, paresthesias. Systemic β-blocker effects (bradycardia, arrhythmias, hypotension, bronchospasm, heart failure). Aphakic maculopathy (rare).

Timoptic Ocudose Clinical Trials

See Literature

Timoptic Ocudose Note

Not Applicable

Timoptic Ocudose Patient Counseling

See Literature