Brimonidine
0.2%
Brinzolamide
1%
Timolol
0.5%
Dosage Form & Strength
1 drop in affected eye(s) twice daily (~12 hours apart)
Adults Brimonidine ~2–3 h; Brinzolamide ~10–12 h; Timolol ~4–5 h – Half life
Open-angle glaucoma or ocular hypertension
Hypersensitivity; severe bronchial asthma/COPD; sinus bradycardia
Ocular irritation, dry mouth, fatigue, bradycardia, bronchospasm
Monitor HR/respiratory status; avoid abrupt withdrawal Long-term use duration
Additive effects with other glaucoma meds
Brimonidine: α2-agonist; Brinzolamide: CAI; Timolol: β-blocker
Lowers IOP by decreasing aqueous humor production and increasing outflow ~60–78% (ocular) Bioavailability
Ocular with systemic absorption Brimonidine hepatic CYP2D6; Brinzolamide unchanged; Timolol hepatic CYP2D6 Metabolism Brimonidine renal; Brinzolamide renal; Timolol renal excretion
Category C
Use with caution in severe renal impairment
Use caution in severe hepatic impairment
Safety not established (<18 yrs)
No dose adjustment needed
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