Brinzolamide with brimonidine
Brand names: Simbrinza
This fixed-combination eye drop pairs brinzolamide, a topical carbonic anhydrase inhibitor, with brimonidine, a selective alpha-2 adrenergic agonist, to lower intraocular pressure in open-angle glaucoma and ocular hypertension when a single agent is insufficient.
Adult dose
Dose adjustments
SPC §4.2/§4.3: contraindicated in severe renal impairment. Not studied in patients with severe renal impairment (CrCl <30 ml/min) or in hyperchloraemic acidosis, as the brinzolamide component and its metabolite are excreted predominantly by the kidney. No numeric dose adjustment is stated for lesser degrees of impairment.
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Hypersensitivity to the active substances or to any of the excipients
- Hypersensitivity to sulphonamides
- Patients receiving monoamine oxidase (MAO) inhibitor therapy
- Patients on antidepressants which affect noradrenergic transmission (e.g. tricyclic antidepressants and mianserin)
- Patients with severe renal impairment
- Patients with hyperchloraemic acidosis
- Neonates and infants under the age of 2 years
Side effects
- Ocular hyperaemia and ocular allergic-type reactions (most common; approximately 6–7% of patients)
- Dysgeusia — bitter or unusual taste in the mouth following instillation (approximately 3% of patients)
- Somnolence, dizziness (common)
- Eye allergy, keratitis, eye pain, ocular discomfort, blurred vision, abnormal vision, conjunctival blanching (common)
- Hypotension (uncommon); bradycardia, tachycardia, arrhythmia, palpitations (uncommon)
- Serious sulphonamide-type reactions including Stevens-Johnson syndrome and toxic epidermal necrolysis (§4.4 — discontinue if they occur)
Interactions
- Monoamine oxidase (MAO) inhibitors — contraindicated (SPC §4.3, cross-referring to §4.5)
- Antidepressants affecting noradrenergic transmission, e.g. tricyclic antidepressants and mianserin — contraindicated (SPC §4.3, cross-referring to §4.5)
- Antihypertensives and/or cardiac glycosides — caution advised, as small decreases in blood pressure were observed in some patients (SPC §4.4)
- Other topical ophthalmic medicinal products — administer at least 5 minutes apart (SPC §4.2)
Clinical monograph
How it works
Brinzolamide inhibits carbonic anhydrase in the ciliary body to reduce aqueous humour formation, while brimonidine both decreases aqueous production and increases uveoscleral outflow, giving additive pressure reduction without a beta-blocker.
Prescribing in practice
- Brimonidine crosses the blood-brain barrier and is contraindicated in neonates and infants because of the risk of apnoea and CNS depression; brinzolamide is a sulfonamide, so avoid in those with sulfonamide hypersensitivity.
- Brinzolamide commonly causes transient blurred vision and a bitter or unusual taste, and brimonidine can cause drowsiness, dry mouth and allergic conjunctivitis.
- Use with caution in significant renal or hepatic impairment and with other systemic carbonic anhydrase inhibitors or CNS depressants.
Monitoring
Monitor intraocular pressure for response and review for sulfonamide-type reactions, ocular allergy and systemic effects such as taste disturbance or drowsiness.
Counselling the patient
- Instil twice daily; shake the bottle and press on the inner corner of the eye after each drop.
- Temporary blurring, a bitter taste, tiredness or a dry mouth may occur.
- Report a red, itchy eye or any rash, and let your clinician know if you are allergic to sulfa medicines.
Evidence & guidelines
This beta-blocker-free fixed combination is supported as an alternative dual therapy in glaucoma where beta-blockade is contraindicated or poorly tolerated.
Reference: NICE NG81; RCOphth; SmPC; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
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