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Brinzolamide

Topical carbonic anhydrase inhibitor (ophthalmic) · Antiglaucoma Agent

START
1 drop 1% in affected eye(s) twice daily
TYPICAL MAX
1 drop three times daily per eye
STOP IF
Hypersensitivity, severe ocular reaction, or corneal oedema
WATCH
IOP response, corneal status; sulfonamide allergy history
CDSCO approvedSchedule HATC S01EC04
Dose laddermg/d
1BID drop1.5TID drop
Renal dose adjustmenteGFR mL/min/1.73m²
FULLUsual topical dosing30AVOIDNot recommended (systemic CAI accumu…90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET2.5hPEAK4.6d10hDURATION
ONSET
1h · IOP fall
PEAK
2.5h · peak IOP effect
4.6d · RBC-bound
DURATION
10h · per dose
EXCRETION
Renal — unchanged drug and metabolite
route + CYP
INTERACTIONS
6 major
SEVERE in our sources
PREGNANCY
Limited data; use only if benefit outweighs risk.
FDA category + note
Top interactionssee all 8
  • AspirinSevereDatabaseDDInter
  • Bismuth SubsalicylateSevereDatabaseDDInter
  • Choline SalicylateSevereDatabaseDDInter
  • DiflunisalSevereDatabaseDDInter
Available in India

6 branded formulations. Look up specific brands in the Drugs workspace.

Mechanism

Inhibits carbonic anhydrase II in the ciliary processes, reducing aqueous humour formation and lowering intraocular pressure.

Indications

Elevated intraocular pressure in ocular hypertensionOpen-angle glaucoma

Dosing

Adult
1 drop of 1% suspension in the affected eye(s) 2–3 times daily.
Pediatric
Safety/efficacy not established (limited use).
Renal adjustment
Not recommended if CrCl <30 mL/min (systemic CAI accumulation).
Hepatic adjustment
Not studied; caution.
Geriatric
No specific adjustment.
Max dose
1 drop three times daily per eye

Pharmacokinetics

Onset
IOP reduction within hours
Peak effect
~2–3 h post-instillation
Duration
~8–12 h
Half-life
Long (RBC carbonic anhydrase binding; ~111 days systemic)
Bioavailability
Low systemic (topical)
Protein binding
~60%
Metabolism
Minimal (N-desethyl active metabolite)
Excretion
Renal (unchanged drug and metabolite)

Contraindications

  • Hypersensitivity to brinzolamide/sulfonamides
  • Severe renal impairment (CrCl <30)
  • Hyperchloraemic acidosis

Side effects

Common
Blurred visionBitter/abnormal tasteOcular discomfortDry eyeForeign-body sensation
Serious
  • Sulfonamide hypersensitivity (Stevens-Johnson, rare)
  • Corneal oedema (endothelial compromise)
  • Systemic acid-base disturbance (rare)

Pregnancy & lactation

Pregnancy

Limited data; use only if benefit outweighs risk.

Lactation

Unknown if excreted in human milk; caution.

Drug interactions

Aspirin
Severe
Database

Drug interaction classified as: distribution.

Source: DDInter

Bismuth Subsalicylate
Severe
Database

Clinical effect not specified

Source: DDInter

Choline Salicylate
Severe
Database

Clinical effect not specified

Source: DDInter

Diflunisal
Severe
Database

Drug interaction classified as: distribution

Source: DDInter

Phenyl Salicylate
Severe
Database

Clinical effect not specified

Source: DDInter

Salsalate
Severe
Database

Drug interaction classified as: distribution

Source: DDInter

High Dose Salicylates
Moderate
Database

CAI–salicylate interaction

Avoid combination

Source: Kimi deep-research + Cla

Oral Carbonic Anhydrase Inhibitors
Moderate
Database

Additive systemic CAI effect

Avoid concurrent systemic CAI

Source: Kimi deep-research + Cla

4 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Other Topical carbonic anhydrase inhibitor (ophthalmic) drugs

Ask House about Brinzolamide

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, BNF·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20