BRINZOLAMIDE

N/A

Manufactured by Sandoz Inc

21,426 FDA adverse event reports analyzed

Last updated: 2026-04-14

About BRINZOLAMIDE

BRINZOLAMIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Sandoz Inc. The most commonly reported adverse reactions for BRINZOLAMIDE include TREATMENT FAILURE, DYSPNOEA, DRUG INEFFECTIVE, DIZZINESS, EYE PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for BRINZOLAMIDE.

Top Adverse Reactions

TREATMENT FAILURE1,429 reports
DYSPNOEA564 reports
DRUG INEFFECTIVE499 reports
DIZZINESS479 reports
EYE PAIN468 reports
DIARRHOEA459 reports
FATIGUE454 reports
FALL433 reports
HEADACHE426 reports
VISION BLURRED418 reports
ASTHENIA410 reports
MALAISE386 reports
BLINDNESS361 reports
NAUSEA361 reports
ARTHRALGIA360 reports
INTRAOCULAR PRESSURE INCREASED328 reports
COUGH311 reports
PRURITUS309 reports
OFF LABEL USE308 reports
VOMITING305 reports
EYE IRRITATION303 reports
SOMNOLENCE293 reports
BLOOD PRESSURE INCREASED284 reports
PYREXIA278 reports
GLAUCOMA277 reports
INSOMNIA277 reports
OCULAR DISCOMFORT274 reports
ABDOMINAL PAIN273 reports
MYALGIA268 reports
SYNCOPE268 reports
TACHYCARDIA263 reports
CHILLS259 reports
DECREASED APPETITE256 reports
HYPERSENSITIVITY242 reports
COMA240 reports
HAEMORRHAGIC STROKE239 reports
HAEMATEMESIS238 reports
ABDOMINAL PAIN UPPER236 reports
SEPSIS233 reports
HEAD DISCOMFORT227 reports
OCULAR HYPERAEMIA226 reports
CARDIO RESPIRATORY ARREST225 reports
TINNITUS224 reports
ALTERED STATE OF CONSCIOUSNESS220 reports
AMAUROSIS FUGAX218 reports
ASCITES218 reports
VISUAL IMPAIRMENT215 reports
CATARACT214 reports
GENERALISED OEDEMA206 reports
DIPLOPIA205 reports
PRESYNCOPE203 reports
HAEMATURIA200 reports
PHOTOPHOBIA199 reports
URINARY TRACT DISORDER191 reports
PAIN186 reports
DRUG INTERACTION162 reports
VISUAL ACUITY REDUCED143 reports
HAEMOGLOBIN DECREASED141 reports
DEATH128 reports
CONDITION AGGRAVATED126 reports
HYPERTENSION123 reports
PAIN IN EXTREMITY117 reports
CONFUSIONAL STATE111 reports
DRY EYE110 reports
PNEUMONIA105 reports
BRADYCARDIA104 reports
EYE PRURITUS104 reports
DRUG HYPERSENSITIVITY103 reports
BACK PAIN96 reports
ACUTE KIDNEY INJURY95 reports
RASH95 reports
ASTHMA93 reports
GAIT DISTURBANCE89 reports
NASOPHARYNGITIS85 reports
ANAEMIA83 reports
ATRIAL FIBRILLATION81 reports
LACRIMATION INCREASED81 reports
TOXIC EPIDERMAL NECROLYSIS76 reports
HYPOTENSION75 reports
ANXIETY74 reports
EYE SWELLING74 reports
GENERAL PHYSICAL HEALTH DETERIORATION74 reports
WEIGHT DECREASED74 reports
ERYTHEMA73 reports
EYE DISORDER73 reports
PRODUCT QUALITY ISSUE73 reports
CHEST PAIN72 reports
DRY MOUTH72 reports
TREMOR72 reports
DEPRESSION69 reports
JOINT SWELLING68 reports
ABDOMINAL DISCOMFORT67 reports
BLINDNESS UNILATERAL67 reports
HYPONATRAEMIA66 reports
PALPITATIONS66 reports
MUSCULAR WEAKNESS65 reports
CEREBROVASCULAR ACCIDENT64 reports
DYSPEPSIA64 reports
FOREIGN BODY SENSATION IN EYES64 reports
CONSTIPATION63 reports

Report Outcomes

Out of 8,461 classified reports for BRINZOLAMIDE:

Serious 59.4%Non-Serious 40.6%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female4,662 (60.8%)
Male2,994 (39.0%)
Unknown18 (0.2%)

Reports by Age

Age 75189 reports
Age 78154 reports
Age 77150 reports
Age 83149 reports
Age 82145 reports
Age 72143 reports
Age 81140 reports
Age 76130 reports
Age 79123 reports
Age 80117 reports
Age 73107 reports
Age 69106 reports
Age 70104 reports
Age 85104 reports
Age 71101 reports
Age 84100 reports
Age 6598 reports
Age 7497 reports
Age 6687 reports
Age 6085 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with BRINZOLAMIDE?

This profile reflects 21,426 FDA FAERS reports that mention BRINZOLAMIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for BRINZOLAMIDE?

Frequently reported terms in FAERS include TREATMENT FAILURE, DYSPNOEA, DRUG INEFFECTIVE, DIZZINESS, EYE PAIN, DIARRHOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures BRINZOLAMIDE?

Labeling and FAERS entries often list Sandoz Inc in connection with BRINZOLAMIDE. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.