Zolaren 1% (Ophthalmic Suspension)
5 ml drop: ৳ 500.00
Medicine Details
Category | Details |
---|---|
Generic | Brinzolamide |
Company | Incepta pharmaceuticals ltd |
Indications
- Treatment of elevated intraocular pressure in patients with ocular hypertension
- Treatment of elevated intraocular pressure in patients with open-angle glaucoma
Pharmacology
- Inhibition of carbonic anhydrase in the ciliary processes of the eye
- Decreases aqueous humor secretion
- Reduction in intraocular pressure
Dosage & Administration
- Shake well before use
- Insert 1 drop in the affected eye(s) three times daily
- Pediatric Use: One drop in the affected eye(s) 2 times daily in pediatric patient (4 weeks to 5 years age)
- Geriatric Use: No overall differences in safety or effectiveness observed between elderly and younger patients
- May be used concomitantly with other topical ophthalmic products to lower intraocular pressure
- If more than one topical ophthalmic drug is being used, the drugs should be administered at least ten minutes apart
Interaction
- Possible drug interactions with high-dose salicylate therapy in patients treated with oral carbonic anhydrase inhibitors
Contraindications
- Hypersensitivity to any component of this product
Side Effects
- Blurred vision
- Bitter, sour or unusual taste
- Blepharitis
- Dermatitis
- Dry eye
- Foreign body sensation
- Headache
- Hyperemia
- Ocular discharge
- Ocular discomfort
- Ocular keratitis
- Ocular pain
- Ocular pruritus
- Allergic reactions
- Alopecia
- Chest pain
- Conjunctivitis
- Dizziness
- Dry mouth
- Dyspnea
- Dyspepsia
- Eye fatigue
- Hypertonia
- Keratoconjunctivitis
- Lid margin crusting or sticky sensation
- Nausea
- Pharyngitis
- Tearing
- Urticaria
Pregnancy & Lactation
- Pregnancy Category C
- Use during pregnancy only if the potential benefit justifies the potential risk to the fetus
Precautions & Warnings
- Zolaren is a sulfonamide and absorbed systemically
- Potential serious adverse reactions including Stevens-Johnson syndrome, toxic epidermal necrolysis, fulminant hepatic necrosis, agranulocytosis, aplastic anemia, and other blood dyscrasias
- Sensitization may occur with repeated administration
- Discontinue use if serious reactions or hypersensitivity occur
- Not recommended in renal impairment patients
- Use with caution in patients with hepatic impairment
Overdose Effects
- Electrolyte imbalance
- Development of an acidosis state
- Possible nervous system effects
Therapeutic Class
- Drugs for miotics and glaucoma
Storage Conditions
- Store at room temperature & protect from light
- Do not touch dropper tip to any surface
- Contents should not be used more than four weeks after first opening of the bottle
- Protect from freezing
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