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Kerolac 0.50% Eye Drop
Kerolac 0.50% Eye Drop
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Kerolac

Eye Drop - (0.50%)
arogga-brand
Gaco Pharmaceuticals(G.A Company Ltd)
Generic: Ketorolac Tromethamine 0.5% Eye prep
Out of Stock
Currently unavailable, please request or choose another variant.
54.70
৳ 60.18
9% OFF

Medicine Overview of Kerolac 0.50% Eye Drop

বাংলা
English
Indication
Allergic conjunctivitis, Postoperative eye inflammation, Cystoid macular oedema
Adult Dose
Allergic Conjunctivitis Indicated for temporary relief of ocular itching caused by seasonal allergic conjunctivitis Instill 1 drop in affected eye(s) q6hr Ocular Pain & Inflammation Indicated for pain and inflammation following catarac surgery Instill 1 drop in affected eye(s) four times daily starting 24 hr after surgery and continue up to 4 days after surgery Ocular Pain & Burning/Stinging Indicated to reduce ocular pain and burning/stinging following corneal refractive surgery Instill 1 drop in the operated eye PRN for up to 4 days postoperatively
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Child Dose
<2 years: Safety and efficacy not established Allergic Conjunctivitis Indicated for temporary relief of ocular itching caused by seasonal allergic conjunctivitis >2 years: Instill 1 drop in affected eye(s) q6hr (Acular) Ocular Pain & Inflammation >2 years: Instill 1 drop (Acular) in affected eye(s) q6hr starting 24 hr after surgery and continue through the first 2 weeks postoperatively Ocular Pain & Burning/Stinging Indicated to reduce ocular pain and burning/stinging following corneal refractive surgery >2 years: Instill 1 drop (Acular LS) in operated eye PRN for up to 4 days postoperatively
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Contraindication
Ketorolac Tromethamine is contraindicated in patients with known hypersensitivity to NSAIDs and any of the components of Ketorolac Tromethamine. Moreover, the patient with the history of asthma, nasal polyp, angioedema, peptic ulcer and bleeding, bleeding disorders are contraindicated for this drug.
Mode of Action
Ketorolac inhibits prostaglandin synthesis by decreasing the activity of the cyclooxygenase enzyme.
Precaution
Elderly, hepatic dysfunction, heart failure, predisposition to reduced blood volume or renal blood flow. Mild renal impairment; monitor renal function closely. Lactation: Unknown; use with caution
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Side Effect
>10% Transient ocular burning/stinging 1-10% Conjunctival hyperemia,Corneal edema,Iritis,Corneal infiltrates,Iritis,Corneal edema,Ocular inflammation,Ocular irritation,Ocular pain,Increased ocular pressure,Superficial keratitis,Superficial ocular infection <1% Blurred vision,Corneal ulcer,Corneal erosion,Corneal thinning,Perforation of cornea,Dry eyes,Epithelial breakdown,Corneal epithelial degeneration
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Interaction
May reduce effects of antihypertensives eg ACE inhibitors or angiotensin II receptor antagonists (AIIA). Increased risk of renal toxicity with ACE inhibitors, diuretics. Increased adverse effects with aspirin or other NSAIDs. Hallucinations may occur when used with fluoxetine, thiothixene, alprazolam. Potentially Fatal: Increased risk of GI bleeding with warfarin. May increase toxicity of methotrexate (MTX) and lithium. Increased plasma concentrations with probenecid.
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Disclaimer
The information provided herein is accurate, updated and complete as per the best practices of the Company. Please note that this information should not be treated as a replacement for physical medical consultation or advice. We do not guarantee the accuracy and the completeness of the information so provided. The absence of any information and/or warning to any drug shall not be considered and assumed as an implied assurance of the Company. We do not take any responsibility for the consequences arising out of the aforementioned information and strongly recommend you for a physical consultation in case of any queries or doubts.