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  2. Travoprost - Wikipedia

    en.wikipedia.org/wiki/Travoprost

    Travoprost, sold under the brand name Travatan among others, is a medication used to treat high pressure inside the eye including glaucoma. [4] Specifically it is used for open angle glaucoma when other agents are not sufficient. [5] [4] It is used as an eye drop. [4] Effects generally occur within two hours. [4]

  3. Travoprost/timolol - Wikipedia

    en.wikipedia.org/wiki/Travoprost/timolol

    Drug Information Portal. U.S. National Library of Medicine. This page was last edited on 31 October 2023, at 11:22 (UTC). Text is available under the Creative Commons ...

  4. Glaucoma medication - Wikipedia

    en.wikipedia.org/wiki/Glaucoma_medication

    Travatan: Increased USO (uveoscleral outflow ) Once daily: blurred vision, eyelid redness, eye discomfort, permanently darken iris, darken/thicken eyelashes Beta blockers: Timolol: Timoptic: Decrease aqueous production: Every 12 hours: 20-30%: bronchospams, bradycardia, depression, impotence Betaxolol: Betoptic: Decrease aqueous production ...

  5. List of drugs: Tr–Tri - Wikipedia

    en.wikipedia.org/wiki/List_of_drugs:_Tr–Tri

    Many drugs have more than one name and, therefore, the same drug may be listed more than once. Brand names and generic names are differentiated by capitalizing brand names. See also the list of the top 100 bestselling branded drugs, ranked by sales. Abbreviations are used in the list as follows: INN = International Nonproprietary Name

  6. Tafluprost - Wikipedia

    en.wikipedia.org/wiki/Tafluprost

    Tafluprost (trade names Taflotan by Santen Pharmaceutical, Zioptan by Merck in the US and Saflutan by Mundipharma in Australia) is a prostaglandin analogue.It is used topically (as eye drops) to control the progression of open-angle glaucoma and in the management of ocular hypertension, alone or in combination with other medication.

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  8. Dorzolamide - Wikipedia

    en.wikipedia.org/wiki/Dorzolamide

    Dorzolamide, developed by Merck, was the first medication in human therapy (market introduction 1995) that resulted from structure-based drug design. It was developed to circumvent the systemic side effects of acetazolamide which has to be taken orally.

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