Matching articles for "ophthalmic cyclosporine"

Perfluorohexyloctane Ophthalmic Solution (Miebo) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • January 22, 2024;  (Issue 1694)
The FDA has approved perfluorohexyloctane ophthalmic solution (Miebo – Bausch+Lomb) for treatment of dry eye disease. Available only by prescription, Miebo is the first ophthalmic product to be approved in...
The FDA has approved perfluorohexyloctane ophthalmic solution (Miebo – Bausch+Lomb) for treatment of dry eye disease. Available only by prescription, Miebo is the first ophthalmic product to be approved in the US that specifically targets tear evaporation caused by meibomian gland dysfunction. An ophthalmic solution with a similar name, Meibo Tears (Vista), which contains 0.6% propylene glycol, is available over the counter for dry eye relief.
Med Lett Drugs Ther. 2024 Jan 22;66(1694):13-4 | Show Full IntroductionHide Full Introduction

Cyclosporine Ophthalmic Emulsion (Verkazia) for Vernal Keratoconjunctivitis

   
The Medical Letter on Drugs and Therapeutics • May 1, 2023;  (Issue 1675)
The FDA has approved Verkazia (Santen), a 0.1% ophthalmic emulsion formulation of the calcineurin inhibitor cyclosporine, for treatment of vernal keratoconjunctivitis (VKC). Verkazia is the first product to...
The FDA has approved Verkazia (Santen), a 0.1% ophthalmic emulsion formulation of the calcineurin inhibitor cyclosporine, for treatment of vernal keratoconjunctivitis (VKC). Verkazia is the first product to be approved in the US for this indication.
Med Lett Drugs Ther. 2023 May 1;65(1675):70-2 | Show Full IntroductionHide Full Introduction

Varenicline Nasal Spray (Tyrvaya) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • December 13, 2021;  (Issue 1639)
Tyrvaya (Oyster Point), a nasal spray formulation of the cholinergic agonist varenicline, has been approved by the FDA for treatment of dry eye disease. It is the first nasal spray to be approved in the...
Tyrvaya (Oyster Point), a nasal spray formulation of the cholinergic agonist varenicline, has been approved by the FDA for treatment of dry eye disease. It is the first nasal spray to be approved in the US for this indication. An oral formulation of varenicline (Chantix, and generics) has been available for years for smoking cessation.
Med Lett Drugs Ther. 2021 Dec 13;63(1639):198-9 | Show Full IntroductionHide Full Introduction

Loteprednol 0.25% (Eysuvis) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • May 17, 2021;  (Issue 1624)
The FDA has approved loteprednol etabonate ophthalmic suspension 0.25% (Eysuvis – Kala) for short-term treatment (≤2 weeks) of dry eye disease. It is the first ocular corticosteroid to be approved...
The FDA has approved loteprednol etabonate ophthalmic suspension 0.25% (Eysuvis – Kala) for short-term treatment (≤2 weeks) of dry eye disease. It is the first ocular corticosteroid to be approved for this indication. Other formulations of loteprednol are approved for treatment of steroid-responsive ocular inflammatory conditions, inflammation after ocular surgery, and seasonal allergic conjunctivitis.
Med Lett Drugs Ther. 2021 May 17;63(1624):75-7 | Show Full IntroductionHide Full Introduction

Drugs for Common Eye Disorders

   
The Medical Letter on Drugs and Therapeutics • December 2, 2019;  (Issue 1586)
This issue includes reviews of drugs for glaucoma, age-related macular degeneration (AMD), bacterial conjunctivitis, and dry eye disease. Allergic conjunctivitis is reviewed in a separate...
This issue includes reviews of drugs for glaucoma, age-related macular degeneration (AMD), bacterial conjunctivitis, and dry eye disease. Allergic conjunctivitis is reviewed in a separate issue.
Med Lett Drugs Ther. 2019 Dec 2;61(1586):187-94 | Show Full IntroductionHide Full Introduction

Cyclosporine 0.09% Solution (Cequa) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • July 29, 2019;  (Issue 1577)
The FDA has approved cyclosporine 0.09% ophthalmic solution (Cequa – Sun) to increase tear production in patients with keratoconjunctivitis sicca (dry eye disease). Restasis, a 0.05% cyclosporine...
The FDA has approved cyclosporine 0.09% ophthalmic solution (Cequa – Sun) to increase tear production in patients with keratoconjunctivitis sicca (dry eye disease). Restasis, a 0.05% cyclosporine emulsion, was approved in the US in 2003 for the same indication.
Med Lett Drugs Ther. 2019 Jul 29;61(1577):116-8 | Show Full IntroductionHide Full Introduction

Lifitegrast (Xiidra) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • August 29, 2016;  (Issue 1502)
The FDA has approved a 5% ophthalmic solution of lifitegrast (Xiidra – Shire), a lymphocyte function-associated antigen-1 (LFA-1) antagonist, for treatment of the signs and symptoms of dry eye...
The FDA has approved a 5% ophthalmic solution of lifitegrast (Xiidra – Shire), a lymphocyte function-associated antigen-1 (LFA-1) antagonist, for treatment of the signs and symptoms of dry eye disease. Lifitegrast is the first LFA-1 antagonist to be approved for any indication in the US.
Med Lett Drugs Ther. 2016 Aug 29;58(1502):110-1 | Show Full IntroductionHide Full Introduction