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Searched for Devices. Results 171 to 180 of 222 total matches.

Perfluorohexyloctane Ophthalmic Solution (Miebo) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • Jan 22, 2024  (Issue 1694)
treatments with Optilight, an FDA-approved device that delivers intense pulsed light, has been shown ...
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   doi:10.58347/tml.2024.1694c |  Show IntroductionHide Introduction

Treatment of Pressure Ulcers

   
The Medical Letter on Drugs and Therapeutics • Feb 23, 1990  (Issue 812)
, and air flow from the device can sharply increase insensible water loss, requiring careful attention ...
Pressure is the most critical factor in the development of pressure ulcers; high pressure applied constantly for two hours produces irreversible tissue ischemia and necrosis. Malnutrition, fecal and urinary incontinence, fractures, and a low serum albumin may be additional risk factors. Frequent turning and mobilization of patients, relieving pressure and allowing tissue reoxygenation, are the most effective means of prevention and treatment (PS Goode and RM Allman, Med Clin North Am, 73:1511, Nov 1989).
Med Lett Drugs Ther. 1990 Feb 23;32(812):17-8 |  Show IntroductionHide Introduction

Lifitegrast (Xiidra) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • Aug 29, 2016  (Issue 1502)
. STANDARD TREATMENT — Treatments for dry eye disease include artificial tears, ocular insert devices ...
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 IntroductionHide Introduction

Revefenacin (Yupelri) for COPD

   
The Medical Letter on Drugs and Therapeutics • Jan 28, 2019  (Issue 1564)
is required to administer the drug and the device may not be portable. Nebulizers and nebulized drugs ...
The FDA has approved revefenacin (Yupelri – Mylan/Theravance Biopharma), a long-acting antimuscarinic agent (LAMA) administered once daily by standard jet nebulizer, for maintenance treatment of chronic obstructive pulmonary disease (COPD). Revefenacin is the second nebulized LAMA to be approved for this indication; glycopyrrolate (Lonhala Magnair), which is administered twice daily with a portable handheld nebulizer, was the first.
Med Lett Drugs Ther. 2019 Jan 28;61(1564):14-5 |  Show IntroductionHide Introduction

Sofpironium (Sofdra) for Primary Axillary Hyperhidrosis

   
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024  (Issue 1709)
, and vesicular rash.5 MiraDry, an in-office device that uses microwave energy, permanently eliminates sweat ...
The FDA has approved a 12.45% gel formulation of the anticholinergic drug sofpironium (Sofdra – Botanix) for treatment of primary axillary hyperhidrosis (excessive underarm sweating) in patients ≥9 years old.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):133-4   doi:10.58347/tml.2024.1709c |  Show IntroductionHide Introduction

Comparison Chart: Correct Use of Inhalers for Asthma (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024  (Issue 1716)
the clear base from the inhaler device • Keep the cap closed • Avoid touching the piercing element ...
View the Comparison Chart: Correct Use of Inhalers for Asthma
Med Lett Drugs Ther. 2024 Nov 25;66(1716):e196-8   doi:10.58347/tml.2024.1716c |  Show IntroductionHide Introduction

Salmeterol

   
The Medical Letter on Drugs and Therapeutics • Apr 29, 1994  (Issue 921)
(200 µg) capsules and a Rotahaler device. 3. Available in 60-ampule packages; each 2-ml ampule ...
Salmeterol xinafoate (Serevent - Allen & Hanburys), a long-acting β 2 -selective adrenergic agonist for inhalation, has been approved by the US Food and Drug Administration for maintenance treatment of asthma, with or without concurrent use of inhaled corticosteroids. Salmeterol is not recommended for acute treatment of bronchospasm.
Med Lett Drugs Ther. 1994 Apr 29;36(921):37-8 |  Show IntroductionHide Introduction

Linezolid (Zyvox)

   
The Medical Letter on Drugs and Therapeutics • May 29, 2000  (Issue 1079)
treatment of VRE infection and the presence of a prosthetic device or undrained abscess (D Clemett ...
Linezolid, the first of a new class of antibiotics, the oxazolidinones, has been marketed for treatment of infection due to vancomycin-resistant Enterococcus faecium, nosocomial and community-acquired pueumonia due to Staphylococcus aureus or penicillin-sucsceptible Streptococcus pneumoniae, and skin and skin structure infections, including those due to methicillin-resistant S. aureus (MRSA).
Med Lett Drugs Ther. 2000 May 29;42(1079):45-6 |  Show IntroductionHide Introduction

More Resistance to Oseltamivir (Tamiflu)

   
The Medical Letter on Drugs and Therapeutics • Jan 26, 2009  (Issue 1304)
reactive airway disease or inability to use the inhaler device, oseltamivir (for treatment of potential ...
Since publication of our recent article on antiviral drugs for influenza, increased levels of resistance to oseltamivir (Tamiflu) have been detected in influenza A H1N1 strains.
Med Lett Drugs Ther. 2009 Jan 26;51(1304):5-6 |  Show IntroductionHide Introduction

Screening for Oral Cancer

   
The Medical Letter on Drugs and Therapeutics • Feb 23, 2009  (Issue 1306)
Plus (Zila Pharmaceuticals) is a combination device that uses fluorescent light and toluidine blue ...
The incidence of oral cancer appears to be increasing, especially in younger patients. Risk factors include use of tobacco and alcohol, and exposure to human papillomavirus. ViziLite Plus (Zila Pharmaceuticals) is a combination device that uses fluorescent light and toluidine blue tissue staining to help dentists identify abnormal changes in the mucous membranes of the oral cavity. Originally developed for detecting abnormal growths on the uterine cervix, in 2001 it received FDA clearance for "identification, evaluation, and monitoring of oral mucosal abnormalities in a patient population at...
Med Lett Drugs Ther. 2009 Feb 23;51(1306):15-6 |  Show IntroductionHide Introduction