Search Results for "Skin"
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Searched for Skin. Results 51 to 60 of 126 total matches.

Emrosi — Low-Dose, Biphasic Oral Minocycline for Rosacea

   
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025  (Issue 1720)
or severe disease) to 0 or 1 at 16 weeks (signifying clear or almost clear skin). A coprimary endpoint. 2 ...
Emrosi (Journey), an oral, low-dose, biphasic-release formulation of the tetracycline antibiotic minocycline, has been approved by the FDA for once-daily treatment of inflammatory lesions of rosacea (papules and pustules) in adults. Low-dose, biphasic-release doxycycline (Oracea, and generics) has been available for years for treatment of papulopustular rosacea.
Med Lett Drugs Ther. 2025 Jan 20;67(1720):10-1   doi:10.58347/tml.2025.1720b |  Show IntroductionHide Introduction

Comparison Chart: Topical Nonsteroidal Drugs for Atopic Dermatitis (online only)

   
The Medical Letter on Drugs and Therapeutics • Mar 02, 2026  (Issue 1749)
≥2 years: bid 2136.00 Nonmelanoma skin cancers have occurred Use restricted to ≤20% of body surface ...
View the Comparison Chart: Topical Nonsteroidal Drugs for Atopic Dermatitis
Med Lett Drugs Ther. 2026 Mar 2;68(1749):e41-2   doi:10.58347/tml.2026.1749d |  Show IntroductionHide Introduction

In Brief: Optune Pax — A Portable Device for Pancreatic Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 13, 2026  (Issue 1752)
ADVERSE EFFECTS — Skin irritation under the transducer arrays occurred in ≥75% of patients ...
Optune Pax (Novocure), a portable device that delivers low-intensity alternating electrical fields to the abdomen, has been approved by the FDA for use with gemcitabine and nab-paclitaxel (GnP) for treatment of locally advanced pancreatic cancer in adults. It is the first device to be approved in the US for treatment of pancreatic cancer. Similar devices are available for treatment of certain lung cancers (Optune Lua) and glioblastoma (Optune Gio).
Med Lett Drugs Ther. 2026 Apr 13;68(1752):e64   doi:10.58347/tml.2026.1752g |  Show IntroductionHide Introduction

Tirzepatide (Zepbound) for Obstructive Sleep Apnea

   
The Medical Letter on Drugs and Therapeutics • Feb 17, 2025  (Issue 1722)
, skin reactions, gastroparesis, ileus, and diabetic retinopathy complications can occur. ▶ Drug ...
The injectable glucose-dependent insulinotropic polypeptide (GIP)/glucagon-like peptide-1 (GLP-1) receptor agonist tirzepatide (Zepbound) has been approved by the FDA for treatment of moderate to severe obstructive sleep apnea (OSA) in adults with obesity. It is the first drug to be approved in the US for this indication. Zepbound is also approved for chronic weight management in adults with obesity and in those who are overweight and have at least one weightrelated comorbidity. Tirzepatide is also available as Mounjaro for treatment of type 2 diabetes.
Med Lett Drugs Ther. 2025 Feb 17;67(1722):29-31   doi:10.58347/tml.2025.1722c |  Show IntroductionHide Introduction

Tirbanibulin 1% Ointment (Klisyri) for Actinic Keratosis

   
The Medical Letter on Drugs and Therapeutics • May 03, 2021  (Issue 1623)
. ACTINIC KERATOSES (AKs) — Common in older, lighter-skinned people with a long history of sun exposure ...
Tirbanibulin, a microtubule inhibitor, has been approved by the FDA as a 1% ointment (Klisyri – Almirall) for topical treatment of actinic keratosis of the face or scalp.
Med Lett Drugs Ther. 2021 May 3;63(1623):70-1 |  Show IntroductionHide Introduction

DaxibotulinumtoxinA (Daxxify) for Frown Lines (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
directly into a muscle that pulls on overlying skin temporarily weakens the contractions of the injected ...
The FDA has approved daxibotulinumtoxinA-lanm (Daxxify – Revance), an acetylcholine release inhibitor and neuromuscular blocking agent, for temporary improvement in the appearance of moderate to severe glabellar (frown) lines associated with corrugator and/or procerus muscle activity. Daxxify is the fifth botulinumtoxin type A product to be approved in the US for this indication (see Table 1). It is also approved for treatment of cervical dystonia in adults
Med Lett Drugs Ther. 2024 Jul 22;66(1707):e121-2   doi:10.58347/tml.2024.1707g |  Show IntroductionHide Introduction

Expanded Table: Some Drugs for Inflammatory Bowel Disease (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 10, 2023  (Issue 1680)
, fluid retention, osteoporosis, osteonecrosis, cataracts, glaucoma, impaired skin healing, acne ...
View the Table: Some Drugs for Inflammatory Bowel Disease
Med Lett Drugs Ther. 2023 Jul 10;65(1680):e115-9   doi:10.58347/tml.2023.1680d |  Show IntroductionHide Introduction

In Brief: Oral Minoxidil for Hair Loss

   
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022  (Issue 1666)
efficacy for androgenetic alopecia: findings from a systematic review with meta-regression analyses. Skin ...
Topical minoxidil (Rogaine, and others), which is available over the counter, has been used for treatment of hair loss in men and women for more than 30 years. Recently published trials suggest that off-label use of a low dose of oral minoxidil may also be effective.
Med Lett Drugs Ther. 2022 Dec 26;64(1666):208 |  Show IntroductionHide Introduction

In Brief: Furoscix - A Subcutaneous Furosemide Infusor for Heart Failure

   
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023  (Issue 1668)
the device on an area of clean, dry skin on either side of the navel. Pressing the start button ...
The FDA has approved Furoscix (scPharmaceuticals), a subcutaneous formulation of the loop diuretic furosemide administered via a single-use, on-body infusor, for treatment of congestion due to fluid overload in adults with New York Heart Association (NYHA) Class II-III chronic heart failure (HF). Furosemide (Lasix, and generics) has been available for years in oral and IV formulations.
Med Lett Drugs Ther. 2023 Jan 23;65(1668):14-5   doi:10.58347/tml.2023.1668d |  Show IntroductionHide Introduction

In Brief: A New Endometrial Cancer Indication for Dostarlimab (Jemperli) (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
dysfunction, and skin reactions, can occur with use of dostarlimab. Serious complications can occur ...
The immune checkpoint inhibitor dostarlimab-gxly (Jemperli – GSK) has been approved by the FDA for use in combination with carboplatin and paclitaxel for treatment of adults with mismatch repair deficient (dMMR) or microsatellite instability-high (MSI-H) primary advanced or recurrent endometrial cancer. Dostarlimab was recently granted regular approval for treatment of adults with dMMR recurrent or advanced endometrial cancer that progressed on or following a prior platinum-containing regimen in any setting and who are not candidates for curative surgery or radiation.
Med Lett Drugs Ther. 2023 Aug 21;65(1683):e138   doi:10.58347/tml.2023.1683f |  Show IntroductionHide Introduction