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Searched for Drug. Results 1421 to 1430 of 2582 total matches.

Ameluz for Actinic Keratoses

   
The Medical Letter on Drugs and Therapeutics • Dec 05, 2016  (Issue 1509)
on the face, forehead, or scalp who received red light treatment with either ALA or the drug vehicle ...
The FDA has approved a 10% nanoemulsion gel formulation of the porphyrin-based photosensitizer aminolevulinic acid hydrochloride (ALA; Ameluz – Biofrontera) for use in combination with a narrowband red light photodynamic therapy (PDT) lamp (BF-RhodoLED) for treatment of actinic keratoses (AKs) of mild to moderate severity on the face and scalp. A 20% ALA solution (Levulan Kerastick) approved for use in combination with blue light PDT (BLU-U) has been available in the US since 2002.
Med Lett Drugs Ther. 2016 Dec 5;58(1509):155-6 |  Show IntroductionHide Introduction

Obalon Balloon System - Another Gastric Balloon for Weight Loss

   
The Medical Letter on Drugs and Therapeutics • Jun 19, 2017  (Issue 1523)
devices for weight loss. Med Lett Drugs Ther 2015; 55:122. 4. FDA summary of safety and effectiveness ...
The FDA has approved the Obalon Balloon System (Obalon), a swallowable intragastric gas-filled balloon device, to facilitate weight loss in adults with a body mass index (BMI) of 30-40 kg/m2 who have not been able to lose weight through diet and exercise. Two other gastric balloon devices, ReShape and Orbera, were approved earlier.
Med Lett Drugs Ther. 2017 Jun 19;59(1523):102-3 |  Show IntroductionHide Introduction

An EUA for Anakinra (Kineret) for COVID-19 (online only)

   
The Medical Letter on Drugs and Therapeutics • Dec 12, 2022  (Issue 1665)
generally receive the antiviral drug remdesivir (Veklury)6 and the corticosteroid dexamethasone; those ...
The recombinant interleukin-1 (IL-1) receptor antagonist anakinra (Kineret – Sobi) has been granted an FDA Emergency Use Authorization (EUA) for treatment of hospitalized adults with confirmed COVID-19 pneumonia who require low- or high-flow supplemental oxygen, are at risk of progressing to severe respiratory failure, and are likely to have elevated plasma levels of soluble urokinase plasminogen activator receptor (suPAR). Anakinra has been available in the US for years; it is FDA-approved for multiple indications, including rheumatoid arthritis. Assays for suPAR are...
Med Lett Drugs Ther. 2022 Dec 12;64(1665):e203-4 |  Show IntroductionHide Introduction

Tenofovir Alafenamide (Vemlidy) for Hepatitis B

   
The Medical Letter on Drugs and Therapeutics • Jan 02, 2017  (Issue 1511)
liver disease. It is the first single-drug product containing tenofovir alafenamide (TAF), a prodrug ...
The FDA has approved tenofovir alafenamide (Vemlidy – Gilead) for treatment of chronic hepatitis B virus (HBV) infection in adults with compensated liver disease. It is the first single-drug product containing tenofovir alafenamide (TAF), a prodrug of the nucleotide reverse transcriptase inhibitor tenofovir, to become available; several combination products containing TAF are approved for treatment of HIV-1 infection. Tenofovir disoproxil fumarate (TDF; Viread – Gilead), another tenofovir prodrug, has been used for many years for treatment of chronic HBV infection; a generic...
Med Lett Drugs Ther. 2017 Jan 2;59(1511):6-8 |  Show IntroductionHide Introduction

Opicapone (Ongentys) - A COMT Inhibitor for Parkinson's Disease

   
The Medical Letter on Drugs and Therapeutics • Jan 11, 2021  (Issue 1615)
a dopa decarboxylase inhibitor such as carbidopa; most patients were also taking other drugs for PD ...
The FDA has approved opicapone (Ongentys – Neurocrine), a peripherally-acting reversible catechol-O-methyltransferase (COMT) inhibitor, for oral use as an adjunct to carbidopa/levodopa in adults with Parkinson’s disease (PD) who experience "off" episodes. It is the third COMT inhibitor to be approved for this indication; tolcapone (Tasmar, and generics) and entacapone (Comtan, and generics) were approved earlier. Opicapone has been available in Europe since 2016.
Med Lett Drugs Ther. 2021 Jan 11;63(1615):3-5 |  Show IntroductionHide Introduction

Bexagliflozin (Brenzavvy) — A Fifth SGLT2 Inhibitor for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
but are summarized in the package insert) in patients with type 2 diabetes that compared the new drug with placebo ...
Bexagliflozin (Brenzavvy – TheracosBio), a sodium-glucose cotransporter 2 (SGLT2) inhibitor, has been approved by the FDA to improve glycemic control in adults with type 2 diabetes. It is the fifth SGLT2 inhibitor to be approved in the US for this indication (see Table 4).
Med Lett Drugs Ther. 2023 Aug 21;65(1683):130-2   doi:10.58347/tml.2023.1683b |  Show IntroductionHide Introduction

Daprodustat (Jesduvroq) for Anemia of Chronic Kidney Disease

   
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024  (Issue 1696)
who have been on dialysis for at least 4 months. It is the first HIF-PHI and the first oral drug ...
The FDA has approved daprodustat (Jesduvroq – GSK), a hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI), for oral treatment of anemia due to chronic kidney disease (CKD) in adults who have been on dialysis for at least 4 months. It is the first HIF-PHI and the first oral drug to be approved in the US for this indication.
Med Lett Drugs Ther. 2024 Feb 19;66(1696):25-7   doi:10.58347/tml.2024.1696a |  Show IntroductionHide Introduction

Chloroxazone Hepatotoxicity

   
The Medical Letter on Drugs and Therapeutics • May 10, 1996  (Issue 974)
The Medical Letter  On Drugs and Therapeutics www.medletter.com Published by The Medical ...
The US Food and Drug Administration (FDA) recently approved a stronger warning about hepatotoxicity in the labeling for chlorzoxazone, a centrally-acting skeletal muscle relaxant.
Med Lett Drugs Ther. 1996 May 10;38(974):46 |  Show IntroductionHide Introduction

In Brief: An Over-the-Counter Retinoid for Acne

   
The Medical Letter on Drugs and Therapeutics • Sep 26, 2016  (Issue 1504)
, scaling, photosensitivity, erythema, burning, and pruritus. Although only small amounts of the drug ...
Differin Gel 0.1% (Galderma), a topical formulation of the retinoid adapalene, will soon be available over the counter (OTC) for once-daily treatment of acne in patients ≥12 years old. It is the first topical retinoid to be approved for sale over the counter.All topical retinoids normalize keratinization and appear to have anti-inflammatory effects; whether any one topical retinoid is more effective than any other is not clear. Many dermatologists now recommend topical retinoids for first-line treatment of acne; they can be used alone or in combination with antibiotics to treat both inflamed...
Med Lett Drugs Ther. 2016 Sep 26;58(1504):126 |  Show IntroductionHide Introduction

Azacitidine (Vidaza) for Myelodysplastic Syndrome

   
The Medical Letter on Drugs and Therapeutics • Jan 31, 2005  (Issue 1201)
Letter ® On Drugs and Therapeutics IN THIS ISSUE Volume 47 (Issue 1201) January 31, 2005 ...
Azacitidine (Vidaza - Pharmion), a pyrimidine nucleoside analog of cytidine, is the first drug approved by the FDA for treatment of myelodysplastic syndrome (MDS). Azacitidine is incorporated into newly synthesized DNA and inhibits DNA methyltransferase. Hypomethylation of DNA can restore the normal expression of genes critical for cell differentiation.
Med Lett Drugs Ther. 2005 Jan 31;47(1201):11 |  Show IntroductionHide Introduction