Search Results for "1"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for 1. Results 491 to 500 of 2658 total matches.

Brolucizumab (Beovu) for Age-Related Macular Degeneration

   
The Medical Letter on Drugs and Therapeutics • Feb 10, 2020  (Issue 1591)
effective and has not been shown to improve vision.1,2 CLINICAL STUDIES — FDA approval of brolucizumab ...
Brolucizumab-dbll (Beovu — Novartis), a vascular endothelial growth factor (VEGF) inhibitor, has been approved by the FDA as an intravitreal injection for treatment of neovascular (wet) age-related macular degeneration (AMD). It is the fourth VEGF inhibitor to be approved in the US for this indication; bevacizumab (Avastin, and others), a VEGF inhibitor FDA-approved for treatment of breast cancer and other malignancies, has been used off-label for this indication for years.
Med Lett Drugs Ther. 2020 Feb 10;62(1591):23-4 |  Show IntroductionHide Introduction

Drugs for Sexually Transmitted Infections

   
The Medical Letter on Drugs and Therapeutics • Jun 27, 2022  (Issue 1653)
of the indications and dosages recommended here have not been approved by the FDA (see Table 1). PARTNER TREATMENT ...
This article includes recommendations for management of most sexually transmitted infections (STIs) other than HIV and viral hepatitis. Some of the indications and dosages recommended here have not been approved by the FDA (see Table 1).
Med Lett Drugs Ther. 2022 Jun 27;64(1653):97-104 |  Show IntroductionHide Introduction

Two New Drugs for Chronic ITP

   
The Medical Letter on Drugs and Therapeutics • Feb 09, 2009  (Issue 1305)
not compete for the same binding site as endogenous thrombopoietin. 1 PHARMACODYNAMICS — Administered ...
Romiplostim (Nplate - Amgen), a recombinant fusion protein injected subcutaneously, and eltrombopag (Promacta - GlaxoSmithKline), a non-peptide taken orally, have been approved by the FDA for treatment of chronic immune thrombocytopenic purpura (ITP) refractory to corticosteroids, immunoglobulins and/or splenectomy.
Med Lett Drugs Ther. 2009 Feb 9;51(1305):10-1 |  Show IntroductionHide Introduction

IV Amisulpride (Barhemsys) for Postoperative Nausea and Vomiting

   
The Medical Letter on Drugs and Therapeutics • Dec 28, 2020  (Issue 1614)
or motion sickness, female sex, nonsmoking status, age ...
The FDA has approved IV amisulpride (Barhemsys – Acacia), a selective dopamine-2 and -3 (D2/D3) receptor antagonist, for prevention and treatment of postoperative nausea and vomiting (PONV) in adults. It is the first antiemetic to be approved for rescue treatment of PONV in patients who have symptoms despite receiving antiemetic prophylaxis. Oral formulations of amisulpride are available in Europe for treatment of schizophrenia and acute psychotic episodes.
Med Lett Drugs Ther. 2020 Dec 28;62(1614):205-8 |  Show IntroductionHide Introduction

Brinzolamide--A New Topical Carbonic Anhydrase Inhibitor for Glaucoma

   
The Medical Letter on Drugs and Therapeutics • Sep 25, 1998  (Issue 1036)
by the FDA in a 1% ophthalmic suspension for treatment of elevated intraocular pressure due to ocular ...
Brinzolamide (Azopt - Alcon), a thieno-thiazine-6-sulfonamide carbonic anhydrase inhibitor, has been approved by the FDA in a 1% ophthalmic suspension for treatment of elevated intraocular pressure due to ocular hypertension or open-angle glaucoma. Brinzolamide is the second FDA-approved topical carbonic anhydrase inhibitor. Dorzolamide (Trusopt) was approved earlier (Medical Letter, 37:76, 1995).
Med Lett Drugs Ther. 1998 Sep 25;40(1036):95-6 |  Show IntroductionHide Introduction

FDA Requires Lower Dosing of Zolpidem

   
The Medical Letter on Drugs and Therapeutics • Jan 21, 2013  (Issue 1408)
and to recommend in their labeling consideration of a lower dose for men.1 No change will be required in the dose ...
On January 10, 2013, the FDA issued a news release to announce that it was requiring the manufacturers of the zolpidem-containing products Ambien, Ambien CR, Edluar and Zolpimist, which are all approved for treatment of insomnia, to lower the doses for women and to recommend in their labeling consideration of a lower dose for men. No change will be required in the dose of Intermezzo, a low-dose sublingual formulation of zolpidem for middle-of-the-night awakening, which is already recommended in a lower dose for women.
Med Lett Drugs Ther. 2013 Jan 21;55(1408):5 |  Show IntroductionHide Introduction

Jentadueto XR for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Aug 01, 2016  (Issue 1500)
The Medical Letter® on Drugs and Therapeutics Volume 58 (Issue 1500) August 1, 2016 Published ...
The FDA has approved Jentadueto XR (Boehringer Ingelheim/Lilly), a once-daily extended-release formulation of the dipeptidyl peptidase-4 (DPP-4) inhibitor linagliptin and the biguanide metformin, for oral treatment of type 2 diabetes. Linagliptin and metformin have been available for years in a twice-daily immediate-release combination (Jentadueto). Once-daily extended-release formulations combining metformin with the DPP-4 inhibitors saxagliptin (Kombiglyze XR) and sitagliptin (Janumet XR) are also available.
Med Lett Drugs Ther. 2016 Aug 1;58(1500):98-100 |  Show IntroductionHide Introduction

Venetoclax (Venclexta) for Chronic Lymphocytic Leukemia

   
The Medical Letter on Drugs and Therapeutics • Aug 01, 2016  (Issue 1500)
The Medical Letter® on Drugs and Therapeutics Volume 58 (Issue 1500) August 1, 2016 Published ...
The FDA has approved venetoclax (Venclexta – Abbvie/Genentech), an oral selective BCL-2 inhibitor, for treatment of chronic lymphocytic leukemia (CLL) in patients with a 17p deletion who have received at least one prior therapy. The 17p deletion is associated with a poor prognosis in patients with CLL; it is prevalent in about 20% of patients with relapsed CLL. Venetoclax is the fi rst BCL-2 inhibitor to become available in the US.
Med Lett Drugs Ther. 2016 Aug 1;58(1500):101-2 |  Show IntroductionHide Introduction

Lyumjev - A New Insulin Lispro for Diabetes

   
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020  (Issue 1609)
– Lilly), a faster-acting formulation of insulin lispro (Humalog), for treatment of type 1 and type 2 ...
The FDA has approved insulin lispro-aabc (Lyumjev – Lilly), a faster-acting formulation of insulin lispro (Humalog), for treatment of type 1 and type 2 diabetes in adults. Fiasp, a faster-acting formulation of insulin aspart (Novolog), was approved in 2017.
Med Lett Drugs Ther. 2020 Oct 19;62(1609):162-3 |  Show IntroductionHide Introduction

DaxibotulinumtoxinA (Daxxify) for Frown Lines (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
in the US for this indication (see Table 1). It is also approved for treatment of cervical dystonia in adults. MECHANISM ...
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