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Searched for establish. Results 531 to 540 of 656 total matches.

Sodium Zirconium Cyclosilicate (Lokelma) for Hyperkalemia

   
The Medical Letter on Drugs and Therapeutics • Dec 03, 2018  (Issue 1561)
has never been established in controlled trials, and its use has been associated with serious adverse ...
The FDA has approved sodium zirconium cyclosilicate (Lokelma – AstraZeneca), an oral potassium binder that exchanges hydrogen and sodium for potassium in the gastrointestinal (GI) lumen, for treatment of non-life-threatening hyperkalemia in adults. Sodium zirconium cyclosilicate (SZC) is the third drug to be approved for this indication; sodium polystyrene sulfonate and patiromer (Veltassa) were approved earlier.
Med Lett Drugs Ther. 2018 Dec 3;60(1561):197-9 |  Show IntroductionHide Introduction

Siponimod (Mayzent) - A New Drug for Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • May 06, 2019  (Issue 1571)
; whether these changes are reversible when the drug is stopped remains to be established. PML, posterior ...
The FDA has approved siponimod (Mayzent – Novartis), a sphingosine 1-phosphate (S1P) receptor modulator, for oral treatment of adults with relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome (initial neurological episode), relapsing-remitting disease, and active secondary progressive MS (SPMS). Siponimod is the second S1P receptor modulator to be approved in the US; fingolimod (Gilenya), which is approved for oral treatment of relapsing forms of MS in patients ≥10 years old, was the first. The purine antimetabolite cladribine (Mavenclad) was also...
Med Lett Drugs Ther. 2019 May 6;61(1571):70-2 |  Show IntroductionHide Introduction

Trifarotene (Aklief) - A New Topical Retinoid for Acne

   
The Medical Letter on Drugs and Therapeutics • Dec 16, 2019  (Issue 1587)
, has not been established. CLINICAL STUDIES — In two 12-week, double-blind trials (PERFECT 1 and PERFECT 2), a total ...
The FDA has approved trifarotene 0.005% cream (Aklief – Galderma) for topical treatment of acne vulgaris in patients ≥9 years old. Trifarotene is the fourth topical retinoid to be approved in the US for treatment of acne; tretinoin (Retin-A, and others), adapalene (Differin, and generics), and tazarotene (Tazorac, and others) have been available by prescription for decades. Adapalene 0.1% gel has been available over the counter since 2016 for treatment of acne in patients ≥12 years old.
Med Lett Drugs Ther. 2019 Dec 16;61(1587):195-7 |  Show IntroductionHide Introduction

Brolucizumab (Beovu) for Age-Related Macular Degeneration

   
The Medical Letter on Drugs and Therapeutics • Feb 10, 2020  (Issue 1591)
. There is no established treatment for dry AMD. The neovascular (wet) form, characterized by an often rapid decrease ...
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

Rimegepant (Nurtec ODT) for Acute Treatment of Migraine

   
The Medical Letter on Drugs and Therapeutics • May 04, 2020  (Issue 1597)
). The safety of treating >15 migraine attacks in a 30-day period with rimegepant has not been established ...
The FDA has approved an orally disintegrating tablet (ODT) formulation of rimegepant (Nurtec ODT – Biohaven), a small-molecule calcitonin gene-related peptide (CGRP) receptor antagonist ("gepant"), for acute treatment of migraine with or without aura in adults. Rimegepant is the second oral gepant to become available in the US; ubrogepant (Ubrelvy), which is approved for the same indication, was the first. Four parenteral CGRP antagonists, erenumab (Aimovig), fremanezumab (Ajovy), galcanezumab (Emgality), and eptinezumab (Vyepti), are approved for prevention of...
Med Lett Drugs Ther. 2020 May 4;62(1597):70-2 |  Show IntroductionHide Introduction

Oliceridine (Olinvyk) - A New Opioid for Severe Pain

   
The Medical Letter on Drugs and Therapeutics • Mar 08, 2021  (Issue 1619)
has not been established. TOLERANCE — Tolerance to the analgesic effect of opioids develops at least as rapidly ...
Oliceridine (Olinvyk - Trevena), an IV opioid agonist, has been approved by the FDA for management of acute pain severe enough to require an opioid and for which alternative treatment options are inadequate.
Med Lett Drugs Ther. 2021 Mar 8;63(1619):37-9 |  Show IntroductionHide Introduction

Vibrant – An Oral Vibrating Capsule for Chronic Idiopathic Constipation

   
The Medical Letter on Drugs and Therapeutics • May 01, 2023  (Issue 1675)
and its long-term efficacy and safety remain to be established. The Vibrant capsule consists of a motor ...
The Vibrant orally administered vibrating capsule (Vibrant Gastro), an FDA-cleared medical device, is now available by prescription for treatment of adults with chronic idiopathic constipation (CIC) who have not experienced relief of their bowel symptoms by using laxative therapies at the recommended dosage for at least one month. It is the first drug-free treatment to be authorized by the FDA for this indication.
Med Lett Drugs Ther. 2023 May 1;65(1675):65-7   doi:10.58347/tml.2023.1675a |  Show IntroductionHide Introduction

Elafibranor (Iqirvo) for Primary Biliary Cholangitis

   
The Medical Letter on Drugs and Therapeutics • Dec 23, 2024  (Issue 1718)
mechanism by which elafibranor treats PBC is not established. It may inhibit bile acid synthesis through ...
Elafibranor (Iqirvo – Ipsen), a peroxisome proliferator-activated receptor (PPAR) agonist, has been granted accelerated approval by the FDA for treatment of primary biliary cholangitis (PBC) in adults. It is indicated for use in combination with ursodeoxycholic acid (ursodiol, UDCA; Urso, and others) in patients with an inadequate response to UDCA alone and as monotherapy in those unable to tolerate UDCA.
Med Lett Drugs Ther. 2024 Dec 23;66(1718):202-4   doi:10.58347/tml.2024.1718b |  Show IntroductionHide Introduction

Drugs for Helicobacter pylori Infection

   
The Medical Letter on Drugs and Therapeutics • Jul 17, 2017  (Issue 1525)
have not been established. 116 The Medical Letter ® Vol. 59 (1525) July 17, 2017 DURATION OF TREATMENT — Because ...
About 50% of the world’s population is infected with Helicobacter pylori. These gastric bacteria can cause chronic inflammation and have been associated with development of gastritis, peptic ulcer disease, gastric adenocarcinoma, and gastric mucosa-associated lymphoid tissue (MALT) lymphoma. Eradication of H. pylori can promote gastric healing, prevent recurrence of duodenal and gastric ulcers, and reduce the incidence of gastric cancer. Guidelines for treatment of H. pylori infection were updated recently.
Med Lett Drugs Ther. 2017 Jul 17;59(1525):113-7 |  Show IntroductionHide Introduction

Comparison Table: Some Drugs for Plaque Psoriasis (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024  (Issue 1712)
; causal relationship not established ▶ New onset and exacerbations of heart failure, pancytopenia ...
View the Comparison Table: Some Drugs for Plaque Psoriasis
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e160-6   doi:10.58347/tml.2024.1712b |  Show IntroductionHide Introduction