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Searched for days. Results 481 to 486 of 486 total matches.

Risks of Tramadol and Gabapentin Use for Pain

   
The Medical Letter on Drugs and Therapeutics • Feb 02, 2026  (Issue 1747)
was associated with an increased risk of dementia; the risk was highest with >90 days of use.5 In a recently ...
Tramadol (Ultram, and others) and gabapentin (Neurontin, and others) are increasingly being prescribed for treatment of chronic pain despite reports of serious adverse events associated with their use. Both drugs are touted as safer and less addictive than strong opioids, but supporting evidence is lacking.
Med Lett Drugs Ther. 2026 Feb 2;68(1747):22-4   doi:10.58347/tml.2026.1747d |  Show IntroductionHide Introduction

Booster Dose of the Pfizer/BioNTech COVID-19 Vaccine (Comirnaty)

   
The Medical Letter on Drugs and Therapeutics • Oct 18, 2021  (Issue 1635)
-CoV-2 infection (by 11.3-fold) and severe COVID-19 (by 19.5- fold) beginning 12 days after ...
On September 22, on the advice of its Vaccines and Related Biologic Products Advisory Committee, the FDA expanded the Emergency Use Authorization (EUA) for the Pfizer/BioNTech mRNA-based COVID-19 vaccine (Comirnaty) to include administration of a booster dose ≥6 months after a 2-dose primary series in adults who are ≥65 years old or at high risk for severe COVID-19 because of an underlying medical condition or frequent institutional or occupational exposure to SARS-CoV-2 (see Table 1). The FDA Advisory Committee recommended against authorization of a booster dose of Comirnaty...
Med Lett Drugs Ther. 2021 Oct 18;63(1635):161-2 |  Show IntroductionHide Introduction

Ublituximab (Briumvi) for Relapsing Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Mar 06, 2023  (Issue 1671)
Metabolism Proteolysis Half-life 22 days STANDARD TREATMENT ― Patients with highly-active relapsing MS ...
The FDA has approved the recombinant chimeric anti-CD20 antibody ublituximab-xiiy (Briumvi – TG Therapeutics) for IV 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). Two other anti-CD20 antibodies, IV ocrelizumab (Ocrevus) and SC ofatumumab (Kesimpta), are also FDA-approved for these indications.
Med Lett Drugs Ther. 2023 Mar 6;65(1671):36-8   doi:10.58347/tml.2023.1671c |  Show IntroductionHide Introduction

Depemokimab (Exdensur) for Severe Eosinophilic Asthma

   
The Medical Letter on Drugs and Therapeutics • Mar 16, 2026  (Issue 1750)
pens and syringes Route Subcutaneous Metabolism Degradation by proteolytic enzymes Half-life 48 days ...
The FDA has approved depemokimab (Exdensur – GSK), a long-acting interleukin-5 (IL-5) antagonist, for add-on maintenance treatment of severe asthma characterized by an eosinophilic phenotype in patients ≥12 years old. Depemokimab is the fourth IL-5-directed treatment to be approved in the US for this indication; the IL-5 antagonists mepolizumab (Nucala) and reslizumab (Cinqair) and the IL-5 receptor alpha antagonist benralizumab (Fasenra) were approved earlier.
Med Lett Drugs Ther. 2026 Mar 16;68(1750):44-6   doi:10.58347/tml.2026.1750b |  Show IntroductionHide Introduction

Risankizumab (Skyrizi) - An IL-23 Antagonist for Crohn's Disease

   
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022  (Issue 1666)
days (in patients with Crohn’s disease) Table 2. Risankizumab Clinical Trial Results Clinical ...
The injectable interleukin (IL)-23 antagonist risankizumab-rzaa (Skyrizi – Abbvie) has been approved by the FDA for treatment of moderately to severely active Crohn's disease (CD) in adults. Risankizumab was approved earlier for treatment of plaque psoriasis and psoriatic arthritis.
Med Lett Drugs Ther. 2022 Dec 26;64(1666):205-7 |  Show IntroductionHide Introduction

Drugs for Open-Angle Glaucoma

   
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025  (Issue 1727)
/day 183.50 Istalol (Bausch + Lomb) 0.5% soln* 2.5, 5 mL 1 drop qAM 208.40 Carbonic Anhydrase ...
Glaucoma is a progressive optic neuropathy associated with increased intraocular pressure (IOP; normal range 8-22 mm Hg), which is the only disease-related factor that can be modified. Topical drugs that lower IOP are the first line of treatment for open-angle glaucoma.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):65-8   doi:10.58347/tml.2025.1727a |  Show IntroductionHide Introduction