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Searched for rapid. Results 11 to 20 of 109 total matches.

Table: Over the Counter At-Home Tests for COVID-19 (online only)

   
The Medical Letter on Drugs and Therapeutics • Oct 20, 2021  (Issue 5041)
test Symptomatic: 94%/98% Yes No N/A Rapid Test (iHealth) (symptomatic) or Asymptomatic: 85-88%/N.D ...
View the Table: Over the Counter At-Home Tests for COVID-19
Med Lett Drugs Ther. 2021 Oct 20;63(5041):e1   doi:10.58347/tml.2021.5041a |  Show IntroductionHide Introduction

Ophthalmic Phentolamine (Ryzumvi) for Drug-Induced Mydriasis

   
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024  (Issue 1705)
. It may be helpful for patients who need a more rapid return to normal vision after dilation. The Medical Letter ...
The FDA has approved a 0.75% ophthalmic solution of the alpha-adrenergic antagonist phentolamine (Ryzumvi – Viatris) for treatment of mydriasis produced by adrenergic agonists such as phenylephrine or parasympatholytic agents such as tropicamide in patients ≥3 years old. Ryzumvi is the first drug to be approved in the US for reversal of pharmacologically induced mydriasis.
Med Lett Drugs Ther. 2024 Jun 24;66(1705):100-1   doi:10.58347/tml.2024.1705c |  Show IntroductionHide Introduction

In Brief: Kirsty — An Insulin Aspart Interchangeable with NovoLog

   
The Medical Letter on Drugs and Therapeutics • Sep 08, 2025  (Issue 5120)
), a biosimilar to rapid-acting insulin aspart (NovoLog), for treatment of type 1 or type 2 diabetes. Kirsty ...
The FDA has approved Kirsty (Biocon), a biosimilar to rapid-acting insulin aspart (NovoLog), for treatment of type 1 or type 2 diabetes. Kirsty is the first rapid-acting insulin to become available in the US that has received interchangeability status with NovoLog; Merilog, another insulin aspart biosimilar, was approved earlier but has not received interchangeability status with NovoLog.
Med Lett Drugs Ther. 2025 Sep 8;67(5120):1-2   doi:10.58347/tml.2025.5120a |  Show IntroductionHide Introduction

Vazalore - A New Aspirin Formulation

   
The Medical Letter on Drugs and Therapeutics • May 02, 2022  (Issue 1649)
in immediaterelease, buffered, and enteric-coated formulations. Immediate-release aspirin is rapidly absorbed ...
The FDA has approved an over-the-counter (OTC) liquid-filled capsule formulation of aspirin (Vazalore – PLx Pharma). The manufacturer has been heavily promoting Vazalore with claims of fast, predictable absorption and antiplatelet activity and improved gastrointestinal safety compared to existing OTC aspirin formulations.
Med Lett Drugs Ther. 2022 May 2;64(1649):70-1 |  Show IntroductionHide Introduction

Benzgalantamine (Zunveyl) for Alzheimer's Disease

   
The Medical Letter on Drugs and Therapeutics • Apr 14, 2025  (Issue 1726)
, headache, and decreased appetite are common with rapid dose escalation of galantamine. Depression, fatigue ...
The FDA has approved Zunveyl (Alpha Cognition), a delayed-release formulation of the prodrug benzgalantamine, for treatment of mild to moderate dementia of Alzheimer's disease (AD). Immediate- and extended-release formulations of the acetylcholinesterase inhibitor galantamine have been available in the US for years for treatment of AD.
Med Lett Drugs Ther. 2025 Apr 14;67(1726):59-60   doi:10.58347/tml.2025.1726b |  Show IntroductionHide Introduction

Comparison Chart: Some Inhaled Drugs for Treatment of Asthma (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024  (Issue 1716)
to perform rapid, deep inhalation ▶ Doses may be wasted if Ellipta inhaler is opened/closed accidently ...
View the Comparison Chart: Some Inhaled Drugs for Treatment of Asthma
Med Lett Drugs Ther. 2024 Nov 25;66(1716):e192-5   doi:10.58347/tml.2024.1716b |  Show IntroductionHide Introduction

A Fixed-Dose Combination of Meloxicam and Rizatriptan (Symbravo) for Migraine

   
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025  (Issue 1727)
. PHARMACOKINETICS — The meloxicam component in Symbravo is absorbed more rapidly than conventional oral meloxicam ...
The FDA has approved Symbravo (Axsome), an oral fixed-dose combination of the nonsteroidal anti-inflammatory drug (NSAID) meloxicam and the 5-HT1B/1D receptor agonist (triptan) rizatriptan (Maxalt, and generics), for acute treatment of migraine with or without aura in adults. It is the second combination of an NSAID and a triptan to be approved for migraine treatment. An oral fixed-dose combination of sumatriptan and naproxen (Treximet, and generics) is approved for use in patients ≥12 years old.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):68-70   doi:10.58347/tml.2025.1727b |  Show IntroductionHide Introduction

Treatment of Common Respiratory Tract Infections

   
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023  (Issue 1674)
Diagnosis – GAS pharyngitis should be diagnosed by nucleic acid amplification test or rapid antigen ...
Most respiratory tract infections are caused by viruses. Bacterial respiratory tract infections are usually treated empirically with antibiotic therapy that targets the most probable causative pathogens. Recommended antibiotic regimens for outpatient treatment of some common respiratory tract infections are listed in Table 1 for adults and Table 2 for children.
Med Lett Drugs Ther. 2023 Apr 17;65(1674):57-62   doi:10.58347/tml.2023.1674a |  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)
of loop diuretics is often used to achieve rapid diuresis in acute decompensation or to overcome ...
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

COVID-19 Update: Tocilizumab (Actemra) FDA-Approved for Treatment of COVID-19 (online only)

   
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023  (Issue 1667)
dexamethasone and have rapidly increasing conventional oxygen needs and systemic inflammation. Dexamethasone ...
The interleukin-6 (IL-6) receptor antagonist tocilizumab (Actemra – Genentech) has been approved by the FDA for IV treatment of COVID-19 in hospitalized adults who are receiving a systemic corticosteroid and require supplemental oxygen, mechanical ventilation, or extracorporeal membrane oxygenation (ECMO). Tocilizumab was previously available for this indication under an Emergency Use Authorization (EUA); it remains available under an EUA for treatment of children 2-17 years old who are hospitalized with COVID-19 and require oxygen support.
Med Lett Drugs Ther. 2023 Jan 9;65(1667):e9   doi:10.58347/tml.2023.1667d |  Show IntroductionHide Introduction