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Searched for days. Results 91 to 100 of 486 total matches.

Antiviral Drugs for Seasonal Influenza for 2025-2026

   
The Medical Letter on Drugs and Therapeutics • Oct 27, 2025  (Issue 1740)
of symptoms by about one day.6-8 Although most controlled trials of antiviral drugs have not been powered ...
Influenza is generally a self-limited illness, but complications including pneumonia, respiratory failure, and death can occur, especially in persons at increased risk (see Table 1).
Med Lett Drugs Ther. 2025 Oct 27;67(1740):169-74   doi:10.58347/tml.2025.1740a |  Show IntroductionHide Introduction

Comparison Chart: Interleukin (IL) Antagonists and Oral JAK Inhibitors for Moderate to Severe Atopic Dermatitis (online only)

   
The Medical Letter on Drugs and Therapeutics • Mar 02, 2026  (Issue 1749)
not controlled with other systemic drugs 100 mg/day with topical therapy: IGA response rate: 37% EASI-75: 56 ...
View the Comparison Chart: Interleukin (IL) Antagonists and Oral JAK Inhibitors for Moderate to Severe Atopic Dermatitis
Med Lett Drugs Ther. 2026 Mar 2;68(1749):e43-4   doi:10.58347/tml.2026.1749e |  Show IntroductionHide Introduction

Molnupiravir - An Oral Antiviral Drug for COVID-19

   
The Medical Letter on Drugs and Therapeutics • Jan 24, 2022  (Issue 1642)
with the Delta variant) with symptom onset within 5 days of randomization and at least one risk factor ...
The investigational oral antiviral drug molnupiravir (Merck/Ridgeback Biotherapeutics) was granted an FDA Emergency Use Authorization (EUA) on December 23, 2021 for treatment of mild to moderate COVID-19 in outpatients ≥18 years old who are at high risk of progressing to severe disease, including hospitalization or death (see Table 1), and for whom alternative treatment options are not available or clinically appropriate. Paxlovid (Pfizer), nirmatrelvir copackaged with ritonavir, was granted an EUA on December 22, 2021. The IV antiviral drug remdesivir (Veklury) was approved by the...
Med Lett Drugs Ther. 2022 Jan 24;64(1642):10-1 |  Show IntroductionHide Introduction

Fruquintinib (Fruzaqla) for Metastatic Colorectal Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024  (Issue 1696)
or placebo once daily for 21 days of each 28-day cycle, each in addition to best supportive care. Median ...
Fruquintinib (Fruzaqla – Takeda), an oral kinase inhibitor, has been approved by the FDA for treatment of adults with metastatic colorectal cancer (mCRC) who received prior fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, anti-VEGF therapy, and, in patients with RAS wild-type mutations, anti-EGFR therapy. The drug can be used in patients with mCRC regardless of biomarker status. Fruquintinib is the first drug to become available in the US for treatment of mCRC that targets 3 VEGF receptor kinases.
Med Lett Drugs Ther. 2024 Feb 19;66(1696):e34-5   doi:10.58347/tml.2024.1696f |  Show IntroductionHide Introduction

Iloprost (Aurlumyn) for Frostbite

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
daily treatment for up to 8 days with aspirin plus either buflomedil 400 mg, iloprost 0.5-2 ng/kg/ min ...
The FDA has approved Aurlumyn (Eicos Sciences), an IV formulation of the prostacyclin analog iloprost, to reduce the risk of digit amputation in adults with severe frostbite. Iloprost is the first drug to be approved by the FDA for treatment of severe frostbite; it has been used off-label for this indication in the EU and elsewhere for decades. In the US, iloprost is also available as an inhaled formulation (Ventavis) for treatment of pulmonary arterial hypertension.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):114   doi:10.58347/tml.2024.1707b |  Show IntroductionHide Introduction

Two Vonoprazan Combinations (Voquezna) for H. pylori

   
The Medical Letter on Drugs and Therapeutics • Oct 31, 2022  (Issue 1662)
in the US, the eradication rate was 87% in patients who had been treated with bismuth quadruple therapy for 14 days.3 H ...
The FDA has approved vonoprazan, a potassium-competitive acid blocker, copackaged with amoxicillin (Voquezna Dual Pak – Phathom) and with amoxicillin and clarithromycin (Voquezna Triple Pak) for treatment of Helicobacter pylori infection in adults. Vonoprazan is the first potassium-competitive acid blocker to be approved in the US. It has been available in Japan for treatment of various acid-related disorders since 2014. Vonoprazan is not available alone in the US.
Med Lett Drugs Ther. 2022 Oct 31;64(1662):169-72 |  Show IntroductionHide Introduction

Drugs for Acne

   
The Medical Letter on Drugs and Therapeutics • Feb 05, 2024  (Issue 1695)
/60 mL generic 1% foam apply once/day 307.10/50 g Evoclin (Mylan) 476.50/50 g Clindamycin phosphate ...
Acne is common among adolescents and adults. Guidelines for treatment of acne were last published by the American Academy of Dermatology in 2016.
Med Lett Drugs Ther. 2024 Feb 5;66(1695):17-20   doi:10.58347/tml.2024.1695a |  Show IntroductionHide Introduction

Three Drugs for Atopic Dermatitis (Adbry, Cibinqo, and Rinvoq)

   
The Medical Letter on Drugs and Therapeutics • Apr 03, 2023  (Issue 1673)
, 30 mg extended-release tabs prefilled syringes Route Subcutaneous Oral Oral Tmax 5-8 days Within 1 ...
The subcutaneously injected interleukin-13 (IL-13) antagonist tralokinumab-ldrm (Adbry – Leo) and the oral Janus kinase (JAK) inhibitors abrocitinib (Cibinqo – Pfizer) and upadacitinib (Rinvoq – Abbvie) have been approved by the FDA for treatment of moderate to severe atopic dermatitis.
Med Lett Drugs Ther. 2023 Apr 3;65(1673):51-5   doi:10.58347/tml.2023.1673b |  Show IntroductionHide Introduction

Mosunetuzumab (Lunsumio) for Follicular Lymphoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Mar 06, 2023  (Issue 1671)
mosunetuzumab in 21-day cycles for up to 17 cycles. After a median follow-up of 18.3 months, the objective ...
Mosunetuzumab-axgb (Lunsumio – Genentech), a bispecific CD20-directed CD3 T-cell engager, has received accelerated approval from the FDA for treatment of relapsed or refractory follicular lymphoma in adults who received ≥2 lines of systemic therapy. It is the first T-cell-engaging bispecific antibody to be approved in the US for this indication.
Med Lett Drugs Ther. 2023 Mar 6;65(1671):e41-2   doi:10.58347/tml.2023.1671f |  Show IntroductionHide Introduction

Relugolix (Orgovyx) for Advanced Prostate Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 24, 2023  (Issue 1681)
levels, liver enzyme elevations, and QT -interval prolongation were common. ▶ Dosage: 360 mg on day 1 ...
The oral gonadotropin-releasing hormone (GnRH) receptor antagonist relugolix (Orgovyx – Myovant Sciences/Pfizer) has been approved by the FDA for treatment of advanced prostate cancer in adults. It is the first oral GnRH receptor antagonist to become available in the US; degarelix (Firmagon), an injectable GnRH receptor antagonist, has been available since 2008 for the same indication.
Med Lett Drugs Ther. 2023 Jul 24;65(1681):e121-2   doi:10.58347/tml.2023.1681e |  Show IntroductionHide Introduction