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Searched for days. Results 51 to 60 of 486 total matches.

COVID-19 Vaccine Comparison Chart (Archived) (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 05, 2021  (Issue 1621)
doses (0.3 mL) 21 days apart 2 doses (0.5 mL) 28 days apart 1 dose (0.5 mL) 2 doses 4-12 weeks ...
View the COVID-19 Vaccine Comparison Chart
Med Lett Drugs Ther. 2021 Apr 5;63(1621):e1-14 |  Show IntroductionHide Introduction

Cefepime/Enmetazobactam (Exblifep) for Complicated Urinary Tract Infections

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
every 8 hours for 7 days (up to 14 days in patients with bacteremia). The rate of clinical cure plus ...
The FDA has approved Exblifep (Allecra), a fixed-dose combination of the cephalosporin cefepime and the beta-lactamase inhibitor enmetazobactam, for IV treatment of adults with complicated urinary tract infections (cUTIs), including pyelonephritis, caused by designated susceptible microorganisms (see Spectrum of Activity). Exblifep is the first product that contains enmetazobactam to be approved in the US.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):117-8   doi:10.58347/tml.2024.1707d |  Show IntroductionHide Introduction

Drugs for Bipolar Disorder

   
The Medical Letter on Drugs and Therapeutics • Apr 01, 2024  (Issue 1699)
of acute manic episodes. Both lithium and valproate may take days to weeks to have a full therapeutic ...
Bipolar disorder is characterized by episodes of mania, hypomania, and depression. Recurrences of manic or (more frequently) depressive symptoms are common. About 15-20% of patients with bipolar disorder die by suicide.
Med Lett Drugs Ther. 2024 Apr 1;66(1699):49-54   doi:10.58347/tml.2024.1699a |  Show IntroductionHide Introduction

Rezafungin (Rezzayo) for Invasive Candida Infections

   
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024  (Issue 1705)
weeks. 2. Approximate WAC for 7 days’ treatment of a 70-kg patient at the highest usual adult dosage ...
The FDA has approved rezafungin (Rezzayo – Cidara/Melinta), an intravenous echinocandin antifungal, for once-weekly treatment of candidemia and invasive candidiasis (IC) in adults with limited or no alternative options. It is the first new drug to become available in the US in more than 15 years for treatment of systemic Candida infections.
Med Lett Drugs Ther. 2024 Jun 24;66(1705):101-4   doi:10.58347/tml.2024.1705d |  Show IntroductionHide Introduction

Neratinib (Nerlynx) for Metastatic HER2-Positive Breast Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022  (Issue 1663)
neratinib 240 mg or lapatinib 1250 mg once daily on days 1-21, each in addition to capecitabine twice ...
The oral tyrosine kinase inhibitor neratinib (Nerlynx – Puma Biotechnology) has been approved by the FDA for use in combination with capecitabine (Xeloda, and generics) for treatment of advanced or metastatic human epidermal growth factor receptor 2 (HER2)-positive breast cancer in adults who received ≥2 prior anti-HER2-based regimens for metastatic disease. It was previously approved for use as monotherapy for extended adjuvant treatment of adults with early-stage, HER2-positive breast cancer following adjuvant trastuzumab (Herceptin)-based therapy. HER2 is overexpressed in...
Med Lett Drugs Ther. 2022 Nov 14;64(1663):e192-3 |  Show IntroductionHide Introduction

Isatuximab (Sarclisa) for Multiple Myeloma (online only)

   
The Medical Letter on Drugs and Therapeutics • Dec 09, 2024  (Issue 1717)
infections and secondary malignancies have been reported. Dosage: 10 mg/kg IV on days 1, 8, 15, 22, and 29 ...
Isatuximab-irfc (Sarclisa – Sanofi), a CD38-directed cytolytic antibody, has been approved by the FDA for treatment of newly diagnosed multiple myeloma in adults who are not eligible for autologous stem cell transplantation (ASCT). The drug was approved earlier for treatment of relapsed or treatment-refractory multiple myeloma.
Med Lett Drugs Ther. 2024 Dec 9;66(1717):e200-1   doi:10.58347/tml.2024.1717e |  Show IntroductionHide Introduction

Sublingual Cyclobenzaprine (Tonmya) for Fibromyalgia

   
The Medical Letter on Drugs and Therapeutics • Jan 19, 2026  (Issue 1746)
taste, and somnolence. ▶ Dosage: 2.8 mg once daily for 14 days, then 5.6 mg once daily. The drug ...
The FDA has approved Tonmya (Tonix), a sublingual tablet formulation of the skeletal muscle relaxant cyclobenzaprine, for treatment of fibromyalgia in adults. Cyclobenzaprine is available in immediate-release tablets and extended-release capsules for short-term treatment of muscle spasms and has been used off-label for treatment of fibromyalgia.
Med Lett Drugs Ther. 2026 Jan 19;68(1746):9-10   doi:10.58347/tml.2026.1746a |  Show IntroductionHide Introduction

An EUA for Bebtelovimab for Treatment of COVID-19

   
The Medical Letter on Drugs and Therapeutics • Mar 21, 2022  (Issue 1646)
confirmatory testing for SARS-CoV-2 infection within the previous 3 days. BLAZE-4 was completed before ...
The investigational monoclonal antibody bebtelovimab (LY-CoV1404 – Lilly) has been granted an FDA Emergency Use Authorization (EUA) for IV treatment of mild to moderate COVID-19 in patients ≥12 years old who weigh ≥40 kg and are at high risk of progressing to severe disease, including hospitalization and death, and for whom alternative treatment options are unavailable or inappropriate. Bebtelovimab is active against the Omicron variant of SARS-CoV-2; sotrovimab (VIR-7831) is the only other monoclonal antibody currently available for treatment of COVID-19 that is active...
Med Lett Drugs Ther. 2022 Mar 21;64(1646):41-2 |  Show IntroductionHide Introduction

Vibrant – An Oral Vibrating Capsule for Chronic Idiopathic Constipation

   
The Medical Letter on Drugs and Therapeutics • May 01, 2023  (Issue 1675)
at night between 9 and 10 pm and was preprogrammed to begin vibrating at noon the next day; it was active ...
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

Comparison Table: Some Drugs for Weight Management (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 04, 2025  (Issue 1734)
Agonists Liraglutide – Saxenda (Novo Nordisk) 18 mg/3 mL pens3 3 mg SC once/day Titration: 0.6 mg once ...
View the Comparison Table: Some Drugs for Weight Management
Med Lett Drugs Ther. 2025 Aug 4;67(1734):e127-30   doi:10.58347/tml.2025.1734b |  Show IntroductionHide Introduction