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An EUA for Casirivimab and Imdevimab for COVID-19

   
The Medical Letter on Drugs and Therapeutics • Dec 28, 2020  (Issue 1614)
1. High-Risk Conditions for COVID-19 Outpatients1 ▶ Age ≥65 years ▶ BMI ≥25 kg/m2 (or, in patients ...
The FDA has issued an Emergency Use Authorization (EUA) for Regeneron's investigational monoclonal antibodies casirivimab and imdevimab (REGEN-COV) to be administered together by IV infusion or SC injection for treatment of mild to moderate COVID-19 in adults and pediatric patients (≥12 years old and weigh ≥40 kg) who are at high risk of progressing to severe COVID-19 and/or hospitalization.
Med Lett Drugs Ther. 2020 Dec 28;62(1614):201-2 |  Show IntroductionHide Introduction

Remimazolam (Byfavo) for Short-Term Procedural Sedation

   
The Medical Letter on Drugs and Therapeutics • Feb 21, 2022  (Issue 1644)
. Initial dose injected IV over 1 minute; additional doses injected IV over 15 seconds at intervals of ≥2 ...
The FDA has approved remimazolam (Byfavo – Acacia Pharma), an ultra-short-acting IV benzodiazepine, for induction and maintenance of sedation in adults undergoing procedures of up to 30 minutes' duration.
Med Lett Drugs Ther. 2022 Feb 21;64(1644):26-8 |  Show IntroductionHide Introduction

Drugs for Rosacea

   
The Medical Letter on Drugs and Therapeutics • Feb 05, 2024  (Issue 1695)
scarring occur rarely.1,2 TOPICAL THERAPY Topical therapies are used for initial treatment of mild ...
Rosacea is a common, chronic inflammatory facial eruption of unknown cause. It is more prevalent in women than in men, and disease onset typically occurs after age 30. Rosacea is characterized by erythema, telangiectasia, and flushing, and sometimes by recurrent, progressive crops of acneiform papules and pustules, usually on the central part of the face. Some patients develop granulomas and tissue hypertrophy, which may lead to rhinophyma (a bulbous nose), particularly in men. Blepharitis and conjunctivitis are common. Keratitis and corneal scarring occur rarely.
Med Lett Drugs Ther. 2024 Feb 5;66(1695):21-2   doi:10.58347/tml.2024.1695b |  Show IntroductionHide Introduction

Automated External Defibrillators

   
The Medical Letter on Drugs and Therapeutics • Aug 14, 2006  (Issue 1241)
cardiac arrest has a survival rate of about 6% without immediate defibrillation. 1 Automated external ...
Sudden cardiac arrest has a survival rate of about 6% without immediate defibrillation. Automated external defibrillators (AEDs) can be found in many public locations such as shopping malls, office buildings and schools. Some patients may ask their physicians whether they should purchase an AED for personal use. One device has been FDA-approved for sale over the counter (HeartStart Home Defibrillator - Philips). Purchase of all other AEDs for public places or home use requires authorization from a physician.
Med Lett Drugs Ther. 2006 Aug 14;48(1241):71-2 |  Show IntroductionHide Introduction

Metformin/Repaglinide (PrandiMet) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Jun 01, 2009  (Issue 1313)
) June 1, 2009 www.medicalletter.org Published by The Medical Letter, Inc. • 1000 Main Street, New ...
A new fixed-dose tablet (PrandiMet - Novo Nordisk) combining metformin (Glucophage, and others) and repaglinide (Prandin) has been approved by the FDA for treatment of type 2 diabetes in patients already taking both metformin and repaglinide, or for patients not adequately controlled on either drug alone.
Med Lett Drugs Ther. 2009 Jun 1;51(1313):41-3 |  Show IntroductionHide Introduction

Ozanimod (Zeposia) for Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Aug 24, 2020  (Issue 1605)
), a sphingosine 1-phosphate (S1P) receptor modulator, for treatment of adults with relapsing forms of multiple ...
The FDA has approved ozanimod (Zeposia – Celgene), a sphingosine 1-phosphate (S1P) receptor modulator, for 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). It is the third oral S1P receptor modulator to be approved in the US for treatment of relapsing forms of MS; siponimod (Mayzent) is also indicated for use in adults, and fingolimod (Gilenya) is approved for use in patients ≥10 years old.
Med Lett Drugs Ther. 2020 Aug 24;62(1605):132-4 |  Show IntroductionHide Introduction

Drugs for Common Eye Disorders

   
The Medical Letter on Drugs and Therapeutics • Dec 02, 2019  (Issue 1586)
is reviewed in a separate issue.1 In general, all eye drops should be given in doses of one drop ...
This issue includes reviews of drugs for glaucoma, age-related macular degeneration (AMD), bacterial conjunctivitis, and dry eye disease. Allergic conjunctivitis is reviewed in a separate issue.
Med Lett Drugs Ther. 2019 Dec 2;61(1586):187-94 |  Show IntroductionHide Introduction

Durysta - A Bimatoprost Implant for Glaucoma

   
The Medical Letter on Drugs and Therapeutics • Jul 27, 2020  (Issue 1603)
(Rhopressa)1 can be added or substituted if IOP fails to reach the target range with a PGA alone.2 Improper ...
The FDA has approved an intracameral implant containing the prostaglandin analog bimatoprost (Durysta – Allergan) for reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. Bimatoprost is also available in 0.01% (Lumigan) and 0.03% (generics) ophthalmic solutions for the same indication and in a 0.03% solution (Latisse, and generics) for eyelash enhancement. Durysta is the first ocular implant to become available in the US for treatment of glaucoma.
Med Lett Drugs Ther. 2020 Jul 27;62(1603):116-7 |  Show IntroductionHide Introduction

Nalmefene Nasal Spray (Opvee) for Reversal of Opioid Overdose

   
The Medical Letter on Drugs and Therapeutics • Oct 16, 2023  (Issue 1687)
(see Table 2).1-3 ADVERSE EFFECTS ― The most common adverse effects of nalmefene nasal spray ...
The FDA has approved an intranasal formulation of the opioid antagonist nalmefene (Opvee – Indivior) for emergency treatment of known or suspected opioid overdose in persons ≥12 years old. Nalmefene, which is available by prescription, is the second opioid antagonist to become available as a nasal spray for this indication; the first was naloxone, which is now available for sale over the counter (Narcan, and generic). Other nasal spray formulations of naloxone and injectable formulations of nalmefene and naloxone are available by prescription (see Table 2).
Med Lett Drugs Ther. 2023 Oct 16;65(1687):166-7   doi:10.58347/tml.2023.1687b |  Show IntroductionHide Introduction

In Brief: OTC Azelastine Nasal Spray 0.15% (Astepro Allergy) for Allergic Rhinitis

   
The Medical Letter on Drugs and Therapeutics • Oct 31, 2022  (Issue 1662)
intranasal antihistamine Table 1. Intranasal H1-Antihistamines Drug Usual Dosage Cost1 Azelastine 0.1%2 ...
The 0.15% nasal spray formulation of the H1- antihistamine azelastine hydrochloride (Astepro Allergy; Children's Astepro Allergy – Bayer) is now available over the counter (OTC) for temporary relief of nasal congestion, runny nose, sneezing, and itchy nose due to allergic rhinitis in adults and children ≥6 years old. It is the first intranasal antihistamine to be approved by the FDA for OTC use. Other drugs that are available OTC for treatment of allergic rhinitis symptoms include oral antihistamines, intranasal corticosteroids, and mast cell stabilizers.
Med Lett Drugs Ther. 2022 Oct 31;64(1662):175-6 |  Show IntroductionHide Introduction