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Searched for Devices. Results 51 to 60 of 220 total matches.

A New Dihydroergotamine Nasal Spray (Trudhesa) for Migraine

   
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021  (Issue 1640)
of migraine. Utilizes a device that delivers the drug to the upper nasal cavity, resulting in greater ...
The FDA has approved Trudhesa (Impel Neuropharma), a new dihydroergotamine nasal spray product, for acute treatment of migraine with or without aura in adults. Another dihydroergotamine nasal spray (Migranal, and generics) has been available for many years for the same indication.
Med Lett Drugs Ther. 2021 Dec 27;63(1640):204-7 |  Show IntroductionHide Introduction

Minimed 670G: A Hybrid Closed-Loop Insulin Delivery System

   
The Medical Letter on Drugs and Therapeutics • Nov 21, 2016  (Issue 1508)
in Spring 2017. RELATED DEVICES — The Minimed 630G system was approved in August 2016 and is currently ...
The FDA has approved the Minimed 670G (Medtronic), a hybrid closed-loop insulin delivery system for use in patients ≥14 years old with type 1 diabetes. The system uses an algorithm to automatically adjust basal insulin doses based on readings from a continuous glucose monitor (CGM). It fully automates basal insulin delivery in "auto" mode, but is considered a "hybrid" system (not a true "artificial pancreas") because it requires some action by the patient. The 670G system is expected to become available in Spring 2017.
Med Lett Drugs Ther. 2016 Nov 21;58(1508):147-8 |  Show IntroductionHide Introduction

In Brief: Epinephrine 1 mg Nasal Spray (neffy)

   
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025  (Issue 1727)
be administered into the same nostril using a new device. The nasal spray should be stored at room temperature ...
The FDA has approved a 1-mg epinephrine nasal spray (neffy - ARS Pharma) for emergency treatment of type 1 hypersensitivity reactions including anaphylaxis in patients ≥4 years old who weigh 15 to <30 kg. A 2-mg formulation of neffy was approved in 2024 for use in patients who weigh ≥30 kg.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):71   doi:10.58347/tml.2025.1727c |  Show IntroductionHide Introduction

iDose TR — A Travoprost Implant for Glaucoma

   
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024  (Issue 1701)
to pharmacologic treatment. THE NEW IMPLANT — iDose TR is a rod-shaped titanium-based device (1.8 mm x 0.5 mm ...
The FDA has approved iDose TR (Glaukos), an intracameral implant containing the prostaglandin analog (PGA) travoprost, for reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. Travoprost is also available as a topical ophthalmic solution (Travatan Z, and generics) for the same indication. iDose TR is the second ocular implant to become available in the US for this indication; Durysta, an intracameral implant containing the prostaglandin analog bimatoprost, was the first.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):70-1   doi:10.58347/tml.2024.1701d |  Show IntroductionHide Introduction

Repetitive Transcranial Magnetic Stimulation (TMS) for Medication-Resistant Depression

   
The Medical Letter on Drugs and Therapeutics • Feb 09, 2009  (Issue 1305)
) for MedicationResistant Depression The FDA has cleared a new device for treatment of major depressive disorder (MDD ...
The FDA has cleared a new device for treatment of major depressive disorder (MDD) resistant to antidepressant medication. The NeuroStar TMS System (Neuronetics) produces pulsed magnetic fields that can induce electrical currents in the brain. Unlike electroconvulsive therapy (ECT), it does not require anesthesia or induction of seizures. Other similar devices are under development.
Med Lett Drugs Ther. 2009 Feb 9;51(1305):11-2 |  Show IntroductionHide Introduction

Automated External Defibrillators

   
The Medical Letter on Drugs and Therapeutics • Aug 14, 2006  (Issue 1241)
” stickers are affixed to the devices), whether it will affect the quality and timeliness of CPR ...
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

Glucagon Nasal Powder (Baqsimi) for Severe Hypoglycemia

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
– Baqsimi is supplied in cartons containing one or two intranasal devices in shrink-wrapped tubes. Each ...
The FDA has approved glucagon nasal powder (Baqsimi – Lilly) for treatment of severe hypoglycemia in patients ≥4 years old with diabetes. Baqsimi is the first noninjectable glucagon formulation to become available in the US. Injectable glucagon emergency kits (GlucaGen Hypokit, and generic) have been available for years, but they require reconstitution of the lyophilized powder by the caregiver immediately before injection. An injectable glucagon formulation that does not require reconstitution was recently approved by the FDA (Gvoke) and is expected to become available...
Med Lett Drugs Ther. 2019 Sep 23;61(1581):148-9 |  Show IntroductionHide Introduction

The Cervical Cap

   
The Medical Letter on Drugs and Therapeutics • Oct 07, 1988  (Issue 776)
of a cervical cap (Prentif Cavity-Rim Cervical Cap — Lamberts Ltd, England), a contraceptive device ...
The US Food and Drug Administration recently approved the marketing of a cervical cap (Prentif Cavity-Rim Cervical Cap - Lamberts Ltd, England), a contraceptive device that has been used in one form or another for many years (JP Koch, Contraception, 25:161, 1982). The cap is being distributed in the USA and Canada by Cervical Cap (CxC), Ltd, PO Box 38003-292, Los Gatos, CA 95031, telephone 408-358-6264; the distributor will make the caps available only to practitioners who have attended training seminars.
Med Lett Drugs Ther. 1988 Oct 7;30(776):93-4 |  Show IntroductionHide Introduction

Implantable Cardioverter Defibrillators

   
The Medical Letter on Drugs and Therapeutics • Jan 26, 2009  (Issue 1304)
) are widely used in patients at risk for sudden cardiac death (SCD) because these devices have been highly ...
Implantable cardioverter defibrillators (ICDs) are widely used in patients at risk for sudden cardiac death (SCD) because these devices have been highly successful in terminating life-threatening ventricular arrhythmias and in increasing survival.
Med Lett Drugs Ther. 2009 Jan 26;51(1304):6-7 |  Show IntroductionHide Introduction

Automated External Defibrillators

   
The Medical Letter on Drugs and Therapeutics • Dec 11, 2000  (Issue 1094)
of these devices for public places or home use requires authorization from a physician. HOW THEY WORK — AEDs ...
Recent studies suggest that timely use of automated external defibrillators operated by laypersons with minimal training can save lives. Purchase of these devices for public places or home use requires authorization from a physician.
Med Lett Drugs Ther. 2000 Dec 11;42(1094):116 |  Show IntroductionHide Introduction