Search Results for "Devices"
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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.
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.
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 Introduction Hide 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 Introduction Hide 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.
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.
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...
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.
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.
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.