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Searched for Devices. Results 81 to 90 of 220 total matches.
Choice of Contraceptives
The Medical Letter on Drugs and Therapeutics • May 15, 2023 (Issue 1676)
.................................................... p 74-75
Comparison of Intrauterine Devices (IUDs) ......................... p 78
Some Oral ...
Intrauterine devices (IUDs) and the etonogestrel
implant are the most effective reversible contraceptive
methods available. Hormonal oral contraceptives,
patches, rings, and injectables are also effective in
preventing pregnancy. When used alone, barrier and
behavioral methods generally have higher failure
rates than other methods (see Table 1). Selection of
a contraceptive method is usually based on patient-specific factors and personal preference
Med Lett Drugs Ther. 2023 May 15;65(1676):73-80 doi:10.58347/tml.2023.1676a | Show Introduction Hide Introduction
MiniMed 530G: An Insulin Pump with Low-Glucose Suspend Automation
The Medical Letter on Drugs and Therapeutics • Dec 09, 2013 (Issue 1431)
sensoraugmented
insulin pump available in the US with this
capability.
THE DEVICE — The MiniMed 530G system ...
The FDA has approved the MiniMed 530G
(Medtronic), an insulin pump used in combination with
a continuous glucose monitoring sensor (Enlite) that
can stop delivery of insulin when interstitial glucose
reaches a prespecified low level. It is the only sensoraugmented
insulin pump available in the US with this
capability.
Esketamine Nasal Spray (Spravato) for Treatment-Resistant Depression
The Medical Letter on Drugs and Therapeutics • Apr 08, 2019 (Issue 1569)
(14 mg/spray) nasal spray devices
Route Intranasal
Bioavailability (mean) 48%
Metabolism Hepatic ...
The FDA has approved esketamine (Spravato –
Janssen), an N-methyl-D-aspartate (NMDA) receptor
antagonist, for intranasal treatment (in conjunction
with an oral antidepressant) of adults with treatment-resistant
depression (TRD). This is the first FDA
approval for esketamine, which is the S-enantiomer
of the intravenous anesthetic ketamine (Ketalar,
and generics). In recent years, IV ketamine has been
increasingly used (off-label) for treatment of TRD.
Correction: Resperate for Hypertension
The Medical Letter on Drugs and Therapeutics • Aug 27, 2007 (Issue 1268)
does not require
proof of effectiveness for approval of devices with minimal
potential for harm ...
(Med Lett Drugs Ther 2007; 49:55) The second sentence in the article ("The FDA does not require proof of effectiveness for approval of devices with minimal potential for harm, such as this one.") should have been omitted. It would apply to a Class I device, but the FDA has classified Resperate as a Class II device.
Safe Needles
The Medical Letter on Drugs and Therapeutics • Apr 05, 1991 (Issue 841)
).
SOME NEW DEVICES — ‘‘Safe’’ needles used with vacuum tubes come in two designs. One
has an external ...
Accidental needlesticks can lead to infection with hepatitis viruses, human immunodeficiency virus, and other blood-borne bacterial, viral, and fungal pathogens (DK Henderson et al, Ann Intern Med, 113:740, 1990). Re-capping used needles is the most frequent cause of needlestick injuries (J Jagger et al, N Engl J Med, 319:284, 1988; MH Becker et al, Am J Infect Control, 18:232, 1990).
Corrections: Drugs for Diabetes & Another Insulin Glargine (Basaglar) for Diabetes
The Medical Letter on Drugs and Therapeutics • Jan 30, 2017 (Issue 1513)
and Administration section, we removed the word
“syringe” to describe Basaglar’s KwikPen device. Basaglar ...
Drugs for Diabetes (Med Lett Drugs Ther 2017; 59:9)In the 4th paragraph of the GLP-1 receptor agonists section, we mistakenly stated that Xultophy 100/3.6 is a combination of insulin degludec and albiglutide; Xultophy 100/3.6 is a combination of insulin degludec and liraglutide.Another Insulin Glargine (Basaglar) for Diabetes (Med Lett Drugs Ther 2017; 59:3)In the Dosage and Administration section, we removed the word "syringe" to describe Basaglar's KwikPen device. Basaglar is not available as a prefilled syringe; it is only available as a KwikPen.Download complete U.S. English...
Drugs for Overactive Bladder
The Medical Letter on Drugs and Therapeutics • Mar 20, 2023 (Issue 1672)
-electrode in the ankle near the tibial nerve and
connection to a stimulator device, is FDA-approved ...
In overactive bladder, involuntary bladder contractions
due to detrusor overactivity result in urinary
urgency, frequency, nocturia, and incontinence.
The prevalence of the disorder increases with age.
Nonpharmacologic treatment, including bladder
training, urge suppression, pelvic floor muscle
exercises, constipation management, modification of
fluid intake, and avoidance of dietary irritants such as
alcohol and caffeine, should be tried first.
Med Lett Drugs Ther. 2023 Mar 20;65(1672):41-5 doi:10.58347/tml.2023.1672a | Show Introduction Hide Introduction
Treatment of Nerve Gas Poisoning
The Medical Letter on Drugs and Therapeutics • May 12, 1995 (Issue 948)
in an automatic injection device called Atropen AutoInjector (Survival Technology, Rockville, MD); pressing ...
The recent attack in the Tokyo subway has led to many questions about the clinical effects, treatment and prevention of nerve gas poisoning.
Spinal Decompression Machines
The Medical Letter on Drugs and Therapeutics • Jun 02, 2008 (Issue 1287)
of mechanical traction. These devices, which are widely
advertised to the public as a noninvasive alternative ...
Spinal decompression machines offer a motorized form of mechanical traction. These devices, which are widely advertised to the public as a noninvasive alternative to surgery, are claimed to relieve low back pain by decompressing discs, improving the flow of nutrients into the disc and rehydrating dried-out discs. Devices cleared by the FDA based on substantial similarity to previously approved power traction devices include the Accu- Spina System, DRS System, DRX9000, Lordex Traction Unit, Spinal Health Elite, SpineMED Decompression Table, SpineRx-LDM and VAX-D Therapeutic Table.
Aclidinium Bromide (Tudorza Pressair) for COPD
The Medical Letter on Drugs and Therapeutics • Dec 10, 2012 (Issue 1405)
% in urine
Bioavailability 6%
Table 1. Pharmacology
Delivery Usual Adult
Drug Formulations Device ...
The FDA has approved aclidinium bromide (Tudorza
Pressair – Forest), an orally-inhaled long-acting anticholinergic,
for long-term maintenance treatment of
bronchospasm associated with chronic obstructive
pulmonary disease (COPD).