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Searched for action. Results 181 to 190 of 1195 total matches.

Fluoxetine (Prozac) and Other Drugs for Treatment of Obesity

   
The Medical Letter on Drugs and Therapeutics • Nov 25, 1994  (Issue 936)
. MECHANISM OF ACTION — Fluoxetine inhibits reuptake and increases availability of serotonin (5 ...
Recent reports have suggested that some obese patients may benefit from long-term pharmacologic treatment (RL Atkinson and VS Hubbard, Am J Clin Nutr, 60:153, August 1994; DJ Goldstein and JH Potvin, Am J Clin Nutr, 60:647, November 1994). Fluoxetine (Prozac), widely used for treatment of depression and near approval by the US Food and Drug Administration (FDA) for treatment of bulimia, is also being tried for treatment of obesity.
Med Lett Drugs Ther. 1994 Nov 25;36(936):107-8 |  Show IntroductionHide Introduction

Zaleplon for Insomnia

   
The Medical Letter on Drugs and Therapeutics • Oct 08, 1999  (Issue 1063)
Onset of action dose 1 Cost 2 Triazolam − average generic price short intermediate 0.25 mg $ 4.62 ...
Zaleplon, a pyrazolopyrimidine hypnotic, was recently approved by the FDA for short-term treatment of insomia. Zaleplon, like zolpidem, is a non-benzodiazepine that binds to benzodiazepine receptors.
Med Lett Drugs Ther. 1999 Oct 8;41(1063):93-4 |  Show IntroductionHide Introduction

Budesonide (Entocort EC) For Crohn's Disease

   
The Medical Letter on Drugs and Therapeutics • Jan 21, 2002  (Issue 1122)
OF ACTION — Budesonide is a synthetic corticosteroid with a strong affinity for glucocorticoid receptors ...
Budesonide (Entocort EC — AstraZeneca), a locally active glucocorticosteriod widely used for inhalation treatment of allergic rhinitis and asthma (Medical Letter 2000; 42:19), has been approved for oral treatment of mild to moderate active Crohn's disease involving the ileum and/or ascending colon. Both oral budesonide and budesonide enemas have been available for years in Europe and Canada for treatment of inflammatory bowel disease.
Med Lett Drugs Ther. 2002 Jan 21;44(1122):6-8 |  Show IntroductionHide Introduction

Insulin-like Growth Factor-1 for Severe Growth Failure

   
The Medical Letter on Drugs and Therapeutics • May 20, 2007  (Issue 1261)
was withdrawn from the market due to patent issues. MECHANISM OF ACTION — IGF-1 is the main mediator ...
Mecasermin (Increlex - Tercica), which is injected subcutaneously, has been approved by the FDA for treatment of growth failure in children with severe primary insulin-like growth factor (IGF-1) deficiency. Mecasermin is recombinant human (rh) IGF-1. It has also been approved to treat children with short stature who are deficient in growth hormone (GH), but have developed neutralizing antibodies in response to GH treatment. A similar product, mecasermin rinfabate (Iplex - Insmed), that was approved by the FDA for the same indications was withdrawn from the market due to patent...
Med Lett Drugs Ther. 2007 May 20;49(1261):43-4 |  Show IntroductionHide Introduction

Two New Drugs for Homozygous Familial Hypercholesterolemia

   
The Medical Letter on Drugs and Therapeutics • Apr 01, 2013  (Issue 1413)
%) Pharmacokinetics of Mipomersen MIPOMERSEN Mechanism of Action – Mipomersen (mi’’ poe mer’ sen) is an antisense ...
The FDA has approved mipomersen (Kynamro – Genzyme) and lomitapide (Juxtapid – Aegerion), each in addition to a low-fat diet and other lipid-lowering medications, to reduce cholesterol levels in patients with homozygous familial hypercholesterolemia (HoFH).
Med Lett Drugs Ther. 2013 Apr 1;55(1413):25-7 |  Show IntroductionHide Introduction

Rolapitant (Varubi) for Prevention of Delayed Chemotherapy-Induced Nausea and Vomiting

   
The Medical Letter on Drugs and Therapeutics • Feb 01, 2016  (Issue 1487)
) MECHANISM OF ACTION — Chemotherapy-induced emesis is mediated by neurotransmitters such as serotonin ...
The FDA has approved rolapitant (Varubi – Tesaro), an oral substance P/neurokinin 1 (NK1) receptor antagonist, for use with other antiemetics to prevent delayed nausea and vomiting associated with cancer chemotherapy in adults. It is the third substance P/NK1 receptor antagonist to be approved in the US; aprepitant (Emend) and netupitant (only available in combination with the 5-HT3 receptor antagonist palonosetron as Akynzeo) were approved earlier for prevention of both acute and delayed chemotherapy-induced nausea and vomiting.
Med Lett Drugs Ther. 2016 Feb 1;58(1487):17-8 |  Show IntroductionHide Introduction

Brivaracetam (Briviact) for Epilepsy

   
The Medical Letter on Drugs and Therapeutics • Jul 18, 2016  (Issue 1499)
: briv" a ra' se tam Briviact: briv' ee akt MECHANISM OF ACTION — Brivaracetam binds selectively ...
Brivaracetam (Briviact – UCB), an analog of levetiracetam (Keppra, and others), has been approved by the FDA for adjunctive treatment of partial-onset seizures in patients ≥16 years old. New drugs for epilepsy are often approved initially only as adjunctive treatment for partial seizures.
Med Lett Drugs Ther. 2016 Jul 18;58(1499):95-6 |  Show IntroductionHide Introduction

Cotempla XR-ODT - Another Long-Acting Methylphenidate for ADHD

   
The Medical Letter on Drugs and Therapeutics • Nov 06, 2017  (Issue 1533)
orally disintegrating tablets Route Oral Tmax ~5 hours Half-life ~4 hours Onset of Action ≤1 hour ...
The FDA has approved an extended-release orally disintegrating tablet formulation of methylphenidate (Cotempla XR-ODT – Neos Therapeutics) for once-daily treatment of attention-defi cit/hyperactivity disorder (ADHD) in children 6-17 years old. Cotempla XR-ODT is the first extended-release orally disintegrating tablet formulation of methylphenidate to become available in the US.
Med Lett Drugs Ther. 2017 Nov 6;59(1533):183-5 |  Show IntroductionHide Introduction

Darolutamide (Nubeqa) for Prostate Cancer

   
The Medical Letter on Drugs and Therapeutics • Dec 16, 2019  (Issue 1587)
months vs 16.2 months; enzalutamide: 36.6 months vs 14.7 months).5,6 MECHANISM OF ACTION — Androgen ...
The FDA has approved darolutamide (Nubeqa – Bayer), an androgen receptor inhibitor, for oral treatment of nonmetastatic castration-resistant prostate cancer (nmCRPC). Darolutamide is the third androgen receptor inhibitor to be approved for this indication; apalutamide (Erleada) and enzalutamide (Xtandi), which are also approved for use in patients with metastatic castration-resistant prostate cancer (mCRPC), were approved earlier.
Med Lett Drugs Ther. 2019 Dec 16;61(1587):201-2 |  Show IntroductionHide Introduction

Nalmefene Nasal Spray (Opvee) for Reversal of Opioid Overdose

   
The Medical Letter on Drugs and Therapeutics • Oct 16, 2023  (Issue 1687)
. Unlike naloxone, nalmefene has a longer duration of action than many opioid analgesics, which could ...
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