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Searched for days. Results 881 to 890 of 1874 total matches.

Tiotropium (Spiriva) for COPD

   
The Medical Letter on Drugs and Therapeutics • May 24, 2004  (Issue 1183)
by CYP2D6 and 3A4. The terminal elimination half-life is 5-6 days. The bronchodilator effect, which ...
Tiotropium bromide inhalation powder (Spiriva HandiHaler - Boehringer Ingelheim), a long-acting anticholinergic agent, has been approved by the FDA for once-daily maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease (COPD). Available in Europe since 2002, it is the first long-acting inhaled anticholinergic drug for treatment of COPD. Ipratropium bromide (Atrovent), an anticholinergic used four times daily, has been available in the US for many years.
Med Lett Drugs Ther. 2004 May 24;46(1183):41-2 |  Show IntroductionHide Introduction

L-Carnitine

   
The Medical Letter on Drugs and Therapeutics • Nov 22, 2004  (Issue 1196)
-controlled trial, among 155 patients with intermittent claudication, propionyl-L-carnitine 2 grams/day ...
Carnitine is a naturally occurring amino acid derivative essential for transport of long-chain fatty acids into mitochondria. It is advertised on the Internet as a dietary supplement that can promote weight loss, increase energy, enhance athletic performance and slow aging. Levocarnitine (Carnitor - Sigma-Tau) has been FDA approved for oral and parenteral treatment of primary carnitine deficiency since 1986. Products containing levocarnitine and its synthetic derivative acetyl-L-carnitine are available as dietary supplements in the US.
Med Lett Drugs Ther. 2004 Nov 22;46(1196):95-6 |  Show IntroductionHide Introduction

Alvimopan (Entereg) for Postoperative Ileus

   
The Medical Letter on Drugs and Therapeutics • Dec 01, 2008  (Issue 1300)
surgery and then twice daily for up to 7 days, compared to placebo, significantly decreased ...
The FDA has approved the marketing of alvimopan (Entereg - Adolor/GlaxoSmithKline), a selective muopioid receptor antagonist, for oral treatment of postoperative ileus after bowel resection. The only other drug in this class available in the US is subcutaneously injected methylnaltrexone (Relistor), which is approved for treatment of opioid-induced constipation in patients with advanced illness receiving palliative care.
Med Lett Drugs Ther. 2008 Dec 1;50(1300):93-4 |  Show IntroductionHide Introduction

A Medical Food for Alzheimer's Disease

   
The Medical Letter on Drugs and Therapeutics • Jun 29, 2009  (Issue 1315)
in the ten apoE4-negative patients. 4 A double-blind, randomized, 90-day, placebo-controlled trial in 152 ...
Axona (Accera), a "medical food" containing a proprietary formulation of medium-chain triglycerides (>95% caprylic triglyceride), is currently being marketed for the "clinical dietary management of the metabolic processes associated with mild to moderate Alzheimer's disease."
Med Lett Drugs Ther. 2009 Jun 29;51(1315):49-50 |  Show IntroductionHide Introduction

Saxagliptin/Metformin (Kombiglyze XR) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Mar 21, 2011  (Issue 1360)
of IR metformin (mean dose about 1800 mg/day) compared the addition of 5 mg daily of saxagliptin ...
Metformin (Glucophage, and others) is generally preferred as the first-line agent for treatment of type 2 diabetes, but most patients subsequently require treatment with more than one drug. Many combination products have been marketed; the latest of these combines saxagliptin with extended-release (ER) metformin as Kombiglyze XR.
Med Lett Drugs Ther. 2011 Mar 21;53(1360):21-2 |  Show IntroductionHide Introduction

Brinzolamide/Brimonidine (Simbrinza) for Glaucoma

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2013  (Issue 1421)
analogs typically lower IOP by 25-30% and stabilize it at a lower level throughout the day ...
The FDA has approved Simbrinza (Alcon), an ophthalmic combination of the carbonic anhydrase inhibitor brinzolamide and the selective alpha2-adrenergic receptor agonist brimonidine, for reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. Simbrinza is the first product to combine drugs from these 2 classes.
Med Lett Drugs Ther. 2013 Jul 22;55(1421):57-8 |  Show IntroductionHide Introduction

Flibanserin (Addyi) for Hypoactive Sexual Desire Disorder

   
The Medical Letter on Drugs and Therapeutics • Sep 28, 2015  (Issue 1478)
— Three randomized, double-blind, 24-week trials compared flibanserin 100 mg/day at bedtime to placebo ...
The FDA has approved flibanserin (Addyi – Sprout) for treatment of premenopausal women with acquired, generalized hypoactive sexual desire disorder (HSDD) not caused by another medical or psychiatric condition, the effects of another drug, or relationship difficulties. Flibanserin is the first drug to be approved for treatment of HSDD. It is not approved for use in men or postmenopausal women. Previous FDA reviews of flibanserin in 2010 and 2013 did not result in approval.
Med Lett Drugs Ther. 2015 Sep 28;57(1478):133-5 |  Show IntroductionHide Introduction

Evolocumab (Repatha) - A Second PCSK9 Inhibitor to Lower LDL-Cholesterol

   
The Medical Letter on Drugs and Therapeutics • Oct 12, 2015  (Issue 1479)
3-4 days Metabolism Probably degradation to small peptides and amino acids Elimination Low ...
Evolocumab (Repatha – Amgen), a subcutaneously injected PCSK9 inhibitor, has been approved by the FDA as an adjunct to diet and maximally tolerated statin therapy for adults with heterozygous familial hypercholesterolemia (HeFH) or clinical atherosclerotic cardiovascular disease who require additional lowering of LDL-cholesterol (LDL-C). It was also approved as an adjunct to diet and other LDL-lowering therapies in patients with homozygous familial hypercholesterolemia (HoFH) who require additional lowering of LDL-C. Evolocumab is the second PCSK9 inhibitor to be approved in the...
Med Lett Drugs Ther. 2015 Oct 12;57(1479):140-1 |  Show IntroductionHide Introduction

Prescription Drug Prices in the US

   
The Medical Letter on Drugs and Therapeutics • May 22, 2017  (Issue 1521)
and uninsured patients. Some pharmacies offer a 30-day supply of certain generic drugs for only $4. Use ...
Per capita spending on prescription drugs in the US is higher than in other industrialized nations, including Canada.
Med Lett Drugs Ther. 2017 May 22;59(1521):81-3 |  Show IntroductionHide Introduction

Another Subcutaneous Immune Globulin (Cuvitru) for Primary Immunodeficiency (online only)

   
The Medical Letter on Drugs and Therapeutics • May 22, 2017  (Issue 1521)
-14 days, depending on the patient's comfort and convenience. The drug can be infused at up to four ...
The FDA has approved a subcutaneously administered 20% solution of human immune globulin (Cuvitru – Shire) for replacement therapy in patients ≥2 years old with a primary humoral immunodeficiency. Hizentra (CSL Behring), another subcutaneously administered 20% immune globulin solution, was approved in 2010 for the same indication. The IgG component of Cuvitru is similar to that of Gammagard Liquid and HyQvia, two subcutaneously administered 10% immune globulin formulations also manufactured by Shire and approved for treatment of primary...
Med Lett Drugs Ther. 2017 May 22;59(1521):e88-9 |  Show IntroductionHide Introduction