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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.
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.
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.
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."
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.
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.
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.
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...
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.
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...