Search Results for "data"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for data. Results 301 to 310 of 1113 total matches.

Montelukast (Singulair) for Perennial Allergic Rhinitis

   
The Medical Letter on Drugs and Therapeutics • Oct 24, 2005  (Issue 1220)
1. Cost for 30 days’ treatment at the lowest initial dosage for adults, based on most recent data ...
Montelukast (Singulair - Merck) is an oral cysteinyl leukotriene D4 receptor antagonist originally marketed for treatment of asthma. It was approved by the FDA in 2003 for treatment of seasonal allergic rhinitis and recently for use in perennial allergic rhinitis in adults and children ≥ 6 months old. Intranasal corticosteroids have generally been considered the most effective drugs available for prevention and treatment of allergic rhinitis.
Med Lett Drugs Ther. 2005 Oct 24;47(1220):87-4 |  Show IntroductionHide Introduction

Omega-3 Polyunsaturated Fatty Acids (Omacor) for Hypertriglyceridemia

   
The Medical Letter on Drugs and Therapeutics • Nov 07, 2005  (Issue 1221)
% and VLDL cholesterol by 30-40% after 48 weeks. 6 No data are available on the effect of Omacor ...
A highly concentrated omega-3 polyunsaturated fatty acid (PUFA) preparation (Omacor - Reliant) has been approved by the FDA as an adjunct to diet for treatment of very high plasma triglyceride concentrations (>=500 mg/dL). Omacor is a combination of the ethyl esters of icosapentaenoic (EPA) and docosahexaenoic (DHA) acids. It is the first drug derived from omega-3 PUFAs to be sold by prescription.
Med Lett Drugs Ther. 2005 Nov 7;47(1221):91-2 |  Show IntroductionHide Introduction

Nilotinib (Tasigna) for CML

   
The Medical Letter on Drugs and Therapeutics • Apr 07, 2008  (Issue 1283)
; survival at 12 months was 79%. 5 No data are available directly comparing nilotinib with dasatinib ...
Nilotinib (Tasigna - Novartis), a tyrosine kinase inhibitor, has been approved by the FDA for treatment of Philadelphia chromosome-positive (Ph+) chronic or accelerated phase chronic myelogenous leukemia (CML) in patients resistant to or intolerant of imatinib (Gleevec).
Med Lett Drugs Ther. 2008 Apr 7;50(1283):26-7 |  Show IntroductionHide Introduction

Extended-Release Fluvoxamine (Luvox CR)

   
The Medical Letter on Drugs and Therapeutics • Jun 30, 2008  (Issue 1289)
of OCD and social anxiety disorder (SAD) in adults. PHARMACOKINETICS — According to data ...
Fluvoxamine maleate, a selective serotonin reuptake inhibitor (SSRI) that has been available for many years in an immediate-release formulation (Luvox, and others) for treatment of obsessive-compulsive disorder (OCD) in children and adults, has now been approved by the FDA in an extended-release formulation (Luvox CR - Jazz Pharmaceuticals) for treatment of OCD and social anxiety disorder (SAD) in adults.
Med Lett Drugs Ther. 2008 Jun 30;50(1289):50-1 |  Show IntroductionHide Introduction

Prostate Cancer Screening

   
The Medical Letter on Drugs and Therapeutics • Nov 03, 2008  (Issue 1298)
of clinically unimportant cancers continues to be a problem. Until more data become available, a male patient ...
The US Preventive Services Task Force (USPSTF) has recently concluded that available evidence is insufficient to assess the balance between potential benefits and harms of using the prostate-specific antigen (PSA) to screen men < 75 years old for prostate cancer and has recommended against screening men > 75 years old.
Med Lett Drugs Ther. 2008 Nov 3;50(1298):85-6 |  Show IntroductionHide Introduction

Cervarix - A Second HPV Vaccine

   
The Medical Letter on Drugs and Therapeutics • May 17, 2010  (Issue 1338)
infections with HPV 45 and other non-vaccine HPV types (but not types 6 and 11). 3 Follow-up data ...
The FDA has approved a recombinant human papillomavirus (HPV) vaccine (Cervarix – GlaxoSmithKline) for use in girls and women 10-25 years old to prevent infection with HPV types 16 and 18, which have been associated with cervical cancer. A recombinant quadrivalent HPV vaccine (Gardasil – Merck) already on the market in the US prevents infection with HPV types 6, 11, 16 and 18.
Med Lett Drugs Ther. 2010 May 17;52(1338):37 |  Show IntroductionHide Introduction

Preservation of Ovarian Function During Chemotherapy

   
The Medical Letter on Drugs and Therapeutics • Jun 28, 2010  (Issue 1341)
for later transplantation, while available at some centers, is experimental, and data on its efficacy ...
Chemotherapy can result in premature menopause and infertility in young women. Pretreatment fertility counseling followed by appropriate action may prevent some of these undesirable consequences.
Med Lett Drugs Ther. 2010 Jun 28;52(1341):49-50 |  Show IntroductionHide Introduction

Ambrisentan (Letairis) and Tadalafil (Adcirca) for Pulmonary Arterial Hypertension

   
The Medical Letter on Drugs and Therapeutics • Jan 04, 2016  (Issue 1485)
; it will be reviewed in a future issue. Combination Therapy – Limited data are available on the effectiveness ...
The FDA has approved the use of ambrisentan (Letairis) and tadalafil (Adcirca) together for treatment of pulmonary arterial hypertension (PAH). It is the first 2-drug regimen to be approved for this indication.
Med Lett Drugs Ther. 2016 Jan 4;58(1485):2-4 |  Show IntroductionHide Introduction

FDA Warns Against Use of Codeine and Tramadol in Children and Breastfeeding Women

   
The Medical Letter on Drugs and Therapeutics • May 22, 2017  (Issue 1521)
and tramadol for children who require an opioid analgesic, but they are both potent opioid agonists and data ...
The FDA has issued new warnings about the use of the opioid analgesics codeine and tramadol in children, particularly those <12 years old, and in breastfeeding women due to concerns about the risk of respiratory depression and death. The FDA previously issued warnings about these drugs in 2013 and 2015.
Med Lett Drugs Ther. 2017 May 22;59(1521):86-8 |  Show IntroductionHide Introduction

Safinamide (Xadago) for Parkinson's Disease

   
The Medical Letter on Drugs and Therapeutics • Sep 11, 2017  (Issue 1529)
; no data on the presence of safinamide in human breast milk are available. DRUG INTERACTIONS — Use ...
The FDA has approved the monoamine oxidase type B (MAO-B) inhibitor safinamide (Xadago – US Worldmeds) as an adjunct to levodopa/carbidopa for management of "off" episodes in patients with Parkinson’s disease (PD). It is the first reversible MAO-B inhibitor to be approved for this indication. Selegiline (Eldepryl, and others) and rasagiline (Azilect, and generics), two irreversible MAO-B inhibitors, have been used alone and as adjuncts to levodopa/carbidopa for many years. Safinamide is not approved for use as monotherapy.
Med Lett Drugs Ther. 2017 Sep 11;59(1529):151-3 |  Show IntroductionHide Introduction