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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.
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.
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).
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.
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.
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.
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.
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.
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.
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.