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Searched for activate. Results 741 to 750 of 1329 total matches.
Rivaroxaban (Xarelto) for Acute Coronary Syndrome
The Medical Letter on Drugs and Therapeutics • Dec 12, 2011 (Issue 1379)
%) treated with the lower
dose of the active drug, in 313 (8.8%) treated with the
higher dose, and in 376 ...
The standard antithrombotic therapy for treatment of
patients with acute coronary syndrome (ACS) is dual
antiplatelet therapy with aspirin and clopidogrel (Plavix)
or another thienopyridine, plus a parenteral anticoagulant
while the patient is hospitalized, followed by antiplatelet
therapy alone after discharge. The addition of the oral
anticoagulant warfarin (Coumadin, and others) to dual
antiplatelet therapy is generally not recommended for this
indication because of fluctuations in its anticoagulant
effect and the risk of bleeding. A recently published trial
found that addition of...
A Transcutaneous Electrical Nerve Stimulation Device (Cefaly) for Migraine Prevention
The Medical Letter on Drugs and Therapeutics • Aug 18, 2014 (Issue 1449)
-primary endpoint of a >50% reduction
in migraine days per month was 13 (38.2%) with active
treatment ...
The FDA has approved the use of a transcutaneous
electrical nerve stimulation device (Cefaly – Cefaly
Technology) for prevention of episodic migraine in
patients ≥18 years old. The first device to be approved
in the US for migraine prevention, it is available in
Canada and Europe for treatment and prevention of
migraines. A transcranial magnetic stimulation device
(SpringTMS - eNeura Therapeutics) recently approved
by the FDA for treatment of migraine preceded by aura
will be reviewed in a future issue.
Durlaza - A 24-Hour Extended-Release Aspirin
The Medical Letter on Drugs and Therapeutics • Jan 18, 2016 (Issue 1486)
into
the systemic circulation after IR aspirin is cleared will
be active until the next dose is taken. Patients ...
The FDA has approved Durlaza (New Haven
Pharmaceuticals), a 24-hour extended-release (ER)
aspirin formulation available only by prescription, for
secondary prevention of myocardial infarction (MI)
and stroke.
Aripiprazole with Digital Ingestion Tracking (Abilify MyCite)
The Medical Letter on Drugs and Therapeutics • Jan 28, 2019 (Issue 1564)
chloride and
magnesium in the new tablets react with gastric
fluid to activate the embedded 1-mm sensor ...
Monitoring adherence of psychiatric patients to
oral medication may be especially difficult. The
FDA has approved Abilify MyCite (Otsuka/Proteus),
an aripiprazole tablet with an embedded sensor
that tracks when patients take the medication. It is
indicated for treatment of adults with schizophrenia,
bipolar disorder, or major depressive disorder. Abilify MyCite is the first drug with a digital ingestion tracking
system to be approved in the US.
In Brief: Shingrix for Immunocompromised Adults
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021 (Issue 1631)
preventing normal daily
activities can occur.1,4 In a postmarketing observa-tional
study in adults ≥65 ...
The FDA has licensed the adjuvanted, recombinant
varicella zoster virus (VZV) vaccine Shingrix (GSK) for
prevention of herpes zoster (shingles) in adults of any
age who are or will be at elevated risk because of disease-
or therapy-induced immunodeficiency or immunosuppression.
Shingrix has been licensed for herpes
zoster prevention in adults ≥50 years old since 2017.1
It is the only VZV vaccine currently available in the US;
Zostavax, a live-attenuated VZV vaccine, was withdrawn
from the market in 2020.
Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Constipation (IBS-C) (online only)
The Medical Letter on Drugs and Therapeutics • Feb 03, 2025 (Issue 1721)
Chloride Channel Activator Lubiprostone – generic Amitiza (SpecGx) 8, 24 mcg caps 71.80 404.50 8 mcg bid ...
View the Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Constipation (IBS-C)
Med Lett Drugs Ther. 2025 Feb 3;67(1721):e1-3 doi:10.58347/tml.2025.1721e | Show Introduction Hide Introduction
New Drugs for Osteoporosis
The Medical Letter on Drugs and Therapeutics • Jan 05, 1996 (Issue 965)
, 34:1, 1992) and alendronate decrease bone turnover, inhibit
osteoclast activity and shift ...
Two new drugs alendronate (Fosamax - Merck) and salmon calcitonin nasalspray (Miacalcin - Sandoz) are now available in the USA for treatment of postmenopausalosteoporosis. A third drug for treatment of osteoporosis, a slow-release fluoridepreparation (Slow Fluoride -Mission Pharmacal), has been recommended for approvalby an advisory committee of the US Food and Drug Administration (FDA). Various formulationsof fluoride have been available in Europe for this indication for many years.
Omalizumab (Xolair): An Anti-IgE Antibody For Asthma
The Medical Letter on Drugs and Therapeutics • Aug 19, 2003 (Issue 1163)
the potential
for mast cell/basophil activation by IgE molecules (DW MacGlashan, Jr et al, J Immunol 1997;
158 ...
The FDA has approved release of omalizumab (oh mah lye zoo mab; Xolair - Genentech, Novartis), a humanized monoclonal antibody given subcutaneously that binds to immunoglobulin E (IgE). The drug is labeled for patients at least 12 years old with moderate to severe persistent asthma who have shown reactivity to an allergen and whose symptoms are inadequately controlled by an inhaled corticosteroid. The manufacturer claims the drug can help stop allergic reactions before they begin.
Performance-Enhancing Drugs
The Medical Letter on Drugs and Therapeutics • Jul 19, 2004 (Issue 1187)
androgenic activity. Testosterone precursors available as nutritional supplements include
androstenediol ...
With the 2004 Olympics only weeks away, performance-enhancing drugs will once again be receiving a great deal of attention. The US Anti-Doping Agency has published a list of drugs banned in Olympic sports (www.usantidoping.org) that includes, at least for some sports, all but 2 of the drugs reviewed here.
Dasatinib (Sprycel) for CML and Ph+ ALL
The Medical Letter on Drugs and Therapeutics • Jan 15, 2007 (Issue 1252)
to ...
Dasatinib (Sprycel - Bristol-Myers Squibb), an inhibitor of multiple tyrosine kinases, has been approved by the FDA for second-line treatment of chronic myelogenous leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) in adults.