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Searched for drug. Results 641 to 650 of 2581 total matches.
Pegaspargase for Acute Lymphoblastic Leukemia
The Medical Letter on Drugs and Therapeutics • Mar 17, 1995 (Issue 944)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Pegaspargase (peg as par jase; PEG-L-asparaginase; Oncaspar - Rh ne-Poulenc Rorer), a polyethylene glycol (PEG) conjugate of L-asparaginase, has been approved by the US Food and Drug Administration for treatment of acute lymphoblastic leukemia (ALL), the most common malignancy of childhood. The new drug is recommended only for patients who have had allergic reactions to asparaginase. Asparaginase is available commercially as Elspar, which is derived from Escherichia coli. A formulation derived from Erwinia chrysanthemi is available on an investigational basis (Ogden Bioservices,...
Tamsulosin for Benign Prostatic Hyperplasia
The Medical Letter on Drugs and Therapeutics • Oct 10, 1997 (Issue 1011)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Tamsulosin (Flomax - Boehringer Ingelheim), an alpha 1 - adrenoreceptor blocker, has been approved by the FDA for treatment of benign prostatic hyperplasia (BPH). It is claimed to bind preferentially to alpha1 receptors in the prostate.
Extended-Release Hydromorphone (Exalgo) for Pain
The Medical Letter on Drugs and Therapeutics • Aug 08, 2011 (Issue 1370)
Letter®
On Drugs and Therapeutics
Volume 53 (Issue 1370)
August 8, 2011
www.medicalletter.org ...
The FDA has approved the opioid agonist hydromorphone in a once-daily extended-release (ER) oral tablet formulation (Exalgo – Covidien) for the management of moderate to severe pain in opioid-tolerant patients requiring continuous, long-term therapy. Another hydromorphone ER formulation (Palladone – Purdue) was available previously, but was withdrawn from the market because taking it with alcohol could interfere with the extended-release mechanism and lead to rapid release of potentially lethal amounts of the drug ("dose-dumping").
Pimavanserin (Nuplazid) for Parkinson's Disease Psychosis
The Medical Letter on Drugs and Therapeutics • Jun 06, 2016 (Issue 1496)
The Medical Letter®
on Drugs and Therapeutics
Volume 58 (Issue 1496) June 6, 2016
Take CME Exams ...
The FDA has approved the atypical antipsychotic
pimavanserin (Nuplazid – Acadia) for treatment
of hallucinations and delusions associated with
Parkinson's disease. It is the first drug to be approved
in the US for this indication.
In Brief: An Asenapine Patch (Secuado) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Jan 11, 2021 (Issue 1615)
with the sublingual
formulation or with any other antipsychotic drug.
Antipsychotic drugs, including asenapine, can ...
A transdermal formulation of the second-generation
(atypical) antipsychotic asenapine (Secuado – Noven)
has been approved by the FDA for once-daily treatment of
schizophrenia in adults. Asenapine is the first antipsychotic
to become available in a transdermal formulation in the US.
A twice-daily sublingual tablet formulation of asenapine
(Saphris) has been available since 2009.
Osimertinib (Tagrisso) for Adjuvant Treatment of NSCLC (online only)
The Medical Letter on Drugs and Therapeutics • Aug 07, 2023 (Issue 1682)
in the US for this
indication. The drug was previously approved for
first-line treatment of adults with NSCLC with EGFR
exon ...
The FDA has approved osimertinib (Tagrisso –
AstraZeneca), an oral kinase inhibitor, for adjuvant
treatment of non-small cell lung cancer (NSCLC)
after tumor resection in adults who have epidermal
growth factor receptor (EGFR) exon 19 deletions or
exon 21 L858R mutations. Osimertinib is the first
targeted therapy to be approved in the US for this
indication. The drug was previously approved for
first-line treatment of adults with NSCLC with EGFR
exon 19 deletions or exon 21 L858R mutations and for
treatment of EGFR T790M mutation-positive NSCLC
in adults whose disease progressed...
Med Lett Drugs Ther. 2023 Aug 7;65(1682):e131-2 doi:10.58347/tml.2023.1682c | Show Introduction Hide Introduction
Mivacurium - A New Neuromuscular Blocker
The Medical Letter on Drugs and Therapeutics • Aug 21, 1992 (Issue 877)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Mivacurium chloride (Mivacron - Burroughs-Wellcome), a short-acting nondepolarizing neuromuscular blocking drug, is now available in the USA for intravenous use in routine intubation and short procedures requiring skeletal muscle relaxation. It can be given in a bolus or a continuous infusion.
Crofelemer (Fulyzaq) for Antiretroviral-Induced Diarrhea
The Medical Letter on Drugs and Therapeutics • Jul 22, 2013 (Issue 1421)
The Medical Letter®
On Drugs and Therapeutics
Volume 55 (Issue 1421)
July 22, 2013 ...
The FDA has approved crofelemer (kroe fel’ e mer;
Fulyzaq – Salix), a chloride channel inhibitor derived
from the red sap of the South American plant Croton
lechleri, for symptomatic relief of noninfectious
diarrhea in patients with HIV taking antiretroviral
drugs. It is the first drug approved for relief of antiretroviral-induced diarrhea and the first oral botanical
drug approved by the FDA.
Clevidipine (Cleviprex) for IV Treatment of Severe Hypertension
The Medical Letter on Drugs and Therapeutics • Sep 22, 2008 (Issue 1295)
Letter
®
On Drugs and Therapeutics
Volume 50 (Issue 1295)
September 22, 2008
www.medicalletter.org ...
Clevidipine (Cleviprex - The Medicines Company), a dihydropyridine calcium channel blocker (CCB), has been approved by the FDA for intravenous (IV) use in lowering high blood pressure. It is the second IV CCB to be marketed in the US; nicardipine has been available in an IV formulation (Cardene IV) for more than 10 years. Like IV nicardipine, clevidipine will probably be used mainly for urgent treatment of hypertension in intensive care units, operating rooms and emergency departments.
Edoxaban (Savaysa) - The Fourth New Oral Anticoagulant
The Medical Letter on Drugs and Therapeutics • Mar 30, 2015 (Issue 1465)
The Medical Letter®
on Drugs and Therapeutics
Objective Drug Reviews Since 1959
Volume 57 (Issue ...
The FDA has approved edoxaban (Savaysa – Daiichi
Sankyo), a once-daily, oral, direct factor Xa inhibitor,
for treatment of venous thromoboembolism (VTE)
and for prevention of stroke and systemic embolism
in patients with nonvalvular atrial fibrillation. It is the
fourth new oral anticoagulant to be approved for VTE
and nonvalvular atrial fibrillation.