Search Results for "drug interactions"
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Searched for drug interactions. Results 491 to 500 of 1152 total matches.
Colesevelam (Welchol) For Hypercholesterolemia
The Medical Letter on Drugs and Therapeutics • Oct 30, 2000 (Issue 1091)
interacts with thyroid hormones, thiazide and furosemide diuretics and other drugs that bind ...
Colesevelam hydrochloride (Welchol - Sankyo Pharma), a nonabsorbed hydrophilic polymer that binds bile acids, has been approved by the FDA for reduction of plasma LDL cholesterol in patients with primary hypercholesterolemia.
Caplacizumab (Cablivi) for iTTP
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020 (Issue 1609)
, and urticaria were also reported with
use of the drug.
DRUG INTERACTIONS — Concomitant use of
caplacizumab ...
Caplacizumab-yhdp (Cablivi – Sanofi /Genzyme), a
von Willebrand factor-directed antibody fragment, has
been approved by the FDA for use in combination with
plasma exchange and immunosuppressive therapy
for treatment of immune-mediated thrombotic
thrombocytopenic purpura (iTTP; formerly called
acquired thrombotic thrombocytopenic purpura
[aTTP]) in adults. It is the first drug to be approved in
the US for this indication.
Oral Balsalazide (Colazal) For Ulcerative Colitis
The Medical Letter on Drugs and Therapeutics • Jul 23, 2001 (Issue 1109)
occurred with mesalamine.
DRUG INTERACTIONS — In vitro, mesalamine from balsalazide or any ...
Balsalazide disodium (Colazal), a prodrug of mesalamine, was marketed in the US this year for oral treatment of mildly to moderately active ulcerative colitis. Oral formulations of mesalamine have been available in the US for nine years for treatment and maintenance of remissions and olsalazine, which is a dimer of mesalamine, is marketed for maintenance of remissions but not for treatment. Balsalazide has been available in Europe for four years.
Fluvoxamine for COVID-19?
The Medical Letter on Drugs and Therapeutics • May 03, 2021 (Issue 1623)
; 11:eaau5266.
5. Drug interactions from The Medical Letter. Available at:
www.medicalletter.org ...
A recent article in JAMA and an interview of its senior
author on 60 Minutes have heightened interest in
off-label use of the oral selective serotonin reuptake
inhibitor (SSRI) fluvoxamine (Luvox, and generics) to
treat COVID-19.
Mifepristone (Korlym) for Cushing's Syndrome
The Medical Letter on Drugs and Therapeutics • Jun 11, 2012 (Issue 1392)
and for 1 month after the last dose.
DRUG INTERACTIONS — Strong inhibitors of
CYP3A4, such as ketoconazole ...
The FDA has approved the antiprogestin mifepristone
(Korlym – Corcept Therapeutics) for control of hyperglycemia
secondary to hypercortisolism in adults with
endogenous Cushing’s syndrome who have type 2 diabetes/
glucose intolerance and have not responded to,
or are not candidates for, surgery. Formerly known as
RU 486, mifepristone is also available in a lower
strength as Mifeprex for use in terminating an early
intrauterine pregnancy.
Orphengesic Forte - An Old Analgesic Combination Returns
The Medical Letter on Drugs and Therapeutics • Nov 16, 2020 (Issue 1611)
as a prescription drug by the FDA for treatment of mild to moderate pain caused by acute musculoskeletal disorders ...
A fixed-dose combination of orphenadrine citrate, aspirin,
and caffeine (Orphengesic Forte – Galt; previously
available as Norgesic Forte) has been approved as
a prescription drug by the FDA for treatment of mild
to moderate pain caused by acute musculoskeletal
disorders. Single-ingredient generic orphenadrine
citrate is available by prescription in oral and injectable
formulations and has been used for years as an adjunct
for treatment of acute musculoskeletal pain. Orphengesic
Forte is being marketed as a non-opioid alternative for
pain relief.
Extended-Release Hydromorphone (Exalgo) for Pain
The Medical Letter on Drugs and Therapeutics • Aug 08, 2011 (Issue 1370)
hydromorphone ER tablets can result in release of a
potentially fatal dose of the drug.
DRUG INTERACTIONS ...
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").
Osimertinib (Tagrisso) for Adjuvant Treatment of NSCLC (online only)
The Medical Letter on Drugs and Therapeutics • Aug 07, 2023 (Issue 1682)
, cutaneous vasculitis,
and aplastic anemia have been reported with use of
the drug.
DRUG INTERACTIONS ...
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
Tesamorelin (Egrifta) for HIV-Associated Lipodystrophy
The Medical Letter on Drugs and Therapeutics • May 02, 2011 (Issue 1363)
Letter®
On Drugs and Therapeutics
Volume 53 (Issue 1363)
May 2, 2011
www.medicalletter.org
Published ...
The FDA has approved tesamorelin (Egrifta – EMD
Serono), an injectable synthetic analog of growth-hormone-
releasing factor (GRF), for reduction of excess
abdominal fat in patients with lipodystrophy associated
with HIV infection. Growth hormone (somatropin –
Serostim; EMD Serono) has been available for years for
treatment of HIV wasting.
Ibrutinib (Imbruvica) for Chronic Lymphocytic Leukemia
The Medical Letter on Drugs and Therapeutics • Apr 14, 2014 (Issue 1440)
,
infection (especially pneumonia), and cytopenias.
DRUG INTERACTIONS — Ibrutinib is a substrate
of CYP3A ...
The FDA has approved ibrutinib (eye broo' ti nib;
Imbruvica – Janssen/Pharmacyclics), an oral kinase
inhibitor, for second-line treatment of chronic
lymphocytic leukemia (CLL). It is the first kinase inhibitor
to be approved for CLL. Ibrutinib was approved earlier
for second-line treatment of mantle cell lymphoma, a
rare form of B-cell non-Hodgkins lymphoma.