Search Results for "drug interactions"
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Searched for drug interactions. Results 981 to 990 of 1134 total matches.
Tenofovir Alafenamide (Vemlidy) for Hepatitis B
The Medical Letter on Drugs and Therapeutics • Jan 02, 2017 (Issue 1511)
in those with other genotypes.
DRUG INTERACTIONS — Like TDF, TAF is a substrate
of the drug transporters ...
The FDA has approved tenofovir alafenamide
(Vemlidy – Gilead) for treatment of chronic hepatitis
B virus (HBV) infection in adults with compensated
liver disease. It is the first single-drug product
containing tenofovir alafenamide (TAF), a prodrug of
the nucleotide reverse transcriptase inhibitor tenofovir,
to become available; several combination products
containing TAF are approved for treatment of HIV-1
infection. Tenofovir disoproxil fumarate (TDF; Viread –
Gilead), another tenofovir prodrug, has been used for
many years for treatment of chronic HBV infection;
a generic...
Opicapone (Ongentys) - A COMT Inhibitor for Parkinson's Disease
The Medical Letter on Drugs and Therapeutics • Jan 11, 2021 (Issue 1615)
with pheochromocytoma, paraganglioma, or other
catecholamine-secreting neoplasms.
DRUG INTERACTIONS — Coadministration ...
The FDA has approved opicapone (Ongentys –
Neurocrine), a peripherally-acting reversible catechol-O-methyltransferase (COMT) inhibitor, for oral use as an
adjunct to carbidopa/levodopa in adults with Parkinson’s
disease (PD) who experience "off" episodes. It is the
third COMT inhibitor to be approved for this indication;
tolcapone (Tasmar, and generics) and entacapone
(Comtan, and generics) were approved earlier. Opicapone
has been available in Europe since 2016.
Bexagliflozin (Brenzavvy) — A Fifth SGLT2 Inhibitor for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023 (Issue 1683)
are available.
DRUG INTERACTIONS — Bexagliflozin is metabolized
primarily by UDP-glucuronosyltransferase
(UGT ...
Bexagliflozin (Brenzavvy – TheracosBio), a sodium-glucose
cotransporter 2 (SGLT2) inhibitor, has been
approved by the FDA to improve glycemic control
in adults with type 2 diabetes. It is the fifth SGLT2
inhibitor to be approved in the US for this indication
(see Table 4).
Med Lett Drugs Ther. 2023 Aug 21;65(1683):130-2 doi:10.58347/tml.2023.1683b | Show Introduction Hide Introduction
Dapagliflozin (Farxiga) for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Feb 17, 2014 (Issue 1436)
as category C (developmental toxicity
in animals; no adequate studies in women).
DRUG INTERACTIONS ...
Dapagliflozin (dap" a gli fl oe' zin; Farxiga – Bristol-Myers
Squibb/AstraZeneca), an SGLT2 (sodium-glucose co-transporter
2) inhibitor, has been approved by the FDA
for oral treatment of type 2 diabetes. Dapagliflozin is the
second SGLT2 inhibitor to be approved for this indication;
canagliflozin (Invokana) was the first .
Tirzepatide (Mounjaro) for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Jul 11, 2022 (Issue 1654)
.
DRUG INTERACTIONS ― Tirzepatide delays gastric
emptying and can delay the absorption of oral drugs ...
The FDA has approved tirzepatide (Mounjaro –
Lilly), a peptide hormone with activity at both
glucose-dependent insulinotropic polypeptide
(GIP) and glucagon-like peptide-1 (GLP-1)
receptors, to improve glycemic control in adults
with type 2 diabetes. Tirzepatide, which is injected
subcutaneously once weekly, is the first dual GIP/GLP-1 receptor agonist to become available in the
US. Selective GIP receptor agonists are not available
in the US; GLP-1 receptor agonists have been
available for years.
Safety of SSRIs in Pregnancy
The Medical Letter on Drugs and Therapeutics • Nov 17, 2008 (Issue 1299)
EDITORIAL FELLOW: Lauren K. Schwartz, M.D., Mount Sinai School of Medicine
DRUG INTERACTIONS FELLOW ...
Depression occurs in up to 20% of pregnant women, and the use of selective serotonin reuptake inhibitors (SSRIs) in these women has been increasing. Maternal depression has itself been associated with intrauterine growth problems and low birth weight, so the risks of exposure to antidepressants during pregnancy must be weighed against the risks of untreated depression, which also include self-harm, poor bonding and poor parenting. SSRIs available in the US for treatment of depression include citalopram (Celexa, and others), escitalopram (Lexapro), fluoxetine (Prozac, and others), paroxetine...
Conjugated Estrogens (Premarin) Vaginal Cream
The Medical Letter on Drugs and Therapeutics • Feb 23, 2009 (Issue 1306)
The Medical Letter
®
On Drugs and Therapeutics
Published by The Medical Letter, Inc. • 1000 ...
An old conjugated estrogens vaginal cream (Premarin Vaginal Cream - Wyeth) has been newly approved by the FDA specifically for treatment of moderate to severe dyspareunia due to vulvar and vaginal atrophy associated with menopause. Synthetic conjugated estrogens A vaginal cream (Barr) has also been approved for this indication, but has not yet been marketed.
Tapentadol (Nucynta) - A New Analgesic
The Medical Letter on Drugs and Therapeutics • Aug 10, 2009 (Issue 1318)
the drug without
tapering the dose has led to symptoms consistent with
withdrawal.
5
DRUG INTERACTIONS ...
The FDA has approved tapentadol hydrochloride (Nucynta - Ortho-McNeil Janssen) for oral treatment of moderate to severe acute pain in patients ≥18 years old. It has been classified as a Schedule II controlled substance
Airsupra: An Inhaled Albuterol/Budesonide Combination for Asthma
The Medical Letter on Drugs and Therapeutics • Mar 18, 2024 (Issue 1698)
. Cataracts, glaucoma, and decreased
bone mineral density have been observed with longterm
use.
DRUG ...
The FDA has approved Airsupra (AstraZeneca), a
metered-dose inhaler containing the short-acting
beta2-agonist (SABA) albuterol and the inhaled
corticosteroid (ICS) budesonide, for use as needed for
treatment or prevention of bronchoconstriction and to
reduce the risk of exacerbations in patients ≥18 years
old with asthma. Airsupra is the first combination of
a SABA and an ICS to become available in the US. It is
not approved for use as maintenance therapy.
Med Lett Drugs Ther. 2024 Mar 18;66(1698):41-3 doi:10.58347/tml.2024.1698a | Show Introduction Hide Introduction
Sofosbuvir/Velpatasvir (Epclusa) for Hepatitis C
The Medical Letter on Drugs and Therapeutics • Aug 15, 2016 (Issue 1501)
; it is contraindicated for use in pregnant
women and in men whose partners are pregnant.
DRUG INTERACTIONS — Sofosbuvir ...
The FDA has approved Epclusa (Gilead), a fixed-dose
combination of sofosbuvir (Sovaldi) and velpatasvir,
a new direct-acting antiviral agent, for oral treatment
of chronic hepatitis C virus (HCV) infection. Epclusa
is the first oral combination to be approved for
treatment of all six major HCV genotypes.