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Searched for Drug. Results 1421 to 1430 of 2582 total matches.
Ameluz for Actinic Keratoses
The Medical Letter on Drugs and Therapeutics • Dec 05, 2016 (Issue 1509)
on the face, forehead, or scalp
who received red light treatment with either ALA or
the drug vehicle ...
The FDA has approved a 10% nanoemulsion gel
formulation of the porphyrin-based photosensitizer
aminolevulinic acid hydrochloride (ALA; Ameluz –
Biofrontera) for use in combination with a narrowband
red light photodynamic therapy (PDT) lamp (BF-RhodoLED)
for treatment of actinic keratoses (AKs)
of mild to moderate severity on the face and scalp.
A 20% ALA solution (Levulan Kerastick) approved for
use in combination with blue light PDT (BLU-U) has
been available in the US since 2002.
Obalon Balloon System - Another Gastric Balloon for Weight Loss
The Medical Letter on Drugs and Therapeutics • Jun 19, 2017 (Issue 1523)
devices for weight loss. Med Lett
Drugs Ther 2015; 55:122.
4. FDA summary of safety and effectiveness ...
The FDA has approved the Obalon Balloon System
(Obalon), a swallowable intragastric gas-filled balloon
device, to facilitate weight loss in adults with a body
mass index (BMI) of 30-40 kg/m2 who have not been
able to lose weight through diet and exercise. Two
other gastric balloon devices, ReShape and Orbera,
were approved earlier.
An EUA for Anakinra (Kineret) for COVID-19 (online only)
The Medical Letter on Drugs and Therapeutics • Dec 12, 2022 (Issue 1665)
generally
receive the antiviral drug remdesivir (Veklury)6
and the corticosteroid dexamethasone; those ...
The recombinant interleukin-1 (IL-1) receptor
antagonist anakinra (Kineret – Sobi) has been
granted an FDA Emergency Use Authorization
(EUA) for treatment of hospitalized adults with
confirmed COVID-19 pneumonia who require low- or
high-flow supplemental oxygen, are at risk of
progressing to severe respiratory failure, and are
likely to have elevated plasma levels of soluble
urokinase plasminogen activator receptor (suPAR).
Anakinra has been available in the US for years; it
is FDA-approved for multiple indications, including
rheumatoid arthritis. Assays for suPAR are...
Tenofovir Alafenamide (Vemlidy) for Hepatitis B
The Medical Letter on Drugs and Therapeutics • Jan 02, 2017 (Issue 1511)
liver disease. It is the first single-drug product
containing tenofovir alafenamide (TAF), a prodrug ...
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)
a dopa decarboxylase
inhibitor such as carbidopa; most patients were also
taking other drugs for PD ...
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)
but
are summarized in the package insert) in patients
with type 2 diabetes that compared the new drug
with placebo ...
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
Daprodustat (Jesduvroq) for Anemia of Chronic Kidney Disease
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024 (Issue 1696)
who have
been on dialysis for at least 4 months. It is the first
HIF-PHI and the first oral drug ...
The FDA has approved daprodustat (Jesduvroq –
GSK), a hypoxia-inducible factor prolyl hydroxylase
inhibitor (HIF-PHI), for oral treatment of anemia due
to chronic kidney disease (CKD) in adults who have
been on dialysis for at least 4 months. It is the first
HIF-PHI and the first oral drug to be approved in the
US for this indication.
Med Lett Drugs Ther. 2024 Feb 19;66(1696):25-7 doi:10.58347/tml.2024.1696a | Show Introduction Hide Introduction
Chloroxazone Hepatotoxicity
The Medical Letter on Drugs and Therapeutics • May 10, 1996 (Issue 974)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
The US Food and Drug Administration (FDA) recently approved a stronger warning about hepatotoxicity in the labeling for chlorzoxazone, a centrally-acting skeletal muscle relaxant.
In Brief: An Over-the-Counter Retinoid for Acne
The Medical Letter on Drugs and Therapeutics • Sep 26, 2016 (Issue 1504)
, scaling,
photosensitivity, erythema, burning, and pruritus.
Although only small amounts of the drug ...
Differin Gel 0.1% (Galderma), a topical formulation of the retinoid adapalene, will soon be available over the counter (OTC) for once-daily treatment of acne in patients ≥12 years old. It is the first topical retinoid to be approved for sale over the counter.All topical retinoids normalize keratinization and appear to have anti-inflammatory effects; whether any one topical retinoid is more effective than any other is not clear. Many dermatologists now recommend topical retinoids for first-line treatment of acne; they can be used alone or in combination with antibiotics to treat both inflamed...
Azacitidine (Vidaza) for Myelodysplastic Syndrome
The Medical Letter on Drugs and Therapeutics • Jan 31, 2005 (Issue 1201)
Letter
®
On Drugs and Therapeutics
IN THIS ISSUE
Volume 47 (Issue 1201)
January 31, 2005 ...
Azacitidine (Vidaza - Pharmion), a pyrimidine nucleoside analog of cytidine, is the first drug approved by the FDA for treatment of myelodysplastic syndrome (MDS). Azacitidine is incorporated into newly synthesized DNA and inhibits DNA methyltransferase. Hypomethylation of DNA can restore the normal expression of genes critical for cell differentiation.