Search Results for ""drugs for""
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Searched for "drugs for". Results 1651 to 1660 of 2581 total matches.
Finerenone (Kerendia) for Chronic Kidney Disease
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021 (Issue 1631)
severe albuminuria;
according to a manufacturer's press release, the drug
significantly reduced ...
Finerenone (Kerendia – Bayer), an oral nonsteroidal
mineralocorticoid receptor antagonist (MRA), has
been approved by the FDA to reduce the risk of
sustained eGFR decline, end-stage renal disease,
nonfatal MI, hospitalization for heart failure (HF), and
cardiovascular death in adults with chronic kidney
disease (CKD) associated with type 2 diabetes. It is the
first nonsteroidal MRA to be approved in the US.
Ruxolitinib Cream (Opzelura) for Nonsegmental Vitiligo
The Medical Letter on Drugs and Therapeutics • Oct 03, 2022 (Issue 1660)
® Vol. 64 (1660) October 3, 2022
159
1. Ruxolitinib (Opzelura) for atopic dermatitis. Med Lett Drugs ...
The 1.5% cream formulation of the Janus kinase
(JAK) inhibitor ruxolitinib (Opzelura – Incyte) has
been approved by the FDA for topical treatment of
nonsegmental vitiligo (NSV) in patients ≥12 years old.
Opzelura is the first product to be approved by the
FDA for this indication. It was previously approved for
treatment of atopic dermatitis.
Tenapanor (Xphozah) for Hyperphosphatemia in Chronic Kidney Disease
The Medical Letter on Drugs and Therapeutics • Mar 04, 2024 (Issue 1697)
with
constipation. Med Lett Drugs Ther 2022; 64:91.
2. MG Vervloet and AJ van Ballegooijen. Prevention ...
The FDA has approved the sodium/hydrogen
exchanger 3 (NHE3) inhibitor tenapanor (Xphozah –
Ardelyx) to reduce serum phosphorus in adults with
chronic kidney disease (CKD) on dialysis as add-on
therapy when phosphate binders are ineffective or
as monotherapy when phosphate binders cannot be
tolerated. Tenapanor is the first NHE3 inhibitor to be
approved in the US for hyperphosphatemia. It was
previously approved as Ibsrela to treat irritable bowel
syndrome with constipation (IBS-C).
Med Lett Drugs Ther. 2024 Mar 4;66(1697):38-9 doi:10.58347/tml.2024.1697b | Show Introduction Hide Introduction
Qlosi — Pilocarpine 0.4% Ophthalmic Solution for Presbyopia
The Medical Letter on Drugs and Therapeutics • Jan 06, 2025 (Issue 1719)
and patients who use it should
avoid driving at night while the drug is active.
Pronunciation Key ...
The FDA has approved pilocarpine 0.4% preservativefree
ophthalmic solution (Qlosi – Orasis) for treatment
of presbyopia in adults. Pilocarpine 1.25% ophthalmic
solution (Vuity) was approved in 2021 for the same
indication. Pilocarpine 1%, 2%, and 4% ophthalmic
solutions (Isopto Carpine, and others) have been
available for years for treatment of glaucoma, but
local (e.g., blurry vision and instillation-site pain)
and systemic (e.g., sweating and GI disturbances)
adverse effects have limited their use.
Med Lett Drugs Ther. 2025 Jan 6;67(1719):5-6 doi:10.58347/tml.2025.1719b | Show Introduction Hide Introduction
Ganaxolone (Ztalmy) for CDKL5 Deficiency Disorder (online only)
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
-dependent
kinase-like 5 (CDKL5) deficiency disorder
in patients ≥2 years old. It is the first drug ...
The FDA has approved ganaxolone (Ztalmy – Marinus)
for oral treatment of seizures associated with cyclin-dependent
kinase-like 5 (CDKL5) deficiency disorder
in patients ≥2 years old. It is the first drug to be
approved in the US for this indication.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):e139-40 doi:10.58347/tml.2024.1709g | Show Introduction Hide Introduction
Iptacopan (Fabhalta) for Paroxysmal Nocturnal Hemoglobinuria (online only)
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024 (Issue 1712)
, and infections were most
common.
▶ Drug Interactions: Concurrent use of CYP2C8 inducers or
inhibitors can ...
The FDA has approved the complement factor B
inhibitor iptacopan (Fabhalta – Novartis) for
treatment of paroxysmal nocturnal hemoglobinuria
(PNH) in adults. Iptacopan is the first oral drug to
be approved in the US for this indication. Three
parenterally administered drugs, the complement
C5 inhibitors eculizumab (Soliris) and ravulizumab
(Ultomiris) and the complement C3 inhibitor
pegcetacoplan (Empaveli), are also approved for
treatment of PNH.
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e171-3 doi:10.58347/tml.2024.1712e | Show Introduction Hide Introduction
Patient-Controlled Analgesia
The Medical Letter on Drugs and Therapeutics • Nov 17, 1989 (Issue 805)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Automated intravenous delivery systems have recently become commercially available for intermittent self-administration of analgesics. Patient-controlled analgesia (PCA) has been used effectively to relieve after a wide variety of surgical procedures. It has also been effective for pain associated with labor, sickle cell crisis, and chronic pain caused by cancer.
Quazepam: A New Hypnotic
The Medical Letter on Drugs and Therapeutics • Apr 20, 1990 (Issue 816)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Quazepam (Doral - Baker Cummins, Wallace) is a trifluoroethyl benzodiazepine made by Schering and approved in 1985 by the US Food and Drug Administration for treatment of insomnia. Like other benzodiazepines, it is a Schedule IV controlled substance.Quazepam (Doral - Baker Cummins, Wallace) is a trifluoroethyl benzodiazepine made by Schering and approved in 1985 by the US Food and Drug Administration for treatment of insomnia. Like other benzodiazepines, it is a Schedule IV controlled substance.
Abciximab to Prevent Vessel Closure After Angioplasty
The Medical Letter on Drugs and Therapeutics • Jun 09, 1995 (Issue 950)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Abciximab (ab sik si mab; ReoPro - Centocor), the Fab (fragment antigen binding) fragment of the chimeric human-murine monoclonal antibody 7E3 (c7E3 Fab), has been approved by the US Food and Drug Administration as an adjunct to percutaneous transluminal coronary angioplasty or atherectomy (PTCA) to prevent abrupt closure of the treated coronary vessel.
Simethicone for Gastrointestinal gas
The Medical Letter on Drugs and Therapeutics • Jun 21, 1996 (Issue 977)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Gastrointestinal gas may cause symptoms when excessive amounts become trapped in the stomach and intestinal tract. Simethicone (Gas-X, Maalox Anti-Gas, Mylanta Gas Relief, Mylicon, Phazyme), sold over-the-counter in capsules, tablets and infant drop formulations, is being heavily advertised to the public for symptomatic treatment of flatulence and gastric bloating. According to a recent press release, 'Phazyme works fast so people can continue living active lives and eating the foods they love without fear of embarrassment.' Products that combine one or more antacids with simethicone...