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Searched for data. Results 141 to 150 of 1144 total matches.

Seladelpar (Livdelzi) for Primary Biliary Cholangitis

   
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025  (Issue 1720)
. PREGNANCY AND LACTATION — No adequate data are available on the use of seladelpar in pregnant women ...
Seladelpar (Livdelzi – Gilead), a peroxisome proliferator-activated receptor (PPAR)-delta agonist, has received accelerated approval from the FDA for use in combination with ursodeoxycholic acid (ursodiol, UDCA; Urso Forte, and generics) for treatment of primary biliary cholangitis (PBC) in adults who had an inadequate response to UDCA and as monotherapy in those unable to tolerate UDCA. Accelerated approval was based on a reduction in alkaline phosphatase (ALP) levels. Seladelpar is the second PPAR agonist to be approved in the US for this indication; elafibranor (Iqirvo)...
Med Lett Drugs Ther. 2025 Jan 20;67(1720):13-5   doi:10.58347/tml.2025.1720d |  Show IntroductionHide Introduction

Comparison Table: Some Drugs for Weight Management (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 04, 2025  (Issue 1734)
for weight loss) ■ Thyroid C-cell tumors (animal data) ■ Acute gallbladder disease ■ Pulmonary aspiration ...
View the Comparison Table: Some Drugs for Weight Management
Med Lett Drugs Ther. 2025 Aug 4;67(1734):e127-30   doi:10.58347/tml.2025.1734b |  Show IntroductionHide Introduction

Delgocitinib Cream (Anzupgo) for Chronic Hand Eczema

   
The Medical Letter on Drugs and Therapeutics • Oct 13, 2025  (Issue 1739)
), cyclosporine, azathioprine, methotrexate, and acitretin, but data on their efficacy are limited and they can ...
The FDA has approved a 2% cream formulation of delgocitinib (Anzupgo – Leo), a Janus kinase (JAK) inhibitor, for treatment of moderate to severe chronic hand eczema (dermatitis) in adults who had an inadequate response to or are unable to use topical corticosteroids. Delgocitinib is the first drug to be approved in the US for this indication. Ruxolitinib, another JAK inhibitor, is available in a 1.5% cream formulation (Opzelura) for treatment of mild to moderate atopic dermatitis in patients ≥2 years old.
Med Lett Drugs Ther. 2025 Oct 13;67(1739):163-5   doi:10.58347/tml.2025.1739b |  Show IntroductionHide Introduction

In Brief: Hyperthermia with Scopolamine Patches

   
The Medical Letter on Drugs and Therapeutics • Aug 18, 2025  (Issue 1735)
with available data. One child and one older adult died; both patients had other risk factors such as use ...
The FDA has required a new warning in the label for the scopolamine transdermal patch (Transderm-Scōp, and generics) about a risk of serious or fatal hyperthermia. Scopolamine, an anticholinergic drug, is FDA-approved for prevention of nausea and vomiting associated with motion sickness or recovery after surgery in adults; it is often used off-label to reduce drooling in children and adolescents with neurologic disorders.
Med Lett Drugs Ther. 2025 Aug 18;67(1735):136   doi:10.58347/tml.2025.1735g |  Show IntroductionHide Introduction

Antiviral Drugs for Seasonal Influenza for 2025-2026

   
The Medical Letter on Drugs and Therapeutics • Oct 27, 2025  (Issue 1740)
of pneumonia, respiratory failure, and death.20-22 No data are available on the efficacy of baloxavir when ...
Influenza is generally a self-limited illness, but complications including pneumonia, respiratory failure, and death can occur, especially in persons at increased risk (see Table 1).
Med Lett Drugs Ther. 2025 Oct 27;67(1740):169-74   doi:10.58347/tml.2025.1740a |  Show IntroductionHide Introduction

Carteolol and Penbutolol For Hypertension

   
The Medical Letter on Drugs and Therapeutics • Jul 28, 1989  (Issue 797)
to data from the manufacturer, carteolol taken once daily in doses of 2.5 to 40 mg lowers blood pressure ...
Carteolol (Cartrol - Abbott) and penbutolol (Levatol - Reed & Carnrick), two oral beta-adrenergic blocking drugs, were recently approved by the US Food and Drug Administration for once-daily treatment of systemic hypertension. Both drugs are non-selective beta-blockers with mild partial agonist activity. Beta-blockers currently available in the USA for treatment of hypertension are listed in the table on the next page.
Med Lett Drugs Ther. 1989 Jul 28;31(797):70-1 |  Show IntroductionHide Introduction

Olsalazine

   
The Medical Letter on Drugs and Therapeutics • Nov 16, 1990  (Issue 831)
to be better tolerated than sulfasalazine, but more data would be welcome, and diarrhea may be a problem ...
Olsalazine sodium (Dipentum - Pharmacia), a dimer (two molecules linked by an azo bond) of 5-aminosalicylic acid, was recently approved by the US Food and Drug Administration for oral use to maintain remission of ulcerative colitis in adult patients who cannot tolerate sulfasalazine (Azulfidine; and others).
Med Lett Drugs Ther. 1990 Nov 16;32(831):105-6 |  Show IntroductionHide Introduction

Celecoxib for Arthritis

   
The Medical Letter on Drugs and Therapeutics • Jan 29, 1999  (Issue 1045)
price (AWP or HCFA) listings in First DataBank NDDF, January 7, 1999 and Drug Topics Red Book Update ...
Celecoxib, a selective COX-2 inhibitor, has been approved by the FDA for treatment of osteoarthritis and rheumatoid arthritis.
Med Lett Drugs Ther. 1999 Jan 29;41(1045):11-2 |  Show IntroductionHide Introduction

A New Long-acting Methylphenidate (Concerta)

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2000  (Issue 1086)
, according to AWP listings in Drug Topics Red Book 2000 and August Update and First DataBank NDDB, August ...
Methylphenidate (Ritalin, and others) is now available in a new extended-release formulation (Concerta--Alza) for treatment of attention deficit/hyperactivity disorder (ADHD).
Med Lett Drugs Ther. 2000 Sep 4;42(1086):80-1 |  Show IntroductionHide Introduction

Caspofungin (Cancidas) For Aspergillosis

   
The Medical Letter on Drugs and Therapeutics • Jul 09, 2001  (Issue 1108)
a complete resolution of all signs and symptoms. In unpublished data presented to the FDA by the manufacturer ...
Caspofungin acetate(Cancidas) is the first of a new class of antifungals, the echinocandins. It has been approved by the FDA for treatment of invasive aspergillosis in patients who fail to respond to or are unable to tolerate other antifungal drugs such as amphotericin B and itraconazole.
Med Lett Drugs Ther. 2001 Jul 9;43(1108):58-9 |  Show IntroductionHide Introduction