Search Results for "Metabolic"
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Searched for Metabolic. Results 831 to 840 of 1047 total matches.

Juluca - A Two-Drug Complete Regimen for HIV (online only)

   
The Medical Letter on Drugs and Therapeutics • Dec 03, 2018  (Issue 1561)
— Rilpivirine is primarily metabolized by CYP3A; concurrent administration of drugs that induce CYP3A ...
The FDA has approved Juluca (ViiV Healthcare/Janssen), a fixed-dose combination of the integrase strand transfer inhibitor (INSTI) dolutegravir (Tivicay) and the non-nucleoside reverse transcriptase inhibitor (NNRTI) rilpivirine (Edurant), as a once-daily complete regimen for treatment of adults with HIV-1 infection who do not have a history of treatment failure or known substitutions associated with resistance to either drug and have been taking a stable suppressive antiretroviral regimen for ≥6 months. Dolutegravir/rilpivirine is the first complete regimen to be approved for...
Med Lett Drugs Ther. 2018 Dec 3;60(1561):e202-4 |  Show IntroductionHide Introduction

Sarecycline (Seysara) - Another Oral Tetracycline for Acne

   
The Medical Letter on Drugs and Therapeutics • Mar 25, 2019  (Issue 1568)
, 100, 150 mg tablets Route Oral Tmax 1.5-2.0 hours Metabolism Minimal ( ...
Sarecycline (Seysara — Allergan), a new oral tetracycline antibiotic, has been approved by the FDA for once-daily treatment of inflammatory lesions of non-nodular moderate to severe acne in patients ≥9 years old.
Med Lett Drugs Ther. 2019 Mar 25;61(1568):43-4 |  Show IntroductionHide Introduction

ZTlido - A New Lidocaine Patch for Postherpetic Neuralgia

   
The Medical Letter on Drugs and Therapeutics • Mar 25, 2019  (Issue 1568)
% patch Route Transdermal Tmax ~14 hours1 Metabolism Primarily hepatic Half-life 1.5-2 hours (IV ...
A lidocaine 1.8% patch (ZTlido – Scilex) has been approved by the FDA for treatment of pain associated with postherpetic neuralgia (PHN). A lidocaine 5% patch (Lidoderm, and generics) was approved earlier for the same indication and has been used off-label for treatment of other types of localized pain. Both of these patches are available only by prescription. Lidocaine 4% patches (Aspercreme, IcyHot, and others) are available over the counter for back, neck, shoulder, and joint pain.
Med Lett Drugs Ther. 2019 Mar 25;61(1568):41-3 |  Show IntroductionHide Introduction

Annovera - A New Contraceptive Vaginal Ring

   
The Medical Letter on Drugs and Therapeutics • Dec 16, 2019  (Issue 1587)
inhibitors, carbamazepine, and St. John’s wort, can increase the metabolism of hormonal contraceptives ...
Annovera (TherapeuticsMD), a contraceptive vaginal ring that releases segesterone acetate, a synthetic progestin, and ethinyl estradiol, was approved by the FDA in 2018 and is now available. It is the first product to contain segesterone and the second vaginal ring to become available in the US; NuvaRing, which delivers etonogestrel and ethinyl estradiol, was the first. Unlike NuvaRing, which requires use of a new ring each month, the Annovera ring can be used for an entire year, but it must be removed for one week each month.
Med Lett Drugs Ther. 2019 Dec 16;61(1587):197-8 |  Show IntroductionHide Introduction

Twirla - A New Contraceptive Patch

   
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021  (Issue 1617)
increase the metabolism of hormonal contraceptives and decrease their effectiveness; backup contraception ...
The FDA has approved Twirla (Agile Therapeutics), a transdermal contraceptive patch containing the estrogen ethinyl estradiol and the progestin levonorgestrel, for use in women with a BMI <30 kg/m2. It is the second contraceptive patch to become available in the US; Xulane, a patch that delivers ethinyl estradiol and the progestin norelgestromin, has been available since 2014.
Med Lett Drugs Ther. 2021 Feb 8;63(1617):17-8 |  Show IntroductionHide Introduction

Low-Dose Colchicine for Coronary Artery Disease

   
The Medical Letter on Drugs and Therapeutics • Apr 05, 2021  (Issue 1621)
) Metabolism Mainly CYP3A4 Elimination Mainly in urine (40-65% unchanged) Half-life 26.6 hours (Colcrys); 31 ...
The centuries-old anti-inflammatory drug colchicine (Colcrys, and others) is FDA-approved for prophylaxis and treatment of gout flares and for treatment of familial Mediterranean fever. It is also used off-label to treat pericarditis, and in recent years has been investigated for reduction of cardiovascular risk in patients with coronary artery disease (CAD).
Med Lett Drugs Ther. 2021 Apr 5;63(1621):54-5 |  Show IntroductionHide Introduction

Finerenone (Kerendia) for Chronic Kidney Disease

   
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021  (Issue 1631)
) Formulation 10, 20 mg tablets Route Oral Cmax 0.5-1.25 hours Metabolism Primarily by CYP3A4 and to a lesser ...
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.
Med Lett Drugs Ther. 2021 Aug 23;63(1631):131-2 |  Show IntroductionHide Introduction

Dasiglucagon (Zegalogue) for Severe Hypoglycemia

   
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021  (Issue 1631)
Subcutaneous Tmax ~35 minutes Metabolism Hydrolyzed to amino acids in blood, liver, and kidneys Half-life ...
The FDA has approved dasiglucagon (Zegalogue – Zealand) for subcutaneous (SC) treatment of severe hypoglycemia in patients ≥6 years old with diabetes. Dasiglucagon is the third glucagon product to be marketed in the US that does not require reconstitution before administration; Gvoke, a SC formulation approved for use in patients ≥2 years old, and Baqsimi, an intranasal powder approved for use in patients ≥4 years old, have been available since 2019. Injectable glucagon emergency kits (GlucaGen HypoKit, and generics) have been available for years, but they require...
Med Lett Drugs Ther. 2021 Aug 23;63(1631):132-4 |  Show IntroductionHide Introduction

Ruxolitinib Cream (Opzelura) for Nonsegmental Vitiligo

   
The Medical Letter on Drugs and Therapeutics • Oct 03, 2022  (Issue 1660)
Topical Metabolism Primarily by CYP3A4 and to a lesser extent by 2C9 in vitro Elimination Urine (74 ...
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.
Med Lett Drugs Ther. 2022 Oct 3;64(1660):158-9 |  Show IntroductionHide Introduction

Relyvrio for ALS

   
The Medical Letter on Drugs and Therapeutics • Nov 28, 2022  (Issue 1664)
CYP1A2, CYP2B6, and CYP3A4 and may alter serum concentrations of drugs that are metabolized ...
The FDA has approved Relyvrio (Amylyx), a fixed-dose combination of sodium phenylbutyrate and taurursodiol, for treatment of amyotrophic lateral sclerosis (ALS). Sodium phenylbutyrate (Buphenyl, and others) has been available by prescription for years for treatment of urea cycle disorders. Taurursodiol (tauroursodeoxycholic acid), a derivative of ursodiol, is an over-the-counter bile acid supplement claimed to have neuroprotective benefits. Relyvrio is the third drug to be approved in the US for treatment of ALS; riluzole (Rilutek, and others) and edaravone (Radicava, Radicava...
Med Lett Drugs Ther. 2022 Nov 28;64(1664):190-1 |  Show IntroductionHide Introduction