Search Results for "moderate concentrate"
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Searched for moderate concentrate. Results 61 to 70 of 149 total matches.

Xanomeline/Trospium (Cobenfy) for Schizophrenia

   
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024  (Issue 1715)
concentrations of xanomeline and its adverse effects. Xanomeline transiently inhibits CYP3A4 and P-glycoprotein ...
The FDA has approved Cobenfy (BMS), an oral fixed-dose combination of the muscarinic agonist xanomeline and the peripheral muscarinic antagonist trospium chloride, for treatment of schizophrenia in adults. It is the first antipsychotic drug to be approved in the US for treatment of schizophrenia that does not block dopamine receptors. This is the first approval for xanomeline; trospium has been available for many years for treatment of overactive bladder.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):177-9   doi:10.58347/tml.2024.1715a |  Show IntroductionHide Introduction

Lodoco: Low-Dose Colchicine for Cardiovascular Event Prevention

   
The Medical Letter on Drugs and Therapeutics • Oct 02, 2023  (Issue 1686)
outcomes. Colchicine is excreted in human breast milk in low concentrations. DRUG INTERACTIONS ...
Colchicine (Colcrys, and others), which has been available in the US for decades for prophylaxis and treatment of gout flares and other indications in oral formulations that contain 0.6 mg of the drug, has now been approved in 0.5-mg tablets as Lodoco (Agepha) to reduce the risk of myocardial infarction (MI), stroke, coronary revascularization, and cardiovascular death in adults with established atherosclerotic disease or multiple risk factors for cardiovascular disease.
Med Lett Drugs Ther. 2023 Oct 2;65(1686):156-7   doi:10.58347/tml.2023.1686b |  Show IntroductionHide Introduction

Zuranolone (Zurzuvae) – An Oral Drug for Postpartum Depression

   
The Medical Letter on Drugs and Therapeutics • Dec 25, 2023  (Issue 1692)
with strong CYP3A4 inhibitors can increase zuranolone concentrations and possibly its toxicity; use ...
The FDA has approved the oral GABAA receptor modulator zuranolone (Zurzuvae – Sage Therapeutics/Biogen) for treatment of postpartum depression (PPD). Zuranolone is the second drug to be approved for this indication; brexanolone (Zulresso), another GABAA receptor modulator, was approved for IV treatment of PPD in 2019.
Med Lett Drugs Ther. 2023 Dec 25;65(1692):201-3   doi:10.58347/tml.2023.1692a |  Show IntroductionHide Introduction

Roflumilast Foam (Zoryve) for Seborrheic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Apr 15, 2024  (Issue 1700)
. Patients were ≥9 years old and had a baseline IGA score of 3 (moderate disease) or 4 (severe disease ...
The FDA has approved a 0.3% foam formulation of the phosphodiesterase-4 (PDE4) inhibitor roflumilast (Zoryve – Arcutis) for topical treatment of seborrheic dermatitis in patients ≥9 years old. Roflumilast is the first PDE4 inhibitor to be approved in the US for this indication. It is also available in a 0.3% cream formulation (Zoryve) for treatment of plaque psoriasis and in an oral formulation (Daliresp, and generics) for treatment of chronic obstructive pulmonary disease. A 0.15% cream formulation for treatment of atopic dermatitis in patients ≥6 years old will be reviewed...
Med Lett Drugs Ther. 2024 Apr 15;66(1700):57-9   doi:10.58347/tml.2024.1700a |  Show IntroductionHide Introduction

Comparison Table: Inhaled Drugs for Treatment of COPD (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 02, 2024  (Issue 1710)
, headache, insomnia, and increases in serum glucose concentrations ▶ HFA MDIs require hand-breath ...
View the Comparison Table: Inhaled Drugs for Treatment of COPD
Med Lett Drugs Ther. 2024 Sep 2;66(1710):e143-7   doi:10.58347/tml.2024.1710b |  Show IntroductionHide Introduction

Two Vonoprazan Combinations (Voquezna) for H. pylori

   
The Medical Letter on Drugs and Therapeutics • Oct 31, 2022  (Issue 1662)
with strong or moderate CYP3A4 inducers can reduce serum concentrations and the efficacy of both drugs ...
The FDA has approved vonoprazan, a potassium-competitive acid blocker, copackaged with amoxicillin (Voquezna Dual Pak – Phathom) and with amoxicillin and clarithromycin (Voquezna Triple Pak) for treatment of Helicobacter pylori infection in adults. Vonoprazan is the first potassium-competitive acid blocker to be approved in the US. It has been available in Japan for treatment of various acid-related disorders since 2014. Vonoprazan is not available alone in the US.
Med Lett Drugs Ther. 2022 Oct 31;64(1662):169-72 |  Show IntroductionHide Introduction

Comparison Table: Some Drugs for Gout (online only)

   
The Medical Letter on Drugs and Therapeutics • Oct 30, 2023  (Issue 1688)
contraceptives Celecoxib is a moderate CYP2D6 inhibitor; it can increase serum concentrations of CYP2D6 ...
View the Comparison Table: Some Drugs for Gout
Med Lett Drugs Ther. 2023 Oct 30;65(1688):e176-9   doi:10.58347/tml.2023.1688c |  Show IntroductionHide Introduction

Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023  (Issue 1684)
concentrate; 40 mg tabs for oral suspension7 80-120 mg PO once/day8 Sedation/respiratory depression ...
View Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e144-5   doi:10.58347/tml.2023.1684b |  Show IntroductionHide Introduction

Sunvozertinib (Zegfrovy) for NSCLC (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 15, 2025  (Issue 1737)
can increase serum concentrations of sunvozertinib and should be avoided; if concomitant use cannot ...
Sunvozertinib (Zegfrovy – Dizal), an oral kinase inhibitor, has received accelerated approval from the FDA for treatment of adults with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion mutations who had disease progression on or after platinum-based chemotherapy.
Med Lett Drugs Ther. 2025 Sep 15;67(1737):e152-3   doi:10.58347/tml.2025.1737f |  Show IntroductionHide Introduction

Olutasidenib (Rezlidhia) for Acute Myeloid Leukemia (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 03, 2023  (Issue 1673)
substrate and an inducer of CYP3A. Coadministration of strong or moderate CYP3A inducers can reduce serum ...
Olutasidenib (Rezlidhia – Rigel), an oral isocitrate dehydrogenase-1 (IDH1) inhibitor, has been approved by the FDA for treatment of relapsed or refractory acute myeloid leukemia (AML) in adults with a susceptible IDH1 mutation. It is the second drug that targets cancer metabolism to be approved for this indication; ivosidenib (Tibsovo) was approved in 2022.
Med Lett Drugs Ther. 2023 Apr 3;65(1673):e58-9   doi:10.58347/tml.2023.1673e |  Show IntroductionHide Introduction