Search Results for "moderate concentrate"
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Searched for moderate concentrate. Results 71 to 80 of 505 total matches.

Two New Drugs for Homozygous Familial Hypercholesterolemia

   
The Medical Letter on Drugs and Therapeutics • Apr 01, 2013  (Issue 1413)
cholesterol concentrations were 439 mg/dL among patients randomized to mipomersen and 400 mg/dL ...
The FDA has approved mipomersen (Kynamro – Genzyme) and lomitapide (Juxtapid – Aegerion), each in addition to a low-fat diet and other lipid-lowering medications, to reduce cholesterol levels in patients with homozygous familial hypercholesterolemia (HoFH).
Med Lett Drugs Ther. 2013 Apr 1;55(1413):25-7 |  Show IntroductionHide Introduction

Zafirlukast for Asthma

   
The Medical Letter on Drugs and Therapeutics • Dec 20, 1996  (Issue 990)
is rapidly absorbed from the gastrointestinal tract, reaching peak concentrations in the blood about three ...
Zafirlukast (za fir loo kast; Accolate - Zeneca), the first leukotriene receptor anta-gonist approved by the US Food and Drug Administration, is now being heavily promoted for oral maintenance treatment of chronic asthma in patients more than 12 years old. It is not recommended for treatment of acute asthma.
Med Lett Drugs Ther. 1996 Dec 20;38(990):111-2 |  Show IntroductionHide Introduction

Erdafitinib (Balversa) for Urothelial Carcinoma (online only)

   
The Medical Letter on Drugs and Therapeutics • May 13, 2024  (Issue 1702)
inhibitor can increase serum concentrations of erdafitinib. Moderate and strong CYP3A4 inducers can ...
Erdafitinib (Balversa – Janssen), an oral kinase inhibitor, has received full approval from the FDA for treatment of locally advanced or metastatic urothelial carcinoma in adults with susceptible FGFR3 (fibroblast growth factor receptor) genetic alterations who had disease progression on or after at least one prior line of systemic therapy. It is not recommended for use in patients who are eligible for but have not received prior PD-1 (programmed death receptor-1) or PD-L1 (programmed death-ligand 1) inhibitor therapy. Erdafitinib is the first oral FGFR kinase inhibitor to be...
Med Lett Drugs Ther. 2024 May 13;66(1702):e83-4   doi:10.58347/tml.2024.1702g |  Show IntroductionHide Introduction

Pioglitazone (Actos)

   
The Medical Letter on Drugs and Therapeutics • Nov 19, 1999  (Issue 1066)
in controlling serum glucose concentrations. Pioglitazone has a longer serum half-life. ADVERSE EFFECTS ...
Pioglitazone is the third thiazolidinedione ("glitazone") to be marketed in the USA for treatment of type 2 diabetes. Thiazolidinediones decrease resistance to insulin.
Med Lett Drugs Ther. 1999 Nov 19;41(1066):112 |  Show IntroductionHide Introduction

Carvedilol for Heart Failure

   
The Medical Letter on Drugs and Therapeutics • Sep 26, 1997  (Issue 1010)
or moderate (NYHA class II or III) heart failure stabilized on other drugs. It is being promoted as an add ...
Carvedilol (Coreg - SmithKline Beecham and Boehringer-Mannheim), a betaadrenergic and alpha-adrenergic blocker approved by the FDA for treatment of hypertension in 1995, but not marketed at that time, has now been approved and marketed for treatment of mild or moderate (NYHA class II or III) heart failure stabilized on other drugs. It is being promoted as an add-on drug that reduces the morbidity and mortality of the disease.
Med Lett Drugs Ther. 1997 Sep 26;39(1010):89-91 |  Show IntroductionHide Introduction

Linagliptin/Metformin (Jentadueto) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • May 14, 2012  (Issue 1390)
and decrease glucagon production, lowering serum glucose concentrations. Metformin decreases hepatic glucose ...
Linagliptin (Tradjenta) and metformin (Glucophage, and others) are now available as a fixed-dose combination (Jentadueto – Boehringer Ingelheim/Lilly) for oral treatment of type 2 diabetes in adults. Metformin is generally the preferred first-line agent for treatment of type 2 diabetes, but most patients eventually require treatment with multiple drugs. Linagliptin is a dipeptidyl peptidase-4 (DDP-4) inhibitor like sitagliptin (Januvia) and saxagliptin (Onglyza). Both sitagliptin and saxagliptin are also available in fixed-dose combinations with...
Med Lett Drugs Ther. 2012 May 14;54(1390):37-9 |  Show IntroductionHide Introduction

Comparison Table: Some Lipid-Lowering Drugs (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 19, 2022  (Issue 1659)
concentrations dramatically ▶ Atorvastatin undergoes less first-pass metabolism by CYP3A4 ▶ Fluvastatin ...
View the Comparison Table: Some Lipid-Lowering Drugs
Med Lett Drugs Ther. 2022 Sep 19;64(1659):e152-6 |  Show IntroductionHide Introduction

A New Dihydroergotamine Nasal Spray (Trudhesa) for Migraine

   
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021  (Issue 1640)
it is still mild to moderate in intensity improves headache response and reduces the risk of recurrence.1 ...
The FDA has approved Trudhesa (Impel Neuropharma), a new dihydroergotamine nasal spray product, for acute treatment of migraine with or without aura in adults. Another dihydroergotamine nasal spray (Migranal, and generics) has been available for many years for the same indication.
Med Lett Drugs Ther. 2021 Dec 27;63(1640):204-7 |  Show IntroductionHide Introduction

Intravenous Acetaminophen/Ibuprofen (Combogesic IV)

   
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024  (Issue 1701)
, to treat mild to moderate pain (alone) or moderate to severe pain (in combination with an opioid ...
The FDA has approved Combogesic IV (Hikma), an IV solution containing acetaminophen and ibuprofen, to treat mild to moderate pain (alone) or moderate to severe pain (in combination with an opioid) in adults when IV analgesia is considered clinically necessary. Single-drug IV solutions containing ibuprofen (Caldolor) and acetaminophen have been available in the US for years.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):68-9   doi:10.58347/tml.2024.1701c |  Show IntroductionHide Introduction

Siponimod (Mayzent) - A New Drug for Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • May 06, 2019  (Issue 1571)
use of a moderate CYP2C9 inducer and strong 3A4 inducer can decrease siponimod serum concentrations ...
The FDA has approved siponimod (Mayzent – Novartis), a sphingosine 1-phosphate (S1P) receptor modulator, for oral treatment of adults with relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome (initial neurological episode), relapsing-remitting disease, and active secondary progressive MS (SPMS). Siponimod is the second S1P receptor modulator to be approved in the US; fingolimod (Gilenya), which is approved for oral treatment of relapsing forms of MS in patients ≥10 years old, was the first. The purine antimetabolite cladribine (Mavenclad) was also...
Med Lett Drugs Ther. 2019 May 6;61(1571):70-2 |  Show IntroductionHide Introduction