Search Results for "moderate concentrate"
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Searched for moderate concentrate. Results 91 to 100 of 512 total matches.

CYP3A and Drug Interactions

   
The Medical Letter on Drugs and Therapeutics • Jul 04, 2005  (Issue 1212)
concentrations. CYP3A inhibitors have been categorized as potent or moderate. A drug is currently considered ...
Serious adverse interactions between drugs continue to be reported. Many of these are due to inhibition or induction of cytochrome P450 (CYP) enzymes, particularly CYP3A4. CYP3A is thought to be involved in the metabolism of more than 50 percent of currently prescribed drugs.2 CYP3A4, which is more abundantly expressed than CYP3A5, accounts for most CYP3A activity in vivo.
Med Lett Drugs Ther. 2005 Jul 4;47(1212):54-5 |  Show IntroductionHide Introduction

Lenacapavir (Sunlenca) for Multidrug-Resistant HIV

   
The Medical Letter on Drugs and Therapeutics • May 01, 2023  (Issue 1675)
reactions occurred in 65% of patients in the CAPELLA trial. Most reactions were mild to moderate; severe ...
The FDA has approved oral and injectable formulations of the HIV-1 capsid inhibitor lenacapavir (Sunlenca – Gilead) for use with other antiretroviral drugs to treat multidrug-resistant HIV-1 infection (MDR-HIV) in heavily treatment-experienced adults whose current regimen is failing. Lenacapavir is the third drug to be approved exclusively for treatment of MDR-HIV; the intravenously administered CD4-directed antibody ibalizumab-uiyk (Trogarzo) and the orally administered HIV-1 gp120-directed attachment inhibitor fostemsavir (Rukobia) were approved earlier.
Med Lett Drugs Ther. 2023 May 1;65(1675):68-70   doi:10.58347/tml.2023.1675c |  Show IntroductionHide Introduction

Once-Monthly Subcutaneous Buprenorphine (Sublocade) for Opioid Use Disorder

   
The Medical Letter on Drugs and Therapeutics • Feb 26, 2018  (Issue 1541)
receptor antagonist buprenorphine (Sublocade – Indivior) for once-monthly treatment of moderate to severe ...
The FDA has approved a subcutaneous (SC) extended-release formulation of the mu-opioid receptor partial agonist and kappa-opioid receptor antagonist buprenorphine (Sublocade – Indivior) for once-monthly treatment of moderate to severe opioid use disorder. Sublocade is the first injectable buprenorphine product to be approved in the US. Buprenorphine is also available in sublingual formulations with or without the opioid antagonist naloxone, in a buccal formulation with naloxone, and as a subdermal implant (Probuphine).
Med Lett Drugs Ther. 2018 Feb 26;60(1541):35-7 |  Show IntroductionHide Introduction

Vardenafil (Levitra) for Erectile Dysfunction

   
The Medical Letter on Drugs and Therapeutics • Sep 29, 2003  (Issue 1166)
% bioavailable after an oral dose. Serum concentrations peak (Cmax) in 30 minutes to 2 hours. The median time ...
Vardenafil (Levitra -Bayer) is the second oral drug approved by the FDA for treatment of erectile dysfunction. Sildenafil (Viagra - Medical Letter 1998; 40:51), the first oral drug, has been available for 5 years. Pharmacokinetics, effectiveness, adverse effects, dosage and cost of the new drug are reviewed. Whether it offers any benefits over sildenafil is discussed.
Med Lett Drugs Ther. 2003 Sep 29;45(1166):77-8 |  Show IntroductionHide Introduction

Comparison Table: H2-Receptor Antagonists and PPIs (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 04, 2022  (Issue 1647)
concentrations of drugs that require gastric acidity for absorption Cimetidine is a moderate inhibitor ...
View the Comparison Table: H2-Receptor Antagonists and PPIs
Med Lett Drugs Ther. 2022 Apr 4;64(1647):e56-7 |  Show IntroductionHide Introduction

Donepezil (Aricept) for Alzheimer's Disease

   
The Medical Letter on Drugs and Therapeutics • Jun 06, 1997  (Issue 1002)
symptoms in patients with mild to moderate dementia due to Alzheimer’s disease. Donepezil is the second ...
Donepezil hydrochloride (Aricept - Eisai), a piperidine-based acetylcholinesterase inhibitor, is now being marketed for oral treatment of cognitive symptoms in patients with mild to moderate dementia due to Alzheimer's disease. Donepezil is the second drug approved for this indication; tacrine hydrochloride (Cognex), also an acetylcholinesterase inhibitor, has been available in the USA for four years (Medical Letter, 35:87, 1993).
Med Lett Drugs Ther. 1997 Jun 6;39(1002):53-4 |  Show IntroductionHide Introduction

Another Once-Daily Formulation of Tramadol (Ryzolt)

   
The Medical Letter on Drugs and Therapeutics • May 17, 2010  (Issue 1338)
(Ryzolt – Purdue) for treatment of moderate to moderately severe chronic pain in adults. Tramadol ...
The FDA has approved tramadol hydrochloride extended-release (Ryzolt – Purdue) for treatment of moderate to moderately severe chronic pain in adults. Tramadol is already available in another extended-release formulation (Ultram ER) and in immediate-release tablets alone (Ultram, and others) and combined with acetaminophen (Ultracet, and others).
Med Lett Drugs Ther. 2010 May 17;52(1338):39-40 |  Show IntroductionHide Introduction

Oteseconazole (Vivjoa) for Recurrent Vulvovaginal Candidiasis

   
The Medical Letter on Drugs and Therapeutics • Aug 08, 2022  (Issue 1656)
of CYP2C9 and 2C19 and a moderate inhibitor of CYP3A4; it can increase serum concentrations of drugs ...
The FDA has approved oteseconazole (Vivjoa – Mycovia), a new oral azole antifungal, to reduce the incidence of recurrent vulvovaginal candidiasis (RVVC) in females with a history of RVVC. Oteseconazole is the first drug to be approved in the US specifically for treatment of RVVC.
Med Lett Drugs Ther. 2022 Aug 8;64(1656):124-6 |  Show IntroductionHide Introduction

Apremilast (Otezla) for Psoriatic Arthritis

   
The Medical Letter on Drugs and Therapeutics • May 26, 2014  (Issue 1443)
(DMARD) methotrexate is generally used for treatment of moderate to severe disease. If there is minimal ...
Apremilast (Otezla – Celgene), an oral phosphodiesterase type-4 (PDE4) inhibitor, has been approved by the FDA for treatment of active psoriatic arthritis in adults. It is the fi rst PDE4 inhibitor to be approved for this indication.
Med Lett Drugs Ther. 2014 May 26;56(1443):41-2 |  Show IntroductionHide Introduction

Transdermal Selegiline (Emsam)

   
The Medical Letter on Drugs and Therapeutics • May 22, 2006  (Issue 1235)
in the systemic circulation can cause a severe hypertensive crisis. In the lower serum concentrations achieved ...
The FDA recently approved the monoamine oxidase inhibitor (MAOI) selegiline in a transdermal (patch) formulation (Emsam - Bristol-Myers Squibb/Somerset) for treatment of major depressive disorder. Selegiline is also available in an oral formulation (Eldepryl, and others) for treatment of Parkinson's disease.
Med Lett Drugs Ther. 2006 May 22;48(1235):41-2 |  Show IntroductionHide Introduction