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Searched for days. Results 1251 to 1260 of 1849 total matches.

Ospemifene (Osphena) for Dyspareunia

   
The Medical Letter on Drugs and Therapeutics • Jul 08, 2013  (Issue 1420)
. Approximate wholesale acquisition cost (WAC) for 90 days’ treatment at the lowest maintenance dose. Source ...
The FDA has approved ospemifene (os pem’ i feen; Osphena – Shionogi), an estrogen agonist/antagonist, for oral treatment of moderate to severe dyspareunia in postmenopausal women. Ospemifene is the fourth estrogen agonist/antagonist to be marketed in the US, but it is the only one that has an estrogen-like effect on vaginal epithelium. The other three, tamoxifen (Nolvadex, and generics), toremifene (Fareston), and raloxifene (Evista), are used for treatment and prevention of breast cancer and osteoporosis.
Med Lett Drugs Ther. 2013 Jul 8;55(1420):55-6 |  Show IntroductionHide Introduction

Vorapaxar (Zontivity) for Prevention of Thrombotic Cardiovascular Events

   
The Medical Letter on Drugs and Therapeutics • Sep 15, 2014  (Issue 1451)
Zontivity2 (Merck) 1. Approximate wholesale acquisition cost (WAC) of 30 days' maintenance treatment ...
The FDA has approved vorapaxar (Zontivity – Merck), an oral protease-activated receptor-1 (PAR-1) antagonist, for use with aspirin and/or clopidogrel to reduce the risk of thrombotic cardiovascular events in patients with peripheral arterial disease or a history of myocardial infarction (MI). It is the first PAR-1 antagonist to be approved by the FDA.
Med Lett Drugs Ther. 2014 Sep 15;56(1451):85-6 |  Show IntroductionHide Introduction

Polidocanol (Varithena) for Varicose Veins

   
The Medical Letter on Drugs and Therapeutics • Aug 03, 2015  (Issue 1474)
then has a shelf-life of 7 days. The freshly generated foam is transferred to a syringe and injected intravenously ...
An injectable foam formulation of the sclerosing agent polidocanol (Varithena – Provensis/BTG) has been approved by the FDA for treatment of incompetent veins and visible varicosities of the great saphenous vein system. It is the first foam therapy to be approved for this indication, but polidocanol and other sclerosants have been used for years as foam formulations compounded by physicians. Polidocanol is also available in a liquid formulation (Asclera) to treat smaller veins. Sodium tetradecyl sulfate (Sotradecol) is FDA-approved in a liquid formulation for use in...
Med Lett Drugs Ther. 2015 Aug 3;57(1474):111-2 |  Show IntroductionHide Introduction

Panobinostat (Farydak) for Multiple Myeloma (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 17, 2015  (Issue 1475)
— The recommended starting dosage of panobinostat is 20 mg orally on days 1, 3, 5, 8, 10, and 12 of a 21-day cycle ...
The FDA has approved panobinostat (Farydak – Novartis), an oral histone deacetylase (HDAC) inhibitor, for use in combination with bortezomib (Velcade) and dexamethasone for treatment of patients with multiple myeloma who have received at least 2 prior therapies including bortezomib and an immunomodulatory drug. It is the first HDAC inhibitor to be approved for this indication.
Med Lett Drugs Ther. 2015 Aug 17;57(1475):e118-9 |  Show IntroductionHide Introduction

A Sumatriptan Patch (Zecuity) for Migraine

   
The Medical Letter on Drugs and Therapeutics • Nov 09, 2015  (Issue 1481)
at the application site, which may take 2 or 3 days to resolve. In an open-label study, 45% of 183 patients ...
The FDA has approved a sumatriptan iontophoretic transdermal system (Zecuity – Teva) for acute treatment of migraine in adults. Sumatriptan, the first of seven serotonin receptor antagonists (triptans) approved for this indication, is the most frequently prescribed migraine treatment in the US. It is also available in oral, intranasal, and injectable formulations.
Med Lett Drugs Ther. 2015 Nov 9;57(1481):151-2 |  Show IntroductionHide Introduction

Mepolizumab (Nucala) for Severe Eosinophilic Asthma

   
The Medical Letter on Drugs and Therapeutics • Jan 18, 2016  (Issue 1486)
by proteolytic enzymes Half-life (terminal) 16-22 days CLINICAL STUDIES — FDA approval of mepolizumab ...
The FDA has approved mepolizumab (Nucala - GSK), a subcutaneously injected humanized interleukin-5 (IL-5) antagonist monoclonal antibody, for maintenance treatment of severe asthma in patients ≥12 years old who have an eosinophilic phenotype.
Med Lett Drugs Ther. 2016 Jan 18;58(1486):11-2 |  Show IntroductionHide Introduction

Low-Dose Meloxicam (Vivlodex) for Osteoarthritis Pain

   
The Medical Letter on Drugs and Therapeutics • Mar 14, 2016  (Issue 1490)
days’ treatment with the lowest usual dosage. WAC = wholesaler acquisition cost or manufacturer’s ...
The FDA has approved Vivlodex (Iroko), a low-dose formulation of the nonsteroidal anti-inflammatory drug meloxicam (Mobic, and generics), for management of osteoarthritis pain. According to the manufacturer, the new formulation aligns with stronger FDA warnings about the cardiovascular risks of NSAIDs and the recommendation to use the lowest possible doses of these drugs.
Med Lett Drugs Ther. 2016 Mar 14;58(1490):35-6 |  Show IntroductionHide Introduction

Lumacaftor/Ivacaftor (Orkambi) for Cystic Fibrosis

   
The Medical Letter on Drugs and Therapeutics • Mar 28, 2016  (Issue 1491)
treatment after an interruption of >7 days, who are currently taking a strong CYP3A inhibitor should take ...
The FDA has approved a fixed-dose combination of lumacaftor and ivacaftor (Orkambi – Vertex) for oral treatment of cystic fibrosis (CF) in patients ≥12 years old who are homozygous for the F508del mutation. About 50% of patients in the US with CF are homozygous for the F508del (also called Phe508del) mutation. This is the first approved indication for lumacaftor; ivacaftor is available alone as Kalydeco for treatment of CF in patients ≥2 years old with other mutations. Orkambi is the first drug to be approved in the US for treatment of patients with the F508del...
Med Lett Drugs Ther. 2016 Mar 28;58(1491):41-2 |  Show IntroductionHide Introduction

Spritam - A New Formulation of Levetiracetam for Epilepsy

   
The Medical Letter on Drugs and Therapeutics • Jun 20, 2016  (Issue 1497)
Immediate-release – Keppra (UCB) 250, 500, 750, 1000 mg tabs; 100 mg/mL 1000-3000 mg/day PO or IV $436.40 ...
The FDA has approved a rapidly disintegrating tablet formulation of the antiepileptic drug levetiracetam (Spritam – Aprecia) for adjunctive treatment of partialonset, myoclonic, and primary generalized tonicclonic seizures. Oral and intravenous formulations of levetiracetam (Keppra, and generics) have been available for years. Although approved by the FDA only as adjunctive therapy, levetiracetam is commonly used as monotherapy for partial-onset and generalized seizures and may also be effective in treating absence seizures and seizures of Lennox-Gastaut syndrome.
Med Lett Drugs Ther. 2016 Jun 20;58(1497):78-9 |  Show IntroductionHide Introduction

Acute Reactions to Drugs of Abuse

   
The Medical Letter on Drugs and Therapeutics • Mar 04, 2002  (Issue 1125)
, but may persist for up to several days with long-acting opioids such as methadone (Dolophine, and others ...
Acute toxic reactions to drugs of abuse continue to be important problems. Some patients may have mixed intoxications with complex combinations of signs and symptoms.
Med Lett Drugs Ther. 2002 Mar 4;44(1125):21-4 |  Show IntroductionHide Introduction