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Searched for action. Results 571 to 580 of 1170 total matches.

Axitinib (Inlyta) for Advanced Renal Cell Carcinoma

   
The Medical Letter on Drugs and Therapeutics • Jun 11, 2012  (Issue 1392)
inhibitor Mechanism of action Inhibits VEGF receptors 1, 2 and 3 Formulation 1-mg and 5-mg tablets Route ...
Axitinib (Inlyta – Pfizer), an oral tyrosine kinase inhibitor, has been approved by the FDA for treatment of advanced renal cell carcinoma after failure of one prior systemic therapy. It is the fourth oral tyrosine kinase inhibitor to be approved for treatment of advanced renal cell carcinoma.
Med Lett Drugs Ther. 2012 Jun 11;54(1392):47-8 |  Show IntroductionHide Introduction

Vismodegib (Erivedge) for Basal Cell Carcinoma

   
The Medical Letter on Drugs and Therapeutics • Jul 09, 2012  (Issue 1394)
OF ACTION — The Hh signaling pathway, which is important in embryonic development and regulation of adult ...
The FDA has approved vismodegib (vis moe deg´ ib; Erivedge – Genentech), the first hedgehog (Hh) pathway inhibitor, for oral treatment of metastatic basal cell cancer, locally advanced basal cell carcinoma that has recurred after surgery, or locally advanced basal cell carcinoma in adults who are not candidates for surgery or radiation.
Med Lett Drugs Ther. 2012 Jul 9;54(1394):53-4 |  Show IntroductionHide Introduction

Ivermectin (Sklice) Topical Lotion for Head Lice

   
The Medical Letter on Drugs and Therapeutics • Aug 06, 2012  (Issue 1396)
Dermatol 2004; 21:670). MECHANISM OF ACTION — Ivermectin is derived from the fermentation of Streptomyces ...
The FDA has approved the antiparasitic drug ivermectin in a 0.5% lotion (Sklice – Sanofi Pasteur) as a single-use topical treatment for head lice in patients ≥6 months old. Oral ivermectin (Stromectol – Merck) is effective for treatment of head lice resistant to other therapies, but it has not been approved by the FDA for this indication.
Med Lett Drugs Ther. 2012 Aug 6;54(1396):61-3 |  Show IntroductionHide Introduction

Raxibacumab for Anthrax

   
The Medical Letter on Drugs and Therapeutics • Apr 01, 2013  (Issue 1413)
, fever and myalgia.2 MECHANISM OF ACTION — Actively dividing Bacillus anthracis produces protective ...
The FDA has approved raxibacumab (rax” ee bak’ ue mab; GSK), a fully human monoclonal antibody given by intravenous infusion, for treatment of inhalational anthrax in combination with appropriate antibacterial drugs, and for prophylaxis of inhalational anthrax when alternative therapies are not available or are not appropriate. It was approved under the Animal Efficacy Rule, which allows the FDA to approve drugs that demonstrate efficacy in animals, providing that they would have a reasonable human health benefit and are safe for human use. Raxibacumab is only available from the...
Med Lett Drugs Ther. 2013 Apr 1;55(1413):27-8 |  Show IntroductionHide Introduction

Icosapent Ethyl (Vascepa) for Severe Hypertriglyceridemia

   
The Medical Letter on Drugs and Therapeutics • Apr 29, 2013  (Issue 1415)
by 20-50%.3 MECHANISM OF ACTION — Omega-3 PUFAs decrease hepatic production of triglycerides ...
Icosapent ethyl (Vascepa [vas EE puh] – Amarin), the ethyl ester of eicosapentaenoic acid (EPA), has been approved by the FDA as an adjunct to diet for treatment of severe hypertriglyceridemia (≥500 mg/dL). Vascepa is the second omega-3 polyunsaturated fatty acid (PUFA) product to become available by prescription for this indication; Lovaza (formerly Omacor), which is a combination of the ethyl esters of EPA and docosahexaenoic acid (DHA), was the first. Many omega-3 PUFA-containing fish oil capsules are sold over the counter as dietary supplements.
Med Lett Drugs Ther. 2013 Apr 29;55(1415):33-4 |  Show IntroductionHide Introduction

Pasireotide (Signifor) for Cushing's Disease

   
The Medical Letter on Drugs and Therapeutics • May 13, 2013  (Issue 1416)
MECHANISM OF ACTION — Pasireotide is a somatostatin analog with high binding affinity for human ...
The FDA has approved the somatostatin analog pasireotide diaspartate (Signifor – Novartis) for treatment of adults with Cushing's disease (cortisol excess caused by an ACTH-secreting pituitary tumor) who are not candidates for pituitary surgery or for whom surgery has not been curative. Pasireotide is the first drug approved in the US specifically to treat Cushing's disease. The antiprogestin mifepristone (Korlym) was approved last year for control of hyperglycemia in patients with Cushing's syndrome, which includes other causes of hypercortisolism, such as exogenous steroids and...
Med Lett Drugs Ther. 2013 May 13;55(1416):39-40 |  Show IntroductionHide Introduction

Lubiprostone (Amitiza) for Opioid-Induced Constipation

   
The Medical Letter on Drugs and Therapeutics • Jun 10, 2013  (Issue 1418)
of post-operative ileus.5 MECHANISM OF ACTION — Exogenous opioids decrease peristalsis and secretion ...
The FDA has approved use of lubiprostone (Amitiza) for treatment of opioid-induced constipation in adults with chronic non-cancer pain. The drug was previously approved for chronic idiopathic constipation and irritable bowel syndrome with constipation.
Med Lett Drugs Ther. 2013 Jun 10;55(1418):47-8 |  Show IntroductionHide Introduction

Tasimelteon (Hetlioz) for Non-24-Hour Sleep-Wake Disorder

   
The Medical Letter on Drugs and Therapeutics • Apr 28, 2014  (Issue 1441)
in the treatment of non-24, with some success.3 MECHANISM OF ACTION — Melatonin acts on two receptors ...
The FDA has approved the melatonin receptor agonist tasimelteon (Hetlioz – Vanda) for treatment of non-24-hour sleep-wake disorder (non-24), which is common in totally blind persons. Tasimelteon is the first drug approved for this indication and the second melatonin receptor agonist approved for use in the US; ramelteon (Rozerem) was approved earlier for treatment of insomnia. Melatonin itself has not been approved by the FDA for any indication; it is available in the US as a dietary supplement and is promoted as a sleep aid.
Med Lett Drugs Ther. 2014 Apr 28;56(1441):34-5 |  Show IntroductionHide Introduction

Apremilast (Otezla) for Psoriatic Arthritis

   
The Medical Letter on Drugs and Therapeutics • May 26, 2014  (Issue 1443)
inhibitors remains to be determined.3 MECHANISM OF ACTION — PDE4 degrades cyclic adenosine monophosphate ...
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

Eslicarbazepine Acetate (Aptiom) for Epilepsy

   
The Medical Letter on Drugs and Therapeutics • May 26, 2014  (Issue 1443)
to eslicarbazepine, the major active metabolite Elimination Urine MECHANISM OF ACTION — As with oxcarbazepine ...
Eslicarbazepine acetate (Aptiom – Sunovion) has been approved by the FDA for adjunctive treatment of partial-onset seizures in adults. New drugs for epilepsy are often approved by the FDA initially only as adjunctive treatment for partial seizures. Eslicarbazepine acetate is a prodrug of eslicarbazepine, which is the S-isomer of the active metabolite of oxcarbazepine. Oxcarbazepine itself is similar to carbamazepine. Both oxcarbazepine and carbamazepine are available generically.
Med Lett Drugs Ther. 2014 May 26;56(1443):42-3 |  Show IntroductionHide Introduction