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Searched for vol. Results 671 to 680 of 1525 total matches.

Trospium (Sanctura): Another Anticholinergic for Overactive Bladder

   
The Medical Letter on Drugs and Therapeutics • Aug 02, 2004  (Issue 1188)
, with a terminal half-life of 18 hours. 63 Vol. 46 (Issue 1188) August 2, 2004 Federal copyright law prohibits ...
Trospium chloride (Sanctura - Indevus/Odyssey) has been approved by the FDA for treatment of overactive bladder with symptoms of urge urinary incontinence, urgency and urinary frequency. It has been available in Europe for many years.
Med Lett Drugs Ther. 2004 Aug 2;46(1188):63-4 |  Show IntroductionHide Introduction

Raloxifene (Evista) for Breast Cancer Prevention in Postmenopausal Women

   
The Medical Letter on Drugs and Therapeutics • May 08, 2006  (Issue 1234)
2006 1234 osteoporosis Postmenopausal volume 48 vol. 48 vol 48 treatment of breast cancer Tamoxifen ...
Preliminary results from a new study, unpublished but reported in a press release from the National Cancer Institute and widely disseminated in the public press, suggest that raloxifene (Evista) might be a better choice than tamoxifen (Nolvadex, and others) for prevention of breast cancer in high-risk postmenopausal women.
Med Lett Drugs Ther. 2006 May 8;48(1234):37 |  Show IntroductionHide Introduction

Extended-Release Oxycodone and Acetaminophen (Xartemis XR)

   
The Medical Letter on Drugs and Therapeutics • Jul 21, 2014  (Issue 1447)
dosing interval (between 36 and 48 hours).2 60 The Medical Letter ® Vol. 56 (1447) July 21, 2014 tion ...
The FDA has approved a fixed-dose extended-release formulation of oxycodone and acetaminophen (Xartemis XR – Mallinckrodt) for oral treatment of acute pain severe enough to require an opioid. Oxycodone is available in the US as a single entity in oral immediate-release (Oxecta, and others) and extendedrelease (OxyContin) formulations. Immediate-release oxycodone is also available in combination with aspirin (Percodan, and others), acetaminophen (Percocet, and others), or ibuprofen (see Table 1).
Med Lett Drugs Ther. 2014 Jul 21;56(1447):59-61 |  Show IntroductionHide Introduction

Maribavir (Livtencity) for Cytomegalovirus Infection (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 28, 2022  (Issue 1664)
The Medical Letter ® Vol. 64 Published online November 28, 2022 1. J Maertens et al. Maribavir for preemptive ...
Maribavir (Livtencity – Takeda), an oral cytomegalovirus (CMV) pUL97 kinase inhibitor, has been approved by the FDA for treatment of post-transplant CMV infection refractory to standard antiviral therapy in patients ≥12 years old who weigh at least 35 kg.
Med Lett Drugs Ther. 2022 Nov 28;64(1664):e193-4 |  Show IntroductionHide Introduction

Altuviiio – A Longer-Acting Factor VIII Product for Hemophilia A

   
The Medical Letter on Drugs and Therapeutics • May 01, 2023  (Issue 1675)
/drug-pricing-policy. The Medical Letter ® Vol. 65 (1675) May 1, 2023 68 In XTEND-1, patients ≥12 ...
The FDA has approved Altuviiio (Sanofi), a von Willebrand Factor (VWF)-independent, recombinant factor VIII concentrate, for routine prophylaxis, on-demand treatment to control bleeding episodes, and perioperative management of bleeding in children and adults with hemophilia A. The manufacturer claims that Altuviiio, which was previously called efanesoctocog alfa, delivers normal to near-normal factor VIII levels for most of the week with once-weekly intravenous dosing.
Med Lett Drugs Ther. 2023 May 1;65(1675):67-8   doi:10.58347/tml.2023.1675b |  Show IntroductionHide Introduction

Toripalimab (Loqtorzi) for Nasopharyngeal Carcinoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Jan 22, 2024  (Issue 1694)
and produced durable responses in those who had treatmentrefractory disease. e17 The Medical Letter ® Vol ...
Toripalimab-tpzi (Loqtorzi – Coherus Biosciences), a programmed death receptor-1 (PD-1)-blocking antibody, has been approved by the FDA for use in combination with cisplatin and gemcitabine for first-line treatment of recurrent locally advanced or metastatic nasopharyngeal carcinoma and for use as monotherapy for treatment of recurrent unresectable or metastatic nasopharyngeal carcinoma in adults with disease progression on or after platinum-based chemotherapy. It is the first immune checkpoint inhibitor to be approved in the US for treatment of nasopharyngeal carcinoma.
Med Lett Drugs Ther. 2024 Jan 22;66(1694):e16-7   doi:10.58347/tml.2024.1694e |  Show IntroductionHide Introduction

Capivasertib (Truqap) for Breast Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024  (Issue 1696)
approved for use in those with AKT pathway-altered tumors. e33 The Medical Letter ® Vol. 66 Published ...
The oral kinase inhibitor capivasertib (Truqap – AstraZeneca), a first-in-class AKT inhibitor, has been approved by the FDA for use in combination with the selective estrogen receptor degrader (SERD) fulvestrant (Faslodex, and generics) for treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer in adults with one or more PIK3CA/AKT1/PTEN-alterations who had disease progression on at least one endocrine-based regimen for metastatic disease or recurrence on or within 12 months of completing...
Med Lett Drugs Ther. 2024 Feb 19;66(1696):e32-3   doi:10.58347/tml.2024.1696e |  Show IntroductionHide Introduction

Repotrectinib (Augtyro) for Non-Small Cell Lung Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024  (Issue 1696)
(steady state) e37 The Medical Letter ® Vol. 66 Published online February 19, 2024 34.1 months. Among ...
The FDA has approved the oral tyrosine kinase inhibitor repotrectinib (Augtyro – BMS) for treatment of locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC) in adults. Repotrectinib is the third oral tyrosine kinase inhibitor to be approved for this indication in the US; crizotinib (Xalkori) and entrectinib (Rozlytrek) were approved earlier.
Med Lett Drugs Ther. 2024 Feb 19;66(1696):e36-7   doi:10.58347/tml.2024.1696g |  Show IntroductionHide Introduction

Resmetirom (Rezdiffra) for Metabolic Dysfunction-Associated Steatohepatitis

   
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024  (Issue 1701)
of MASH resolution with no worsening of fibrosis The Medical Letter ® Vol. 66 (1701) April 29, 2024 66 ...
Resmetirom (Rezdiffra – Madrigal), a thyroid hormone receptor-beta agonist, has received accelerated approval from the FDA for treatment of noncirrhotic nonalcoholic steatohepatitis (NASH) with moderate to advanced fibrosis in adults. NASH has recently been renamed metabolic dysfunction-associated steatohepatitis (MASH). Resmetirom is the first drug to be approved in the US for this indication.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):65-6   doi:10.58347/tml.2024.1701a |  Show IntroductionHide Introduction

Drugs for Assisted Reproduction

   
Treatment Guidelines from The Medical Letter • Oct 01, 2003  (Issue 14)
. (ISSN 1541-2784) Vol. 1 (Issue 14) October 2003 Published by The Medical Letter, Inc. 1000 Main ...
Infertility occurs in about 15% of couples. About one third of infertility is due to problems with ovulation or an anatomic abnormality of the fallopian tube or peritoneum, such as scarring, adhesions or endometriosis. Another third is due to a male infertility factor, most commonly insufficient sperm production or abnormal motility or morphology. The remaining third is unexplained. In older women unexplained infertility is probably caused by diminished quality and quantity of oocytes, decreased implantation and spontaneous pregnancy wastage.
Treat Guidel Med Lett. 2003 Oct;1(14):89-92 |  Show IntroductionHide Introduction