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Searched for days. Results 1501 to 1510 of 1849 total matches.

Osimertinib (Tagrisso) for Adjuvant Treatment of NSCLC (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 07, 2023  (Issue 1682)
-day supply of Tagrisso is $16,134.70.4 CONCLUSION — In one small trial, the oral kinase inhibitor ...
The FDA has approved osimertinib (Tagrisso – AstraZeneca), an oral kinase inhibitor, for adjuvant treatment of non-small cell lung cancer (NSCLC) after tumor resection in adults who have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R mutations. Osimertinib is the first targeted therapy to be approved in the US for this indication. The drug was previously approved for first-line treatment of adults with NSCLC with EGFR exon 19 deletions or exon 21 L858R mutations and for treatment of EGFR T790M mutation-positive NSCLC in adults whose disease progressed...
Med Lett Drugs Ther. 2023 Aug 7;65(1682):e131-2   doi:10.58347/tml.2023.1682c |  Show IntroductionHide Introduction

Talazoparib (Talzenna) for Prostate Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 07, 2023  (Issue 1682)
acquisition cost of a 30-day supply of Talzenna is about $17,515.3 CONCLUSION — In one clinical trial in men ...
The oral poly(ADP-ribose) polymerase (PARP) inhibitor talazoparib (Talzenna – Pfizer) has been approved by the FDA for use in combination with the androgen receptor blocker enzalutamide (Xtandi) for treatment of adults with homologous recombination repair (HRR) gene-mutated metastatic castration-resistant prostate cancer (mCRPC). The drug has been available since 2018 for treatment of deleterious or suspected deleterious germline BRCA-mutated (gBRCAm), HER2-negative locally advanced or metastatic breast cancer.
Med Lett Drugs Ther. 2023 Aug 7;65(1682):e134-5   doi:10.58347/tml.2023.1682e |  Show IntroductionHide Introduction

In Brief: GI Effects of GLP-1 Receptor Agonists

   
The Medical Letter on Drugs and Therapeutics • Nov 27, 2023  (Issue 1690)
on the day of elective surgery for those that are administered daily, or for one week prior to the procedure ...
Glucagon-like peptide-1 (GLP-1) receptor agonists and the dual glucose-dependent insulinotropic polypeptide (GIP)/GLP-1 receptor agonist tirzepatide (Mounjaro) are widely prescribed for treatment of type 2 diabetes and weight management (see Table 1), but they delay gastric emptying and commonly cause nausea and vomiting. Gastroparesis and bowel obstruction (ileus) have also been reported with their use.
Med Lett Drugs Ther. 2023 Nov 27;65(1690):191-2   doi:10.58347/tml.2023.1690e |  Show IntroductionHide Introduction

In Brief: A New OTC Naloxone Nasal Spray (RiVive)

   
The Medical Letter on Drugs and Therapeutics • Mar 18, 2024  (Issue 1698)
(MME) per day. Have respiratory conditions such as chronic obstructive pulmonary disease (COPD ...
The FDA has approved RiVive (Harm Reduction Therapeutics), a 3-mg naloxone nasal spray, as an over-the-counter (OTC) product for emergency treatment of opioid overdose. Two 4-mg naloxone nasal spray formulations, Narcan and one of its generics, were approved for OTC sale in 2023.
Med Lett Drugs Ther. 2024 Mar 18;66(1698):47-8   doi:10.58347/tml.2024.1698d |  Show IntroductionHide Introduction

Nabilone (Cesamet) for Chemotherapy-Induced Nausea and Vomiting

   
The Medical Letter on Drugs and Therapeutics • Dec 04, 2006  (Issue 1249)
– 2.5, 5 and 5 mg/m 2 211.44 2 Marinol (Solvay) 10 mg caps 4-6x/d 1. Cost based on 3 days treatment ...
Nabilone, an oral synthetic cannabinoid similar to delta-9-tetrahydrocannabinol (THC), the active ingredient in marijuana, has recently been reintroduced to the US market (Cesamet - Valeant) after a 17-year absence. The previous manufacturer discontinued marketing of the drug for commercial reasons. Nabilone is classified as a Schedule II controlled substance.
Med Lett Drugs Ther. 2006 Dec 4;48(1249):103-4 |  Show IntroductionHide Introduction

Proton Pump Inhibitors for GERD in Children

   
The Medical Letter on Drugs and Therapeutics • Feb 26, 2007  (Issue 1255)
mg once 6,10 5–16 yrs 10 122.40 1. Cost for 30 days’ treatment with tablets or capsules ...
A recent advertisement for the proton pump inhibitor (PPI) lansoprazole (Prevacid - TAP) suggests that children who cough at night, complain of abdominal pain, refuse to eat, or have a bad taste in their mouths may all have gastroesophageal reflux disease (GERD). A Bunny's Tummy Trouble, a children's book about GERD published by TAP, is now available as a patient handout in pediatricians' waiting rooms. The use of acid-suppressive drugs in infants and children has increased markedly in recent years and many of these drugs are now available in child-friendly formulations. A table in the article...
Med Lett Drugs Ther. 2007 Feb 26;49(1255):17-8 |  Show IntroductionHide Introduction

Two New Drugs for Renal Cell Carcinoma

   
The Medical Letter on Drugs and Therapeutics • Feb 26, 2007  (Issue 1255)
and warfarin concurrently. Dosage and Cost – The recommended dose of sorafenib is 400 mg twice a day until ...
Sunitinib (Sutent - Pfizer) and sorafenib (Nexavar - Bayer), two oral tyrosine kinase inhibitors, have been approved by the FDA for treatment of advanced renal cell carcinoma (RCC). Sunitinib is also approved for use in patients with gastrointestinal stromal tumor (GIST) who are not responding to or are intolerant of standard therapy with imatinib (Gleevec).
Med Lett Drugs Ther. 2007 Feb 26;49(1255):18-20 |  Show IntroductionHide Introduction

Safety of SSRIs in Pregnancy

   
The Medical Letter on Drugs and Therapeutics • Nov 17, 2008  (Issue 1299)
: 800-211-2769 nificant only in women who took more than 25 mg per day (the usual dose is 20 mg per ...
Depression occurs in up to 20% of pregnant women, and the use of selective serotonin reuptake inhibitors (SSRIs) in these women has been increasing. Maternal depression has itself been associated with intrauterine growth problems and low birth weight, so the risks of exposure to antidepressants during pregnancy must be weighed against the risks of untreated depression, which also include self-harm, poor bonding and poor parenting. SSRIs available in the US for treatment of depression include citalopram (Celexa, and others), escitalopram (Lexapro), fluoxetine (Prozac, and others), paroxetine...
Med Lett Drugs Ther. 2008 Nov 17;50(1299):89-91 |  Show IntroductionHide Introduction

PPI Interactions with Clopidogrel

   
The Medical Letter on Drugs and Therapeutics • Jan 12, 2009  (Issue 1303)
on the ability of clopidogrel to inhibit platelet activation in blood samples from the patients. After 7 days ...
Clopidogrel (Plavix), which prevents arterial thrombosis by inhibiting platelet activation, is commonly prescribed (usually with aspirin) for months after acute coronary syndromes and stent implantation. It may also, however, increase the risk of bleeding. Therefore, a proton pump inhibitor (PPI) such as omeprazole (Prilosec, and others) is often given concurrently to decrease the risk of gastrointestinal (GI) bleeding. Some reports have suggested that omeprazole may interfere with the antiplatelet effect of clopidogrel.
Med Lett Drugs Ther. 2009 Jan 12;51(1303):2-3 |  Show IntroductionHide Introduction

Golimumab (Simponi) for Inflammatory Arthritis

   
The Medical Letter on Drugs and Therapeutics • Jul 13, 2009  (Issue 1316)
concentrations 2-7 days after subcutaneous (SC) injection. Its mean terminal half-life is about 2 weeks ...
Golimumab (Simponi - Centocor), a fully humanized anti-tumor necrosis factor (TNF)-a antibody, has been approved by the FDA for the treatment of: (1) moderate to severe active rheumatoid arthritis (RA) in combination with methotrexate; (2) active psoriatic arthritis (PsA) alone or in combination with methotrexate; and (3) active ankylosing spondylitis (AS).
Med Lett Drugs Ther. 2009 Jul 13;51(1316):55-6 |  Show IntroductionHide Introduction