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Searched for Lung. Results 121 to 130 of 220 total matches.

Vandetanib (Caprelsa) for Medullary Thyroid Cancer

   
The Medical Letter on Drugs and Therapeutics • Jan 09, 2012  (Issue 1381)
tachycardia and sudden deaths have been reported. Fatal interstitial lung disease has occurred. Fatal ...
The FDA recently approved vandetanib [van det´ a nib] (Caprelsa – AstraZeneca) for oral treatment of symptomatic or progressive medullary thyroid cancer (MTC) in patients with unresectable locally advanced or metastatic disease. Vandetanib is the first drug approved in the US for medullary thyroid cancer.
Med Lett Drugs Ther. 2012 Jan 9;54(1381):3-4 |  Show IntroductionHide Introduction

Ado-Trastuzumab Emtansine (Kadcyla) for HER2-Positive Metastatic Breast Cancer

   
The Medical Letter on Drugs and Therapeutics • Sep 16, 2013  (Issue 1425)
from pretreatment values and does not recover within 3 weeks of holding therapy, if interstitial lung disease ...
Ado-trastuzumab emtansine (Kadcyla – Genentech), a human epidermal growth factor receptor 2 (HER2)-targeted antibody and microtubule inhibitor conjugate, has been approved by the FDA for intravenous (IV) treatment of HER2-positive metastatic breast cancer in patients previously treated with trastuzumab (Herceptin) and a taxane. The prefix was added to the new conjugate’s name at the request of the FDA to distinguish it from trastuzumab.
Med Lett Drugs Ther. 2013 Sep 16;55(1425):75-6 |  Show IntroductionHide Introduction

Rilonacept (Arcalyst) for Recurrent Pericarditis

   
The Medical Letter on Drugs and Therapeutics • Sep 06, 2021  (Issue 1632)
, cardiac procedures (especially coronary artery bypass grafting), autoimmune disorders, lung or breast ...
Rilonacept (Arcalyst – Kiniksa), an interleukin-1 (IL-1) antagonist that has been available for years for treatment of cryopyrin-associated periodic syndromes, has now been approved by the FDA for treatment of recurrent pericarditis and prevention of further recurrences in patients ≥12 years old. It is the first drug to be approved in the US for this indication. Anakinra (Kineret), an IL-1 receptor antagonist FDA-approved for treatment of rheumatoid arthritis, has been used off-label for years for treatment of recurrent pericarditis.
Med Lett Drugs Ther. 2021 Sep 6;63(1632):143-4 |  Show IntroductionHide Introduction

Enfortumab Vedotin (Padcev) for Urothelial Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • May 22, 2023  (Issue 1677)
, pneumonitis/interstitial lung disease, peripheral neuropathy, ocular disorders, and infusion-site reactions ...
Enfortumab vedotin-ejfv (Padcev – Astellas), a nectin-4-directed antibody and microtubule inhibitor conjugate, has received accelerated approval from the FDA for use with the immune checkpoint inhibitor pembrolizumab (Keytruda) for treatment of locally advanced or metastatic urothelial cancer in adults who are ineligible for cisplatin-containing chemotherapy. Accelerated approval was based on tumor response rates and the durability of response.
Med Lett Drugs Ther. 2023 May 22;65(1677):e91-2   doi:10.58347/tml.2023.1677g |  Show IntroductionHide Introduction

Insulins for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • May 06, 2019  (Issue 1571)
or in patients with lung cancer and is contraindicated for use in patients with chronic lung disease ...
The goal of drug therapy for type 2 diabetes is to achieve and maintain a near-normal glycated hemoglobin (A1C) concentration without inducing hypoglycemia; for most patients, the target A1C is <7%. Metformin is the preferred first-line treatment, but most patients with type 2 diabetes eventually require multidrug therapy and/or insulin to achieve glycemic control.
Med Lett Drugs Ther. 2019 May 6;61(1571):65-8 |  Show IntroductionHide Introduction

Carboplatin

   
The Medical Letter on Drugs and Therapeutics • Sep 08, 1989  (Issue 800)
COPYRIGHT LAWS Other studies have found carboplatin active in small-cell and non-small-cell lung cancer ...
Carboplatin (Paraplatin - Bristol-Myers), a cytotoxic platinum-containing drug chemically related to cisplatin (Platinol), was recently approved by the US Food and Drug Administration (FDA) for palliative treatment of patients with recurrent ovarian cancer, including those previously treated with cisplatin.
Med Lett Drugs Ther. 1989 Sep 8;31(800):83-4 |  Show IntroductionHide Introduction

Rifabutin

   
The Medical Letter on Drugs and Therapeutics • Apr 30, 1993  (Issue 895)
, and widely distributed, with high concentrations in the lungs. The drug is metabolized in the liver ...
Rifabutin (formerly ansamycin; Mycobutin - Adria), a rifamycin antibiotic similar to rifampin (Rifadin, Rimactane) was recently approved by the US Food and Drug Administration for prevention of disseminated Mycobacterium avium complex (MAC) disease in patients with advanced HIV infection.
Med Lett Drugs Ther. 1993 Apr 30;35(895):36-8 |  Show IntroductionHide Introduction

Bronchial Thermoplasty for Asthma

   
The Medical Letter on Drugs and Therapeutics • Aug 23, 2010  (Issue 1345)
. An unpublished 5-year follow-up found no deterioration of lung function as assessed by FEV1.6 No deaths ...
The FDA has approved the marketing of the Alair Bronchial Thermoplasty System (Asthmatx) for treatment of severe persistent asthma in patients ≥18 years old whose asthma is not well controlled with inhaled corticosteroids and long-acting beta2-agonists.
Med Lett Drugs Ther. 2010 Aug 23;52(1345):65-6 |  Show IntroductionHide Introduction

OTC Primatene Mist Returns

   
The Medical Letter on Drugs and Therapeutics • Jan 28, 2019  (Issue 1564)
and Immunology, American College of Chest Physicians, American Lung Association, American Thoracic Society ...
The FDA has approved over-the-counter (OTC) sale of inhaled epinephrine (Primatene Mist – Amphastar), a nonselective alpha and beta agonist, for temporary relief of mild symptoms of intermittent asthma in patients ≥12 years old who have been diagnosed with mild intermittent asthma by a healthcare professional. The original version of Primatene Mist, which was approved by the FDA in 1967, was removed from the market in 2011 because the metered-dose inhaler (MDI) contained ozone-depleting chlorofluorocarbon (CFC) propellants; the new MDI contains hydrofluoroalkane (HFA)...
Med Lett Drugs Ther. 2019 Jan 28;61(1564):9-10 |  Show IntroductionHide Introduction

In Brief: Dabrafenib (Tafinlar) and Trametinib (Mekinist) for Glioma (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023  (Issue 1674)
and involvement of lymph nodes following complete resection ▶ Metastatic non-small cell lung cancer (NSCLC ...
The oral kinase inhibitors dabrafenib (Tafinlar – GSK) and trametinib (Mekinist – Novartis) have been approved by the FDA for use together for a sixth indication: treatment of low-grade glioma (LGG) with a BRAF V600E mutation in patients ≥1 years old who require systemic therapy. This combination is the first systemic therapy to be approved in the US for first-line treatment of LGG with a BRAF V600E mutation in pediatric patients. The FDA also approved new oral formulations of both drugs for patients who are unable to swallow dabrafenib capsules or trametinib...
Med Lett Drugs Ther. 2023 Apr 17;65(1674):e75-6   doi:10.58347/tml.2023.1674i |  Show IntroductionHide Introduction