Search Results for "Lung"
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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.
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.
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.
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 Introduction Hide 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.
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.
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.
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.
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)...
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 Introduction Hide Introduction