Search Results for "Growth"
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Searched for Growth. Results 51 to 60 of 296 total matches.
Brolucizumab (Beovu) for Age-Related Macular Degeneration
The Medical Letter on Drugs and Therapeutics • Feb 10, 2020 (Issue 1591)
.
Brolucizumab-dbll (Beovu — Novartis), a vascular
endothelial growth factor (VEGF) inhibitor ...
Brolucizumab-dbll (Beovu — Novartis), a vascular
endothelial growth factor (VEGF) inhibitor, has been
approved by the FDA as an intravitreal injection for
treatment of neovascular (wet) age-related macular
degeneration (AMD). It is the fourth VEGF inhibitor to
be approved in the US for this indication; bevacizumab
(Avastin, and others), a VEGF inhibitor FDA-approved
for treatment of breast cancer and other malignancies,
has been used off-label for this indication for years.
Laser Treatment of Onychomycosis
The Medical Letter on Drugs and Therapeutics • Feb 18, 2013 (Issue 1410)
can increase clear linear nail growth.4 In one 3
month trial in 7 patients, 4 of 13 nails showed >25 ...
Fungal infections of the fingernails or toenails can persist
for months or years despite topical and systemic
antimicrobial therapy. The FDA has cleared several
short-pulse laser systems for treatment of this mainly
cosmetic disorder.
Low-Dose Aspirin for Prevention of Preeclampsia
The Medical Letter on Drugs and Therapeutics • Jun 23, 2014 (Issue 1445)
. In the fetus, preeclampsia can
cause intrauterine growth restriction, premature delivery,
and death. Delivery ...
The American College of Obstetricians and Gynecologists
(ACOG) and the US Preventive Services Task
Force (USPSTF) have recommended that women at
risk for preeclampsia take low-dose aspirin daily after
the first trimester.
Avacincaptad Pegol (Izervay) for Geographic Atrophy in Age-Related Macular Degeneration
The Medical Letter on Drugs and Therapeutics • Jan 22, 2024 (Issue 1694)
into the subretinal space. Vascular endothelial
growth factor (VEGF) inhibitors can markedly reduce
vision loss ...
The FDA has approved the complement C5 inhibitor
avacincaptad pegol (Izervay – Iveric) for intravitreal
treatment of geographic atrophy (GA) secondary
to age-related macular degeneration (AMD).
Avacincaptad pegol is the second complement
inhibitor to be approved in the US for this indication;
pegcetacoplan (Syfovre), a complement C3 and C3b
inhibitor, was approved earlier.
Med Lett Drugs Ther. 2024 Jan 22;66(1694):15-6 doi:10.58347/tml.2024.1694d | Show Introduction Hide Introduction
In Brief: A New Indication for Pemigatinib (Pemazyre) (online only)
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023 (Issue 1674)
myeloid/lymphoid neoplasms (MLNs) with fibroblast growth
factor receptor 1 (FGFR1) rearrangements ...
The oral kinase inhibitor pemigatinib (Pemazyre –
Incyte) has been approved by the FDA for treatment
of adults with relapsed or refractory myeloid/lymphoid neoplasms (MLNs) with fibroblast growth
factor receptor 1 (FGFR1) rearrangements. It is the
first targeted therapy to be approved in the US for this
indication. The drug received accelerated approval
from the FDA in 2020 for treatment of adults with
previously treated, unresectable, locally advanced or
metastatic cholangiocarcinoma with FGFR2 fusions
or other rearrangements.
Med Lett Drugs Ther. 2023 Apr 17;65(1674):e71-2 doi:10.58347/tml.2023.1674g | Show Introduction Hide Introduction
Perinatal Toxicity of Cocaine
The Medical Letter on Drugs and Therapeutics • Jun 03, 1988 (Issue 767)
of spontaneous abortion, abruptio
placentae, prematurity, and intrauterine growth retardation have been reported ...
As cocaine continues to be widely available in the USA (Medical Letter, 28:69, 1986), new problems associated with its use continue to emerge. Some recent reports indicate that use of the drug during pregnancy can damage the fetus, lead to abortion or premature labor, and cause toxic effects in the newborn infant.
In Brief: Olmesartan and Sprue-Like Enteropathy
The Medical Letter on Drugs and Therapeutics • Jan 29, 2018 (Issue 1539)
with earlystage,
human epidermal growth factor receptor 2
(HER2)-positive breast cancer, following adjuvant ...
A reader asked whether healthcare providers should avoid prescribing the angiotensin receptor blocker (ARB) olmesartan medoxomil (Benicar, and others) because it can cause severe GI adverse effects.In 2013, the FDA warned that olmesartan can cause sprue-like enteropathy, a condition characterized by intestinal villous atrophy, severe chronic diarrhea, and significant unintended weight loss. The warning was based on 23 cases of serious sprue-like enteropathy associated with use of olmesartan, some occurring years after starting the drug. All patients improved after stopping olmesartan; 10 had a...
Neratinib (Nerlynx) for HER2-Positive Breast Cancer
The Medical Letter on Drugs and Therapeutics • Jan 29, 2018 (Issue 1539)
with earlystage,
human epidermal growth factor receptor 2
(HER2)-positive breast cancer, following adjuvant ...
The FDA has approved the oral tyrosine kinase
inhibitor neratinib (Nerlynx – Puma Biotechnology)
for extended adjuvant treatment of adults with early-stage,
human epidermal growth factor receptor 2
(HER2)-positive breast cancer, following adjuvant
trastuzumab (Herceptin)-based therapy. HER2 is
overexpressed in about 20% of breast cancers. Up
to 30% of early-stage, HER2-positive breast cancer
cases treated with trastuzumab-based adjuvant
therapy recur.
Zanidatamab (Ziihera) for Biliary Tract Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025 (Issue 1720)
by the ERBB2 gene.
HER2, a transmembrane receptor protein involved
in normal cell growth, is mutated ...
Zanidatamab-hrii (Ziihera – Jazz), a bispecific HER2-directed antibody, has received accelerated approval
from the FDA for treatment of unresectable or metastatic
HER2-positive (IHC 3+) biliary tract cancer in patients
who received prior therapy. Biliary tract cancer includes
gallbladder cancer and intrahepatic and extrahepatic
cholangiocarcinoma. Zanidatamab is the first dual
HER2-targeted therapy to be approved in the US for
this indication. Accelerated approval was based on the
overall response rate and duration of response.
Med Lett Drugs Ther. 2025 Jan 20;67(1720):e16-7 doi:10.58347/tml.2025.1720f | Show Introduction Hide Introduction
Treatment of Pressure Ulcers
The Medical Letter on Drugs and Therapeutics • Feb 23, 1990 (Issue 812)
growth. Appropriate debridement technique is determined by the degree of
necrosis, with choices ...
Pressure is the most critical factor in the development of pressure ulcers; high pressure applied constantly for two hours produces irreversible tissue ischemia and necrosis. Malnutrition, fecal and urinary incontinence, fractures, and a low serum albumin may be additional risk factors. Frequent turning and mobilization of patients, relieving pressure and allowing tissue reoxygenation, are the most effective means of prevention and treatment (PS Goode and RM Allman, Med Clin North Am, 73:1511, Nov 1989).