Search Results for "Diabetes"
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Searched for Diabetes. Results 101 to 110 of 381 total matches.
Minimed 670G: A Hybrid Closed-Loop Insulin Delivery System
The Medical Letter on Drugs and Therapeutics • Nov 21, 2016 (Issue 1508)
≥14 years old with type 1 diabetes. The system
uses an algorithm to automatically adjust basal ...
The FDA has approved the Minimed 670G (Medtronic),
a hybrid closed-loop insulin delivery system for use in
patients ≥14 years old with type 1 diabetes. The system
uses an algorithm to automatically adjust basal insulin
doses based on readings from a continuous glucose
monitor (CGM). It fully automates basal insulin
delivery in "auto" mode, but is considered a "hybrid"
system (not a true "artificial pancreas") because it
requires some action by the patient. The 670G system
is expected to become available in Spring 2017.
In Brief: Exenatide (Byetta) for Weight Loss
The Medical Letter on Drugs and Therapeutics • Mar 13, 2006 (Issue 1230)
from
pancreatic beta cells, has been used by diabetics and
non-diabetics to lose weight. Approved by the FDA ...
Patients may be asking about reports in the lay press that exenatide (Byetta - Med Lett Drugs Ther 2005; 47:45), a synthetic peptide that stimulates release of insulin from pancreatic beta cells, has been used by diabetics and non-diabetics to lose weight. Approved by the FDA to improve glycemic control in patients with type 2 diabetes not controlled by metformin, a sulfonylurea or both, it is given by subcutaneous injection before the morning and evening meals. In clinical trials, some diabetic patients treated with the drug lost weight. No data are available on use in non-diabetics....
MiniMed 530G: An Insulin Pump with Low-Glucose Suspend Automation
The Medical Letter on Drugs and Therapeutics • Dec 09, 2013 (Issue 1431)
diabetes and
nocturnal hypoglycemia were randomized to sensoraugmented
insulin pump therapy ...
The FDA has approved the MiniMed 530G
(Medtronic), an insulin pump used in combination with
a continuous glucose monitoring sensor (Enlite) that
can stop delivery of insulin when interstitial glucose
reaches a prespecified low level. It is the only sensoraugmented
insulin pump available in the US with this
capability.
Insulin Glargine (Lantus) and Cancer Risk
The Medical Letter on Drugs and Therapeutics • Aug 24, 2009 (Issue 1319)
insulin.
1
DIABETES AND CANCER — Type 2 diabetes has
been associated with an increased risk of breast ...
Several large European observational studies published on-line this summer have raised questions about whether use of insulin glargine increases the risk of cancer.
A New Indication for Semaglutide (Wegovy)
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
the risk of MACE in adults with type 2 diabetes
and established CVD. The GLP-1 receptor agonists ...
The injectable glucagon-like peptide-1 (GLP-1)
receptor agonist semaglutide (Wegovy) has been
approved by the FDA to reduce the risk of major
adverse cardiovascular events (MACE) in adults with
established cardiovascular disease (CVD) and either
obesity or overweight. Semaglutide is the first drug
to be approved for cardiovascular risk reduction in
this population. It is also approved in a lower-dose
injectable formulation as Ozempic and in an oral
formulation as Rybelsus (see Table 1).
Med Lett Drugs Ther. 2024 Apr 29;66(1701):66-7 doi:10.58347/tml.2024.1701b | Show Introduction Hide Introduction
Liraglutide (Saxenda) for Weight Loss
The Medical Letter on Drugs and Therapeutics • Jun 22, 2015 (Issue 1471)
liraglutide, previously approved by the
FDA for treatment of type 2 diabetes as Victoza,1 has
now also ...
The injectable glucagon-like peptide-1 (GLP-1)
receptor agonist liraglutide, previously approved by the
FDA for treatment of type 2 diabetes as Victoza, has
now also been approved at a higher dose as Saxenda
(Novo Nordisk) for chronic weight management
in adults with a BMI ≥30, or a BMI ≥27 with a
weight-related comorbidity such as hypertension,
dyslipidemia, or diabetes.
In Brief: A New Glucagon Injection (Gvoke) for Severe Hypoglycemia
The Medical Letter on Drugs and Therapeutics • Nov 18, 2019 (Issue 1585)
years old with diabetes.
Conscious patients with symptoms of hypoglycemia can
take oral glucose ...
The FDA has approved a new formulation of glucagon
(Gvoke – Xeris) for subcutaneous treatment of severe
hypoglycemia in patients ≥2 years old with diabetes.
Conscious patients with symptoms of hypoglycemia can
take oral glucose. Glucagon is usually administered by a
caregiver to an unresponsive patient. The new formulation is
available in a single-use prefilled syringe (Gvoke PFS) and is
expected to become available in a single-use auto-injector
(Gvoke HypoPen) in 2020. Unlike previously available
injectable glucagon products (Glucagon Emergency Kit,
and others), Gvoke does not...
Table: GLP-1 and GIP/GLP-1 Receptor Agonists for Chronic Weight Management (online only)
The Medical Letter on Drugs and Therapeutics • Aug 05, 2024 (Issue 1708)
disease,
hypertension, obstructive sleep apnea,
type 2 diabetes, dyslipidemia
COMMENTS
▶Saxenda ...
View the Table: GLP-1 and GIP/GLP-1 Receptor Agonists for Chronic Weight Management
Med Lett Drugs Ther. 2024 Aug 5;66(1708):e1-2 doi:10.58347/tml.2024.1708d | Show Introduction Hide Introduction
In Brief: Semglee - Insulin Glargine Interchangeable with Lantus
The Medical Letter on Drugs and Therapeutics • Oct 04, 2021 (Issue 1634)
trial (INSTRIDE 3) in patients with
type 1 diabetes, switching between Lantus and
Semglee resulted ...
Insulin glargine-yfgn (Semglee – Viatris), a follow-on
insulin glargine product, has now received
interchangeability status with the reference product
Lantus from the FDA. It is the first biosimilar insulin
product to receive this designation in the US. Now a
pharmacist can substitute Semglee for Lantus as a
lower-cost alternative without permission from the
prescriber.
Semaglutide (Ozempic) for Weight Loss
The Medical Letter on Drugs and Therapeutics • Apr 05, 2021 (Issue 1621)
Nordisk), which is FDA-approved for treatment of
type 2 diabetes and to reduce the risk of major adverse ...
In recently published clinical trials, once-weekly
subcutaneous injection of the glucagon-like peptide 1
(GLP-1) receptor agonist semaglutide (Ozempic – Novo Nordisk), which is FDA-approved for treatment of
type 2 diabetes and to reduce the risk of major adverse
cardiovascular events in adults with type 2 diabetes
and established cardiovascular disease, has reduced
body weight significantly in patients with and without
type 2 diabetes when given in addition to lifestyle
intervention. Liraglutide (Saxenda), another GLP-1
receptor agonist, has been FDA-approved for chronic
weight...