Search Results for "Diabetes"
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Searched for Diabetes. Results 201 to 210 of 381 total matches.
Ceftaroline Fosamil (Teflaro) - A New IV Cephalosporin
The Medical Letter on Drugs and Therapeutics • Jan 24, 2011 (Issue 1356)
, diabetes mellitus,
infected pressure ulcers and traumatic or surgical
wound infections, may also ...
The FDA has approved ceftaroline fosamil (Teflaro –
Forest), an intravenous (IV) cephalosporin, for treatment
of acute bacterial skin and skin structure infections,
including those caused by methicillin-resistant
Staphylococcus aureus (MRSA), and for treatment of
community-acquired bacterial pneumonia in adults. It
is the first beta-lactam antibiotic approved for treatment
of MRSA.
Long-Acting Injectable Aripiprazole (Abilify Maintena) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Apr 29, 2013 (Issue 1415)
antipsychotics
includes warnings about hyperglycemia and diabetes,
but aripiprazole has a relatively low risk ...
An extended-release injectable formulation of the
second-generation antipsychotic aripiprazole
(Abilify) has been approved by the FDA (Abilify
Maintena – Otsuka/Lundbeck) for once-monthly treatment of schizophrenia. It is the fourth second-generation
antipsychotic to become available in a
long-acting parenteral formulation. Long-acting parenteral
antipsychotics, given at intervals of 2-4
weeks, are generally used for patients with a history
of relapse due to poor adherence to oral maintenance
therapy.
Avanafil (Stendra) - Another PDE5 Inhibitor for Erectile Dysfunction
The Medical Letter on Drugs and Therapeutics • May 12, 2014 (Issue 1442)
with diabetes
mellitus. Mayo Clin Proc 2012; 87:843.
5. JP Mulhall et al. A phase 3, placebo-controlled study ...
The FDA has approved avanafil (Stendra – Vivus),
an oral phosphodiesterase type-5 (PDE5) inhibitor,
for treatment of erectile dysfunction. It is the fifth
PDE5 inhibitor to be approved for this indication.
Advertisements on Stendra’s website imply that
it has a faster onset of action than other PDE5
inhibitors.
A Ranibizumab Ocular Implant (Susvimo) for Age-Related Macular Degeneration
The Medical Letter on Drugs and Therapeutics • May 02, 2022 (Issue 1649)
-2 (Ang-2), recently became available for
intravitreal treatment of nAMD and diabetic macular
edema ...
The FDA has approved Susvimo (Genentech), a
refillable permanent ocular implant containing the
vascular endothelial growth factor (VEGF) inhibitor
ranibizumab, for treatment of neovascular (wet) age-related
macular degeneration (nAMD) in patients who
have previously responded to at least two intravitreal
injections of a VEGF inhibitor. Ranibizumab intravitreal
injection (Lucentis) has been available since 2006 for
monthly treatment of nAMD. The FDA has approved
ranibizumab-nuna (Byooviz), a biosimilar of Lucentis
and the first ophthalmologic biosimilar; it will be
available in June...
Two New Intra-Articular Injections for Knee Osteoarthritis
The Medical Letter on Drugs and Therapeutics • Aug 27, 2018 (Issue 1554)
to the active control (-3.12 vs -2.86).10
Approximately 30% of patients with type 2 diabetes
also have knee OA ...
The FDA has approved a single-injection hyaluronic
acid gel (Durolane – Bioventus) and an extended-release
(ER) formulation of the synthetic corticosteroid
triamcinolone acetonide (Zilretta – Flexion) for intra-articular
(IA) treatment of osteoarthritic knee pain.
Peginterferon Alfa-2b (Sylatron) for Melanoma
The Medical Letter on Drugs and Therapeutics • Sep 19, 2011 (Issue 1373)
and diabetes mellitus.
DOSAGE, ADMINISTRATION AND COST — The recommended
dosage of peginterferon alfa-2b ...
The FDA has approved peginterferon alfa-2b (Sylatron – Merck) for adjuvant treatment of node-positive melanoma after surgical resection. Pegylated interferon has a longer duration of action than interferon alfa-2b (Intron A), which is also FDA-approved for adjuvant treatment of malignant melanoma after surgery, and can be given once a week, compared to 3-5 times a week for standard interferon.
In Brief: Avelumab (Bavencio) for Metastatic Merkel Cell Carcinoma (online only)
The Medical Letter on Drugs and Therapeutics • Jul 17, 2017 (Issue 1525)
insufficiency,
type 1 diabetes) can occur.
The recommended dosage of Bavencio is 10 mg/kg infused
IV over 60 ...
The FDA has approved the fully-human programmed death ligand 1 (PD-L1) blocking antibody avelumab (Bavencio – EMD Serono/Pfizer) for treatment of metastatic Merkel cell carcinoma (MCC) in patients ≥12 years old. Avelumab is the first drug to be approved in the US for this rare skin cancer. About 1600 people in the US, most commonly older adults (mean age at presentation is 75 years), are diagnosed each year with MCC. Most of these patients can be treated with surgical resection, but ~50% will have a recurrence and >30% will eventually have metastatic disease. Median progression-free...
Intravenous Immune Globulin
The Medical Letter on Drugs and Therapeutics • Dec 25, 1992 (Issue 886)
Contraindicated in IgA
deficiency
Freeze-dried
May be given to diabetics (stabilized with sucrose)
3
620.00 ...
Intravenous formulations of immune globulin (IVIG) have been available for more than ten years for treatment of immune deficiency (Medical Letter, 24:81, 1982). Seven preparations are now licensed in the USA, with additional indications for their use.
A Two-Dose Hepatitis B Vaccine for Adults (Heplisav-B)
The Medical Letter on Drugs and Therapeutics • Jan 29, 2018 (Issue 1539)
(Heplisav-B has not been studied
in hemodialysis patients), diabetes (particularly
in persons 19-59 years ...
The FDA has approved a two-dose hepatitis B virus
(HBV) vaccine (Heplisav-B – Dynavax) for use in adults
≥18 years old. The three other HBV vaccines marketed
in the US are usually administered in 3 doses. Engerix-B
and Recombivax HB are licensed for use in persons of
all ages. A combination hepatitis A/B vaccine (Twinrix)
contains the same hepatitis B component as Engerix-B
and is licensed for use only in adults.
Osilodrostat (Isturisa) for Cushing's Disease
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021 (Issue 1617)
. Lancet Diabetes Endocrinol 2018; 7:300.
3. NA Tritos and BMK Biller. Current management of Cushing ...
The FDA has approved osilodrostat (Isturisa –
Recordati), a cortisol synthesis inhibitor, for oral
treatment of adults with Cushing's disease when
surgical resection of the pituitary adenoma is not an
option or has not been curative. Osilodrostat is the
first cortisol synthesis inhibitor to be approved in
the US for this indication. Other oral steroidogenesis
inhibitors such as ketoconazole and metyrapone have
been used off-label for this indication for many years.