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Difelikefalin (Korsuva) for Chronic Kidney Disease-Associated Pruritus
The Medical Letter on Drugs and Therapeutics • Feb 07, 2022 (Issue 1643)
,
and generics), and montelukast (Singulair, and
generics) have been used (off-label) in patients ...
Difelikefalin (Korsuva – Vifor), an IV kappa opioid
receptor (KOR) agonist, has been approved by the
FDA for treatment of moderate to severe pruritus
associated with chronic kidney disease (CKD) in
adults on hemodialysis. It is the first drug to be
approved for this indication and the first KOR agonist
to become available in the US. Difelikefalin has not
been studied in patients on peritoneal dialysis.
COVID-19 Update: Metformin to Prevent Long Covid?
The Medical Letter on Drugs and Therapeutics • May 29, 2023 (Issue 1677)
that off-label
use of the oral antihyperglycemic drug metformin
in patients with COVID-19 may decrease ...
Results from a double-blind trial suggest that off-label
use of the oral antihyperglycemic drug metformin
in patients with COVID-19 may decrease the risk
of post-acute sequelae of SARS-CoV-2 infection
("long COVID").
Med Lett Drugs Ther. 2023 May 29;65(1677):87-8 doi:10.58347/tml.2023.1677e | Show Introduction Hide Introduction
Ribociclib (Kisqali) for Early Breast Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Dec 09, 2024 (Issue 1717)
by 7 days off.
Cost: One 28-day treatment cycle costs $14,148.30.
Conclusion: Addition ...
The oral cyclin-dependent kinase (CDK) 4/6 inhibitor
ribociclib (Kisqali – Novartis), which was approved by
the FDA in 2017 for use with an aromatase inhibitor
or fulvestrant for treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor
2 (HER2)-negative advanced or metastatic breast
cancer, has now been approved for use with an
aromatase inhibitor for adjuvant treatment of HR-positive,
HER2-negative stage II or III early breast
cancer at high risk of recurrence. Kisqali can be used in
patients with node-positive or node-negative disease.
The CDK 4/6...
Med Lett Drugs Ther. 2024 Dec 9;66(1717):e202-3 doi:10.58347/tml.2024.1717f | Show Introduction Hide Introduction
Brexpiprazole (Rexulti) for Agitation in Alzheimer's Dementia
The Medical Letter on Drugs and Therapeutics • Jun 26, 2023 (Issue 1679)
treatment of choice has
been off-label use of an antipsychotic drug such
as aripiprazole (Abilify ...
The FDA has approved the oral second-generation
antipsychotic drug brexpiprazole (Rexulti – Otsuka/Lundbeck) for once-daily treatment of agitation associated
with dementia due to Alzheimer's disease (AD).
Brexpiprazole is the first drug to be approved in the US
for this indication. It is also approved for treatment of
schizophrenia and as an adjunct to antidepressants for
treatment of major depressive disorder.
Med Lett Drugs Ther. 2023 Jun 26;65(1679):99-101 doi:10.58347/tml.2023.1679b | Show Introduction Hide Introduction
Teprotumumab (Tepezza) for Thyroid Eye Disease
The Medical Letter on Drugs and Therapeutics • May 31, 2021 (Issue 1625)
)
have been used off-label to reduce inflammation, but
they are not effective long-term and adverse effects
limit ...
Teprotumumab-trbw (Tepezza - Horizon), an insulin-like
growth factor-1 receptor (IGF-1R) inhibitor, has
been approved by the FDA for IV treatment of thyroid
eye disease. It is the first drug to be approved in the US
for this indication.
Iloprost (Aurlumyn) for Frostbite
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024 (Issue 1707)
of severe frostbite; it has been used off-label for this indication in the EU and elsewhere for decades ...
The FDA has approved Aurlumyn (Eicos Sciences),
an IV formulation of the prostacyclin analog iloprost,
to reduce the risk of digit amputation in adults
with severe frostbite. Iloprost is the first drug to be
approved by the FDA for treatment of severe frostbite;
it has been used off-label for this indication in the EU
and elsewhere for decades. In the US, iloprost is also
available as an inhaled formulation (Ventavis) for
treatment of pulmonary arterial hypertension.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):114 doi:10.58347/tml.2024.1707b | Show Introduction Hide Introduction
Drugs for Sexually Transmitted Infections
The Medical Letter on Drugs and Therapeutics • Jun 27, 2022 (Issue 1653)
3 days, then 4 days off,
repeat up to 4x2
Sinecatechins 15% tid up to 16 weeks2,38
MU = million ...
This article includes recommendations for management
of most sexually transmitted infections (STIs)
other than HIV and viral hepatitis. Some of the
indications and dosages recommended here have
not been approved by the FDA (see Table 1).
Treatment of Clostridioides difficile Infection
The Medical Letter on Drugs and Therapeutics • Sep 06, 2021 (Issue 1632)
of additional doses of vancomycin
rectally as a retention enema (off-label route) can
be considered.13 Data ...
Clostridioides (formerly Clostridium) difficile infection
(CDI) is the most common infectious cause of
healthcare-associated diarrhea in adults. Guidelines
on management of CDI have recently been updated.
Lodoco: Low-Dose Colchicine for Cardiovascular Event Prevention
The Medical Letter on Drugs and Therapeutics • Oct 02, 2023 (Issue 1686)
may
prescribe generic colchicine 0.6-mg tablets off-label as a
more affordable alternative.
patients were also ...
Colchicine (Colcrys, and others), which has been
available in the US for decades for prophylaxis
and treatment of gout flares and other indications
in oral formulations that contain 0.6 mg of the
drug, has now been approved in 0.5-mg tablets as
Lodoco (Agepha) to reduce the risk of myocardial
infarction (MI), stroke, coronary revascularization,
and cardiovascular death in adults with established
atherosclerotic disease or multiple risk factors for
cardiovascular disease.
Med Lett Drugs Ther. 2023 Oct 2;65(1686):156-7 doi:10.58347/tml.2023.1686b | Show Introduction Hide Introduction
Capivasertib (Truqap) for Breast Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024 (Issue 1696)
.
Dosage: 400 mg twice daily for 4 days, followed by 3 days off
until disease progression or unacceptable ...
The oral kinase inhibitor capivasertib (Truqap –
AstraZeneca), a first-in-class AKT inhibitor, has
been approved by the FDA for use in combination
with the selective estrogen receptor degrader (SERD)
fulvestrant (Faslodex, and generics) for treatment of
hormone receptor (HR)-positive, human epidermal
growth factor receptor 2 (HER2)-negative, locally
advanced or metastatic breast cancer in adults with
one or more PIK3CA/AKT1/PTEN-alterations who had
disease progression on at least one endocrine-based
regimen for metastatic disease or recurrence on or
within 12 months of completing...
Med Lett Drugs Ther. 2024 Feb 19;66(1696):e32-3 doi:10.58347/tml.2024.1696e | Show Introduction Hide Introduction