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Brolucizumab (Beovu) for Age-Related Macular Degeneration
The Medical Letter on Drugs and Therapeutics • Feb 10, 2020 (Issue 1591)
effective and has not
been shown to improve vision.1,2
CLINICAL STUDIES — FDA approval of brolucizumab ...
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.
Drugs for Sexually Transmitted Infections
The Medical Letter on Drugs and Therapeutics • Jun 27, 2022 (Issue 1653)
of the
indications and dosages recommended here have
not been approved by the FDA (see Table 1).
PARTNER TREATMENT ...
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).
Two New Drugs for Chronic ITP
The Medical Letter on Drugs and Therapeutics • Feb 09, 2009 (Issue 1305)
not
compete for the same binding site as endogenous
thrombopoietin.
1
PHARMACODYNAMICS — Administered ...
Romiplostim (Nplate - Amgen), a recombinant fusion protein injected subcutaneously, and eltrombopag (Promacta - GlaxoSmithKline), a non-peptide taken orally, have been approved by the FDA for treatment of chronic immune thrombocytopenic purpura (ITP) refractory to corticosteroids, immunoglobulins and/or splenectomy.
IV Amisulpride (Barhemsys) for Postoperative Nausea and Vomiting
The Medical Letter on Drugs and Therapeutics • Dec 28, 2020 (Issue 1614)
or motion sickness,
female sex, nonsmoking status, age ...
The FDA has approved IV amisulpride (Barhemsys –
Acacia), a selective dopamine-2 and -3 (D2/D3) receptor
antagonist, for prevention and treatment of postoperative
nausea and vomiting (PONV) in adults. It is the first
antiemetic to be approved for rescue treatment of
PONV in patients who have symptoms despite receiving
antiemetic prophylaxis. Oral formulations of amisulpride
are available in Europe for treatment of schizophrenia
and acute psychotic episodes.
Brinzolamide--A New Topical Carbonic Anhydrase Inhibitor for Glaucoma
The Medical Letter on Drugs and Therapeutics • Sep 25, 1998 (Issue 1036)
by the FDA in a 1% ophthalmic suspension for treatment of elevated intraocular pressure due to ocular ...
Brinzolamide (Azopt - Alcon), a thieno-thiazine-6-sulfonamide carbonic anhydrase inhibitor, has been approved by the FDA in a 1% ophthalmic suspension for treatment of elevated intraocular pressure due to ocular hypertension or open-angle glaucoma. Brinzolamide is the second FDA-approved topical carbonic anhydrase inhibitor. Dorzolamide (Trusopt) was approved earlier (Medical Letter, 37:76, 1995).
FDA Requires Lower Dosing of Zolpidem
The Medical Letter on Drugs and Therapeutics • Jan 21, 2013 (Issue 1408)
and to recommend in their labeling consideration of a
lower dose for men.1 No change will be required in the
dose ...
On January 10, 2013, the FDA issued a news release
to announce that it was requiring the manufacturers of
the zolpidem-containing products Ambien, Ambien
CR, Edluar and Zolpimist, which are all approved for
treatment of insomnia, to lower the doses for women
and to recommend in their labeling consideration of a
lower dose for men. No change will be required in the
dose of Intermezzo, a low-dose sublingual formulation
of zolpidem for middle-of-the-night awakening, which
is already recommended in a lower dose for women.
Jentadueto XR for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Aug 01, 2016 (Issue 1500)
The Medical Letter®
on Drugs and Therapeutics
Volume 58 (Issue 1500) August 1, 2016
Published ...
The FDA has approved Jentadueto XR (Boehringer
Ingelheim/Lilly), a once-daily extended-release formulation
of the dipeptidyl peptidase-4 (DPP-4) inhibitor
linagliptin and the biguanide metformin, for oral
treatment of type 2 diabetes. Linagliptin and metformin
have been available for years in a twice-daily immediate-release combination (Jentadueto). Once-daily
extended-release formulations combining metformin
with the DPP-4 inhibitors saxagliptin (Kombiglyze XR)
and sitagliptin (Janumet XR) are also available.
Venetoclax (Venclexta) for Chronic Lymphocytic Leukemia
The Medical Letter on Drugs and Therapeutics • Aug 01, 2016 (Issue 1500)
The Medical Letter®
on Drugs and Therapeutics
Volume 58 (Issue 1500) August 1, 2016
Published ...
The FDA has approved venetoclax (Venclexta –
Abbvie/Genentech), an oral selective BCL-2 inhibitor,
for treatment of chronic lymphocytic leukemia (CLL) in
patients with a 17p deletion who have received at least
one prior therapy. The 17p deletion is associated with a
poor prognosis in patients with CLL; it is prevalent in
about 20% of patients with relapsed CLL. Venetoclax is
the fi rst BCL-2 inhibitor to become available in the US.
Lyumjev - A New Insulin Lispro for Diabetes
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020 (Issue 1609)
–
Lilly), a faster-acting formulation of insulin lispro
(Humalog), for treatment of type 1 and type 2 ...
The FDA has approved insulin lispro-aabc (Lyumjev –
Lilly), a faster-acting formulation of insulin lispro
(Humalog), for treatment of type 1 and type 2 diabetes
in adults. Fiasp, a faster-acting formulation of insulin
aspart (Novolog), was approved in 2017.
DaxibotulinumtoxinA (Daxxify) for Frown Lines (online only)
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024 (Issue 1707)
in the US for this indication (see Table 1). It is also approved for treatment of cervical dystonia in adults.
MECHANISM ...
The FDA has approved daxibotulinumtoxinA-lanm
(Daxxify – Revance), an acetylcholine release inhibitor
and neuromuscular blocking agent, for temporary
improvement in the appearance of moderate to severe
glabellar (frown) lines associated with corrugator
and/or procerus muscle activity. Daxxify is the fifth
botulinumtoxin type A product to be approved in the
US for this indication (see Table 1). It is also approved
for treatment of cervical dystonia in adults
Med Lett Drugs Ther. 2024 Jul 22;66(1707):e121-2 doi:10.58347/tml.2024.1707g | Show Introduction Hide Introduction
