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Searched for vol. Results 201 to 210 of 395 total matches.
Tramadol Oral Solution (Qdolo) for Pain
The Medical Letter on Drugs and Therapeutics • May 31, 2021 (Issue 1625)
increase
tramadol levels and the risk of seizures. Concurrent
84
The Medical Letter ® Vol. 63 (1625 ...
The opioid agonist tramadol is now available in an oral
solution (Qdolo – Athena Bioscience) for management
of pain severe enough to require an opioid and for
which alternative treatment options are inadequate.
Tramadol has been available for years in immediate-release
tablets and capsules, extended-release
capsules (Ultram, and others), and in a fixed-dose
combination tablet with acetaminophen (Ultracet,
and generics).
Setmelanotide (Imcivree) for Rare Genetic Forms of Obesity (online only)
The Medical Letter on Drugs and Therapeutics • Jul 26, 2021 (Issue 1629)
The Medical Letter ® Vol. 63 (1629) July 26, 2021
DOSAGE, ADMINISTRATION, AND COST —
Setmelanotide ...
The FDA has approved setmelanotide (Imcivree –
Rhythm), a subcutaneously injected melanocortin 4
(MC4) receptor agonist, for chronic weight management
in patients ≥6 years old with obesity due to
pro-opiomelanocortin (POMC) deficiency, proprotein
subtilisin/kexin type 1 (PCSK1) deficiency, or leptin
receptor (LEPR) deficiency.
Xywav - A Mixed-Salt Oxybate Oral Solution for Idiopathic Hypersomnia
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021 (Issue 1640)
of Xywav costs $5110.
The Medical Letter ® Vol. 63 (1640) December 27, 2021Medical
Letter
1. E ...
Xywav (Jazz), an oral solution that contains calcium,
magnesium, potassium, and sodium oxybates, has
been approved by the FDA for treatment of idiopathic
hypersomnia in adults. It is the first drug to be
approved in the US for this indication. Xywav was
approved in 2020 for treatment of excessive daytime
sleepiness or cataplexy in patients ≥7 years old with
narcolepsy. It contains about 92% less sodium than
sodium oxybate oral solution (Xyrem), which has
been available in the US for years for use in patients
≥7 years old with narcolepsy.
A Drug-Eluting Contact Lens for Allergic Conjunctivitis
The Medical Letter on Drugs and Therapeutics • Apr 18, 2022 (Issue 1648)
; they can be reinserted after 10 minutes.
The Medical Letter ® Vol. 64 (1648) April 18, 2022
61 ...
The FDA has approved Acuvue Theravision with
Ketotifen (Johnson & Johnson Vision Care), a daily-wear,
disposable, vision-correcting soft contact
lens that releases the H1-antihistamine ketotifen, for
prevention of ocular itch due to allergic conjunctivitis
in contact lens users. This is the first approval for a
drug-eluting contact lens. Ketotifen eye drops (Alaway,
Zaditor, and others) are available over the counter.
Vazalore - A New Aspirin Formulation
The Medical Letter on Drugs and Therapeutics • May 02, 2022 (Issue 1649)
to immediate- release or enteric-coated aspirin, and
it costs much more.
The Medical Letter ® Vol. 64 (1649 ...
The FDA has approved an over-the-counter (OTC)
liquid-filled capsule formulation of aspirin (Vazalore –
PLx Pharma). The manufacturer has been heavily
promoting Vazalore with claims of fast, predictable
absorption and antiplatelet activity and improved
gastrointestinal safety compared to existing OTC
aspirin formulations.
In Brief: Higher-Dose Semaglutide (Ozempic) for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • May 16, 2022 (Issue 1650)
, randomised, phase 3B trial. Lancet
Diabetes Endocrinol 2021; 9:563.
The Medical Letter ® Vol. 64 (1650 ...
The FDA has approved a higher-dose injectable
formulation of the long-acting glucagon-like
peptide-1 (GLP-1) receptor agonist semaglutide
(Ozempic) for treatment of type 2 diabetes in adults.
A single SC injection of the new 8 mg/3 mL
formulation delivers 2 mg of semaglutide.
Alpelisib (Vijoice) for PIK3CA-Related Overgrowth Spectrum (online only)
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022 (Issue 1663)
® Vol. 64 Published online November 14, 2022
1. G Canaud et al. LBA23 EPIK-P1: retrospective chart ...
The oral kinase inhibitor alpelisib (Vijoice – Novartis)
has been approved by the FDA for treatment of
patients ≥2 years old with severe manifestations of
PIK3CA-related overgrowth spectrum (PROS) who
require systemic treatment. Alpelisib is the first
drug to be approved in the US for this indication.
It was also approved in 2019 as Piqray for use in
combination with fulvestrant for treatment of certain
types of breast cancer.
Neratinib (Nerlynx) for Metastatic HER2-Positive Breast Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022 (Issue 1663)
with neratinib and
for at least one month after the last dose.
e193
The Medical Letter ® Vol. 64 Published ...
The oral tyrosine kinase inhibitor neratinib (Nerlynx –
Puma Biotechnology) has been approved by the FDA
for use in combination with capecitabine (Xeloda, and
generics) for treatment of advanced or metastatic
human epidermal growth factor receptor 2 (HER2)-positive breast cancer in adults who received ≥2 prior
anti-HER2-based regimens for metastatic disease.
It was previously approved for use as monotherapy
for extended adjuvant treatment of adults with early-stage,
HER2-positive breast cancer following adjuvant
trastuzumab (Herceptin)-based therapy. HER2 is
overexpressed in...
In Brief: Zanubrutinib (Brukinsa) for CLL or SLL (online only)
The Medical Letter on Drugs and Therapeutics • Feb 20, 2023 (Issue 1670)
) for CLL or SLL e34
The Medical Letter ® Vol. 65 Published online February 20, 2023
1. CS Tam et al ...
The Bruton's tyrosine kinase (BTK) inhibitor
zanubrutinib (Brukinsa), which was previously
approved by the FDA for treatment of mantle cell
lymphoma, Waldenström's macroglobulinemia,
and relapsed or refractory marginal zone
lymphoma, has now been approved for treatment
of chronic lymphocytic leukemia (CLL) or small
lymphocytic lymphoma (SLL) in adults. The BTK
inhibitors ibrutinib (Imbruvica) and acalabrutinib
(Calquence) were approved earlier for treatment of
CLL and SLL.
Med Lett Drugs Ther. 2023 Feb 20;65(1670):e33-4 doi:10.58347/tml.2023.1670e | Show Introduction Hide Introduction
In Brief: OTC Ivermectin for Head Lice
The Medical Letter on Drugs and Therapeutics • Jun 26, 2023 (Issue 1679)
to
ivermectin is rare.6
The Medical Letter ® Vol. 65 (1679) June 26, 2023Medical
Letter
Table 1. Some OTC ...
Topical ivermectin lotion 0.5% (Sklice, and generics),
which has been available by prescription since 2012,
is now FDA-approved for sale over the counter (OTC)
for treatment of head lice in patients ≥6 months old.
Ivermectin is also available by prescription as a 1%
cream (Soolantra) approved for topical treatment of
inflammatory lesions of rosacea and in oral tablets
(Stromectol, and generics) for treatment of various
parasitic infections.
Med Lett Drugs Ther. 2023 Jun 26;65(1679):103-4 doi:10.58347/tml.2023.1679e | Show Introduction Hide Introduction