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Searched for days. Results 241 to 250 of 479 total matches.
Talicia - A 3-Drug Combination for Helicobacter pylori Infection
The Medical Letter on Drugs and Therapeutics • Jun 01, 2020 (Issue 1599)
, double-blind, 14-
day trials in a total of 573 treatment-naive adults with
recurrent epigastric pain ...
The FDA has approved a fixed-dose combination
of omeprazole, amoxicillin, and rifabutin (Talicia –
RedHill) for treatment of Helicobacter pylori infection
in adults. Talicia is the first rifabutin-based product to
be approved for this indication.
Osilodrostat (Isturisa) for Cushing's Disease
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021 (Issue 1617)
.
The wholesale acquisition cost of a 30-day supply at the lowest
usual maintenance dosage is $14,388.
22 ...
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.
Oliceridine (Olinvyk) - A New Opioid for Severe Pain
The Medical Letter on Drugs and Therapeutics • Mar 08, 2021 (Issue 1619)
regimen
should be used until oliceridine can be administered
the next day. In the clinical trials ...
Oliceridine (Olinvyk - Trevena), an IV opioid agonist,
has been approved by the FDA for management of
acute pain severe enough to require an opioid and for
which alternative treatment options are inadequate.
Zavegepant (Zavzpret) for Acute Treatment of Migraine
The Medical Letter on Drugs and Therapeutics • Jul 24, 2023 (Issue 1681)
orally disintegrating tabs3 75 mg PO (max 75 mg/day) $118.90
Ubrogepant – Ubrelvy (Abbvie) 50, 100 mg ...
The FDA has approved zavegepant nasal spray
(Zavzpret – Pfizer) for acute treatment of migraine
with or without aura in adults. Zavzpret is the first
nasal spray formulation of a calcitonin gene-related
peptide (CGRP) receptor antagonist ("gepant") to
become available in the US.
Med Lett Drugs Ther. 2023 Jul 24;65(1681):116-8 doi:10.58347/tml.2023.1681c | Show Introduction Hide Introduction
Drugs for Type 2 Diabetes
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022 (Issue 1663)
mg tabs 1500-2550 mg/day PO divided bid-tid4 $2.70
Riomet (Sun) 500 mg/5 mL soln (4, 16 oz) 665.205 ...
Diet, exercise, and weight loss can improve glycemic
control, but almost all patients with type 2 diabetes
require antihyperglycemic drug therapy. Treating to
a target A1C of <7% while minimizing hypoglycemia
is recommended to prevent microvascular complications
of diabetes (retinopathy, nephropathy, and
neuropathy). An A1C target of <8% may be appropriate
for some older patients.
Lemborexant (Dayvigo) for Insomnia
The Medical Letter on Drugs and Therapeutics • Jun 29, 2020 (Issue 1601)
5 mg was not significantly
different from placebo in next-day postural stability, memory ...
The FDA has approved lemborexant (Dayvigo – Eisai),
an orexin receptor antagonist, for treatment of sleep-onset
and/or sleep-maintenance insomnia in adults. It
is the second orexin receptor antagonist to be approved
for this indication; suvorexant (Belsomra) was the first.
Rilonacept (Arcalyst) for Recurrent Pericarditis
The Medical Letter on Drugs and Therapeutics • Sep 06, 2021 (Issue 1632)
singlevials
use prefilled syringes
Usual Dosage ≥18 years: 320 mg SC 1-2 mg/kg SC once/day
once,2 then 160 ...
Rilonacept (Arcalyst – Kiniksa), an interleukin-1 (IL-1)
antagonist that has been available for years for
treatment of cryopyrin-associated periodic syndromes,
has now been approved by the FDA for treatment
of recurrent pericarditis and prevention of further
recurrences in patients ≥12 years old. It is the first drug
to be approved in the US for this indication. Anakinra
(Kineret), an IL-1 receptor antagonist FDA-approved for
treatment of rheumatoid arthritis, has been used off-label
for years for treatment of recurrent pericarditis.
Xywav - A Mixed-Salt Oxybate Oral Solution for Idiopathic Hypersomnia
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021 (Issue 1640)
depression can occur.
No head-to-head trials comparing it with stimulants are
available.
A 30-day supply ...
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.
Vazalore - A New Aspirin Formulation
The Medical Letter on Drugs and Therapeutics • May 02, 2022 (Issue 1649)
-coated aspirin, each given at
a dose of 325 mg once daily for 3 days. The time
to complete inhibition ...
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.
Vimseltinib (Romvimza) for Tenosynovial Giant Cell Tumor (online only)
The Medical Letter on Drugs and Therapeutics • Apr 14, 2025 (Issue 1726)
twice weekly.
Cost: A 28-day supply costs $26,128.
Conclusion: Vimseltinib produced durable ...
Vimseltinib (Romvimza – Deciphera), an oral kinase
inhibitor, has been approved by the FDA for treatment
of symptomatic tenosynovial giant cell tumor in adults
for whom surgical resection would cause worsening
functional limitation or severe morbidity. The kinase
inhibitor pexidartinib (Turalio) was approved for a
similar indication in 2019.
Med Lett Drugs Ther. 2025 Apr 14;67(1726):e66-7 doi:10.58347/tml.2025.1726h | Show Introduction Hide Introduction