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Searched for days. Results 801 to 810 of 1911 total matches.
Abemaciclib (Verzenio) - A Third CDK 4/6 Inhibitor for Breast Cancer
The Medical Letter on Drugs and Therapeutics • Nov 06, 2017 (Issue 1533)
in post- for 21 days, then
menopausal women 7 days off3,4
In combination with fulvestrant in women ...
The FDA has approved abemaciclib (Verzenio – Lilly),
an oral cyclin-dependent kinase (CDK) 4/6 inhibitor,
for treatment of hormone receptor (HR)-positive,
human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer.
Abemaciclib is the third CDK 4/6 inhibitor to be
approved in the US for this indication.
Benralizumab (Fasenra) for Severe Eosinophilic Asthma
The Medical Letter on Drugs and Therapeutics • Feb 26, 2018 (Issue 1541)
by proteolytic enzymes
Half-life ~15 days 16-22 days ~24 days
Dosage 30 mg SC q4 wks x 3, then q8 wks 100 mg SC ...
The FDA has approved benralizumab (Fasenra –
AstraZeneca), a humanized monoclonal antibody
selective for the interleukin-5 (IL-5) receptor, for
add-on maintenance treatment of severe asthma in
patients ≥12 years old with an eosinophilic phenotype.
Benralizumab is the third anti-IL-5 antibody to be
approved for treatment of severe eosinophilic asthma;
mepolizumab (Nucala) and reslizumab (Cinqair), which
target IL-5 itself, were approved earlier.
Brigatinib (Alunbrig) for Non-Small Cell Lung Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Apr 23, 2018 (Issue 1545)
Clin Oncol 2017; 35:2490.
2. Patients first received brigatinib 90 mg once daily for 7 days.
3 ...
The FDA has approved brigatinib (Alunbrig – Takeda),
an oral tyrosine kinase inhibitor, for treatment of
patients with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC)
who have progressed on or are intolerant to crizotinib
(Xalkori). Translocations of the ALK gene are found in
about 5% of lung cancers; they occur predominantly
in nonsmokers with adenocarcinoma. Brigatinib is the
third tyrosine kinase inhibitor to be approved for this
indication; ceritinib (Zykadia) and alectinib (Alecensa)
were approved earlier, and subsequently were...
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
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.
Drugs for Psychotic Disorders
The Medical Letter on Drugs and Therapeutics • Dec 19, 2016 (Issue 1510)
for renal or hepatic impairment.
2. Approximate WAC for 30 days’ treatment with the lowest usual adult ...
Oral antipsychotic drugs used for treatment of
schizophrenia, schizoaffective disorder, delusional
disorder, and other manifestations of psychosis or
mania are listed in Table 1. Parenteral
antipsychotic drugs used for treatment of these
disorders are listed in Table 2.
Methylphenidate Revisited
The Medical Letter on Drugs and Therapeutics • May 06, 1988 (Issue 765)
be started with a 5-mg methylphenidate tablet at breakfast.
Dosage can be increased at three- to seven-day ...
Methylphenidate (Ritalin and others), a Schedule II controlled substance in the USA, is a short-acting central-nervous-system stimulant widely used for treatment of children with school performance or behavior problems, or what is now called Attention Deficit-Hyperactivity Disorder, or AD-HD (American Psychiatric Association, Diagnostic and Statistical Manual of Mental Disorders, third ed., revised [DSM-III R], Washington, DC:authors, 1987, p 50). Some studies have estimated that more than 3% of elementary school students are taking methylphenidate, and one parents' group has brought a...
