Search Results for "moderate concentrate"
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Searched for moderate concentrate. Results 81 to 90 of 149 total matches.
Ganaxolone (Ztalmy) for CDKL5 Deficiency Disorder (online only)
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
, and seasonal allergy are most common.
▶ Drug Interactions: Moderate or strong CYP3A4 inducers can
decrease ...
The FDA has approved ganaxolone (Ztalmy – Marinus)
for oral treatment of seizures associated with cyclin-dependent
kinase-like 5 (CDKL5) deficiency disorder
in patients ≥2 years old. It is the first drug to be
approved in the US for this indication.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):e139-40 doi:10.58347/tml.2024.1709g | Show Introduction Hide Introduction
Lipid-Lowering Drugs
The Medical Letter on Drugs and Therapeutics • Sep 19, 2022 (Issue 1659)
concentrations. Atorvastatin undergoes less firstpass
metabolism by CYP3A4, but rhabdomyolysis has
occurred ...
Cholesterol management guidelines from the
American College of Cardiology/American Heart
Association Task Force were last published in 2019.
Comparison Chart: Some Drugs for HFrEF
The Medical Letter on Drugs and Therapeutics • May 26, 2025 (Issue 1729)
...
View the Comparison Chart: Some Drugs for HFrEF
Med Lett Drugs Ther. 2025 May 26;67(1729):e1-15 doi:10.58347/tml.2025.1729b | Show Introduction Hide Introduction
Deuruxolitinib (Leqselvi) for Severe Alopecia Areata
The Medical Letter on Drugs and Therapeutics • Oct 27, 2025 (Issue 1740)
has not been studied in lactating
women. Because the drug is highly protein-bound,
concentrations in breast milk ...
The FDA has approved the oral Janus kinase (JAK)
inhibitor deuruxolitinib (Leqselvi – Sun) for treatment
of severe alopecia areata in adults. Two other oral
JAK inhibitors are approved for treatment of severe
alopecia areata: baricitinib (Olumiant) is approved for
use in adults, and ritlecitinib (Litfulo) is approved for
use in patients ≥12 years old.
Med Lett Drugs Ther. 2025 Oct 27;67(1740):174-6 doi:10.58347/tml.2025.1740b | Show Introduction Hide Introduction
Tapinarof Cream (Vtama) for Psoriasis
The Medical Letter on Drugs and Therapeutics • Aug 08, 2022 (Issue 1656)
% of
patients with mainly moderate plaque psoriasis. Comparative
trials are lacking.
TOPICAL TREATMENT ...
The FDA has approved Vtama (Dermavant), a 1%
cream formulation of the aryl hydrocarbon receptor
(AhR) agonist tapinarof, for treatment of adults with
plaque psoriasis. It is the first AhR agonist to be
approved by the FDA.
Taletrectinib (Ibtrozi) — Another Kinase Inhibitor for Non-Small Cell Lung Cancer (NSCLC) (online only)
The Medical Letter on Drugs and Therapeutics • Aug 04, 2025 (Issue 1734)
,
dizziness, rash, constipation, and fatigue.
▶ Drug Interactions: Concurrent use of strong or moderate CYP3A ...
Taletrectinib (Ibtrozi – Nuvation Bio), an oral kinase
inhibitor, has been approved by the FDA for treatment
of locally advanced or metastatic ROS1-positive non-small
cell lung cancer (NSCLC) in adults. It is the fourth
oral kinase inhibitor to be approved in the US for this
indication; crizotinib (Xalkori), entrectinib (Rozlytrek),
and repotrectinib (Augtyro) were approved earlier.
Med Lett Drugs Ther. 2025 Aug 4;67(1734):e130-1 doi:10.58347/tml.2025.1734d | Show Introduction Hide Introduction
Sevabertinib (Hyrnuo) for NSCLC (online only)
The Medical Letter on Drugs and Therapeutics • Feb 16, 2026 (Issue 1748)
: Concurrent use of sevabertinib and strong
CYP3A4 inhibitors or moderate or strong CYP3A4 inducers
should ...
Sevabertinib (Hyrnuo – Bayer), an oral kinase inhibitor,
has received accelerated approval from the FDA for
treatment of adults with locally advanced or metastatic
nonsquamous non-small cell lung cancer (NSCLC)
with human epidermal growth factor 2 (HER2) tyrosine
kinase domain activating mutations who had received
prior systemic therapy. It is the second oral targeted
therapy to be approved in the US for this indication;
the oral kinase inhibitor zongertinib (Hernexeos) was
approved in August 2025.
Med Lett Drugs Ther. 2026 Feb 16;68(1748):e34-5 doi:10.58347/tml.2026.1748g | Show Introduction Hide Introduction
Vonoprazan (Voquezna) for Nonerosive GERD
The Medical Letter on Drugs and Therapeutics • Oct 14, 2024 (Issue 1713)
; use with strong or moderate CYP3A4
inducers can decrease serum concentrations of
vonoprazan ...
The potassium-competitive acid blocker vonoprazan
(Voquezna – Phathom), which was approved earlier
for treatment of erosive esophagitis, has now been
approved by the FDA for relief of heartburn associated
with nonerosive gastroesophageal reflux disease
(GERD) in adults. Vonoprazan is also available
copackaged with amoxicillin (Voquezna Dual Pak) and
with amoxicillin and clarithromycin (Voquezna Triple
Pak) for treatment of Helicobacter pylori infection.
Med Lett Drugs Ther. 2024 Oct 14;66(1713):164-6 doi:10.58347/tml.2024.1713c | Show Introduction Hide Introduction
Nonopioid Drugs for Pain
The Medical Letter on Drugs and Therapeutics • Mar 07, 2022 (Issue 1645)
to moderate pain,
nonopioid analgesics such as acetaminophen and
nonsteroidal anti-inflammatory drugs ...
Nonopioid drugs can be used in the treatment of
many nociceptive and neuropathic pain conditions.
For severe pain, especially severe chronic cancer
pain, use of opioids may be necessary. Noninvasive
nonpharmacologic treatments, including physical
and psychological therapies, have been shown to
improve pain and function in patients with some
common chronic pain conditions and are unlikely
to cause serious harms. A multimodal approach to
analgesic therapy can increase pain control while
reducing opioid use and adverse effects.
Daridorexant (Quviviq) for Insomnia
The Medical Letter on Drugs and Therapeutics • Jul 11, 2022 (Issue 1654)
, and
hallucinations have occurred.
▶ Drug Interactions: Use with strong CYP3A4 inhibitors or strong
or moderate ...
The FDA has approved daridorexant (Quviviq –
Idorsia), an orexin receptor antagonist, for treatment
of sleep-onset and/or sleep-maintenance insomnia
in adults. Daridorexant is the third orexin receptor
antagonist to be approved for this indication;
suvorexant (Belsomra) and lemborexant (Dayvigo)
were approved earlier.
