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Searched for data. Results 51 to 60 of 1100 total matches.
Comparison Table: Some Lipid-Lowering Drugs (online only)
The Medical Letter on Drugs and Therapeutics • Sep 19, 2022 (Issue 1659)
▶ No data on presence in human breast milk or on its effects on the
breastfed infant
Drug Interactions ...
View the Comparison Table: Some Lipid-Lowering Drugs
Comparison Table: Some Oral Antiseizure Medications (online only)
The Medical Letter on Drugs and Therapeutics • Aug 05, 2024 (Issue 1708)
or inhibit CYP1A2
and 2B6
No adequate data
in pregnant women;
developmental toxicity in
animals ...
View the Comparison Table: Some Oral Antiseizure Medications
Med Lett Drugs Ther. 2024 Aug 5;66(1708):e133-40 doi:10.58347/tml.2024.1708b | Show Introduction Hide Introduction
Expanded Table: Some Oral Drugs for Chronic Insomnia (online only)
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023 (Issue 1667)
, cataplexy-like
symptoms
Pregnancy and Lactation:
No adequate data in pregnant
women
Administration ...
View the Expanded Table: Some Oral Drugs for Chronic Insomnia
Med Lett Drugs Ther. 2023 Jan 9;65(1667):e6-10 doi:10.58347/tml.2023.1667b | Show Introduction Hide Introduction
Citalopram (Celexa) and QT Interval Prolongation
The Medical Letter on Drugs and Therapeutics • Sep 03, 2012 (Issue 1398)
interval prolongation.1
THE DATA — The FDA based its warnings on postmarketing
reports of QT interval ...
The FDA has asked the manufacturers of the selective
serotonin reuptake inhibitor (SSRI) antidepressant
citalopram (Celexa, and others) to revise the labeling
of the drug to include new warnings about the risk of
QT interval prolongation.
Aripiprazole with Digital Ingestion Tracking (Abilify MyCite)
The Medical Letter on Drugs and Therapeutics • Jan 28, 2019 (Issue 1564)
of the rib cage.
The patch transmits ingestion data via Bluetooth
technology to a smartphone app; the data ...
Monitoring adherence of psychiatric patients to
oral medication may be especially difficult. The
FDA has approved Abilify MyCite (Otsuka/Proteus),
an aripiprazole tablet with an embedded sensor
that tracks when patients take the medication. It is
indicated for treatment of adults with schizophrenia,
bipolar disorder, or major depressive disorder. Abilify MyCite is the first drug with a digital ingestion tracking
system to be approved in the US.
Three New Oral Contraceptives
The Medical Letter on Drugs and Therapeutics • Sep 25, 2006 (Issue 1244)
recent data available
(August 31, 2006) from Wolters Kluwer Health.
SEASONIQUE vs. SEASONALE
LOESTRIN ...
Three new combination oral contraceptives (COCs) with shortened hormone-free intervals, Seasonique, Loestrin 24 Fe and Yaz, have recently been approved by the FDA. All 3 are derivatives of older products.
Dasatinib (Sprycel) for CML and Ph+ ALL
The Medical Letter on Drugs and Therapeutics • Jan 15, 2007 (Issue 1252)
has been
reported, possibly related to the inhibition of tyrosine
kinase.
10
No data are available on the safety ...
Dasatinib (Sprycel - Bristol-Myers Squibb), an inhibitor of multiple tyrosine kinases, has been approved by the FDA for second-line treatment of chronic myelogenous leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) in adults.
Losartan for Hypertension
The Medical Letter on Drugs and Therapeutics • Jun 23, 1995 (Issue 951)
1995), no data are available to indicate that losartan, like ACE inhibitors, prolongs
survival ...
Losartan potassium (Cozaar - Merck), the first angiotensin II receptor antagonist, has been approved for oral treatment of hypertension by the US Food and Drug Administration. It will be marketed both alone and in a fixed-dose combination with the diuretic hydrochlorothiazide (Hyzaar).
A Mometasone-Eluting Sinus Implant (Sinuva) for Nasal Polyps
The Medical Letter on Drugs and Therapeutics • Sep 10, 2018 (Issue 1555)
to intranasal corticosteroid
therapy. Limited data suggest that the anti-IgE
antibody omalizumab (Xolair ...
The FDA has approved Sinuva (Intersect ENT), a sinus
implant that gradually releases the corticosteroid
mometasone furoate over a 90-day period, for
treatment of nasal polyps in adults who have had
ethmoid sinus surgery. Propel, a sinus implant that
releases mometasone furoate over 30 days, is FDA-approved
to maintain the sinus opening after ethmoid
sinus surgery; it is marketed by the same manufacturer
as Sinuva.
Drugs Past Their Expiration Date
The Medical Letter on Drugs and Therapeutics • Jul 27, 2020 (Issue 1603)
on the label. Since our last article on this
subject,1 more data have become available.
SAFETY ...
Healthcare providers are often asked if drugs can
be used past their expiration date. Because of legal
restrictions and liability concerns, manufacturers do
not sanction such use and usually do not comment
on the safety or effectiveness of their products beyond
the date on the label. Since our last article on this
subject, more data have become available.