Search Results for "moderate concentrate"
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Searched for moderate concentrate. Results 271 to 280 of 512 total matches.
Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Diarrhea (IBS-D) (online only)
The Medical Letter on Drugs and Therapeutics • Feb 03, 2025 (Issue 1721)
serum concentrations; INR changes in patients taking warfarin and rifaximin Bile Acid Sequestrants ...
View the Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Diarrhea (IBS-D)
Med Lett Drugs Ther. 2025 Feb 3;67(1721):e1-3 doi:10.58347/tml.2025.1721f | Show Introduction Hide Introduction
Once-Daily Mesalamine (Lialda) for Ulcerative Colitis
The Medical Letter on Drugs and Therapeutics • Mar 26, 2007 (Issue 1257)
with mild to moderate
ulcerative colitis.
MECHANISM OF ACTION — Mesalamine (5-ASA)
acts locally against ...
A once-daily oral formulation of mesalamine (Lialda - Shire) was recently approved by the FDA for induction of remission in patients with mild to moderate ulcerative colitis.
Dexmedetomidine Sublingual Film (Igalmi) for Acute Agitation
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022 (Issue 1666)
, plasma concentrations of
dexmedetomidine were generally quantifiable 5-20
minutes aftertaking Igalmi ...
The FDA has approved a sublingual film formulation
of the alpha-2 adrenergic receptor agonist
dexmedetomidine (Igalmi — BioXcel Therapeutics)
for acute treatment of agitation associated with
schizophrenia or bipolar I or II disorder in adults. It is
the first alpha-2 agonist and the only sublingual film
to be approved for this indication. Dexmedetomidine
has been available for many years in an injectable
formulation (Precedex) for sedation in the intensive
care unit and to facilitate procedures such as
mechanical ventilation.
Drugs for Atopic Dermatitis
The Medical Letter on Drugs and Therapeutics • Jun 15, 2020 (Issue 1600)
effective in two 28-day clinical trials in patients with mild to
moderate atopic dermatitis ...
Atopic dermatitis (AD; also known as eczema) is
frequently associated with other atopic disorders
such as allergic rhinitis, asthma, and food allergy. It
commonly presents in infancy and early childhood
and has a relapsing course, often improving by
adolescence, but sometimes persisting into (or first
appearing in) adulthood or even old age.
Comparison Table: Some Oral Antiseizure Medications (online only)
The Medical Letter on Drugs and Therapeutics • Aug 05, 2024 (Issue 1708)
concentrations fall
after the first few weeks of
treatment
Risk of developmental
toxicity unclear; studies ...
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
Azithromycin Extended-Release (Zmax) for Sinusitis and Pneumonia
The Medical Letter on Drugs and Therapeutics • Sep 28, 2005 (Issue 1218)
, has been approved by the FDA for single-dose treatment of mild to moderate community-acquired pneumonia (CAP ...
Zmax (Pfizer), an extended-release oral suspension of azithromycin, has been approved by the FDA for single dose treatment of mild to moderate community acquired pneumonia (CAP) and acute bacterial sinusitis (ABS) in adults. Immediate-release azithromycin will probably become available generically later this year when its patent expires.
Lumateperone (Caplyta) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Jul 27, 2020 (Issue 1603)
of
moderate or strong CYP3A4 inhibitors can increase
lumateperone serum concentrations and should
be avoided ...
The FDA has approved lumateperone (Caplyta —
Intracellular Therapies), an oral second-generation
antipsychotic, for once-daily treatment of schizophrenia
in adults. It is the 13th second-generation antipsychotic
drug to be approved by the FDA for this indication.
Venlafaxine - A New Antidepressant
The Medical Letter on Drugs and Therapeutics • Jun 10, 1994 (Issue 924)
metabolite reach steady-state concentrations in plasma within three days.
CLINICAL TRIALS — A double-blind ...
Venlafaxine hydrochloride (Effexor - Wyeth-Ayerst) was recently approved by the US Food and Drug Administration for treatment of depression. An aminomethyl-benzyl- cyclohexanol, it is chemically related to bupropion (Wellbutrin).
Tasimelteon (Hetlioz) for Non-24-Hour Sleep-Wake Disorder
The Medical Letter on Drugs and Therapeutics • Apr 28, 2014 (Issue 1441)
dreams (10%). Serum concentrations
of tasimelteon are 2-fold higher in patients >65 years
old, which ...
The FDA has approved the melatonin receptor agonist
tasimelteon (Hetlioz – Vanda) for treatment of non-24-hour sleep-wake disorder (non-24), which is common
in totally blind persons. Tasimelteon is the first drug
approved for this indication and the second melatonin
receptor agonist approved for use in the US; ramelteon
(Rozerem) was approved earlier for treatment of
insomnia. Melatonin itself has not been approved by
the FDA for any indication; it is available in the US as a
dietary supplement and is promoted as a sleep aid.
Valdecoxib (Bextra) - a New Cyclooxygenase-2 Inhibitor
The Medical Letter on Drugs and Therapeutics • Apr 29, 2002 (Issue 1129)
)
that decreases proinflammatory prostaglandin synthesis by inhibiting COX-2. At therapeutic
plasma concentrations ...
Valdecoxib (Bextra - Pharmacia/Pfizer), a selective cyclooxygenase (COX-2) inhibitor similar to celecoxib (Celebrex) and rofecoxib (Vioxx), was recently approved by the FDA for treatment of osteoarthritis, rheumatoid arthritis and primary dysmenorrhea.