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Searched for days. Results 31 to 40 of 479 total matches.
Crexont — Extended-Release Carbidopa/Levodopa for Parkinson's Disease
The Medical Letter on Drugs and Therapeutics • Dec 23, 2024 (Issue 1718)
Adult Maintenance Dosage1 Cost2
Generic 25/100, 50/200 tabs3 400-1600 mg levodopa/day, divided $30.30 ...
The FDA has approved Crexont (Amneal), an
extended-release capsule formulation of carbidopa/levodopa, for treatment of Parkinson's disease (PD),
postencephalitic parkinsonism, and parkinsonism
associated with carbon monoxide or manganese
intoxication. Crexont contains a combination of
immediate-release carbidopa/levodopa granules and
extended-release levodopa pellets. An extended-release
carbidopa/levodopa oral capsule (Rytary) has
been available from the same manufacturer for years;
the patent for Rytary expires in 2025.
Med Lett Drugs Ther. 2024 Dec 23;66(1718):206-8 doi:10.58347/tml.2024.1718e | Show Introduction Hide Introduction
Twirla - A New Contraceptive Patch
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021 (Issue 1617)
-label trial
(SECURE) that included 1736 women 18-35 years old
who completed 15,165 evaluable 28-day ...
The FDA has approved Twirla (Agile Therapeutics),
a transdermal contraceptive patch containing the
estrogen ethinyl estradiol and the progestin
levonorgestrel, for use in women with a BMI <30 kg/m2.
It is the second contraceptive patch to become
available in the US; Xulane, a patch that delivers
ethinyl estradiol and the progestin norelgestromin,
has been available since 2014.
COVID-19 Updates
The Medical Letter on Drugs and Therapeutics • Feb 21, 2022 (Issue 1644)
days previously and
had one or more risk factors for progression to
severe COVID-19 (e.g., age ≥60 ...
The IV antiviral drug remdesivir (Veklury – Gilead)
has been available for treatment of COVID-19 in
hospitalized patients since 2020. Now, the FDA has
approved remdesivir for treatment of mild to moderate
COVID-19 in outpatients ≥12 years old who weigh
≥40 kg and are at high risk for progression to severe
disease, including hospitalization or death; they
also issued an Emergency Use Authorization (EUA)
allowing its use in any other high-risk outpatient who
weighs ≥3.5 kg.
Teplizumab (Tzield) to Delay Onset of Type 1 Diabetes
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023 (Issue 1667)
peptides
Half-life (elimination) 4.5 days
Teplizumab-mzwv (Tzield – Provention Bio), an anti-
CD3 ...
Teplizumab-mzwv (Tzield – Provention Bio), an anti-CD3 monoclonal antibody, has been approved by the
FDA to delay the onset of stage 3 type 1 diabetes
in patients ≥8 years old who have stage 2 type 1
diabetes. It is the first drug to become available in the
US that delays the onset of type 1 diabetes.
Med Lett Drugs Ther. 2023 Jan 9;65(1667):7-8 doi:10.58347/tml.2023.1667c | Show Introduction Hide Introduction
Lumateperone (Caplyta) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Jul 27, 2020 (Issue 1603)
mg/mL soln 10-15 mg once/day 10-30 mg once/day $2.10
Abilify (Otsuka) 2, 5, 10, 15, 20, 30 mg tabs ...
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.
Ganaxolone (Ztalmy) for CDKL5 Deficiency Disorder (online only)
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
/day titrated to
63 mg/kg/day; >28 kg: 450 mg/day titrated to 1800 mg/day.
Cost: 30 days ...
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
Drugs for Hypertension
The Medical Letter on Drugs and Therapeutics • May 27, 2024 (Issue 1703)
such as the Dietary Approaches
to Stop Hypertension (DASH) diet,2 limiting intake
of sodium (ideally ...
American College of Cardiology/American Heart
Association (ACC/AHA) guidelines for treatment of
hypertension were last published in 2018. Treatment
of hypertensive urgencies and emergencies is not
discussed here.
Med Lett Drugs Ther. 2024 May 27;66(1703):81-8 doi:10.58347/tml.2024.1703a | Show Introduction Hide Introduction
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)
)
5.8 g/teaspoon powder; 5.8 g
packets; 1.8 g caps; 2 g wafers
$29.00
10-35 g/day in 2-3 divided ...
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
Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder (online only)
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023 (Issue 1684)
buprenorphine levels with 32 mg
once weekly or 128 mg once
monthly ~60% higher than those
with 24 mg/day ...
View Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e144-5 doi:10.58347/tml.2023.1684b | Show Introduction Hide Introduction
COVID-19 Update: Metformin to Prevent Long Covid?
The Medical Letter on Drugs and Therapeutics • May 29, 2023 (Issue 1677)
years old with
an elevated body mass index who had tested positive
for SARS-CoV-2 infection ≤3 days ...
Results from a double-blind trial suggest that off-label
use of the oral antihyperglycemic drug metformin
in patients with COVID-19 may decrease the risk
of post-acute sequelae of SARS-CoV-2 infection
("long COVID").
Med Lett Drugs Ther. 2023 May 29;65(1677):87-8 doi:10.58347/tml.2023.1677e | Show Introduction Hide Introduction