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Searched for Drug. Results 121 to 130 of 618 total matches.
Two Vonoprazan Combinations (Voquezna) for H. pylori
The Medical Letter on Drugs and Therapeutics • Oct 31, 2022 (Issue 1662)
TREATMENT — In clinical trials,
combinations of antibacterial drugs have been
successful in eradicating H ...
The FDA has approved vonoprazan, a potassium-competitive
acid blocker, copackaged with amoxicillin
(Voquezna Dual Pak – Phathom) and with amoxicillin
and clarithromycin (Voquezna Triple Pak) for
treatment of Helicobacter pylori infection in adults.
Vonoprazan is the first potassium-competitive acid
blocker to be approved in the US. It has been available
in Japan for treatment of various acid-related
disorders since 2014. Vonoprazan is not available
alone in the US.
Dexmedetomidine Sublingual Film (Igalmi) for Acute Agitation
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022 (Issue 1666)
hours after taking the drug.
Hypotension, including orthostatic hypotension, and
bradycardia ...
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.
Tirzepatide (Zepbound) for Chronic Weight Management
The Medical Letter on Drugs and Therapeutics • Dec 25, 2023 (Issue 1692)
Elimination Primarily in urine and feces
Half-life ~5 days
Tirzepatide vs Other Weight-Loss Drugs ...
The injectable glucose-dependent insulinotropic
polypeptide (GIP)/glucagon-like peptide-1 (GLP-1)
receptor agonist tirzepatide, which was approved by
the FDA as Mounjaro for treatment of type 2 diabetes
in 2022, has now been approved as Zepbound (Lilly)
for chronic weight management in adults who have
a BMI ≥30 kg/m2 or a BMI ≥27 kg/m2 and at least
one weight-related comorbidity. The injectable
GLP-1 receptor agonists liraglutide (Saxenda) and
semaglutide (Wegovy) are approved for chronic
weight management in patients ≥12 years...
Med Lett Drugs Ther. 2023 Dec 25;65(1692):205-7 doi:10.58347/tml.2023.1692c | Show Introduction Hide Introduction
Intravenous Acetaminophen/Ibuprofen (Combogesic IV)
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
) in adults
when IV analgesia is considered clinically necessary.
Single-drug IV solutions containing ...
The FDA has approved Combogesic IV (Hikma), an IV
solution containing acetaminophen and ibuprofen, to
treat mild to moderate pain (alone) or moderate to
severe pain (in combination with an opioid) in adults
when IV analgesia is considered clinically necessary.
Single-drug IV solutions containing ibuprofen
(Caldolor) and acetaminophen have been available in
the US for years.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):68-9 doi:10.58347/tml.2024.1701c | Show Introduction Hide Introduction
Sebetralstat (Ekterly) for Treatment of Hereditary Angioedema Attacks
The Medical Letter on Drugs and Therapeutics • Feb 16, 2026 (Issue 1748)
. It is the first oral
drug to be approved in the US for this indication. The
intravenous C1 esterase inhibitors ...
Sebetralstat (Ekterly – Kalvista), an oral plasma
kallikrein inhibitor, has been approved by the FDA
for treatment of acute hereditary angioedema (HAE)
attacks in patients ≥12 years old. It is the first oral
drug to be approved in the US for this indication. The
intravenous C1 esterase inhibitors (C1INHs) Berinert
and Ruconest, the subcutaneous plasma kallikrein
inhibitor ecallantide (Kalbitor), and the subcutaneous
bradykinin B2 receptor antagonist icatibant (Firazyr)
have been available for years for on-demand
treatment of HAE attacks; all of these drugs except
ecallantide can...
Med Lett Drugs Ther. 2026 Feb 16;68(1748):29-30 doi:10.58347/tml.2026.1748c | Show Introduction Hide Introduction
Donidalorsen (Dawnzera) for Prevention of Hereditary Angioedema Attacks
The Medical Letter on Drugs and Therapeutics • Jan 19, 2026 (Issue 1746)
) attacks in patients
≥12 years old. It is the first RNA-targeted drug to be
approved ...
Donidalorsen (Dawnzera – Ionis), a subcutaneously
injected prekallikrein-directed antisense oligonucleotide,
has been approved by the FDA for prevention
of hereditary angioedema (HAE) attacks in patients
≥12 years old. It is the first RNA-targeted drug to be
approved in the US for this indication.
Med Lett Drugs Ther. 2026 Jan 19;68(1746):12-4 doi:10.58347/tml.2026.1746c | Show Introduction Hide Introduction
Comparison Table: Some Parenteral Anticoagulants for VTE (online only)
The Medical Letter on Drugs and Therapeutics • Jul 25, 2022 (Issue 1655)
Drug
FDA-Approved
Indications
Usual Adult
Treatment Dosage
Usual Adult
Prophylaxis Dosage1
Some ...
View the Comparison Table: Some Parenteral Anticoagulants for VTE
Lecanemab (Leqembi) Granted Full Approval for Early Alzheimer's Disease
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023 (Issue 1683)
contains a boxed warning about
the risk of ARIA associated with use of the drug. Most
cases of ARIA-E ...
Lecanemab-irmb (Leqembi – Eisai/Biogen), the IV
amyloid-directed monoclonal antibody that received
accelerated approval from the FDA in January 2023
for treatment of early Alzheimer's disease, has now
received full approval from the FDA based on a trial
showing that it slowed cognitive and functional decline
in patients with mild cognitive impairment (MCI) or
mild Alzheimer's disease dementia and confirmed
presence of brain amyloid. The IV amyloid-directed
monoclonal antibody aducanumab (Aduhelm) has
received only an accelerated FDA-approval for the
same indication.
Med Lett Drugs Ther. 2023 Aug 21;65(1683):129-30 doi:10.58347/tml.2023.1683a | Show Introduction Hide Introduction
A Fixed-Dose Combination of Finasteride and Tadalafil (Entadfi) for BPH (online only)
The Medical Letter on Drugs and Therapeutics • Sep 05, 2022 (Issue 1658)
) in men with an enlarged
prostate; use of the drug is limited to 26 weeks.
Entadfi is the first 5α ...
The FDA has approved Entadfi (Veru), a fixed-dose
combination of the 5α-reductase inhibitor
finasteride and the phosphodiesterase type 5 (PDE5)
inhibitor tadalafil, for initial treatment of benign
prostatic hyperplasia (BPH) in men with an enlarged
prostate; use of the drug is limited to 26 weeks.
Entadfi is the first 5α-reductase inhibitor/PDE5
inhibitor combination to become available in the
US. Finasteride (Proscar, and generics) and tadalafil
(Cialis, and generics) are also available separately.
Stiripentol (Diacomit) for Dravet Syndrome (online only)
The Medical Letter on Drugs and Therapeutics • Mar 24, 2021 (Issue 1620)
).
Stiripentol, which has been available in Europe, Canada,
and Japan for many years, is the second drug ...
The FDA has approved stiripentol (Diacomit – Biocodex)
for treatment of seizures in patients ≥2 years old with
Dravet syndrome who are also taking clobazam (Onfi).
Stiripentol, which has been available in Europe, Canada,
and Japan for many years, is the second drug to be
approved in the US for this indication; cannabidiol oral
solution (Epidiolex), a purified marijuana product, was
the first.
