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Searched for Infection. Results 331 to 340 of 842 total matches.
Cantharidin Topical Solution (Ycanth) for Molluscum Contagiosum
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024 (Issue 1696)
― A skin infection
caused by a poxvirus, molluscum contagiosum is
most common in preschool ...
The FDA has approved cantharidin 0.7% solution
(Ycanth – Verrica) for topical treatment of molluscum
contagiosum in patients ≥2 years old. Ycanth
was the first drug to be approved in the US for this
indication. A 10.3% gel formulation of berdazimer
(Zelsuvmi), a nitric oxide-releasing agent, has
also been approved by the FDA for treatment of
molluscum contagiosum (in patients ≥1 year old); it
will be reviewed in a future issue.
Med Lett Drugs Ther. 2024 Feb 19;66(1696):27-9 doi:10.58347/tml.2024.1696b | Show Introduction Hide Introduction
In Brief: New Indications for Secukinumab (Cosentyx)
The Medical Letter on Drugs and Therapeutics • Jun 06, 2016 (Issue 1496)
infection. In general, infections occurred at
a higher rate in secukinumab-treated patients than in
those ...
The FDA has approved the subcutaneous IL-17A antagonist secukinumab (Cosentyx - Novartis), which was first approved in 2015 for treatment of plaque psoriasis, for treatment of psoriatic arthritis and ankylosing spondylitis in adults.1 Secukinumab is one of the most effective drugs available for treatment of plaque psoriasis.2FDA approval of secukinumab for treatment of psoriatic arthritis was based on two randomized, double-blind trials with a primary endpoint of at least a 20% improvement in the American College of Rheumatology response criteria (ACR20) at 24 weeks. In both trials, ACR20...
The Viralizer For The Common Cold
The Medical Letter on Drugs and Therapeutics • Jan 27, 1989 (Issue 784)
from cold symptoms. Another clinical study in 80 private patients with acute upper respiratory infections ...
Recently, full-page advertisements have appeared in the New York Times and other newspapers promoting the Viralizer (Viral Response Systems, Greenwich, CT), a heated nebulizer-sprayer device marketed for treatment of colds, sore throats, allergy and sinusitis symptoms. The device is available without a prescription for about $30 to $40.
Empagliflozin (Jardiance) for Type 2 Diabetes in Children (online only)
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023 (Issue 1683)
ADVERSE EFFECTS ― Adverse effects of SGLT2
inhibitors include genital mycotic infections, urinary
tract ...
The sodium-glucose cotransporter 2 (SGLT2)
inhibitor empagliflozin has been available for years
alone (Jardiance – Boehringer Ingelheim) and in
combination with metformin (Synjardy) to improve
glycemic control in adults with type 2 diabetes. Both
products have now been approved for use in children
≥10 years old. Empagliflozin is the second oral drug
to become available in the US for treatment of type
2 diabetes in children; metformin has been available
since 2000 for this indication. The injectable
glucagon-like peptide-1 (GLP-1) receptor agonists
liraglutide (Victoza) and...
Med Lett Drugs Ther. 2023 Aug 21;65(1683):e137 doi:10.58347/tml.2023.1683e | Show Introduction Hide Introduction
Caspofungin (Cancidas) For Aspergillosis
The Medical Letter on Drugs and Therapeutics • Jul 09, 2001 (Issue 1108)
in other fungal infections, particularly
deep Candida infections, and whether it would be more effective ...
Caspofungin acetate(Cancidas) is the first of a new class of antifungals, the echinocandins. It has been approved by the FDA for treatment of invasive aspergillosis in patients who fail to respond to or are unable to tolerate other antifungal drugs such as amphotericin B and itraconazole.
Empagliflozin (Jardiance) for Diabetes
The Medical Letter on Drugs and Therapeutics • Oct 13, 2014 (Issue 1453)
, has been associated
with genitourinary symptoms and genital mycotic
infections. According to the package insert ...
Empagliflozin (Jardiance – Boehringer Ingelheim/Lilly),
an SGLT2 inhibitor, has been approved by the FDA for
oral treatment of type 2 diabetes. It is the third SGLT2
inhibitor to be approved for this indication.
OTC Fluticasone Nasal Spray for Allergic Rhinitis
The Medical Letter on Drugs and Therapeutics • Mar 30, 2015 (Issue 1465)
infection (thrush),
mucosal atrophy, and septal perforation have been
reported rarely. Intranasal fungal ...
The nasal spray formulation of the corticosteroid
fluticasone propionate is now available over the
counter (OTC) as Flonase Allergy Relief (GSK) in
the same strength as the prescription product
(Flonase, and generics) for patients ≥4 years old with
seasonal or perennial allergic rhinitis. It is the second
corticosteroid nasal spray to become available OTC;
triamcinolone acetonide (Nasacort Allergy 24HR) was
the first. Unlike prescription Flonase, the OTC product
is FDA-approved for reduction of ocular as well as
nasal symptoms. Brand-name prescription Flonase
has been...
Eflapegrastim (Rolvedon) for Prevention of Chemotherapy-Induced Febrile Neutropenia
The Medical Letter on Drugs and Therapeutics • May 29, 2023 (Issue 1677)
the incidence of infection, as manifested by febrile
neutropenia, in adults with nonmyeloid malignancies ...
Eflapegrastim-xnst ((Rolvedon) [Spectrum]; previously
called Rolontis), a granulocyte colony-stimulating
factor (G-CSF) conjugated to an Fc fragment of human
IgG4, has been approved by the FDA to decrease
the incidence of infection, as manifested by febrile
neutropenia, in adults with nonmyeloid malignancies
receiving myelosuppressive chemotherapy that can
cause clinically significant febrile neutropenia.
Med Lett Drugs Ther. 2023 May 29;65(1677):83-4 doi:10.58347/tml.2023.1677b | Show Introduction Hide Introduction
Lifileucel (Amtagvi): A Cellular Therapy for Melanoma (online only)
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
cytopenias, severe infection, and cardiopulmonary and
renal impairment can occur.
▶ Dosage: A single IV ...
Lifileucel (Amtagvi – Iovance), a tumor-derived
autologous T-cell immunotherapy, has received
accelerated approval from the FDA for one-time
treatment of adults with unresectable or metastatic
melanoma previously treated with a programmed
death receptor-1 (PD-1) inhibitor, and if BRAF V600
mutation-positive, a BRAF inhibitor with or without
a mitogen-activated kinase (MEK) inhibitor. It is the
first cellular therapy to be approved for use in solid
tumors. Accelerated approval of lifileucel was based
on objective response rates.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):e77-8 doi:10.58347/tml.2024.1701h | Show Introduction Hide Introduction
Gatifloxacin and Moxifloxacin: Two New Fluoroquinolones
The Medical Letter on Drugs and Therapeutics • Feb 21, 2000 (Issue 1072)
sinusitis. Gatifloxacin has also received FDA approval for treatment of urinary tract infections ...
Gatifloxacin and moxifloxacin are now available for once-daily treatment of patients with community-acquired pneumonia, acute bacterial exacerbations of chronic bronchitis, or acute sinusitis.