Search Results for "Glaucoma"
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Searched for Glaucoma. Results 11 to 20 of 30 total matches.
Sofpironium (Sofdra) for Primary Axillary Hyperhidrosis
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
%).
Sofpironium gel is contraindicated for use in patients
with glaucoma, paralytic ileus, unstable ...
The FDA has approved a 12.45% gel formulation of the
anticholinergic drug sofpironium (Sofdra – Botanix) for
treatment of primary axillary hyperhidrosis (excessive
underarm sweating) in patients ≥9 years old.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):133-4 doi:10.58347/tml.2024.1709c | Show Introduction Hide Introduction
Expanded Table: Some Drugs for Inflammatory Bowel Disease (online only)
The Medical Letter on Drugs and Therapeutics • Jul 10, 2023 (Issue 1680)
, fluid retention, osteoporosis,
osteonecrosis, cataracts, glaucoma, impaired skin healing,
acne ...
View the Table: Some Drugs for Inflammatory Bowel Disease
Med Lett Drugs Ther. 2023 Jul 10;65(1680):e115-9 doi:10.58347/tml.2023.1680d | Show Introduction Hide Introduction
Qlosi — Pilocarpine 0.4% Ophthalmic Solution for Presbyopia
The Medical Letter on Drugs and Therapeutics • Jan 06, 2025 (Issue 1719)
of glaucoma, but
local (e.g., blurry vision and instillation-site pain)
and systemic (e.g., sweating and GI ...
The FDA has approved pilocarpine 0.4% preservativefree
ophthalmic solution (Qlosi – Orasis) for treatment
of presbyopia in adults. Pilocarpine 1.25% ophthalmic
solution (Vuity) was approved in 2021 for the same
indication. Pilocarpine 1%, 2%, and 4% ophthalmic
solutions (Isopto Carpine, and others) have been
available for years for treatment of glaucoma, but
local (e.g., blurry vision and instillation-site pain)
and systemic (e.g., sweating and GI disturbances)
adverse effects have limited their use.
Med Lett Drugs Ther. 2025 Jan 6;67(1719):5-6 doi:10.58347/tml.2025.1719b | Show Introduction Hide Introduction
Xanomeline/Trospium (Cobenfy) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024 (Issue 1715)
,
or untreated narrow-angle glaucoma. Cobenfy is not
recommended for use in patients with mild hepatic ...
The FDA has approved Cobenfy (BMS), an oral
fixed-dose combination of the muscarinic agonist
xanomeline and the peripheral muscarinic antagonist
trospium chloride, for treatment of schizophrenia in
adults. It is the first antipsychotic drug to be approved
in the US for treatment of schizophrenia that does not
block dopamine receptors. This is the first approval
for xanomeline; trospium has been available for many
years for treatment of overactive bladder.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):177-9 doi:10.58347/tml.2024.1715a | Show Introduction Hide Introduction
Loteprednol 0.25% (Eysuvis) for Dry Eye Disease
The Medical Letter on Drugs and Therapeutics • May 17, 2021 (Issue 1624)
may result in glaucoma, cataract
formation, and an increased risk of secondary ocular
infections.
Like ...
The FDA has approved loteprednol etabonate ophthalmic suspension 0.25% (Eysuvis – Kala) for
short-term treatment (≤2 weeks) of dry eye disease.
It is the first ocular corticosteroid to be approved for
this indication. Other formulations of loteprednol are
approved for treatment of steroid-responsive ocular
inflammatory conditions, inflammation after ocular
surgery, and seasonal allergic conjunctivitis.
Comparison Table: Some Drugs for Migraine Prevention in Adults (online only)
The Medical Letter on Drugs and Therapeutics • Jun 12, 2023 (Issue 1678)
,
nephrolithiasis
▶ Secondary narrow-angle glaucoma, oligohydrosis,
and symptomatic metabolic
acidosis are rare ...
View the Comparison Table: Some Drugs for Migraine Prevention in Adults
Med Lett Drugs Ther. 2023 Jun 12;65(1678):e100-2 doi:10.58347/tml.2023.1678c | Show Introduction Hide Introduction
Drugs and Devices for Weight Management
The Medical Letter on Drugs and Therapeutics • May 30, 2022 (Issue 1651)
Uncontrolled hypertension
Glaucoma
Hyperthyroidism
History of drug abuse/agitation
Within 14 days of a MAOI ...
Adults with a body mass index (BMI) between 25
and 29.9 kg/m2 are considered overweight. Those
with a BMI ≥30 are considered obese. The initial
recommendation for any weight loss effort is to
achieve a 5-10% reduction in weight, which has been
associated with a reduction in the risk of developing
type 2 diabetes, hypertension, and dyslipidemia. Diet,
exercise, and behavior modification are the preferred
methods for losing weight, but long-term weight
maintenance can be difficult. Several drugs and
devices are FDA-approved for weight reduction and
maintenance of weight...
Dextromethorphan/Bupropion (Auvelity) for Depression
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022 (Issue 1666)
. Bupropion
monotherapy (at higher doses than in Auvelity)
has caused hypertension, angle-closure glaucoma ...
The FDA has approved an extended-release fixed-dose
combination of dextromethorphan and
bupropion (Auvelity – Axsome) for treatment of major
depressive disorder (MDD) in adults.
Airsupra: An Inhaled Albuterol/Budesonide Combination for Asthma
The Medical Letter on Drugs and Therapeutics • Mar 18, 2024 (Issue 1698)
. Cataracts, glaucoma, and decreased
bone mineral density have been observed with longterm
use.
DRUG ...
The FDA has approved Airsupra (AstraZeneca), a
metered-dose inhaler containing the short-acting
beta2-agonist (SABA) albuterol and the inhaled
corticosteroid (ICS) budesonide, for use as needed for
treatment or prevention of bronchoconstriction and to
reduce the risk of exacerbations in patients ≥18 years
old with asthma. Airsupra is the first combination of
a SABA and an ICS to become available in the US. It is
not approved for use as maintenance therapy.
Med Lett Drugs Ther. 2024 Mar 18;66(1698):41-3 doi:10.58347/tml.2024.1698a | Show Introduction Hide Introduction
Fenfluramine (Fintepla) for Dravet Syndrome
The Medical Letter on Drugs and Therapeutics • Aug 09, 2021 (Issue 1630)
, a risk factor
for angle-closure glaucoma. No cases have been
reported to date with use of fenfluramine ...
The FDA has approved fenfluramine oral solution
(Fintepla – Zogenix) for treatment of seizures in
patients ≥2 years old with Dravet syndrome. It is the
third drug to be approved for this indication. Stiripentol
(Diacomit) and cannabidiol (Epidiolex), a purified
product derived from marijuana, were approved earlier.