Search Results for "MAO Inhibitors"
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Searched for MAO Inhibitors. Results 121 to 130 of 144 total matches.
Opioids for Pain
The Medical Letter on Drugs and Therapeutics • Dec 12, 2022 (Issue 1665)
.20
Use of an opioid with or within 14 days of a monoamine
oxidase (MAO) inhibitor can cause ...
A new CDC guideline for prescribing opioids for pain
recently became available. Nonopioid drugs for pain
were reviewed in a previous issue.
In Brief: One Drop or Two
The Medical Letter on Drugs and Therapeutics • Jun 19, 2006 (Issue 1237)
not be used with a monoamine oxidase
inhibitor (MAOI) or within 14 days of stopping one.
Methylphenidate ...
Many prescriptions for eye drops call for instillation of 1-2 drops. But Medical Letter consultants in ophthalmology seem to agree that all eye drops should generally be given in doses of only one drop. The volume of a single drop can vary with the viscosity of the solution, the design of the dropper, and patient technique. The average volume of a drop is 35-50 microliters, but can be as high as 75 microliters. An eye brimming with fluid holds 30 microliters at best, so even one drop is often an overdose. A second either washes out the first or increases the possibility of systemic toxicity,...
Two Drugs for Weight Loss
The Medical Letter on Drugs and Therapeutics • Sep 03, 2012 (Issue 1398)
.
Phentermine is contraindicated for 14 days
after starting a monoamine oxidase (MAO) inhibitor
because ...
In 2013 the FDA approved one new drug and a new combination of 2 old drugs as adjuncts to lifestyle changes for chronic weight management. Lorcaserin (lor-ca-SER-in; Belviq – Arena/Esai) is a selective serotonin 2C receptor agonist. Qsymia (Vivus) is a fixed-dose combination of the weight-loss drug phentermine and an extended-release (ER) formulation of topiramate. The new products are approved for use in obese patients (body mass index [BMI] of ≥30 kg/m2) and for patients who are overweight (BMI ≥27 kg/m2) and have one weight-related risk factor such as hypertension, dyslipidemia or...
Glycopyrrolate/Formoterol (Bevespi Aerosphere) for COPD
The Medical Letter on Drugs and Therapeutics • Oct 10, 2016 (Issue 1505)
(MAO) inhibitors, tricyclic antidepressants,
or other drugs that prolong the QT interval8 could ...
The FDA has approved a fixed-dose combination of
the long-acting anticholinergic glycopyrrolate and
the long-acting beta2-adrenergic agonist (LABA)
formoterol (Bevespi Aerosphere – AstraZeneca) for
long-term maintenance treatment of patients with
chronic obstructive pulmonary disease (COPD).
Glycopyrrolate/formoterol is the fourth long-acting
anticholinergic/LABA combination to be approved in
the US, but the first to become available in a metered-dose
inhaler. Glycopyrrolate/indacaterol (Utibron
Neohaler), umeclidinium/vilanterol (Anoro Ellipta),
and tiotropium/olodaterol (Stiolto...
Expanded Table: Some Drugs for Smoking Cessation (online only)
The Medical Letter on Drugs and Therapeutics • Jul 15, 2019 (Issue 1576)
(MAO)
inhibitor or within 2 weeks of stopping
one is contraindicated
▶ Drugs that lower the seizure ...
View the Expanded Table: Some Drugs for Smoking Cessation
Drugs for Cough
The Medical Letter on Drugs and Therapeutics • Dec 17, 2018 (Issue 1562)
and they should not be used with or within
14 days of a monoamine oxidase (MAO) inhibitor.
OTC phenylephrine ...
Acute cough (<3 weeks in duration) generally does
not require pharmacologic treatment, especially in
children. Suppression of productive cough may be
harmful. Management of patients with cough should
include elimination of any precipitating factor (e.g.,
cigarette smoking) and treatment of any underlying
cause such as upper airway cough syndrome,
gastroesophageal reflux disease, asthma, or other
pulmonary disease.
Trelegy Ellipta - A Three-Drug Inhaler for COPD
The Medical Letter on Drugs and Therapeutics • May 21, 2018 (Issue 1547)
with potassiumwasting
diuretics (e.g., furosemide) can exacerbate
hypokalemia and cause ECG changes, and use with
MAO ...
The FDA has approved Trelegy Ellipta (GSK), a fixed-dose
combination of the inhaled corticosteroid (ICS)
fluticasone furoate, the long-acting antimuscarinic
agent (LAMA) umeclidinium, and the long-acting
beta2-agonist (LABA) vilanterol. It is available as a dry
powder inhaler for once-daily maintenance treatment
of COPD and to reduce COPD exacerbations in patients
with a history of exacerbations. Trelegy Ellipta is
the first three-drug inhaler for treatment of COPD to
become available in the US.
Fenfluramine (Fintepla) for Dravet Syndrome
The Medical Letter on Drugs and Therapeutics • Aug 09, 2021 (Issue 1630)
, or dextromethorphan. It is contraindicated for
use with or within 14 days of a monoamine oxidase
(MAO) inhibitor ...
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.
A Fixed-Dose Combination of Meloxicam and Rizatriptan (Symbravo) for Migraine
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025 (Issue 1727)
oxidase (MAO) inhibitor or within 2 weeks of stopping
one is contraindicated. The combination should ...
The FDA has approved Symbravo (Axsome), an oral
fixed-dose combination of the nonsteroidal anti-inflammatory
drug (NSAID) meloxicam and the
5-HT1B/1D receptor agonist (triptan) rizatriptan (Maxalt,
and generics), for acute treatment of migraine with or
without aura in adults. It is the second combination
of an NSAID and a triptan to be approved for migraine
treatment. An oral fixed-dose combination of
sumatriptan and naproxen (Treximet, and generics) is
approved for use in patients ≥12 years old.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):68-70 doi:10.58347/tml.2025.1727b | Show Introduction Hide Introduction
Lisdexamfetamine dimesylate (Vyvanse) for ADHD
The Medical Letter on Drugs and Therapeutics • Jul 16, 2007 (Issue 1265)
INTERACTIONS — Monoamine oxidase
(MAO) inhibitors and lisdexamfetamine dimesylate
used together or within 2 ...
Lisdexamfetamine dimesylate (Vyvanse - Shire), a prodrug in which d-amphetamine is covalently bonded to L-lysine, has been approved by the FDA for treatment of attention-deficit/hyperactivity disorder (ADHD) in children 6-12 years old. It was designed to have less potential than amphetamine itself for abuse, diversion or overdose toxicity. Like methylphenidate and amphetamines, lisdexamfetamine is a Schedule II controlled substance.