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Searched for prepared. Results 61 to 70 of 236 total matches.
Focalin XR for ADHD
The Medical Letter on Drugs and Therapeutics • Mar 23, 2009 (Issue 1308)
or stigmatizing. Long-acting MPH preparations with once-daily dosing have therefore become
the mainstay ...
Short-acting methylphenidate (MPH) is effective for treatment of attention-deficit/hyperactivity disorder (ADHD), but its 3-5 hour duration of action usually requires mid-day dosing in school, which children may find disruptive or stigmatizing.
Problems With Dietary Supplements
The Medical Letter on Drugs and Therapeutics • Sep 30, 2002 (Issue 1140)
dietary supplements that meet the same Good Manufacturing Practices (GMPs) used to prepare prescription ...
Millions of people now take herbal products and other "dietary supplements." The Physicians' Desk Reference has published a PDR for Herbal Medicines listing their ingredients and indications, and the Drug Topics Red Book lists their prices.
Generic Levothyroxine
The Medical Letter on Drugs and Therapeutics • Sep 20, 2004 (Issue 1192)
IN THIS ISSUE
Levothyroxine Addendum
In preparing the Canadian edition of the
September 27 issue, we noticed ...
The FDA has determined that 3 generic formulations of levothyroxine are therapeutically equivalent to brand-name formulations. Some brand-name manufacturers have objected, and endocrine organizations have expressed their concern.
See levothyroxine addendum
See levothyroxine addendum
In Brief: Two New Seasonal Influenza Vaccines
The Medical Letter on Drugs and Therapeutics • Feb 04, 2013 (Issue 1409)
to the manufacturer.
2. Sold in boxes of 10.
Table 1. New Influenza Vaccines
Flucelvax is prepared in a similar ...
Two new trivalent influenza vaccines, Flucelvax (Novartis) and Flublok (Protein Sciences), will soon be available for prevention of seasonal influenza in adults ≥18 years old (Flucelvax) and 18-49 years old (Flublok). Unlike other available influenza vaccines, neither vaccine is produced in eggs, removing any concern regarding use in egg-allergic patients. Avoiding the use of eggs should allow for faster production of these 2 new vaccines, which could be especially beneficial during a pandemic.Flucelvax is prepared in a similar manner to other influenza vaccines, but the influenza virus is...
Foods Interacting With MAO Inhibitors
The Medical Letter on Drugs and Therapeutics • Feb 10, 1989 (Issue 785)
, prepared from fermented bean curd, all contain tyramine in large
amounts; miso soup has caused reactions ...
Many fermented foods contain tyramine as a byproduct formed by the bacterial breakdown of the amino acid tyrosine; it can also be formed by para-hydroxylation of phenylethylamine or dehydroxylation of DOPA and dopamine. Tyramine and some other amines found in food can cause hypertensive reactions in patients taking monoamine oxidase (MAO)inhibitors.
VEGF Inhibitors for AMD and Diabetic Macular Edema
The Medical Letter on Drugs and Therapeutics • Mar 16, 2015 (Issue 1464)
Clin Pharmacol 2014;
70:1505.
11. BA Frost and MA Kainer. Safe preparation and administration ...
Vascular endothelial growth factor (VEGF) is a principal
mediator of neovascularization in wet age-related
macular degeneration (AMD) and diabetic macular
edema. It induces angiogenesis and increases vascular
permeability and inflammation. VEGF inhibitors reduce
leakage from blood vessels, prevent proliferation of
new abnormal vessels, decrease swelling of the retina,
and improve visual acuity in patients with neovascular
(wet) AMD and diabetic macular edema. These drugs
are given as periodic intravitreal injections with topical
anesthesia.
An EUA for Casirivimab and Imdevimab for COVID-19
The Medical Letter on Drugs and Therapeutics • Dec 28, 2020 (Issue 1614)
minutes before dose preparation.
The two antibodies are only authorized for
administration together ...
The FDA has issued an Emergency Use Authorization
(EUA) for Regeneron's investigational monoclonal
antibodies casirivimab and imdevimab (REGEN-COV)
to be administered together by IV infusion or SC
injection for treatment of mild to moderate COVID-19
in adults and pediatric patients (≥12 years old and
weigh ≥40 kg) who are at high risk of progressing to
severe COVID-19 and/or hospitalization.
Relyvrio for ALS
The Medical Letter on Drugs and Therapeutics • Nov 28, 2022 (Issue 1664)
within 1 hour of preparation. The
suspension can be taken orally or via feeding tube.
The recommended ...
The FDA has approved Relyvrio (Amylyx), a fixed-dose
combination of sodium phenylbutyrate and
taurursodiol, for treatment of amyotrophic lateral
sclerosis (ALS). Sodium phenylbutyrate (Buphenyl,
and others) has been available by prescription
for years for treatment of urea cycle disorders.
Taurursodiol (tauroursodeoxycholic acid), a derivative
of ursodiol, is an over-the-counter bile acid
supplement claimed to have neuroprotective
benefits. Relyvrio is the third drug to be approved
in the US for treatment of ALS; riluzole (Rilutek, and
others) and edaravone (Radicava, Radicava...
Table: Correct Use of Inhalers for COPD (online only)
The Medical Letter on Drugs and Therapeutics • Sep 07, 2020 (Issue 1606)
Prepare the dose by sliding the lever next to the mouthpiece away
from you until it clicks
Exhale fully ...
View the Table: Correct Use of Inhalers for COPD
Fat Substitutes
The Medical Letter on Drugs and Therapeutics • Jun 15, 1990 (Issue 820)
is apparently not altered by the process used to prepare
Simplesse (PS Tang et al and R Dudley et al, FASEB ...
Two new substitutes for fat will soon be available in supermarkets in the USA, not directly, but incorporated into low-fat foods. Simplesse (NutraSweet) has already been approved for use by the US Food and Drug Administration (FDA) and is commercially available in some areas, but only in an ice-cream-like product called Simple Pleasures. Trailblazer (Kraft General Foods) is expected to be approved soon.