Search Results for "rapid"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for rapid. Results 81 to 90 of 541 total matches.
Conivaptan (Vaprisol) for Hyponatremia
The Medical Letter on Drugs and Therapeutics • Jun 19, 2006 (Issue 1237)
used in euvolemic patients, but it can be nephrotoxic. Overly rapid correction of serum sodium ...
Conivaptan hydrochloride (Vaprisol - Astellas), a vasopressin antagonist, has been approved by the FDA for short-term intravenous (IV) treatment of euvolemic hyponatremia in hospitalized patients. Euvolemic hyponatremia is most often caused by the syndrome of inappropriate ADH secretion (SIADH), or by hypothyroidism or adrenal insufficiency. The drug has not been approved for treatment of hypervolemic hyponatremia, which is associated with congestive heart failure (CHF), cirrhosis and renal disease. It should not be used in hypovolemic hyponatremia, such as occurs when fluid losses are...
Seebri Neohaler and Utibron Neohaler for COPD
The Medical Letter on Drugs and Therapeutics • Mar 28, 2016 (Issue 1491)
is dependent
upon ability to perform a rapid, deep inhalation
▶ Once-daily dosing
▶ No assembly or priming ...
The FDA has approved two new inhalers for long-term
maintenance treatment of chronic obstructive
pulmonary disease (COPD). Seebri Neohaler
(Novartis) contains the long-acting anticholinergic
glycopyrrolate. Utibron Neohaler (Novartis) contains
both glycopyrrolate and the long-acting beta2-adrenergic agonist (LABA) indacaterol. Glycopyrrolate/indacaterol is the third fixed-dose combination of a
long-acting anticholinergic and a LABA to become
available in the US; umeclidinium/vilanterol (Anoro
Ellipta) and tiotropium/olodaterol (Stiolto Respimat)
were approved...
FDA Warns Against Use of Codeine and Tramadol in Children and Breastfeeding Women
The Medical Letter on Drugs and Therapeutics • May 22, 2017 (Issue 1521)
determined and varies among patients. Patients can
be categorized as ultra-rapid, extensive (normal ...
The FDA has issued new warnings about the use of the
opioid analgesics codeine and tramadol in children,
particularly those <12 years old, and in breastfeeding
women due to concerns about the risk of respiratory
depression and death. The FDA previously issued
warnings about these drugs in 2013 and 2015.
Management of Opioid Withdrawal Symptoms
The Medical Letter on Drugs and Therapeutics • Aug 27, 2018 (Issue 1554)
, may
require a slower taper.
4. Some CYP rapid metabolizers may require more frequent dosing.
5. Cost of oral ...
Pharmacologic management of opioid withdrawal
symptoms can reduce the intensity of drug craving
and improve treatment retention in patients with opioid
use disorder who will receive maintenance treatment.
Withdrawal management without subsequent maintenance
treatment is associated with high rates of
relapse, overdose death, and HIV and/or hepatitis C
virus infection. Several guidelines on management
of opioid withdrawal are available. Maintenance
treatment of opioid use disorder was reviewed in a
previous issue.
Treatment of Heat Injury
The Medical Letter on Drugs and Therapeutics • Jul 13, 1990 (Issue 822)
by fairly rapid intravenous administration of one liter of a glucose-in-hypotonic saline solution
over 30 ...
Summer heat waves cause thousands of cases of heat-related illness in the USA each year and hundreds of heat-related deaths, especially among the elderly. A few principles may be helpful in preventing and treating heat injury.
Loratadine - A New Antihistamine
The Medical Letter on Drugs and Therapeutics • Aug 06, 1993 (Issue 902)
Pharmacol, 127:153, 1986).
The drug is well absorbed after oral administration, extensively and rapidly ...
Loratadine (Claritin - Schering), a new H 1 -receptor antagonist, has been approved by the U.S. Food and Drug Administration for treatment of seasonal allergic rhinitis in patients more than 12 years old. It will compete with older, relatively sedating drugs such as chlorpheniramine (Chlor-Trimeton, and others) and clemastine (Tavist - Medical Letter, 35:9, 1993) and with newer relatively non-sedating agents such as terfenadine (Seldane) and astemizole (Hismanal).
Extended-Release Isosorbide Mononitrate for Angina
The Medical Letter on Drugs and Therapeutics • Feb 04, 1994 (Issue 915)
Wholesale Price listings in Red Book MicREData, January 1994.
TOLERANCE — All nitrates cause rapid ...
Isosorbide mononitrate, the major active metabolite of isosorbide dinitrate, was first approved in the USA for oral use in patients with chronic stable angina in 1992 (Medical Letter, 34:61, 1992). Now an extended-release formulation of isosorbide mononitrate (Imdur -Key) has been approved by the US Food and Drug Administration.
Melatonin
The Medical Letter on Drugs and Therapeutics • Nov 24, 1995 (Issue 962)
are highest during the normal hours of
sleep, increasing rapidly in the late evening, peaking after midnight ...
Several readers have asked the Medical Letter to evaluate the effectiveness and safety of exogenous melatonin for treatment of insomnia and jet lag. Melatonin has not been approved by the US Food and Drug Administration (FDA), but is available in health food stores and apparently is being used as self-medication to treat a wide variety of disorders.
Intravenous, Amiodarone
The Medical Letter on Drugs and Therapeutics • Dec 08, 1995 (Issue 963)
is rapidly distributed.
No minimal effective or maximal tolerated plasma concentrations ...
An intravenous formulation of amiodarone (Cordarone IV -Wyeth-Ayerst) has been approved by the US Food and Drug Administration (FDA) for treatment and prophylaxis of recurrent ventricular fibrillation (VF) or hemodynamically unstable ventricular tachycardia (VT) in patients refractory to other therapy.
Zileuton for Asthma
The Medical Letter on Drugs and Therapeutics • Feb 28, 1997 (Issue 995)
— Zileuton taken with or without food is rapidly absorbed from the
gastrointestinal tract, reaching peak ...
Zileuton (zye loo' ton; Zyflo - Abbott), an inhibitor of leukotriene synthesis, has been approved by the US Food and Drug Administration (FDA) for prophylaxis and maintenance treatment of chronic asthma in adults and children more than 12 years old. A related drug—zafirlukast (Accolate), a leukotriene receptor antagonist—was recently reviewed in the Medical Letter (vol. 38, page 111, December 20, 1996). Neither of these drugs is recommended for treatment of acute asthma.