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Searched for data. Results 881 to 890 of 1113 total matches.

Mometasone (Asmanex Twisthaler) for Asthma

   
The Medical Letter on Drugs and Therapeutics • Dec 05, 2005  (Issue 1223)
with the lowest usual adult dosage, based on most recent data (October 31, 2005) from retail pharmacies nationwide ...
The FDA has approved marketing of the corticosteroid mometasone furoate in an orally inhaled dry powder formulation (Asmanex Twisthaler - Schering-Plough) for maintenance treatment of asthma in patients at least 12 years old. Mometasone is also available as a mid-potency topical corticosteroid cream (Elocon) and as an intranasal spray (Nasonex) for treatment of allergic rhinitis.
Med Lett Drugs Ther. 2005 Dec 5;47(1223):98-9 |  Show IntroductionHide Introduction

A Combination of Oxycodone and Ibuprofen (Combunox) for Pain

   
The Medical Letter on Drugs and Therapeutics • Jan 02, 2006  (Issue 1225)
2005; 27:418. 6. Based on most recent data (October 31, 2005) from retail pharmacies nationwide ...
A fixed-dose combination of oxycodone 5 mg and ibuprofen 400 mg (Combunox - Forest Laboratories) is now available and is being heavily advertised for short-term treatment of moderate to severe acute pain.
Med Lett Drugs Ther. 2006 Jan 2;48(1225):3-4 |  Show IntroductionHide Introduction

A New Indication for Gamma Hydroxybutyrate (Xyrem) in Narcolepsy

   
The Medical Letter on Drugs and Therapeutics • Jan 30, 2006  (Issue 1227)
for the treatment of narcolepsy. Sleep 2003; 26:31. 9. Price according to the most recent data (December 31, 2005 ...
Gamma hydroxybutyrate (GHB), a central-nervous-system depressant notorious for its use in "date rape", was approved by the FDA in 2002 as sodium oxybate (Xyrem - Jazz Pharmaceuticals) for oral treatment of cataplexy in patients with narcolepsy. Now it has also been approved for treatment of excessive daytime sleepiness (EDS) in these patients. Xyrem is a Schedule III controlled substance.
Med Lett Drugs Ther. 2006 Jan 30;48(1227):11-2 |  Show IntroductionHide Introduction

Lubiprostone (Amitiza) for Chronic Constipation

   
The Medical Letter on Drugs and Therapeutics • Jun 05, 2006  (Issue 1236)
, (Novartis) abdominal pain 1. Cost for 30 days’ treatment at lowest usual dosage, based on most recent data ...
The FDA has approved lubiprostone (Amitiza - Sucampo/Takeda), a chloride channel activator, for treatment of chronic idiopathic constipation in adults. The only other prescription drug approved by the FDA for this indication (in 2004 for adults <= 65 years old) is tegaserod (Zelnorm), a partial agonist of serotonin that is also approved for constipation-predominant irritable bowel syndrome in women. Of course, numerous over-the-counter products are available for treatment of constipation.
Med Lett Drugs Ther. 2006 Jun 5;48(1236):47-8 |  Show IntroductionHide Introduction

Conivaptan (Vaprisol) for Hyponatremia

   
The Medical Letter on Drugs and Therapeutics • Jun 19, 2006  (Issue 1237)
treatment of euvolemic hyponatremia. Data supporting its use are limited, and overly rapid correction ...
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...
Med Lett Drugs Ther. 2006 Jun 19;48(1237):51-2 |  Show IntroductionHide Introduction

A Human Papillomavirus Vaccine

   
The Medical Letter on Drugs and Therapeutics • Aug 14, 2006  (Issue 1241)
among the women who received placebo, and one among those who were vaccinated. No clinical data ...
A recombinant quadrivalent human-papillomavirus-like particle vaccine, Gardasil (Merck), has been approved by the FDA for use in girls and women 9-26 years old to prevent diseases associated with infection with human papillomavirus (HPV) types 6, 11, 16, and 18, including genital warts, precancerous cervical, vaginal or vulvar lesions, and cervical cancer.
Med Lett Drugs Ther. 2006 Aug 14;48(1241):65-6 |  Show IntroductionHide Introduction

Oral Oxymorphone (Opana)

   
The Medical Letter on Drugs and Therapeutics • Jan 01, 2007  (Issue 1251)
treatment at the lowest starting dosage, according to the most recent data (October 31, 2006) from retail ...
Oxymorphone hydrochloride, a semi-synthetic opioid agonist, has been available for many years in the US as Numorphan (Endo) for parenteral use and as a rectal suppository. Now it has been approved by the FDA for oral administration as an immediate-release (IR) tablet (Opana) for treatment of moderate to severe acute pain, and as an extended-release tablet (Opana ER) for treatment of moderate to severe pain in patients requiring continuous opioid treatment for an extended period of time.
Med Lett Drugs Ther. 2007 Jan 1;49(1251):3-4 |  Show IntroductionHide Introduction

A Low-Dose Doxycycline (Oracea) for Rosacea

   
The Medical Letter on Drugs and Therapeutics • Jan 15, 2007  (Issue 1252)
, based on the most recent data (November 30, 2006) from retail pharmacies nationwide available ...
A new once-daily, low-dose oral formulation of doxycycline monohydrate (Oracea - CollaGenex) has been approved by the FDA for treatment of inflammatory papules and pustules associated with rosacea in adults.
Med Lett Drugs Ther. 2007 Jan 15;49(1252):5-6 |  Show IntroductionHide Introduction

Angeliq for Treatment of Menopausal Symptoms

   
The Medical Letter on Drugs and Therapeutics • Feb 12, 2007  (Issue 1254)
on most recent data (December 31, 2006) from retail pharmacies nationwide available from Wolters Kluwer ...
A combination tablet containing estradiol and drospirenone (Angeliq - Berlex) recently became available for treatment of moderate to severe menopausal symptoms in women with an intact uterus. Since the last Medical Letter issue reviewing such devices,1 more continuous glucose monitoring (CGM) systems have become available. Five devices available now, and two expected to be marketed soon, are listed in the table on page 14. The FDA has approved continuous glucose devices only for the observation of glucose trends.
Med Lett Drugs Ther. 2007 Feb 12;49(1254):15-6 |  Show IntroductionHide Introduction

Ixabepilone (Ixempra) for Breast Cancer

   
The Medical Letter on Drugs and Therapeutics • Jan 28, 2008  (Issue 1278)
with the combination was 6.4 months compared to 5.6 months with monotherapy. 3 No data are available on use ...
Ixabepilone (ix ab ep' i lone; Ixempra - Bristol-Myers Squibb), a semisynthetic epothilone analog, has been approved by the FDA for treatment of advanced breast cancer. It is indicated for use in combination with capecitabine (Xeloda - Roche) for treatment of locally advanced or metastatic breast cancer after failure of an anthracycline such as doxorubicin (Adriamycin) and a taxane such as paclitaxel (Taxol, and others). It is also approved as monotherapy for treatment of metastatic or locally advanced breast cancer after an anthracycline, a taxane and capecitabine have...
Med Lett Drugs Ther. 2008 Jan 28;50(1278):7-8 |  Show IntroductionHide Introduction