نتایج جستجو برای: chewable tablet

تعداد نتایج: 32928  

2014
M. Franc E. Bouhsira C. Böhm S. Wolken O. Wolf W. Löhlein S. Wiseman B. Hayes B. Schnitzler M. Fisher

METHODS An ectoparasiticide containing spinosad was evaluated as an oral formulation for cats. Two European laboratory studies and a European multicentre field efficacy and safety study assessed the use of a chewable tablet formulation of spinosad at a dose range of 50-75 mg/kg for treatment and control of flea infestations on cats. RESULTS The studies with experimentally infested cats consis...

Journal: :The Veterinary record 2012
S Wolken M Franc E Bouhsira S Wiseman B Hayes B Schnitzler D E Jacobs

The novel ectoparasiticide spinosad is a naturally occurring mixture of spinosyns A and D formed during a fermentation process. The spinosyns are tetracyclic macrolides with a unique ring system. Their mode of action differs from that of other commercially available insecticides. Laboratory and field trials were conducted to evaluate the use of spinosad in a chewable tablet at a dose range of 4...

2010
Albert Wertheimer Larry Radican Michael Robert Jacobs

Numerous pharmaceutical products are launched each year for the treatment of various medical conditions. The prescriber is in a difficult position to determine which the optimal product is for a specific patient, when he has available immediate release as well as sustained action capsules and tablets, chewable tablets and liquid dosage forms. Some have activity within 15 minutes while others ta...

2012
Edith Weisberg

A new chewable combined oral contraceptive pill containing ethinyl estradiol (EE) 0.025 mg and norethindrone (NE) 0.8 mg in a 24/4 regimen was approved for marketing in December 2010. Each of the four inactive tablets contains 75 mg ferrous fumarate, which has no therapeutic benefit. The tablet can be taken with food but not water as this affects the absorption of EE. The Pearl index based on i...

2017
Sharon B. Wigal Ann Childress Sally A. Berry Heidi Belden Faith Walters Phillip Chappell Nancy Sherman John Orazem Donna Palumbo

OBJECTIVE This phase 3, laboratory classroom study assessed the efficacy and safety of methylphenidate hydrochloride extended-release chewable tablets (MPH ERCT) compared with placebo in children with attention-deficit/hyperactivity disorder (ADHD). METHODS Following a 6-week, open-label, dose-optimization period, children 6-12 years of age (n = 90) with ADHD were randomly assigned to double-...

Journal: :International Research Journal of Pharmacy 2016

Journal: :Chest 1982
J R Wilson N Ferraro

The effect of chewable isosorbide dinitrate on submaximal bicycle exercise capacity was evaluated in a double-blind randomized study involving 13 patients with chronic heart failure. All patients had impaired maximal exercise capacity (VO2 max = 12.0 +/- 2.6 ml/kg/min) due to fatigue and dyspnea but not angina. The administration of isosorbide dinitrate lowered the resting mean blood pressure (...

2006
M. PAYNE-JOHNSON T. P. MAITLAND J. BULLARD J. GOSSELLIN

A series of six palatability studies, employing acceptance (three studies) and preference (three studies) tests, were used to compare the voluntary acceptance, preference and consumption of a palatable formulation of carprofen (Rimadyl® Chewable Tablets or Rimadyl® Palatable Tablets; Pfizer Animal Health) with those of two generic formulations of carprofen (Carprodyl® Tablets; Ceva and Norocarp...

2016
Yiming Yuan Zhongcheng Xin

After launching of sildenafil citrate, the last invention of 20 century, in 1998, oral phosphodiesterase type 5 (PDE5) inhibitor has been established as first line treatment of erectile dysfunction and shift new paradigm of diagnosis and treatment of erectile dysfunction. The big success of sildenafil in pharmaceutical R&D induced the consecutive development of the so-called ‘The second Viagra’...

Journal: :Alternative medicine review : a journal of clinical therapeutic 2011
Michael R Lyon Mahendra P Kapoor Lekh R Juneja

INTRODUCTION The purpose of this study was to investigate the efficacy and safety of L-theanine as an aid to the improvement of objectively measured sleep quality in a population of 98 male children formally diagnosed with attention-deficit/hyperactivity disorder (ADHD). METHODS A randomized, double-blind, placebo-controlled trial was conducted involving boys, ages 8-12 years, who had been pr...

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