نتایج جستجو برای: oral dosing

تعداد نتایج: 277969  

2013
Kunal Srivastava Anamika Arora Aditi Kataria Joseph C Cappelleri Alesia Sadosky Andrew M Peterson

OBJECTIVES To assess the impact of reduced frequency of oral therapies from multiple-dosing schedules to a once-daily (OD) dosing schedule on adherence, compliance, persistence, and associated economic impact. METHODS A meta-analysis was performed based on relevant articles identified from a comprehensive literature review using MEDLINE® and Embase®. The review included studies assessing adhe...

2013
Matthew Matava D. Craig Brater Nancy Gritter Robert Heyer Douglas Rollins Theodore Schlegel Robert Toto Anthony Yates

T hank you for the opportunity to respond to the points put forth by the reader regarding the use of SPRIX ® (ketorolac tromethamine) nasal spray. As the developer of SPRIX ® , the reader points out that prior pharmacokinetic data comparing oral with intramuscular (IM) ketorolac indicate that the time for the drug to reach maximum plasma concentration (t max) is as low as 20 minutes in fasted i...

Journal: :Scientia Pharmaceutica 2022

There is a need to develop dosage forms suitable for children improve drug treatment. Extemporaneous compounding of drugs one way meet these needs. However, excipients generally considered as safe in adults may not be appropriate intended children. The aim was optimize the composition two pediatric liquid preparations by substituting paraben microbiological preservative and ethanol solubilizer,...

Journal: :Revista da Sociedade Brasileira de Medicina Tropical 1989
N Katz E P Dias C P de Souza J I Bruce G C Coles

Mice infected with adult Schistosoma mansoni were dosed with a single oral dose of 125 or 250 mg/kg oltipraz, 50 or 100 mg/kg oxamniquine, or 200 or 400 mg/kg praziquantel. The mortality rate of worms and oogram changes were determined between 1 and 16 weeks after dosing. The time required between dosing and postmortem to obtain maximum effectiveness was 1 week for praziquantel, 2 weeks for oxa...

Journal: :Postgraduate medical journal 1981
R T Dorr J R Powell M Heick D W Barry

A 24-year-old female with Hodgkin's disease and Pneumocystis carinii pneumonia was tested with trimethoprim/sulphamethoxazole (TMP/SMX) tablets. Because treatment failure was feared owing to chronic emesis potentially resulting in incomplete drug absorption, the same TMP/SMX dose was administered by rectal suppositories after the 5th day of oral dosing. The relative fractions (rectal/oral) or t...

2015
Eric Laille Tao Shi Guillermo Garcia-Manero Christopher R. Cogle Steven D. Gore Joel Hetzer Keshava Kumar Barry Skikne Kyle J. MacBeth M Consuelo del Cañizo

UNLABELLED CC-486 (oral azacitidine) is an epigenetic modifier in development for patients with myelodysplastic syndromes and acute myeloid leukemia. In part 1 of this two-part study, a 7-day CC-486 dosing schedule showed clinical activity, was generally well tolerated, and reduced DNA methylation. Extending dosing of CC-486 beyond 7 days would increase duration of azacitidine exposure. We hypo...

Journal: :British journal of clinical pharmacology 2005
Martin Brunner Pejman Dehghanyar Bernd Seigfried Wolfgang Martin Georg Menke Markus Müller

AIMS The study was designed to evaluate the relative bioavailability of diclofenac in plasma, subcutaneous adipose and skeletal muscle tissue after repeated topical administration using MIKA Diclofenac Spray Gel (4%), a novel formulation, and after oral dosing using VOLTAREN 50 mg enteric coated tablets. METHODS Diclofenac (48 mg) was administered topically three times daily for 3 days onto a...

Journal: :Environmental Science and Pollution Research 2021

Antibiotics are considered an important primary therapy for bacterial diseases in aquaculture. This study evaluated the influence of oral administration oxytetracycline (OTC) on feed intake, growth, mortality, residue accumulation and clearance, histopathological changes vital organs six groups Nile tilapia Oreochromis niloticus when fed at 0–10 times therapeutic dose (1×: 80 mg/kg biomass/day)...

2009
Kristina Casadei Carolyn Becker

Bisphosphonates are the mainstay of treatment for postmenopausal women with osteoporosis. Despite numerous clinical trials documenting efficacy, tolerability, and safety of bisphosphonate therapy, long-term persistence and adherence to these agents remains low. This has serious consequences for patients with osteoporosis in that medication non-compliance is associated with significantly higher ...

2009
Richard Derman Joseph D Kohles Ann Babbitt

Data from two open-label trials (PRIOR and CURRENT) of women with postmenopausal osteoporosis or osteopenia were evaluated to assess whether monthly oral and quarterly intravenous (IV) ibandronate dosing improved self-reported gastrointestinal (GI) tolerability for patients who had previously experienced GI irritation with bisphosphonate (BP) use. In PRIOR, women who had discontinued daily or w...

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