نتایج جستجو برای: tramadol hydrochloride

تعداد نتایج: 47017  

2017
Jian Tang Jin Fan Yilun Yao Weihua Cai Guoyong Yin Wei Zhou

This study aimed to investigate the perioperative analgesic effect of a buprenorphine transdermal patch in patients who underwent simple lumbar discectomy.In total, 96 patients were randomly divided into parecoxib intravenous injection (Group A), oral celecoxib (Group B), and buprenorphine transdermal patch groups (Group C). The pain status, degree of satisfaction, adverse effects, and conditio...

Journal: :The Journal of pharmacology and experimental therapeutics 2008
Robert B Raffa Dennis J Stone

Tramadol is one of the most widely used centrally acting analgesics worldwide. Because of its multimodal analgesic mechanism (opioid plus nonopioid), the adverse effects profile of tramadol, similar to its analgesic profile, can be atypical compared with single-mechanism opioid analgesics. The comparison is often favorable (e.g., less respiratory depression or abuse), but it is sometimes cited ...

2013
Rajesh Shukla

A specific, rapid and simple UV spectrophotometric method with good sensitivity was developed and validated for the simultaneous quantification of tramadol HCl and paracetamol in bulk and marketed product by simultaneous equation method. From the optical characteristics of the proposed methods, it was found that the λmax of tramadol·HCl and paracetamol was found to 271 nm and 248 nm respectivel...

Journal: :Polish journal of veterinary sciences 2010
M Giorgi S Del Carlo B Łebkowska-Wieruszewska C J Kowalski G Saccomanni

The aim of this study was to determine the pharmacokinetics of tramadol and its main metabolites after i.v. and i.m. injections. The pharmacokinetic cross-over study was carried out on 6 healthy male beagle dogs. Tramadol was administered by intravenous (i.v.) and intramuscular (i.m.) injection at 4 mg/kg. Tramadol and its main metabolites O-desmethyl-tramadol (M1), N-,N-didesmethyl-tramadol (M...

2012
Hyun-Young Lee Sang Hun Kim Keum Yung So Dong Jun Kim

BACKGROUND Although arthroscopic shoulder surgery is less invasive and painful than open shoulder surgery, it can often cause intra-operative hemodynamic instability and severe post-operative pain. This study was conducted to investigate the efficacy of the interscalene brachial plexus block (IBPB) on intra-operative hemodynamic changes and post-operative pain during arthroscopic shoulder surge...

2013
Y. N. Gavhane A. V. Yadav

Tramadol hydrochloride, highly water soluble drug was chosen as candidate drug for formulation of controlled release drug delivery owing to its undesirable side effects like abdominal pain, anorexia which were likely to happen after administration of conventional drug delivery of tramadol. The objective of present study was to design and investigate the performance of hydrophilic and hydrophobi...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2001
V Subrahmanyam A B Renwick D G Walters P J Young R J Price A P Tonelli B G Lake

The metabolism of cis-tramadol has been studied in human liver microsomes and in cDNA-expressed human cytochrome P-450 (CYP) isoforms. Human liver microsomes catalyzed the NADPH-dependent metabolism of tramadol to the two primary tramadol metabolites, namely, O-desmethyl-tramadol (metabolite M1) and N-desmethyl-tramadol (metabolite M2). In addition, tramadol was also metabolized to two minor se...

In this study 50 samples of ecstasy tablets seized in Iran during the period of 2007 through 2008 were examined and their physical characteristics (appearance, marking, scored/not scored, color, weight, diameter, thickness) were determined. In order to determine the chemical characteristics of these tablets, color tests (Marquis test, Simon’s test, Chen’s test and Gallic acid test), Thin Layer ...

2006
Kader Keskinbora

Tramadol, a centrally acting analgesic, consists of two enantiomers, both of which contribute to analgesic activity via different mechanisms. (+) Tramadol and the metabolite (+) -Odesmethyl-tramadol (M1) are agonists of the mu opioid receptor. (+) Tramadol also stimulates presinaptic release of serotonin and inhibits serotonin reuptake weheres (-) tramadol inhibits norepinephrine reuptake. Thus...

2011

In most cancer patients, pain is successfully treated with pharmacological measures using opioid analgesics for moderate to severe pain (strong opioids) alone or in combination with adjuvant analgesics (coanalgesics). Opioids for mild to moderate pain (weak opioids) are usually recommended in the treatment of cancer pain of mild to moderate intensity. There is a debate whether the second step o...

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