메뉴 건너뛰기




Volumn 54, Issue 5, 2004, Pages 293-297

Pharmacokinetic assessment of a fast-release orodispersible tramadol tablet compared to a conventional tramadol capsule

Author keywords

CAS 27203 92 5; Tramadol, orodispersible, pharmacokinetics; Zamadol Melt, bioavailability, bioequivalence, drug delivery

Indexed keywords

DRUG METABOLITE; O NORTRAMADOL; TRAMADOL; UNCLASSIFIED DRUG; ZAMADOL;

EID: 2542579404     PISSN: 00044172     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0031-1296973     Document Type: Article
Times cited : (7)

References (12)
  • 1
    • 0031764451 scopus 로고    scopus 로고
    • The clinical use of tramadol hydrochloride
    • Bamigbade, T. A., Langford, R. M., The clinical use of tramadol hydrochloride. Pain Rev. 5, 155 (1998)
    • (1998) Pain Rev. , vol.5 , pp. 155
    • Bamigbade, T.A.1    Langford, R.M.2
  • 2
    • 0023720412 scopus 로고
    • Receptor binding, analgesic and antitussive potency of tramadol and other selected opioids
    • Hennies, H. H., Friderichs, E., Schneider, J., Receptor binding, analgesic and antitussive potency of tramadol and other selected opioids. Arzneim.-Forsch./Drug Res. 38, 877 (1988)
    • (1988) Arzneim.-Forsch./Drug Res. , vol.38 , pp. 877
    • Hennies, H.H.1    Friderichs, E.2    Schneider, J.3
  • 3
    • 0026512239 scopus 로고
    • Opioid and nonopioid components independently contribute to the mechanism of action of tramadol, an 'atypical' opioid analgesic
    • Raffa, R. B., Friderichs, E., Reimann, W. et al., Opioid and nonopioid components independently contribute to the mechanism of action of tramadol, an 'atypical' opioid analgesic. J. Pharmacol. Exp. Ther. 260, 275 (1992)
    • (1992) J. Pharmacol. Exp. Ther. , vol.260 , pp. 275
    • Raffa, R.B.1    Friderichs, E.2    Reimann, W.3
  • 4
    • 0026585612 scopus 로고
    • Interaction of the central analgesic, tramadol, with the uptake and release of 5-hydroxytryptamine in the rat brain in vitro
    • Driessen, B., Reimann, W., Interaction of the central analgesic, tramadol, with the uptake and release of 5-hydroxytryptamine in the rat brain in vitro. Br. J. Pharmacol. 105, 147 (1992)
    • (1992) Br. J. Pharmacol. , vol.105 , pp. 147
    • Driessen, B.1    Reimann, W.2
  • 5
    • 0036128113 scopus 로고    scopus 로고
    • Tramadol in musculoskeletal pain - A survey
    • Reig, E., Tramadol in musculoskeletal pain - a survey. Clin. Rheumatol. Suppl. 1, S9 (2002)
    • (2002) Clin. Rheumatol. Suppl. , vol.1
    • Reig, E.1
  • 6
    • 0028209877 scopus 로고
    • Chronic pain - Challenge and response
    • Budd, K., Chronic pain - challenge and response. Drugs. 47 (Suppl. 1), 33 (1994)
    • (1994) Drugs , vol.47 , Issue.1 SUPPL. , pp. 33
    • Budd, K.1
  • 7
    • 0032824204 scopus 로고    scopus 로고
    • A postmarketing surveillance program to monitor Ultram (tramadol hydrochloride) abuse in the United States
    • Cicero, T. J., Adams, E. H., Geller, A. et al., A postmarketing surveillance program to monitor Ultram (tramadol hydrochloride) abuse in the United States. Drug Alcohol Depend. 57, 7 (1999)
    • (1999) Drug Alcohol Depend. , vol.57 , Issue.7
    • Cicero, T.J.1    Adams, E.H.2    Geller, A.3
  • 9
    • 0033868693 scopus 로고    scopus 로고
    • Tramadol-present and future
    • Shipton, E. A., Tramadol-present and future. Anaesth. Intensive Care 28, 363 (2000)
    • (2000) Anaesth. Intensive Care , vol.28 , pp. 363
    • Shipton, E.A.1
  • 10
    • 0032946793 scopus 로고    scopus 로고
    • Slowing the initial titration rate of tramadol improves tolerability
    • Ruoff, G. E., Slowing the initial titration rate of tramadol improves tolerability. Pharmacotherapy 19, 388 (1999)
    • (1999) Pharmacotherapy , vol.19 , pp. 388
    • Ruoff, G.E.1
  • 12
    • 0022497847 scopus 로고
    • Bioavailability of enterai tramadol formulations
    • Lintz, W., Barth, H., Osterloh, G. et al., Bioavailability of enterai tramadol formulations. Arzneim.-Forsch./Drug Res. 36 (II), 1278 (1986)
    • (1986) Arzneim.-Forsch./Drug Res. , vol.36 , Issue.2 , pp. 1278
    • Lintz, W.1    Barth, H.2    Osterloh, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.