1978
DOI: 10.1007/978-3-642-66896-8_73
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Pharmacokinetics of Dextropropoxyphene in Acute Poisoning

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Cited by 16 publications
(10 citation statements)
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“…Moreover, the quotient dxp/ndxp (= K) may be used to differentiate between an acute and a chronic poisoning. This is possible because the half life of the metabolite is much greater than the half life of dxp, which means that in most cases the metabolite will be present in a concentration higher than the concentration of dxp [8]. An exception to this is found in acute poisonings or chronic/ intermittent poisonings in combination with an acute poisoning.…”
Section: Blood Concentrations In Fatal Dxp Intoxicationsmentioning
confidence: 89%
See 1 more Smart Citation
“…Moreover, the quotient dxp/ndxp (= K) may be used to differentiate between an acute and a chronic poisoning. This is possible because the half life of the metabolite is much greater than the half life of dxp, which means that in most cases the metabolite will be present in a concentration higher than the concentration of dxp [8]. An exception to this is found in acute poisonings or chronic/ intermittent poisonings in combination with an acute poisoning.…”
Section: Blood Concentrations In Fatal Dxp Intoxicationsmentioning
confidence: 89%
“…For many years dextropropoxyphene (dxp) has been a frequently used and misused drug in Denmark [1][2][3][4][5][6][7][8]. During the period from 1981 to 1985 its sale in daily doses of 0.2 g increased from 7.7 to 9.3 per 1000 inhabitants.…”
Section: Introductionmentioning
confidence: 99%
“…The speed of onset of CNS depression appears incompatible with animal studies which show that dextropropoxyphene, in common with most opioids, delays gastric emptying. Clearly lethal quantities can be absorbed rapidly, perhaps before gastric emptying is significantly reduced and particularly if alcohol or other brain depressants are ingested simultaneously (Carson & Carson, 1977;Schou et al, 1978).…”
Section: Dextropropoxyphene Poisoning Due To Distalgesicmentioning
confidence: 99%
“…Previous reports suggest dextropropoxyphene is rapidly absorbed from the gastrointestinal tract and detectable in plasma 5 min after administration of the napthylate and hydrochloride by mouth (19), the peak concentration in plasma is reached between 1 and 2 h after oral administration to an empty stomach (20). Long plasma half-lives of dextropropoxyphene and norpropoxyphene have been reported in overdose (21), following repeated doses (22) and in the elderly (23). Half-lives of 14.6 h (24), 17.9 to 30.5 (21), 35.5 (23), for dextropropoxyphene and 6.1 to 32.9 (22), 53.3 (23) for norpropoxyphene have been reported.…”
Section: Discussionmentioning
confidence: 95%