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Addicts addiction

Krenz S, Zimmermann G, Kolly S, et al Ether a forgotten addiction. Addiction 98 1167-1168,2003... [Pg.308]

Robinson TE, Berridge KC (2001) Incentive-sensitization and addiction. Addiction 96 103-114 Robinson JH, Pritchard WS (1992) The role of nicotine in tobacco use. Psychopharmacology 108 397 07... [Pg.364]

Btewet, D.D., Catalano, R.F., Haggerty, K., Gainey, R.R., and Fleming, C.B. (1998) A meta-analysis of ptedictots of continued drug use during and after treatment for opiate addiction. Addiction 93-J3-91. [Pg.248]

Farrell M, Neeleman J, Griffiths P Strang J (1996). Suicide and overdose among opiate addicts. Addiction, 91, 321-3... [Pg.155]

The same goes for attachment to acquired appetites. As we have seen, some people can manage their addictions. Addiction is in principle compatible with temperance.40 We cannot dismiss a regulated devotion to tobacco or drink as demeaning or enslaving just on the grounds that it involves dependence. That would presuppose an ideal of self-mastery that would condemn much of what we value in human life. [Pg.18]

For this term, see Wolf (1990,129). In Wolf s terms, the addict s will is less intelligent than it would be in the absence of addiction. Addictions can impair normative competence not only by distorting probabilistic judgment or instrumental rationality, but also by affecting our fundamental values and prefects—what we find meaningful in life. [Pg.23]

Eiser, Richard, Stephen Sutton, and Mallory Weber. 1978. " Consonant and Dissonant Smokers and the Self-Attribution of Addiction." Addictive Behaviors 3 99-106. [Pg.273]

How is a drug addicts addiction similar to our need for food How is it different ... [Pg.515]

Wildeboer KM, Stevens KE (2008) Stimulation of the alpha4beta2 nicotinic receptor by 5-1 A-85380 improves auditory gating in DBA/2 mice. Brain Res 1224 29-36 Wilhams JM, Ziedonis D (2004) Addressing tobacco among individuals with a mental illness or an addiction. Addict Behav 29 1067-1083... [Pg.784]

Abstinence on its own is not enough for the addict. Addiction is a function of the lower brain and cannot be controlled by force of will. Craving will wear down the addict s resolve and in an attempt to resist can create a rigidity known in the field as white-knuckle sobriety, in which the abstinent addict is clinging so hard that it is like the driver with such a grip on the wheel that his or her knuckles are bloodless. That is no way to drive a car or to maintain recovery from addiction. Recovery for the addict is a lifelong undertaking and requires help. ... [Pg.1039]

Medication abuse occurs gradually, so much so that the patient is unable to recognize the addiction and steadfastly denies that he or she is addicted. Addiction results in an altered mental state that leads to deviation from normal behavioral patterns. These deviations are ... [Pg.42]

Levran O, Peles E, Hamon S, Randesi M, Adelson M, Kreek MJ (2013) CYP2B6 SNPs are associated with methadone dose required for effective treatment of opioid addiction. Addict Biol 18 709-716... [Pg.622]

Petrakis IF, Carroll KM, Nich C, Gordon FT, McCance-Katz EF, Frankforter T, Rounsaville BJ (2000) Disulfiram treatment for cocaine dependence in methadone-maintained opioid addicts. Addiction 95 219-228... [Pg.624]

Morphine and its salts are very valuable analgesic drugs but are highly addictive. In addition to suppression of pain, morphine causes constipation, decreases pupillary size and depresses respiration. Only the (-l-)-stereoisoraer is biologically active. They appear to produce their effects on the brain by activating neuronal mechanisms normally activated by... [Pg.266]

The reasons Strike wrote this book. The reasons you re reading this book. Ecstasy is the most benign drug Strike has ever encountered. It is passive yet powerful. By powerful Strike does not mean that it incapacitates or makes one dangerous. It is, in fact, quite the opposite. Its power is in its ability to evoke a total sensory bath of tactile, visual and mental enhancement. One s perception is perfectly clear. Hallucinations are nonexistent. The feeling one has is, literally, ecstasy. Plus, it is one of the few narcotics in the world that is not physically addictive. Why this substance was taken away from the people is a question that only government-funded scientists can answer. [Pg.7]

An opium alkaloid Although it is an excellent analgesic its use is restricted because of the potential for addiction Heroin is the diacetate ester of morphine )... [Pg.924]

Anhydride has been used for the illegal manufacture of heroin [561-27-3] (acetyknorphine) and certain other addictive dmgs. Regulations on acetic anhydtide commerce have long been a feature of European practice. After passage in 1988 of the Chemical Diversion and Trafficking Act, there is also U.S. control. Orders for as much as 1,023 kg acetic anhydtide, for either domestic sale or export, require a report to the Department of Justice, Dmg Enforcement Administration (54). [Pg.79]

U.S. Laws and Regulations Related to Drug Product Development and Manufacture. Until early in the twentieth century, dmg products were made and sold in the United States having virtually no imposed control. QuaUty was generally poor. Many products were patent medicines of dubious value. Some were harmful and addicting. [Pg.225]

Codeine, mol wt 299.3, is a significantly less potent analgesic than morphine, requiring 60 mg (0.20 mmol) to equal the effectiveness of 10 mg (0.04 mmol) of morphine. However, codeine is orally effective, and it is less addictive and associated with less nausea than morphine. Codeine is used as an antitussive agent, although newer, nonaddictive agents are preferred (see Expectorants, antitussives, and related agents). [Pg.381]

Introduced in 1898, heroin was heralded as a nonaddictive alternative to morphine. Subsequent clinical experience showed it to be highly addictive and preferred by addicts over morphine (13). Heroin is approximately ten times more potent than morphine, with quicker onset and shorter duration of... [Pg.381]

A common strategy for treating chronic opiate addiction iavolves the substitution of methadone which can either be provided as maintenance therapy or tapered until abstinence is achieved. Naltrexone and buprenorphine [52485-79-7] have also been used ia this manner. The a2 adrenergic agonist clonidine [4205-90-7] provides some rehef from the symptoms of opiate withdrawal, probably the result of its mimicking the inhibitory effect of opiates on the activity of locus coerukus neurons. [Pg.238]

Group for the Advancement of Psychiatry Committee on AlcohoHsm and the Addictions, / Psychiaty 148, 1291 (1991). [Pg.244]

M. R. Jacobs and K. O B. P r. A.ddiction Research Foundation s Drugs andDrugAbuse 2nd ed.. Addiction Research Foundation, Toronto, Canada,... [Pg.245]

Nicotine Delivery Systems. For all transdermal nicotine products, the hypothesis is that continuous deflvery of nicotine [34-11-3] ne t trough levels during smoking should alleviate physical nicotine withdrawal symptoms and allow the smoker to concentrate on eliminating the behavioral aspects of addiction. [Pg.230]

Codeine, like morphine, is isolated from the opium poppy. However, the low yield of 0.7—2.5% does not provide sufficient material to meet commercial demands. The majority of marketed codeine is prepared by methylating the phenolic hydroxyl group of morphine. Morphine yields from opium poppy are 4—21%. When prescribed for cough, the usual oral dose is 10—20 mg, three to four times daily. At these doses, adverse side effects are very few. Although the abuse potential for codeine is relatively low, the compound can substitute for morphine in addicts (47). [Pg.522]

Hydromorphone [466-99-9] (31) and hydrocodone [125-29-1] (32) are isomers of morphine and codeine, respectively. Hydromorphone can be prepared by catalytic rearrangement of morphine (49) or by oxidation of the aliphatic hydroxyl group of dihydromorphine (50). Hydrocodone can be similarly prepared. As an antitussive, hydromorphone is several times more active than morphine and hydrocodone is slightly more active than codeine. Hydromorphone has a much higher addiction potential than hydrocodone. [Pg.522]

Dihydrocodeine [125-28-0] (33), introduced in Germany before 1930, and dihydrocodeinone enol acetate [466-90-0] (34) both have clinical activity and addiction potential comparable to codeine. [Pg.522]

Nonnarcotic Antitussives. The most centrally active, noimarcotic antitussive is dextromethorphan [125-71-3] (39). It is similar to codeine in terms of potency and mechanism of action, ie, it is a direct depressant of the cough center. It is unique in that even though it is stmcturaHy related to codeine, it is not addictive. [Pg.523]

Levopropoxyphene [2338-37-6] (42), the optical antipode of the dextrorotatory analgetic propoxyphene, is an antitussive without analgetic activity. The 2-naphthalenesulfonate salt has a less unpleasant taste than the hydrochloride salt, and is widely used. Clinical effectiveness has been demonstrated against pathological and artificially induced cough, but the potency is somewhat less than codeine. The compound is reported not to cause addiction. Levopropoxyphene can be prepared (62) by first resolving [ -dimethylamino-CX-methylpropiophenone with dibenzoyl-(+)-tartaric acid. The resolved... [Pg.523]

Except for the addiction HabiUty of some of the narcotic antitussives, side effects for most of the centrally acting compounds are relatively few and mild at therapeutic doses. QuaUtative comparisons of both side effects and pharmacological profiles have been summarized for many of the compounds described above (97). [Pg.527]

Meprobamate [2,2-di(carbamoyloxymethyl)pentane] [57-53-4] M 246.3, m 104-106°. Crystd from hot water. Could be an addictive drug. [Pg.282]

The hydrochloride of a natural product which is intoxicating and addictive produced the set of NMR results 53. What is the structure of the material What additional information can be derived from the NOE difference spectrum ... [Pg.168]

A series of papers dealing with the investigation of cocaine addiction may also be noted. [Pg.112]

These early observations on the correlation of structure and pharmacological action in the morphine group have been greatly extended as a result of chemical, pharmacological and clinical work done under the auspices of the American National Committee on Drug Addiction. In addition to numerous papers, contributed by experts serving this Committee, to chemical and pharmacological journals, two important reports have been published —... [Pg.260]

Studies on Drug Addiction, with special reference to Chemical Structure of Opium Derivatives and Allied Synthetic Substances and their Physiological Action, by Small, Eddy, Mosettig and Himmelsbach. ... [Pg.260]

Apart from the study of drug addiction in its clinical aspects, much... [Pg.262]

Codeine (morphine methyl ether) resembles morphine in its general effect, but is less toxic and its depressant action less marked and less prolonged, whilst its stimulating action involves not only the spinal cord, but also the lower parts of the brain. In small doses in man it induces sleep, which is not so deep as that caused by morphine, and in large doses it causes restlessness and increased reflex excitability rather than sleep. The respiration is slowed less than by morphine (cf. table, p. 261). Cases of addiction for codeine can occur but according to Wolff they are rare. The best known ethers of morphine are ethylmorphine and benzyl-morphine [cf., table, p. 261), both used to replace morphine or codeine for special purposes. [Pg.265]


See other pages where Addicts addiction is mentioned: [Pg.719]    [Pg.105]    [Pg.115]    [Pg.250]    [Pg.21]    [Pg.308]    [Pg.43]    [Pg.174]    [Pg.385]    [Pg.32]    [Pg.537]    [Pg.539]    [Pg.545]    [Pg.545]    [Pg.557]    [Pg.532]    [Pg.381]    [Pg.382]    [Pg.383]    [Pg.383]    [Pg.383]    [Pg.228]    [Pg.521]    [Pg.523]    [Pg.448]    [Pg.495]    [Pg.313]    [Pg.260]    [Pg.262]    [Pg.262]    [Pg.263]    [Pg.264]    [Pg.265]    [Pg.266]    [Pg.267]    [Pg.791]   


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