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Haloperidol Opioids

Our results suggest that the numerically predominant 153 nM 3H-(+)SKF-10,047 site represents the PCP opioid receptor. The much less abundant haloperidol - sensitive 3.6 nM 3H-SKF-10,047 binding site that we have described appears to represent the same entity as a class of sites reported by several other groups utilizing diverse strategies, including use of H-SKF-10,047 in the presence of etorphine (Su 1982) 3H-ethylketoSycl azocine (EKC) in the presence of excess naloxone (Tam 1983) 3H-(+)SKF-10,047 or (+)3H-... [Pg.32]

The answer is c. (Hardman, pp 574—575.) Phencyclidine is a hallucinogenic compound with no opioid activity Its mechanism of action is amphetamine-like. A withdrawal syndrome has not been described for this drug in human subjects. In overdose, the treatment of choice for the psychotic activity is the antipsychotic drug haloperidol. [Pg.160]

Other indications. Acutely, there is sedation with anxiolysis after neurolep-tization has been started. This effect can be utilized for psychosomatic uncoupling in disorders with a prominent psychogenic component neuroleptanalgesia (p. 216) by means of the buty-rophenone droperidol in combination with an opioid tranquilization of overexcited, agitated patients treatment of delirium tremens with haloperidol as well as the control of mania (see p. 234). [Pg.236]

Temazepam (Restoril) [C-IV] [Sedative/Hypnotic/ Benzodiazepine] Uses Insomnia, anxiety, depression, panic attacks Action Benzodiaz ine Dose 15-30 mg PO hs PRN X in elderly Caution [X, /-] Potentiates CNS dqjressive effects of opioids, barbs, EtOH, antihistamines, MAOIs, TCAs Contra NAG Disp Caps SE Confusion, dizziness, drowsiness, hangover Interactions T Effects W/ cimetidine, disulfiram, kava kava, valerian T CNS depression W/ anticonvulsants, CNS depressants, EtOH t effects OF haloperidol, phenytoin X effects W/ aminophylline, dyphylline, OCPs, oxtriphylline, rifampin, theophylline, tobacco X effects OF levodopa EMS Use caution w/ other benzodiazepines, antihistamines, opioids and verapamil, can T CNS depression concurrent EtOH can T CNS depression abruptly D/C after >10 d use may cause withdrawal OD May cause profound CNS depression, confusion, bradycardia, hypotension, and altered reflexes flumazenil can be used as antidote, activated charcoal may be effective... [Pg.296]

Heparin and its salts are incompatible with many drugs including alteplase, amikacin sulfate, amiodarone hydrochloride, ampicillin sodium, aprotinin, benzylpenicillin potassium or sodium, cephalothin sodium, ciprofloxacin lactate, cytarabine, dacarbazine, daunorubicin hydrochloride, diazepam, dobutamine hydrochloride, doxorubicin hydrochloride, droperidol, erythromycin lactobionate, gentamicin sulfate, haloperidol lactate, hyaluronidase, hydrocortisone sodium succinate, kanamycin sulfate, methicillin sodium, netilmicin sulfate, some opioid analgesics, oxytetracycline hydrochloride, some phenothiazines, polymyxin B sulfate, streptomycin sulfate, tetracycline hydrochloride, tobramycin sulfate, vancomycin hydrochloride, vinblastine sulfate, cisatracurium besylate, labetalol hydrochloride, nicardipine hydrochloride, cefmetazole, sodium ions, and fat emulsion.110 112... [Pg.349]

Figure 2.3 Dextromethorphan 6, the unnatural enantiomer of a narcotic morphine analog, is an antitussive drug. The antidiarrhea drug loperamide 7 and the neuroleptic drug haloperidol 8 also resulted from structural modification of morphine. The morphine antagonist nalorphine 9 differs from the opioid agonist morphine 3 (Figure 2.2) only by having an N-allyl group instead of the N-methyl group. Figure 2.3 Dextromethorphan 6, the unnatural enantiomer of a narcotic morphine analog, is an antitussive drug. The antidiarrhea drug loperamide 7 and the neuroleptic drug haloperidol 8 also resulted from structural modification of morphine. The morphine antagonist nalorphine 9 differs from the opioid agonist morphine 3 (Figure 2.2) only by having an N-allyl group instead of the N-methyl group.
As well as oral use, i.v. administration (with the pleasurable flash as with opioids) is employed. Severe dependence induces behaviour disorders, hallucinations and even florid psychosis, which can be controlled by haloperidol. Withdrawal is accompanied by lethargy, sleep, desire for food and sometimes severe depression, which leads to an urge to resume the drug. [Pg.193]


See other pages where Haloperidol Opioids is mentioned: [Pg.372]    [Pg.372]    [Pg.572]    [Pg.1274]    [Pg.16]    [Pg.29]    [Pg.32]    [Pg.33]    [Pg.101]    [Pg.46]    [Pg.165]    [Pg.109]    [Pg.244]    [Pg.255]    [Pg.266]    [Pg.186]    [Pg.473]    [Pg.552]    [Pg.109]    [Pg.244]    [Pg.255]    [Pg.266]    [Pg.296]    [Pg.453]    [Pg.453]    [Pg.608]    [Pg.353]    [Pg.331]    [Pg.1274]    [Pg.2623]    [Pg.615]    [Pg.140]    [Pg.266]    [Pg.1418]    [Pg.142]    [Pg.604]    [Pg.314]    [Pg.336]    [Pg.39]    [Pg.109]    [Pg.244]    [Pg.255]    [Pg.266]   
See also in sourсe #XX -- [ Pg.172 ]




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Haloperidol

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