1989
DOI: 10.1001/archinte.149.11.2486
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Metoclopramide-induced movement disorders. Clinical findings with a review of the literature

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Cited by 101 publications
(74 citation statements)
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“…Treatment of patients with metoclopramide leads to a very high incidence (and severity) of EPS, including tardive dyskinesia (Ganzini et al, 1991(Ganzini et al, , 1993Miller and Jankovic, 1989). The high incidence and severity of EPS that accompanies metoclopramide treatment is seen at doses at least 40-fold lower than those that have been suggested to have antipsychotic effects (Makra et al, 1975;Stanley et al, 1980); there are no double-blind trials indicating that metoclopramide possesses antipsychotic efficacy.…”
Section: Clinical Correlates and Conclusionmentioning
confidence: 99%
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“…Treatment of patients with metoclopramide leads to a very high incidence (and severity) of EPS, including tardive dyskinesia (Ganzini et al, 1991(Ganzini et al, , 1993Miller and Jankovic, 1989). The high incidence and severity of EPS that accompanies metoclopramide treatment is seen at doses at least 40-fold lower than those that have been suggested to have antipsychotic effects (Makra et al, 1975;Stanley et al, 1980); there are no double-blind trials indicating that metoclopramide possesses antipsychotic efficacy.…”
Section: Clinical Correlates and Conclusionmentioning
confidence: 99%
“…These two D2 antagonists differ in their pharmacological profile and in their clinical actions: haloperidol is an effective antipsychotic drug that produces EPS, whereas metoclopramide potently produces EPS but has not been shown in double-blind studies to possess antipsychotic efficacy (Ganzini et al, 1991;Makra et al, 1975;Miller and Jankovic, 1989;Stanley et al, 1980;see Deutch, 1996).…”
Section: Introductionmentioning
confidence: 99%
“…Finally, we examined the effects of acute administration of metoclopramide, a substituted benzamide that is an antagonist at D2 and H-HT 3 receptors. Metoclopramide treatment is marked by a high incidence of EPS and tardive dyskinesia (Ganzini et al, 1991;Miller and Jankovic, 1989). Metoclopramide, while having parkinsonian side effect liability, may be antipsychotic at very high (at least ten fold higher than required to elicit EPS) doses (Makra etal., 1975;Stanley etal., 1980); to date there have been no controlled double-blind trials of the antipsychotic properties of metoclopramide.…”
Section: Antipsychotic Drug Administration and The Nucleus Accumbens mentioning
confidence: 99%
“…Metoclopramide (e.g., Paspertin, Solvay, Germany; Gastrosil, Heumann, Germany) has been shown to be only poorly efficient (adding no significant benefit over cimetidine alone [19,34]), and documented incidences of side effects such as fatigue, restlessness, tremor, parkinsonism, and tardive dyskinesia range from 20 to 50% [21].…”
Section: Prokineticsmentioning
confidence: 99%