chronically remitted, chronically stable, etc.), as well as baseline turnover of NE may play a role in determining the type of change in psychosis. The results imply that the clinical state (severely psychotic vs. This study raises questions of how d-amphetamine affects psychotic behavior ( Angrist and Gershon, 1977 van Kammen and others, 1977 Angrist and associates, 1980 Janowsky and Davis, 1976). van Kammen, in Recent Advances in Neuropsycho-Pharmacology, 1981 DISCUSSION The clinical study data on the use of quetiapine in DLB, however, are very limited so far.Д.P. Quetiapine may therefore prove to be an easier to use option with a starting dose of 25В mg which generally has to be increased in a range between 50 and 150В mg/d. Weekly blood count monitoring is cumbersome but inevitable for the first 4 months (to be follow by monthly blood counts). Clozapine with starting bedtime doses of 6.25В mg/d and incomense in a range between 6.25 and 50В mg/d (rarely 75вЂ“150В mg/d) is probably the currently best option although it may be less well tolerated in DLB patients compared to psychotic PD patients. Unfortunately, this is also true for the atypical neuroleptics risperidone and olanzapine. As in PD patients classic neuroleptics should be avoided due to their potential to significantly worsen motor symptoms. Still add-on treatment with antipsychotics is frequently needed. Visual hallucinations, delusions, and psychotic behavior may improve when DLB patients are put on cholinesterase inhibitors like rivastigmine or donepezil. Wenning, in Primer on the Autonomic Nervous System (Third Edition), 2012 Hallucinations and Psychosis

Amphetamine induced psychosis f code