Abstract | AIM: METHODS: The study included patients with schizophrenia and related psychotic disorders who commenced LAI-SGA therapy between January/1//2009 and March/31/2020 at Fujita Health University Hospital in Toyoake, Japan. RESULTS: We conducted a chart review of 157 patients with schizophrenia. At the time of this survey, 4 (6.9%), 5 (12.2%), and 10 (17.2%) of the patients in the aripiprazole once monthly, paliperidone palmitate, and risperidone-LAI groups, respectively, discontinued due to AEs since the start of LAI-SGA therapy. Three patients required hospitalization for AE treatment. CONCLUSION: The severity of these AEs in most patients is moderate (ie, no hospital treatment required). Due to the small sample size, a larger study is needed to confirm/replicate our study results.
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Authors | Taro Kishi, Kenji Sakuma, Makoto Okuya, Masakazu Hatano, Nakao Iwata |
Journal | Neuropsychopharmacology reports
(Neuropsychopharmacol Rep)
Vol. 41
Issue 3
Pg. 422-425
(09 2021)
ISSN: 2574-173X [Electronic] United States |
PMID | 34212530
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2021 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. |
Chemical References |
- Antipsychotic Agents
- Delayed-Action Preparations
- Aripiprazole
- Paliperidone Palmitate
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Topics |
- Antipsychotic Agents
(adverse effects)
- Aripiprazole
(adverse effects)
- Delayed-Action Preparations
(therapeutic use)
- Humans
- Paliperidone Palmitate
(adverse effects)
- Schizophrenia
(drug therapy)
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