Pericyazine 2.5mg/5ml oral solution
Requires a prescription from a doctor or prescriber
Periciazine is a phenothiazine of the piperidine group.
Official documents, adverse reaction reporting, and safety monitoring
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Drug safety updates
MHRA alerts for Pericyazine
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Pericyazine
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
WHO defined daily dose (DDD)
50 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
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Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing all 21 studies.
1965–2022
Showing all 21 studies, sorted by most relevant.
Hua-lin Cai, Yang Deng, P. Fang, et al.
Journal of Pharmaceutical and Biomedical Analysis, 2017
- Asian People
- Sulfoxides
- Phenothiazines
D. S. Danilov
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova, 2017
- Phenothiazines
- Ambulatory Care
- Patient Admission
Louis A. Pagliaro, Ann Marie Pagliaro
Psychologists’ Psychotropic Drug Reference, 2020
Brian MacKenna, Helen J Curtis, Alex J Walker, et al.
2022
BACKGROUND Data analysis can be used to identify signals suggestive of variation in treatment choice or clinical outcome. Analyses to date have generally focused on an hypothesis-driven approach. OBJECTIVE Develop hypothesis-blind data driven approaches to identify outlier prescribing behaviour. METHODS Here we report an innovative hypothesis-blind approach (calculating chemical-class proportions for every chemical substance prescribed in each Clinical Commissioning Group and ranking chemicals by (a) their kurtosis and (b) a ratio between inter-centile differences) applied to England’s national prescribing data, and demonstrate how this identified unusual prescribing of two antipsychotics. RESULTS We identified that, while promazine and pericyazine are barely used by most clinicians, they make up a substantial proportion of all antipsychotic prescribing in two small geographic regions in England. CONCLUSIONS Data-driven approaches can be effective at identifying unusual clinical choices. More widespread adoption of such approaches, combined with clinician and decision-maker engagement could lead to better optimised patient care. CLINICALTRIAL n/a
Abstract licence: CC BY
Brian MacKenna, Helen J Curtis, Alex J Walker, et al.
2022
Abstract Background Data analysis can be used to identify signals suggestive of variation in treatment choice or clinical outcome. Analyses to date have generally focused on an hypothesis-driven approach. Methods Here we report an innovative hypothesis-blind approach (calculating chemical-class proportions for every chemical substance prescribed in each Clinical Commissioning Group and ranking chemicals by (a) their kurtosis and (b) a ratio between inter-centile differences) applied to England’s national prescribing data, and demonstrate how this identified unusual prescribing of two antipsychotics. Outcomes We identified that, while promazine and pericyazine are barely used by most clinicians, they make up a substantial proportion of all antipsychotic prescribing in two small geographic regions in England. Interpretation Data-driven approaches can be effective at identifying unusual clinical choices. More widespread adoption of such approaches, combined with clinician and decision-maker engagement could lead to better optimised patient care. Funding NIHR Biomedical Research Centre, Oxford; Health Foundation; National Institute for Health Research (NIHR) School of Primary Care Research and Research for Patient Benefit Research in context Evidence before this study Identifying variation in clinical activity typically employs a traditional approach whereby measures are prospectively defined, and adherence then assessed in data. We are aware of no prior work using data science techniques hypothesis-blind to systematically identify outliers for any given treatment choice or clinical outcome (numerators) as a proportion of automatically generated denominators. Added value of this study Here we report an innovative hypothesis-blind approach applied to England’s national prescribing data, to identify chemical substances with substantial prescribing patterns between organisations. As illustrative examples we show that promazine and pericyazine, while rarely used by most clinicians, made up a substantial proportion of all antipsychotic prescribing in two small geographic regions in England. Implications of all the available evidence The choice of antipsychotics between English regions could be further investigated using qualitative methods to explore the implications for patient care. More broadly, data-driven approaches can be effective at identifying unusual clinical choices. More widespread adoption of such approaches, combined with clinician and decision-maker engagement could lead to better optimised patient care.
Abstract licence: CC BY
J. Barker, Mabel Miller
British Journal of Psychiatry, 1969
- Chronic Disease
- Phenothiazines
- Thioridazine
T. W. H. Weir, G. A. Kernohan, D. N. Mackay
British Journal of Psychiatry, 1968
- Intellectual Disability
- Chlorpromazine
- Tranquilizing Agents
Hosam E Matar, Muhammad Qutayba Almerie, Samer Makhoul, et al.
Cochrane Database of Systematic Reviews, 2014
- Tremor
- Spasm
- Akathisia, Drug-Induced
R. Ionescu, S. U. Nica, L. Oproiu, et al.
Pharmacopsychiatry, 1973
- Dibenzazepines
- Phenothiazines
- Social Behavior
B. Tischler, K. Patriasz, J. Beresford, et al.
Canadian Medical Association journal, 1972
- Nitriles
- Piperidines
- Phenothiazines
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
90 found
Half-life
Not available
Mechanism
Pericyazine, like other phenothiazines, is presumed to act principally in the su…
Food interactions
2 warnings
Human targets
4 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 1249 interactions
Proteins and enzymes this drug interacts with in the body
PMID:19022849
Transcription factor activity is modulated by bound coactivator and corepressor proteins like ZBTB7A that recruits NCOR1 and NCOR2 to the androgen response elements/ARE on target genes, negatively regulating androgen receptor signaling and androgen-induced cell proliferation .
PMID:20812024
Transcription activation is also down-regulated by NR0B2. Activated, but not phosphorylated, by HIPK3 and ZIPK/DAPK3
ATC N05AC01
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Periciazine
Matched from: Pericyazine
Additional database identifiers
Drugs Product Database (DPD)
13098
ChemSpider
4585
BindingDB
50346422
ZINC
ZINC000000538159
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3020
GenAtlas
DRD1
GeneCards
DRD1
GenBank Gene Database
X55760
GenBank Protein Database
30397
Guide to Pharmacology
214
UniProt Accession
DRD1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:281
GenAtlas
ADRA2A
GeneCards
ADRA2A
GenBank Gene Database
M23533
GenBank Protein Database
178196
Guide to Pharmacology
25
UniProt Accession
ADA2A_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:278
GenAtlas
ADRA1B
GeneCards
ADRA1B
GenBank Gene Database
M99589
Guide to Pharmacology
23
UniProt Accession
ADA1B_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:644
GenAtlas
AR
GeneCards
AR
GenBank Gene Database
M20132
GenBank Protein Database
178628
Guide to Pharmacology
628
UniProt Accession
ANDR_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72