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Quetiapine: Difference between revisions

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Dedupe migration per interface-claude 2026-05-20: Antipsychotics / Neuroleptics merged into canonical Neuroleptics. Member retagged.
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[[Category:Antipsychotics / Neuroleptics]]
[[Category:Second-Generation Antipsychotics (SGAs / Atypicals)]]
[[Category:Second-Generation Antipsychotics (SGAs / Atypicals)]]
[[Category:Neuroleptics]]
[[Category:Neuroleptics]]

Revision as of 18:00, 19 May 2026

Antipsychotic, Neuroleptic
Quetiapine
Seroquel

Experience

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Problems

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Titration strategies

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Effects

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Interactions

Pharmacogenomic + mechanism interactions2 edges
Pharmacogenomic guideline recommendationsCPIC and Dutch Pharmacogenetics Working Group clinical guidelines
Phenotype:CYP3A4 poor metabolizer prefer alternative DPWG 60 / 100
DPWG guideline: Patients who are CYP3A4 poor metabolizers and being treated for depression should be given an alternative drug. Patients being treated for other indications and who are CYP3A4 poor metabolizers should be given a reduced dose of quetiapine. No action is needed for patients who are CYP3A4 intermediate metabolizers. ClinPGx uses CYP3A4 allele nomenclature as defined by PharmVar , while the current version of this guideline issued by the DPWG uses retired allele names. Further details are given on the DPWG curation page .
Phenotype:CYP3A4 intermediate metabolizer prefer alternative DPWG 60 / 100
DPWG guideline: Patients who are CYP3A4 poor metabolizers and being treated for depression should be given an alternative drug. Patients being treated for other indications and who are CYP3A4 poor metabolizers should be given a reduced dose of quetiapine. No action is needed for patients who are CYP3A4 intermediate metabolizers. ClinPGx uses CYP3A4 allele nomenclature as defined by PharmVar , while the current version of this guideline issued by the DPWG uses retired allele names. Further details are given on the DPWG curation page .

Patient experience

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Relevant Literature

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Summary
Classes
Antipsychotic, Neuroleptic
Common uses
+ 2 more uses →
Pharmacy
Pharmacology
Purported mechanism
D2/5-HT2A antagonist; strong H1 antagonist