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Drug Use Investigation for PAXIL Tablet

Drug Use Investigation for PAXIL Tablet

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01371435
Enrollment
3708
Registered
2011-06-10
Start date
2001-04-30
Completion date
2005-12-31
Last updated
2017-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Disorders

Brief summary

This post-marketing surveillance study is designed to detect adverse events (particularly clinically significant adverse drug reactions) occurring in clinical settings and to examine factors likely to affect the safety and efficacy of paroxetine.

Interventions

DRUGParoxetine

Sponsors

GlaxoSmithKline
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* Patients with depression/depressed state or panic disorder

Exclusion criteria

* Patients who had been taking PAXIL since before the start of the survey * Patients with hypersensitivity to paroxetine * Patients taking monoamine oxidase inhibitors (MAOIs) or within 2 weeks of stopping treatment with MAOIs * Concomitant use in patients taking pimozide

Design outcomes

Primary

MeasureTime frameDescription
Incidence of adverse events in Japanese subjects treated with paroxetine tablet based on prescribing information under the conditions of general clinical practice8 weeks
Presence/absence of concomitant use of drugs metabolized by CYP2D6Within 2 weeks after discontinuation or completion of treatmentPAXIL inhibits drug-metabolizing enzyme CYP2D6, and it takes about 1 week following discontinuation of PAXIL for this CYP2D6 function to recover from the inhibiting effect. Since it requires attention if drugs that are metabolized by CYP2D6 are administered during this recovery period, it was decided to investigate the presence/absence of use of drugs metabolized by CYP2D6 within 2 weeks after discontinuation of treatment in patients for whom treatment with PAXIL was discontinued, as well as the safety thereof.
Presence/absence of concomitant use of products containing Saint John's Wort (Hypericum perforatum; SJW, hereinafter)8 weeksAlthough the action mechanism for this is not clear, SJW has been reported to have the action of inhibiting reuptake of serotonin, noradrenaline and dopamine, and to exhibit an antidepressant effect. Since PAXIL also acts to inhibit serotonin reuptake, concomitant use of products containing SJW is thought to have an effect upon the serotonin reuptake inhibiting action of PAXIL, so it was decided to check for concomitant use of products containing SJW and investigate the safety of such concomitant use.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026