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The objectives of this survey was to retrospectively collect and evaluate the information on the efficacy and safety of PAXIL tablets ("PAXIL", hereinafter) in pediatric subjects (aged under 18) with panic disorder under conditions of actual use.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Subjects prescribed PAXIL | Pediatric subjects with panic disorder prescribed PAXIL during study period |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Paroxetine | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of adverse events in Japanese pediatric subjects with panic disorder treated with paroxetine tablet based on prescribing information under the conditions of general clinical practice | From the starting day of the treatment to the time of treatment termination/discontinuation was assessed from 1 month at minimum up to 2 years | |
| Efficacy evaluation based on overall improvement | From the starting day of the treatment to the time of treatment termination/discontinuation was assessed from 1 month at minimum up to 2 years |
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Inclusion Criteria:
Exclusion Criteria:
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Male and female Japanese subjects whose age is under 18 with panic disorder, who are considered appropriate to prescribe paroxetine tablet according to the prescribing information
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| Name | Affiliation | Role |
|---|---|---|
| GSK Clinical Trials | GlaxoSmithKline | Study Director |
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| ID | Term |
|---|---|
| D016584 | Panic Disorder |
| ID | Term |
|---|---|
| D001008 | Anxiety Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D017374 | Paroxetine |
| ID | Term |
|---|---|
| D010880 | Piperidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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