Comparison · NCT00962104-sae
Atomoxetine vs Placebo: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Atomoxetine vs Placebo: serious adverse events. Trial comparisons, record NCT00962104-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00962104-sae
On this page
Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.00518 | 0.000915 | 0.0288 | wilson | |
| Risk in group 2 | 0.0103 | 0.00282 | 0.0366 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00508 | -0.0318 | 0.0197 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.505 | 0.0462 | 5.53 | log | |
| Odds ratio, group 1 over group 2 | 0.503 | 0.0452 | 5.59 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Atomoxetine than on Placebo | 197 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Atomoxetine | Treatment was started at 40 milligrams (mg) taken by mouth, once daily. The treatment period was 10 weeks, during which the dosage was up-titrated to a maximum of 120 mg by mouth, once daily. | 1 | 193 | EG000 |
| Group 2 | Placebo | Taken by mouth, once daily for 10 weeks. | 2 | 195 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Source ClinicalTrials.gov
Trial
- Title
- Atomoxetine to Treat Asian Adult Patients With Attention-Deficit/Hyperactivity Disorder
- NCT number
- NCT00962104
- Phases
- PHASE3
- Conditions
- Attention Deficit Hyperactivity Disorder
- Interventions
- Atomoxetine, Placebo
- Lead sponsor
- Eli Lilly and Company
- Results first posted
- 2012-09-11
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00962104?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
For software
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT00962104-sae