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Comparison · NCT00884117-sae

Participants Treated With Oseltamivir vs Participants Not Treated With Oseltamivir: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Participants Treated With Oseltamivir vs Participants Not Treated With Oseltamivir: serious adverse events. Trial comparisons, record NCT00884117-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00884117-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.009310.006260.0138wilson
Risk in group 20.005570.003110.00995wilson
Risk difference, group 1 minus group 20.00374-0.001590.00887newcombe hybrid score
Risk ratio, group 1 over group 21.670.8213.4log
Odds ratio, group 1 over group 21.680.823.43log
Number needed to harm, for one more participant with a serious adverse event on Participants Treated With Oseltamivir than on Participants Not Treated With Oseltamivir267from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Participants Treated With Oseltamivir
Otherwise healthy/non-immunocompromised adults and children with a positive diagnostic test of influenza and/or displaying symptoms suggestive of influenza-like illness were enrolled during Years 1 to 7 of the overall study. Participants receiving antiviral treatment with oseltamivir (according to local practice standards) were followed for up to 10 days after informed consent for virological surveillance and assessment of clinical outcomes.
242,578EG000
Group 2Participants Not Treated With Oseltamivir
Otherwise healthy/non-immunocompromised adults and children with a positive diagnostic test of influenza and/or displaying symptoms suggestive of influenza-like illness were enrolled during Years 1 to 7 of the overall study. Participants not receiving oseltamivir, including no treatment or other antiviral treatment, were followed for up to 10 days after informed consent for virological surveillance and assessment of clinical outcomes.
111,975EG001

Harm

What it counts
Total, serious adverse events
Time frame
From Baseline (Day 1) to Day 10; assessed on Days 1, 3, 6, 10

Source ClinicalTrials.gov

Trial

Title
Influenza Resistance Information Study
NCT number
NCT00884117
Phases
Conditions
Influenza
Interventions
Oseltamivir
Lead sponsor
Hoffmann-La Roche
Results first posted
2016-07-19

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.

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