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Trial · NCT01201798

Adverse events12

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherIridocyclitisEye disordersDurezol356
otherIridocyclitisEye disordersPred Forte254
otherPunctate keratitisEye disordersDurezol356
otherPunctate keratitisEye disordersPred Forte054
otherIntraocular Pressure IncreasedInvestigationsDurezol556
otherIntraocular Pressure IncreasedInvestigationsPred Forte254
otherHeadacheNervous system disordersDurezol356
otherHeadacheNervous system disordersPred Forte454
seriousNecrotising retinitisEye disordersDurezol156
seriousNecrotising retinitisEye disordersPred Forte054
seriousHypertensionVascular disordersDurezol156
seriousHypertensionVascular disordersPred Forte054

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01201798/events