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Comparison · NCT00981045-sae

Ferric Carboxymaltose (FCM) vs Iron Sucrose (Venofer): 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. Ferric Carboxymaltose (FCM) vs Iron Sucrose (Venofer): serious adverse events. Trial comparisons, record NCT00981045-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00981045-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 10.1580.1390.179wilson
Risk in group 20.1530.1350.174wilson
Risk difference, group 1 minus group 20.005-0.02310.0331newcombe hybrid score
Risk ratio, group 1 over group 21.030.8621.24log
Odds ratio, group 1 over group 21.040.8391.29log
Number needed to harm, for one more participant with a serious adverse event on Ferric Carboxymaltose (FCM) than on Iron Sucrose (Venofer)200from 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 1Ferric Carboxymaltose (FCM)Ferric Carboxymaltose (FCM) : 2 doses at 15 mg/kg to a maximum 750 mg per dose for a total maximum cumulative dose of 1500 mg2021,276EG000
Group 2Iron Sucrose (Venofer)Iron Sucrose (Venofer) : 5 doses of 200 mg for a total cumulative dose of 1000 mg1971,285EG001

Harm

What it counts
Total, serious adverse events
Time frame
September 4, 2009 through June 15, 2011

Source ClinicalTrials.gov

Trial

Title
Evaluation of Efficacy and Safety of Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia and Impaired Renal Function
NCT number
NCT00981045
Phases
PHASE3
Conditions
Iron Deficiency Anemia, Impaired Renal Function
Interventions
Ferric Carboxymaltose (FCM), Iron Sucrose (Venofer)
Lead sponsor
American Regent, Inc.
Results first posted
2013-10-18

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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