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. 2015 Jul 8;38(10):895–908. doi: 10.1007/s40264-015-0314-8

Table 1.

Subsets of the OMOP reference standard used in the three experiments

Reference Set 1
FAERS and NYP/CUMC EHR
Reference Set 2
FAERS and GE EHR
Reference Set 3
FAERS and claims data
P N P N P N
Acute renal failure 16 37 21 48 21 51
Acute liver injury 52 16 75 30 77 32
Acute myocardial infarction 10 28 33 51 33 58
Upper GI bleed 17 38 24 57 24 63
Total 95 119 153 186 155 204

EHR electronic health record, FAERS FDA Adverse Event Reporting System, GE EHR GE Healthcare MQIC (Medical Quality Improvement Consortium) database, N negative controls, NYP/CUMC New York Presbyterian Hospital at Columbia University Medical Center, OMOP Observational Medical Outcomes Partnership, P positive controls in the reference standard