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Table 1 Two-by-two contingency table for disproportionality analysis

From: Risk comparison of adverse reactions between gemcitabine monotherapy and gemcitabine combined with albumin-bound paclitaxel in pancreatic cancer: insights from the FDA Adverse Event Reporting System (FAERS) database

Drug

Target AEs

Other AEs

Total

Gemcitabine combined with albumin-bound paclitaxel

a

b

a + b

Gemcitabine

c

d

c + d

Total

a + c

b + d

a + b + c + d

  1. Abbreviation AEs, adverse events; a, number of reports containing both the gemcitabine combined with albumin-bound paclitaxel and target adverse drug reaction; b, number of reports containing other adverse drug reaction of the gemcitabine combined with albumin-bound paclitaxel; c, number of reports containing the target adverse drug reaction of gemcitabine; d, number of reports containing other adverse drug reactions of gemcitabine