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Table 1

From: Adverse event reporting in randomised trials of neuropathic pain: challenges for clinical usefulness of safety data

  All (N=53) n (%) Post-2004 (N=12) n (%)
Reported total number who withdrew & withdrew due to AE 48 (91) 12 (100%)
Reported that grading for AEs were assigned 30 (57) 9 (75)
Reported mode of collection (e.g. questionnaire, patient reported, observation) 23 (43) 5 (42)
Distinction between severe/life threatening AEs and those that were not. 29 (55) 11 (92)
Reported the dictionary used for coding AEs 1 (1.9) 0 (0.0)