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Table 1 Basic characteristics of included systematic reviews on adverse events

From: Utilization of the evidence from studies with no events in meta-analyses of adverse events: an empirical investigation

Basic characteristics

No. of systematic reviews (N = 640)

Year

 2008–2011

184 (28.75%)

 2015–2020

456 (71.25%)

Region of corresponding author

 Africa

15 (2.34%)

 America (North and South)

193 (30.16%)

 Asia

193 (30.16%)

 European

219 (34.22%)

 Oceania

20 (3.13%)

Intervention

 Drug

483 (75.47%)

 Surgery or device

108 (16.88%)

 Others (e.g., complementary medicine)

49 (7.66%)

Type of meta-analysis

 Pairwise meta-analysis

585 (91.41%)

 Network meta-analysis

17 (2.66%)

 Both pairwise and network meta-analyses

32 (5.0%)

 Association

2 (0.31%)

 Individual participant data

4 (0.63%)

Protocol

 Yes

166 (25.94%)

 No

474 (74.06%)

Type of study for meta-analysis

 Randomized controlled trial (RCT)

460 (71.88%)

 Non-randomized study of intervention (NRSI)

89 (13.91%)

 Both RCT and NRSI

87 (13.59%)

 Not reported

4 (0.63%)

Effect estimator

 Odds ratio, including Peto’s OR

266 (41.56%)

 Risk ratio or relative risk

316 (49.38%)

 Hazard ratio

9 (1.41%)

 Risk difference

15 (2.34%)

 Others (e.g., mixed use, Chi2, coef.)

34 (5.31%)

Systematic review with zero-events studies in meta-analysis

 Yes

406 (63.45%)

 No

88 (13.75%)

 No data available for judgment

146 (22.80%)

Power analysis

 Yes

16 (2.50%)

 No

624 (97.5%)