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. Author manuscript; available in PMC: 2024 Mar 21.
Published in final edited form as: N Engl J Med. 2023 Jul 17;389(12):1096–1107. doi: 10.1056/NEJMoa2305032

Table 3.

Adverse Events.*

Event Solanezumab (N = 572) Placebo (N = 591)
number (percent)
Any adverse event 560 (97.9) 577 (97.6)
Adverse event definitely related to solanezumab or placebo 6 (1.0) 8 (14)
Serious adverse event 172 (30.1) 158 (26.7)
Death 6 (1.0) 7 (12)
Adverse event leading to discontinuation of solanezumab or placebo 28 (4.9) 34 (5.8)
ARIA 167 (29.2) 194 (32.8)
ARIA with edema 1 (02) 2 (0.3)
ARIA with microhemorrhage or hemosiderosis 167 (29.2) 194 (32.8)
Microhemorrhage 158 (27.6) 189 (32.0)
Superficial siderosis 19 (3.3) 19 (3.2)
*

Shown are adverse events that emerged or worsened after the first dose of solanezumab or placebo. ARIA denotes amyloid-related imaging abnormalities.

The relatedness of the adverse event to solanezumab or placebo was determined by the site investigator.