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. 2019 Feb 15;16(2):e1002745. doi: 10.1371/journal.pmed.1002745

Table 3. Adverse events recorded within day 0 to day 3 after MDA using dihydroartemisinin-piperaquine.

Adverse event Month Day 0 Day 1 Day 2 Overall
Number taking drug Number of events Percent of events Number taking drug Number of events Percent of events Number taking drug Number of events Percent of events Number of doses taken Number of events Percent of events
Vomiting M0 6,866* 51 0.74% 6,769 26 0.38% 6,721 6 0.09%
M1 6,583 8 0.12% 6,454 11 0.17% 6,389 4 0.06% 59,375 121 0.20%
M2 6,583 12 0.18% 6,518 3 0.05% 6,492 0 0.00%
Dizziness M0 NA NA NA 4,690 176 3.75% 4,680 129 2.76%
M1 NA NA NA 4,285 87 2.03% 4,247 55 1.30% 26,898 586 2.18%
M2 NA NA NA 4,505 86 1.91% 4,491 53 1.18%
Itching M0 NA NA NA 4,690 3 0.06% 4,680 6 0.13%
M1 NA NA NA 4,285 0 0.00% 4,247 1 0.02% 26,898 12 0.04%
M2 NA NA NA 4,505 0 0.00% 4,491 2 0.04%

*The tolerability data included villages that had MDA but no follow-up (Cambodia and Lao People’s Democratic Republic after M12).

No recorded data from Vietnam for dizziness and itching; data from 1 deferred MDA village from Cambodia included.

M[number], month [number]; MDA, mass drug administration; NA, not applicable.