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. 2019 May 20;13(5):e0007325. doi: 10.1371/journal.pntd.0007325

Table 2. Adverse events (AEs) following treatment with a single dose of IVM, DEC, and ALB.

Number of participants with AEs (percent)
Infected Uninfected
(n = 32) (n = 24)
At least one AE 32 (100) 24 (100)
Individuals with two or more AEs 30 (94) 20 (88)
Severe or Serious AEs 0 0
Fever ≥ 37.5°C§ 16 (50) 4 (17)
Hemodynamic changes 7 (22) 6 (25)
Hematuria 10 (31) 3 (13)
Overall Grade 1 AEs (subjective) 32 (100) 23 (96)
Overall Grade 2 AEs (subjective) 9 (28) 6 (25)
Subjective AEs by symptoms
    Headache 15 (47) 11 (46)
    Abdominal Pain 14 (44) 11 (46)
    Diarrhea 14 (44) 7 (29)
    Fatigue 10 (31) 6 (25)
    Muscle/Joint ache 10 (31) 4 (17)
    Lightheaded 3 (9) 7 (29)
    Scrotal pain/swelling* 6/20 (30) 0
    Itching 4 (13) 1 (4)
    Cough 2 (6) 3 (13)
    Swelling 3 (9) 1 (4)
    Back pain 1 (3) 3 (13)
    Rash 1 (3) 2 (8)
    Nausea/vomiting 0 1 (4)
    Other 4 (13) 0

§Temperature increased ≥0.9°C post-treatment relative to pre-treatment to at least 37.5°C based on auricular temperature

Systolic blood pressure decrease of 20mmHg and <100 or diastolic blood pressure decrease of 10mmHg and <50, P = 0.278

*P = 0.025

one person each with eye selling, lymph node swelling, insomnia and paresthesia