Skip to main content
. 2019 Jul 5;6(8):1383–1394. doi: 10.1002/acn3.50820

Table 2.

Adverse events occurring in HAM/TSP patients during HuMikβ1 trial.

Group Adverse event Grade Number of events
0.5mg pruritus 1 1
  flu‐like syndrome 1 1
  hypotension 1 1
  hypokalemia 1 1
  tachycardia 1 1
  fever 1 1
  palpitation 1 1
  diarrhea 1 1
  infection 2 1
  decubitus ulcer 2 1
  limb edema 2 1
  substernal pain 2 1
  rash/desquamation 1 2 1
  thrombosis 1 3 2
1.0mg headache, chills, fatigue 1 1
  flu‐like symptoms 1 2
  paresthesias 1 1
  herpes labialis 1 1
  prolonged QTCB on EKG 1 1
  rash 1 1
  tooth abscess 2 1
  infection/UTI 2 1
  elevated ALT 2 1
  shoulder pain 3 1
  thrombosis 3 1
1.5 mg bradycardia 1 1
  low b12 1 1
  elevated RSVP on echo 1 1
  contact dermatitis 1 1
  anemia 1 1
  vaginal spotting 1 1
  lymphopenia 1 1
  lymphopenia 2 1
  elevated troponin 2 1
  elevated troponin 2 1
  post dural puncture headache 4 1
1

Post study