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Table 4 Font trial: serious adverse events

From: Efficacy of galactose and adalimumab in patients with resistant focal segmental glomerulosclerosis: report of the font clinical trial group

Event

Adalimumab (N = 7)

Galactose (N = 7)

Standard Therapy (N = 7)

 

N PTs with events

% Rand PTs

N Events

N PTs with events

% Rand PTs

N events

N PTs with events

% Rand PTs

N events

Fatal

0

0

0

0

0

0

0

0

0

Immediate Life Threatening

0

0

0

0

0

0

0

0

0

Required Hospitalization

3

42.9

32

1

14.3

9

1

14.3

1

Prolonged Existing Hospitalization

0

0

0

0

0

0

0

0

0

Persistent or Significant Disability/Incapacity

0

0

0

1

14.3

1

0

0

0

Congenital Anomaly / Birth Defect

1

14.3

1

1

14.3

1

0

0

0

Causes Cancer

0

0

0

0

0

0

0

0

0

Overdose of Study Medication

0

0

0

0

0

0

0

0

0

  1. This Table summarizes the serious adverse events that occurred throughout the study period from screening through to the end of the 6 month observation period after the completion of the experimental therapy