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Table 4 Frequency of the most common adverse events during the multiple dose study

From: Phase I randomized dose-ascending placebo-controlled trials of ferroquine - a candidate anti-malarial drug - in adults with asymptomatic Plasmodium falciparum infection

System organ class

Preferred term

Multiple Dose Study

  

Placebo

Ferroquine

  

(N = 7)

400 mg (N = 6)

600 mg (N = 6)

800 mg (N = 6)

1000 mg (N = 1)

Any class

Any TEAE

6 (86)

6 (100)

6 (100)

6 (100)

1 (100)

Gastrointestinal disorders

Any TEAE

4 (57)

3 (50)

4 (67)

5 (83)

1 (100)

 

Abdominal pain

3 (43)

1 (17)

1 (17)

2 (33)

1 (100)

 

Diarrhoea

0

0

0

2 (33)

0

 

Nausea

1 (14)

2 (33)

2 (33)

3 (50)

0

 

Toothache

1 (14)

1 (17)

0

2 (33)

0

 

Vomiting

0

1 (17)

2 (33)

1 (17)

1 (100)

system disorders

Any TEAE

1 (14)

1 (17)

3 (50)

1 (17)

0

 

Dizziness

0

0

1 (17)

0

0

 

Headache

1 (14)

1 (17)

2 (33)

1 (17)

0

  1. NOTE: N (%): count of patients (percentage per group); TEAE: treatment emergent adverse event