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Table 2 Number of participants in each AZD0530 treatment group experiencing an adverse event

From: A phase Ib multiple ascending dose study of the safety, tolerability, and central nervous system availability of AZD0530 (saracatinib) in Alzheimer’s disease

 

Treatment group (AZD0539 dose; n = 6 per group)

 

Adverse event

Placebo

50 mg

100 mg

125 mg

Total

Any adverse event*

3

4

5

4

16

Diarrhea

2

0

1

2

5

Headache

2

1

1

1

5

Fatigue

1

0

0

2

3

Nausea

2

0

0

1

3

Pneumonia, atypical/bronchitis

0

0

0

1

1

Congestive heart failure

0

0

0

1

1

Renal insufficiency, worsened

0

0

0

1

1

Elevated serum creatinine

0

0

0

1

1

Cough, worsened

0

0

0

1

1

Postnasal drip

0

0

0

1

1

Pulmonary hypertension

0

0

0

1

1

Anorexia

0

0

0

1

1

Tinnitus

0

0

0

1

1

Myalgias

0

0

0

1

1

Squamous cell carcinoma

0

0

1

0

1

Basal cell carcinoma

0

0

1

0

1

Wrist pain

0

0

1

0

1

Noncardiac chest pain

0

0

1

0

1

Upper respiratory infection

0

1

0

0

1

Flu-like symptoms

0

1

0

0

1

Lightheadedness

0

1

0

0

1

Vomiting

1

0

0

0

1

  1. *Includes participants who reported at least one adverse event. The effect of treatment group is not significant for any adverse event or individual adverse events (Fisher’s exact test, P > 0.05).