Skip to main content

Table 5 Characteristics of adverse drug events (N = 148)

From: Improving patient self-reporting of antihypertensive adverse drug events in primary care: a stepped wedge cluster randomised trial

 

Control

(N = 65)

Intervention

(N = 83)

ADEs reported by the patient and/or his GPa

 ADE reported by GPs only, % (n)

20.0 (13)

16.8 (14)

 ADE reported by patients only, % (n)

52.3 (34)

68.7 (57)

 ADE reported by GPs and patients, % (n)

27.7 (18)

14.5 (12)

 ADE total, % (n)

100.0 (65)

100.0 (83)

Symptomsb

 Dizziness or light-headedness or Syncope (fainting) or vertigo, % (n)

30.8 (20)

12.1 (10)

 Fatigue or asthenia or drowsiness, % (n)

23.1 (15)

15.7 (13)

 Leg oedema, % (n)

15.4 (10)

12.1 (10)

 Abdominal discomfort or diarrhoea or gastric irritation (upset stomach) or abdominal pain or nausea or vomiting or dyspepsia, % (n)

15.4 (10)

9.7 (8)

 Restlessness or nervousness or anxiety or depression, % (n)

13.9 (9)

9.6 (8)

 Respiratory disorder, % (n)

9.2 (6)

14.5 (12)

 Myalgia (muscle pain) or muscle spasm, % (n)

7.7 (5)

7.2 (6)

 Skin rashes, % (n)

3.1 (2)

9.6 (8)

 Other symptoms, % (n)

44.7 (29)

38.6 (32)

 Symptoms total, % (n)

100.0 (100)

100.0 (107)

  1. a ADEs reported by GPs in the study online form but not reported by patients to the research assistant (GPs only), ADEs reported by patients to the research assistant but not by the GPs in the online form (Patients only) and ADEs reported both by the GPs and by their patients
  2. b One or more symptoms could be described for one AD. ADE adverse drug event