Skip to main content

Table 2 Treatment-related adverse events

From: Long-term safety and effectiveness of a continuous erythropoietin receptor activator (CERA) in patients with renal anemia: a prospective, observational, multicenter study

 

Disease stage

ND (n = 1599)

HD (n = 1408)

PD (n = 336)

ADRs, n (%)

SADRs, n (%)

ADRs, n (%)

SADRs, n (%)

ADRs, n (%)

SADRs, n (%)

Any

49 (3.06)

21 (1.31)

59 (4.19)

35 (2.48)

15 (4.46)

6 (1.78)

Number of cases that had ≥ 2 ADRs

 Hypertension

15 (0.93)

0

16 (1.13)

1 (0.07)

5 (1.48)

0

 Increased BP

1 (0.06)

0

4 (0.28)

0

1 (0.29)

0

 IDA

4 (0.25)

0

3 (0.21)

0

0

0

 Anemia

2 (0.12)

2 (0.12)

10 (0.71)

10 (0.71)

2 (0.59)

2 (0.59)

 Cerebral infarction

1 (0.06)

1 (0.06)

4 (0.28)

4 (0.28)

0

0

 Shunt occlusion

1 (0.06)

1 (0.06)

5 (0.35)

5 (0.35)

0

0

 Cerebral hemorrhage

0

0

2 (0.14)

2 (0.14)

0

0

 Subdural hematoma

2 (0.12)

2 (0.12)

0

0

0

0

 Diabetic nephropathy

2 (0.12)

2 (0.12)

0

0

0

0

 Increased Hb

2 (0.12)

0

0

0

0

0

 Decreased platelets

2 (0.12)

0

1 (0.07)

1 (0.07)

0

0

 Decreased appetite

0

0

2 (0.14)

2 (0.14)

0

0

  1. ADRs adverse drug reactions, BP blood pressure, Hb hemoglobin, HD hemodialysis, IDA iron deficiency anemia, ND not on dialysis, PD peritoneal dialysis, SADRs serious adverse drug reactions