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Table 5 Adverse events leading to discontinuations of T2D study medication at 1-year ± 2-months of treatment (Full Analysis Set)

From: Real-world characteristics, modern antidiabetic treatment patterns, and comorbidities of patients with type 2 diabetes in central and Eastern Europe: retrospective cross-sectional and longitudinal evaluations in the CORDIALLY® study

AE leading to discontinuation, n (%)

Empagliflozin (N = 1697)

GLP-1 RA (N = 332)

Other SGLT2i (N = 536)

Total (N = 3618)

Total AEs

32 (1.89)

3 (0.90)

8 (1.49)

43 (1.19)

Gastrointestinal AEs

 Nausea

1 (0.06)

2 (0.60)

 

3 (0.08)

 Dyspepsia

2 (0.12)

  

2 (0.06)

 Vomiting

2 (0.12)

  

2 (0.06)

 Abdominal pain

3 (0.18)

  

3 (0.08)

 Other

 

1 (0.30)

 

1 (0.03)

Genitourinary infections

 Vaginal moniliasis

  

1 (0.19)

1 (0.03)

 Vulvovaginitis

4 (0.24)

 

1 (0.19)

5 (0.14)

 Balanitis and other genital infections

6 (0.35)

 

1 (0.19)

7 (0.19)

 Urinary tract infection (including pyelonephritis and urosepsis)

4 (0.24)

 

1 (0.19)

5 (0.14)

Renal AEs

 Glomerular filtration rate decreased

1 (0.06)

  

1 (0.03)

Urinary AEs

 Increased urination

3 (0.18)

 

1 (0.19)

4 (0.11)

 Dysuria

9 (0.53)

 

2 (0.37)

11 (0.30)

 Other

1 (0.06)

 

1 (0.19)

2 (0.06)

Metabolic AEs

 Thirst

1 (0.06)

  

1 (0.03)

Cardiovascular AEs

 Cerebrovascular event

1 (0.06)

  

1 (0.03)

  1. AE adverse event, DPP4i dipeptidyl peptidase-4 inhibitor, GLP-1 RA glucagon-like peptide-1 receptor agonist, SGLT2i sodium-glucose cotransporter-2 inhibitor