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. 2021 Jul 19;38(8):4599–4601. doi: 10.1007/s12325-021-01813-8

Correction to: Safety and Effectiveness of Ipragliflozin for Type 2 Diabetes in Japan: 12-Month Interim Results of the STELLA-LONG TERM Post-Marketing Surveillance Study

Ichiro Nakamura 1,, Hiroshi Maegawa 2, Kazuyuki Tobe 3, Satoshi Uno 1
PMCID: PMC8496576  PMID: 34279807

Correction to: Adv Ther (2019) 36:923–949 10.1007/s12325-019-0895-1

In the original article, the Table 6 was published with some errors. The correct Table 6 is below.

Original

Table 6 Adverse drug reactions of special interest

STELLA-LONG TERM (safety analysis set n = 11,051) Pre-approval clinical trials
Total number of patients experiencing an ADR Serious Non-serious Total (n = 1669)
All ADRs 1616 (14.6) 107 (0.97) 1539 (13.9) (32.9)
ADRs of special interest
 Polyuria/pollakiuria 571 (5.2) 1 (0.01) 570 (5.2) (10.0)
 Volume depletion-related events, including dehydration 196 (1.8) 9 (0.08) 189 (1.7) (4.5)
 Skin complications 166 (1.5) 4 (0.04) 162 (1.5) (4.0)
 Genital infection 135 (1.2) 2 (0.02) 133 (1.2) (2.0)
 Urinary tract infection 115 (1.0) 5 (0.05) 110 (1.0) (1.8)
 Renal disorder 115 (1.0) 3 (0.03) 112 (1.0) (4.8)
 Hepatic disorder 82 (0.74) 6 (0.05) 78 (0.71) (1.0)
 Hypoglycemia 39 (0.35) 3 (0.03) 36 (0.33) (1.4)
 Cardiovascular diseasea 30 (0.27) 19 (0.17) 11 (0.10) (1.0)
 Cerebrovascular diseaseb 23 (0.21) 20 (0.18) 3 (0.03) (0.2)
 Malignant tumor 22 (0.20) 19 (0.17) 3 (0.03) (0.2)
 Ketoacidosis, events related to ketone-body increase 3 (0.03) 0 (0.00) 3 (0.03) (1.0)
 Fracture 2 (0.02) 1 (0.01) 1 (0.01) 0

Data are presented as number of events (%), unless otherwise indicated

ADR adverse drug reaction

aIncidence of cardiovascular disease was 4.4/1000 person-years [34] and 9.59/1000 person-years [35] in the JDDM and JDCS studies, respectively

bIncidence of cerebrovascular disease was 3.1/1000 person-years [34] and 7.45/1000 person-years [35] in the JDDM and JDCS studies, respectively

Corrected

Table 6 Adverse drug reactions of special interest

STELLA-LONG TERM (safety analysis set n = 11,051) Pre-approval clinical trials
Total number of patients experiencing an ADR Serious Non-serious Total (n = 1669)
All ADRs 1616 (14.6) 107 (0.97) 1539 (13.9) (32.9)
ADRs of special interest
 Polyuria/pollakiuria 571 (5.2) 1 (0.01) 570 (5.2) (10.0)
 Volume depletion-related events, including dehydration 196 (1.8) 9 (0.08) 189 (1.7) (4.5)
 Skin complications 166 (1.5) 4 (0.04) 162 (1.5) (3.5)
 Genital infection 135 (1.2) 2 (0.02) 133 (1.2) (2.0)
 Urinary tract infection 115 (1.0) 5 (0.05) 110 (1.0) (1.8)
 Renal disorder 115 (1.0) 3 (0.03) 112 (1.0) (4.6)
 Hepatic disorder 82 (0.74) 6 (0.05) 78 (0.71) (1.0)
 Hypoglycemia 39 (0.35) 3 (0.03) 36 (0.33) (1.4)
 Cardiovascular diseasea 30 (0.27) 19 (0.17) 11 (0.10) (1.0)
 Cerebrovascular diseaseb 23 (0.21) 20 (0.18) 3 (0.03) (0.2)
 Malignant tumor 22 (0.20) 19 (0.17) 3 (0.03) (0.2)
 Ketoacidosis, events related to ketone-body increase 3 (0.03) 0 (0.00) 3 (0.03) (0.7)
 Fracture 2 (0.02) 1 (0.01) 1 (0.01) 0

Data are presented as number of events (%), unless otherwise indicated

ADR adverse drug reaction

aIncidence of cardiovascular disease was 4.4/1000 person-years [34] and 9.59/1000 person-years [35] in the JDDM and JDCS studies, respectively

bIncidence of cerebrovascular disease was 3.1/1000 person-years [34] and 7.45/1000 person-years [35] in the JDDM and JDCS studies, respectively


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