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Table 1 Analysis of All Drug-Related and Post-Therapy Adverse Events

From: Assessment of safety and tolerability of remogliflozin etabonate (GSK189075) when administered with total daily dose of 2000 mg of metformin

Adverse Event

Placebo + Metformin

(N = 17)

RE 500 mg + Metformin

(N = 16)

RE 750 mg + Metformin

(N = 17)

All Adverse Event (AE) N(%)

 Any AE

3 (18%)

6 (38%)

4 (24%)

 Diarrhoea

1 (6%)

3a (19%)

1 (6%)

 Nausea

1a (6%)

1 (6%)

1 (6%)

 Thirst

1 (6%)

0

1a (6%)

 Vomiting

0

1a (6%)

1 (6%)

 Dizziness

0

1 (6%)

1 (6%)

 Supraventricular tachycardia

0

1a (6%)

0

 Urinary tract infection

1b (6%)

 

0

 Dyslipidemia

0

1b (6%)

0

  1. AE Adverse event, RE Remogliflozinetabonate a determined to be drug related adverse event, one of 3 events of diarrhoea with RE 500 mg + Met determined to be drug related, b post therapy adverse events occurred after last dose