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Fig. 1 | BMC Gastroenterology

Fig. 1

From: Transient alterations in plasma sodium concentrations with NER1006 bowel preparation: an analysis of three phase III, randomized clinical trials

Fig. 1

Patient populations. *All patients randomly assigned to treatment for whom patient diary data could not rule out that they received at least one dose of NER1006. Patients included in the safety population who had a normal sodium concentration at baseline and an increase from baseline to above the upper limit of normal (ULN) for sodium (143–148 mmol/L). Reported as an adverse event based on test results on the day of colonoscopy; medical intervention was not required, and sodium levels returned to normal range within 2 ± 1 days post-colonoscopy. DAYB Day Before Arm MORA Morning Arm NOCT Nocturnal Pause Arm

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