A Health Economic Trial in Adult Patients Undergoing Ileostomy Reversal MA402S23B504

Exclusion Criteria

• •Patients with a history of hypersensitivity or idiosyncratic reactions or intolerance to any local anesthetic, opioid, or propofol.
• •Patients who abuse alcohol or other drug substance.
• •Patients with severe hepatic impairment.
• •Patients currently pregnant or who may become pregnant during the course of the study or who are unwilling to use acceptable means of contraception for at lest one month before and one month after dosing.
• •Patients with any psychiatric, psychological, or other condition that the Investigator feels may make the patient an inappropriate candidate for this clinical study.
• •Patients who have participated in an EXPAREL study within the last 30 days.
• •Patients who have received an investigational drug within 30 days prior to study drug administration, or planned administration of another investigational product or procedure during the patient's participation in this study.