I have searched and searched and asked several people and can't seem to get a satisfactory answer. On my MAR for a specific patient who is on Reglan 10 mg four times daily for GERD it says it requires an AIMS assessment. I don't have any other patients who I have to do this on who take this medication, only this one in particular. Does anyone know why this might be? No one else seems to know and it's not a big deal but it's one of those things that is just driving me crazy because I don't understand. Thanks in advance!
What is an AIMS assessment's purpose?
What are the adverse side effects of Reglan?