MEDTRONIC Adverse Event — Other (MDR MW5005540)

Name: MEDTRONIC Adverse Event — Other (MDR MW5005540)
Creator: DeviceEvents

MEDTRONIC Adverse Event — Other (MDR MW5005540) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDTRONIC; Generic name: PARADIGM 715; Report number: MW5005540.

Device	MEDTRONIC
Generic name	PARADIGM 715
Report number	MW5005540
Event type	Other
Product problem	N
Date received	2008-02-18
Narrative	PATIENT PRESENTED TO CLINIC WITH MEDTRONIC PUMP, ORDERED BY HER PRIMARY CARE DOCTOR. PT HAD NO KNOWLEDGE OF: MULTIPLE DOSE INJECTION THERAPY, CARBOHYDRATE COUNTING, CHECKS BLOOD SUGARS 1-2 TIMES A DAY, DID NOT KNOW SIGNS/SYMPTOMS OF HYPOGLYCEMIA OR HOW TO TREAT HYPOGLYCEMIA. DID NOT KNOW HOW TO CORRECT HYPERGLYCEMIA.
Source	openFDA MAUDE (device adverse events)

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