CT SCAN CONTRAST *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1996-10-17 for CT SCAN CONTRAST * manufactured by Unk.

Event Text Entries

[27833] Upon termination of an abdominal cat scan, the pt manifested hives without pruritus. 50 mg benadryl given iv with no further progression.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: MW1010082
• MDR Report Key: 43167
• Date Received: 1996-10-17
• Date of Report: 1995-05-15
• Date of Event: 1995-04-25
• Date Added to Maude: 1996-10-21
• Event Key: 0
• Report Source Code: Voluntary report
• Manufacturer Link: N
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 0
• Health Professional: 3
• Initial Report to FDA: 0
• Report to FDA: 0
• Event Location: 3
• Single Use: 0
• Previous Use Code: 0
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: CT SCAN CONTRAST
• Generic Name: COMPUTED CONTRAST MEDIA, TOMOGRAPHY
• Product Code: KTA
• Date Received: 1996-10-17
• Model Number: *
• Catalog Number: *
• Lot Number: *
• ID Number: *
• Operator: HEALTH PROFESSIONAL
• Device Availability: *
• Implant Flag: N
• Date Removed: *
• Device Sequence No: 1
• Device Event Key: 44138
• Manufacturer: UNK
• Manufacturer Address: * * *

Patients

Patient Number	Treatment	Outcome	Date
1	0		1996-10-17