FDA Adverse Event Injury Summary report: N

INRATIO

MDR report key: 2071740 · Received April 13, 2011

Report

Report Number
2027969-2011-00889
Event Type
Injury
Date Received
April 13, 2011
Date of Event
March 8, 2011
Report Date
April 21, 2011
Manufacturer
ALERE SAN DIEGO, INC.
Product Code
GJS
PMA / PMN Number
K021923
Removal / Correction Number
NI
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

PENDING INVESTIGATION.

Description of Event or Problem · 1

CALLER ALLEGED IMPRECISION WITH INRATIO METER. ON THIS DAY, THE PATIENT STARTED A REGIMEN OF TWO STRONG ANTIBIOTICS; TRICLOCYCLIN AND METRONIDAZOLE. PATIENT'S THERAPEUTIC RANGE IS (2-3).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100071 247456

Patients

Seq Age Sex Outcome Treatment
1 NI Other