| Subject: | FDA Issues Safety Information on Interference With Blood Glucose Measurement Following Use of Parenteral Maltose/Parenteral Galactose/Oral Xylose-Containing Products |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 11 Nov 2005 - 11:43 am |
| The FDA has issued safety information about the potential for life-threatening falsely elevated glucose readings in patients who have received parenteral products containing maltose or galactose, or oral xylose, and are subsequently tested using glucose dehydrogenase pyrroloquinolinequinone, GDH-PQQ, based glucose monitoring systems.
The GDH-PQQ method of glucose determination is non-specific for glucose and, in the presence of maltose, xylose, or galactose, may yield falsely elevated glucose... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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