Dexcom G4 Professional User Manual Download Page 3

Dexcom G4 PLATINUM User’s Guide 

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CHAPTER 2:  INDICATIONS FOR USE AND 
SAFETY STATEMENT

2.1  INDICATIONS FOR USE

The Dexcom G4 PLATINUM Continuous Glucose Monitoring 
System is a glucose monitoring device indicated for 
detecting trends and tracking patterns in persons 

(age 18 

and older)

 with diabetes. The system is intended for single 

patient use and requires a prescription.

The Dexcom G4 PLATINUM System is indicated for use as 
an adjunctive device to complement, not replace, information 
obtained from standard home glucose monitoring devices.

The Dexcom G4 PLATINUM System aids in the detection 
of episodes of hyperglycemia and hypoglycemia, facilitating 
both acute and long-term therapy adjustments, which may 
minimize these excursions. Interpretation of the Dexcom G4 
PLATINUM System results should be based on the trends 
and patterns seen with several sequential readings over 
time.

2.2  IMPORTANT USER INFORMATION

Please review your product instructions before using your 
continuous glucose monitoring system. Contraindications, 
warnings, precautions, cautions, and other important user 
information can be found in your product instructions. 
Discuss with your healthcare professional how you should 
use your sensor trend information to help manage your 
diabetes. Your product instructions contain important 
information on troubleshooting your system and on the 
performance characteristics of the device.

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  Dexcom G4 PLATINUM Continuous Glucose Monitoring System

2

2.3  CONTRAINDICATIONS

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and Receiver before Magnetic Resonance Imaging (MRI), 
Computed Tomography (CT) scan, or diathermy treatment. 
The Dexcom G4 PLATINUM System has not been tested 
during MRI or CT scans or with diathermy treatment. The 
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might not display sensor glucose readings or provide alerts, 
and you might miss a low or high blood glucose value.

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while wearing the sensor may falsely raise your sensor 
glucose readings. The level of inaccuracy depends on the 
amount of acetaminophen active in your body and may be 
different for each person.

2.4  WARNINGS

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with your CGM system before using the Dexcom G4 
PLATINUM CGM System. Incorrect use might lead to you 
misunderstanding the information provided by your system, 
or might affect system performance, and you might miss a 
low or high blood glucose value.

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treatment decisions, such as how much insulin you should 
take. The Dexcom G4 PLATINUM System does not replace 
a blood glucose meter. Always use the values from your 
blood glucose meter for treatment decisions. Blood glucose 
values may differ from sensor glucose readings. Using the 
sensor glucose readings for treatment decisions could lead 
to low or high blood glucose value.

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sensor glucose readings do not match your symptoms, 

Dexcom, 

Inc. 

P120005, 

180-Day 

Supplement

Volume 

Page 

219 
of 

309

Confidential. 

Do 
not 
disclose 

without 

written 

permission 

from 

Dexcom, 

Inc.

Summary of Contents for G4 Professional

Page 1: ...Between the Lines Dexcom Inc 6340 Sequence Drive San Diego CA 92121 USA 1 858 200 0200 1 877 339 2664 www dexcom com 3 LBL012514 Rev X01 MT21686 Dexcom Inc P120005 180 Day Supplement Volume 8 Page 20...

Page 2: ...2 INDICATIONS FOR USE AND SAFETY STATEMENT 18 Dexcom G4 PLATINUM Continuous Glucose Monitoring System 2 Dexcom Inc P120005 180 Day Supplement Volume 8 Page 218 of 309 Confidential Do not disclose with...

Page 3: ...on troubleshooting your system and on the performance characteristics of the device 20 Dexcom G4 PLATINUM Continuous Glucose Monitoring System 2 2 3 CONTRAINDICATIONS _ Z Z and Receiver before Magnet...

Page 4: ...ge The sensor should not be stored in a freezer Storing the sensor improperly might cause the sensor 22 Dexcom G4 PLATINUM Continuous Glucose Monitoring System 2 glucose readings to be inaccurate and...

Page 5: ...an obstruction they might not communicate or the communication distance may be shorter and you might miss a low or high blood glucose value the USB cable is not attached If water gets into the 24 Dex...

Page 6: ...chapter fourteen TECHNICAL INFORMATION...

Page 7: ...linical studies the Original Receiver Software Study SW10050 and the Software 505 Receiver Software Study SW10505 Differences between the studies include the number of subjects enrolled the number of...

Page 8: ...ays Day 1 Day 4 and Day 7 of the 7 day wear period In the Software 505 Study subjects were evaluated in one of the three clinic days so there are fewer data samples than in the Original Study While us...

Page 9: ...fter the YSI was collected The agreement of the System to blood glucose value was assessed by calculating the percentage of System readings that were within 15 20 30 and greater than 40 of the YSI val...

Page 10: ...ot display glucose values below 40 mg dL or above 400 mg dL the comparisons to the actual blood glucose levels as determined by the YSI analyzer when CGM is classified as LOW or HIGH are included sepa...

Page 11: ...umber of Paired CGM YSI 40 6 48 37 7 1 0 0 0 0 0 0 155 40 60 4 49 36 11 1 0 0 0 0 0 0 512 61 80 0 22 51 24 1 0 0 0 0 0 0 781 81 120 0 2 17 66 13 1 0 0 0 0 0 1706 121 160 0 0 1 25 60 13 2 0 0 0 0 1492...

Page 12: ...01 250 0 0 0 0 0 16 70 13 1 0 0 376 251 300 0 0 0 0 0 2 16 61 14 7 0 281 301 350 0 0 0 0 0 0 2 28 59 10 1 229 351 400 0 0 0 0 0 0 0 4 47 45 5 152 400 0 0 0 0 0 0 0 0 20 38 42 45 Concurrence of System...

Page 13: ...n absolute percent difference is the average distance regardless if positive or negative between System readings and YSI values Accuracy measures in differences for both the Original and Software 505...

Page 14: ...2 4 0 4 11 4 8 6 Software 505 226 0 8 1 4 6 7 5 4 81 180 Original 3853 4 8 3 0 13 8 9 8 Software 505 738 3 9 4 1 9 6 8 2 181 300 Original 2784 2 1 0 0 11 9 9 2 Software 505 798 0 6 0 4 8 0 6 1 301 35...

Page 15: ...e period before or after your alarm sounds Based on the Software 505 Study if your alarm sounds you can expect your blood sugar to be below 70 mg dL approximately 92 of the time and not be below 70 mg...

Page 16: ...Detection Rate 55 Original 50 50 71 29 Software 505 71 29 68 32 60 Original 64 36 75 25 Software 505 85 15 83 17 70 Original 79 21 83 17 Software 505 92 8 91 9 80 Original 87 13 86 14 Software 505 95...

Page 17: ...of the time within the 15 minute period before or after your alarm sounds Hyperglycemia Detection Rate The Detection Rate shows how often the device recognizes and alerts you to an episode of hypergl...

Page 18: ...ftware 505 98 2 100 0 140 Original 94 6 97 3 Software 505 97 3 99 1 180 Original 92 8 97 3 Software 505 97 3 99 1 200 Original 92 8 97 3 Software 505 96 4 98 2 220 Original 91 9 95 5 Software 505 94 6...

Page 19: ...1068 65 77 91 4 Software 505 295 80 90 98 0 12 14 hours Original 17 65 76 82 12 Software 505 0 1 CGM readings are within 40 to 400 mg dL inclusive 2 Both sets of study data are presented and are label...

Page 20: ...le The average and median of the absolute percent differences are included in Table 8 showing consistent accuracy and sensor stability over the 7 day life of the sensor Precision of System Readings In...

Page 21: ...100 100 100 100 100 STD Original 5 3 9 8 10 3 11 8 Software 505 3 2 8 11 15 2 13 9 1 Both sets of study data are presented and are labeled as Original SW10050 or Software 505 SW10505 2 A total of 108...

Page 22: ...rovided between 1 497 and 1 992 valid glucose readings or more than 75 of the expected number of readings Adjusted within each system wear day the Software 505 System provided an average of 98 of all...

Page 23: ...ood glucose values is also characterized using paired System and SMBG results The System and SMBG values were compared by pairing the comparative SMBG value to a System glucose reading that occurred i...

Page 24: ...00 mg dL inclusive 2 Both sets of study data are presented and are labeled as Original SW10050 or Software 505 SW10505 For CGM 80 mg dL the differences in mg dL are included instead of percent differe...

Page 25: ...an SMBG values Adverse Events No serious adverse events or device related serious adverse events occurred during either study Mild or very slight skin irritation such as erythema or edema occurred in...

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