Does DEVICE Cause Blood creatinine increased? 140 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 140 reports of Blood creatinine increased have been filed in association with DEVICE. This represents 1.1% of all adverse event reports for DEVICE.
140
Reports of Blood creatinine increased with DEVICE
1.1%
of all DEVICE reports
6
Deaths
22
Hospitalizations
How Dangerous Is Blood creatinine increased From DEVICE?
Of the 140 reports, 6 (4.3%) resulted in death, 22 (15.7%) required hospitalization, and 2 (1.4%) were considered life-threatening.
Is Blood creatinine increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 140 reports have been filed with the FAERS database.