Does DULOXETINE\REPAGLINIDE\TICAGRELOR Cause Hypoglycaemia? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Hypoglycaemia have been filed in association with DULOXETINE\REPAGLINIDE\TICAGRELOR. This represents 35.0% of all adverse event reports for DULOXETINE\REPAGLINIDE\TICAGRELOR.
7
Reports of Hypoglycaemia with DULOXETINE\REPAGLINIDE\TICAGRELOR
35.0%
of all DULOXETINE\REPAGLINIDE\TICAGRELOR reports
3
Deaths
0
Hospitalizations
How Dangerous Is Hypoglycaemia From DULOXETINE\REPAGLINIDE\TICAGRELOR?
Of the 7 reports, 3 (42.9%) resulted in death, and 3 (42.9%) were considered life-threatening.
Is Hypoglycaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULOXETINE\REPAGLINIDE\TICAGRELOR. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does DULOXETINE\REPAGLINIDE\TICAGRELOR Cause?
What Other Drugs Cause Hypoglycaemia?
METFORMIN (5,047)
INSULIN GLARGINE (4,212)
INSULIN LISPRO (2,141)
INSULIN ASPART (1,647)
GLIMEPIRIDE (1,403)
INSULIN HUMAN (1,350)
INSULIN DEGLUDEC (762)
GLICLAZIDE (756)
ACETAMINOPHEN (684)
SITAGLIPTIN (674)