1,568 reports of this reaction
2.3% of all INSULIN DETEMIR reports
#3 most reported adverse reaction
BLOOD GLUCOSE DECREASED is the #3 most commonly reported adverse reaction for INSULIN DETEMIR, manufactured by Novo Nordisk. There are 1,568 FDA adverse event reports linking INSULIN DETEMIR to BLOOD GLUCOSE DECREASED. This represents approximately 2.3% of all 67,881 adverse event reports for this drug.
Patients taking INSULIN DETEMIR who experience blood glucose decreased should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BLOOD GLUCOSE DECREASED is a less commonly reported adverse event for INSULIN DETEMIR, but still significant enough to appear in the safety profile.
In addition to blood glucose decreased, the following adverse reactions have been reported for INSULIN DETEMIR:
The following drugs have also been linked to blood glucose decreased in FDA adverse event reports:
BLOOD GLUCOSE DECREASED has been reported as an adverse event in 1,568 FDA reports for INSULIN DETEMIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
BLOOD GLUCOSE DECREASED accounts for approximately 2.3% of all adverse event reports for INSULIN DETEMIR, making it one of the most commonly reported side effect.
If you experience blood glucose decreased while taking INSULIN DETEMIR, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.