DYSPNOEA is the #9 most commonly reported adverse reaction for INSULIN HUMAN, manufactured by Eli Lilly and Company. There are 1,273 FDA adverse event reports linking INSULIN HUMAN to DYSPNOEA. This represents approximately 1.5% of all 82,903 adverse event reports for this drug.
Patients taking INSULIN HUMAN who experience dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
DYSPNOEA1,273 of 82,903 reports
DYSPNOEA is a less commonly reported adverse event for INSULIN HUMAN, but still significant enough to appear in the safety profile.
Other Side Effects of INSULIN HUMAN
In addition to dyspnoea, the following adverse reactions have been reported for INSULIN HUMAN:
DYSPNOEA has been reported as an adverse event in 1,273 FDA reports for INSULIN HUMAN. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is DYSPNOEA with INSULIN HUMAN?
DYSPNOEA accounts for approximately 1.5% of all adverse event reports for INSULIN HUMAN, making it a notable side effect.
What should I do if I experience DYSPNOEA while taking INSULIN HUMAN?
If you experience dyspnoea while taking INSULIN HUMAN, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.