DYSPNOEA is the #4 most commonly reported adverse reaction for Xarelto, manufactured by Janssen Pharmaceuticals, Inc.. There are 7,247 FDA adverse event reports linking Xarelto to DYSPNOEA. This represents approximately 2.4% of all 302,183 adverse event reports for this drug.
Patients taking Xarelto 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
DYSPNOEA7,247 of 302,183 reports
DYSPNOEA is a less commonly reported adverse event for Xarelto, but still significant enough to appear in the safety profile.
Other Side Effects of Xarelto
In addition to dyspnoea, the following adverse reactions have been reported for Xarelto:
DYSPNOEA has been reported as an adverse event in 7,247 FDA reports for Xarelto. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is DYSPNOEA with Xarelto?
DYSPNOEA accounts for approximately 2.4% of all adverse event reports for Xarelto, making it a notable side effect.
What should I do if I experience DYSPNOEA while taking Xarelto?
If you experience dyspnoea while taking Xarelto, 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.