DYSPNOEA is the #9 most commonly reported adverse reaction for RABEPRAZOLE SODIUM, manufactured by Waylis Therapeutics LLC. There are 1,159 FDA adverse event reports linking RABEPRAZOLE SODIUM to DYSPNOEA. This represents approximately 2.0% of all 58,263 adverse event reports for this drug.
Patients taking RABEPRAZOLE SODIUM 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
DYSPNOEA1,159 of 58,263 reports
DYSPNOEA is a less commonly reported adverse event for RABEPRAZOLE SODIUM, but still significant enough to appear in the safety profile.
Other Side Effects of RABEPRAZOLE SODIUM
In addition to dyspnoea, the following adverse reactions have been reported for RABEPRAZOLE SODIUM:
DYSPNOEA has been reported as an adverse event in 1,159 FDA reports for RABEPRAZOLE SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is DYSPNOEA with RABEPRAZOLE SODIUM?
DYSPNOEA accounts for approximately 2.0% of all adverse event reports for RABEPRAZOLE SODIUM, making it a notable side effect.
What should I do if I experience DYSPNOEA while taking RABEPRAZOLE SODIUM?
If you experience dyspnoea while taking RABEPRAZOLE SODIUM, 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.