DYSPNOEA is the #7 most commonly reported adverse reaction for GLATIRAMER ACETATE, manufactured by Teva Neuroscience, Inc.. There are 2,881 FDA adverse event reports linking GLATIRAMER ACETATE to DYSPNOEA. This represents approximately 2.7% of all 108,384 adverse event reports for this drug.
Patients taking GLATIRAMER ACETATE 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
DYSPNOEA2,881 of 108,384 reports
DYSPNOEA is a less commonly reported adverse event for GLATIRAMER ACETATE, but still significant enough to appear in the safety profile.
Other Side Effects of GLATIRAMER ACETATE
In addition to dyspnoea, the following adverse reactions have been reported for GLATIRAMER ACETATE:
DYSPNOEA has been reported as an adverse event in 2,881 FDA reports for GLATIRAMER ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is DYSPNOEA with GLATIRAMER ACETATE?
DYSPNOEA accounts for approximately 2.7% of all adverse event reports for GLATIRAMER ACETATE, making it a notable side effect.
What should I do if I experience DYSPNOEA while taking GLATIRAMER ACETATE?
If you experience dyspnoea while taking GLATIRAMER ACETATE, 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.