14 reports of this reaction
1.8% of all ARNICA MONTANA reports
#11 most reported adverse reaction
DYSPNOEA is the #11 most commonly reported adverse reaction for ARNICA MONTANA, manufactured by Laboratoires Boiron. There are 14 FDA adverse event reports linking ARNICA MONTANA to DYSPNOEA. This represents approximately 1.8% of all 789 adverse event reports for this drug.
Patients taking ARNICA MONTANA 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.
DYSPNOEA is a less commonly reported adverse event for ARNICA MONTANA, but still significant enough to appear in the safety profile.
In addition to dyspnoea, the following adverse reactions have been reported for ARNICA MONTANA:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 14 FDA reports for ARNICA MONTANA. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 1.8% of all adverse event reports for ARNICA MONTANA, making it a notable side effect.
If you experience dyspnoea while taking ARNICA MONTANA, 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.