1 reports of this reaction
0.8% of all ECHINACEA ANGUSTIFOLIA reports
#18 most reported adverse reaction
ACUTE RESPIRATORY FAILURE is the #18 most commonly reported adverse reaction for ECHINACEA ANGUSTIFOLIA, manufactured by Boiron. There are 1 FDA adverse event reports linking ECHINACEA ANGUSTIFOLIA to ACUTE RESPIRATORY FAILURE. This represents approximately 0.8% of all 118 adverse event reports for this drug.
Patients taking ECHINACEA ANGUSTIFOLIA who experience acute respiratory failure should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ACUTE RESPIRATORY FAILURE is a less commonly reported adverse event for ECHINACEA ANGUSTIFOLIA, but still significant enough to appear in the safety profile.
In addition to acute respiratory failure, the following adverse reactions have been reported for ECHINACEA ANGUSTIFOLIA:
The following drugs have also been linked to acute respiratory failure in FDA adverse event reports:
ACUTE RESPIRATORY FAILURE has been reported as an adverse event in 1 FDA reports for ECHINACEA ANGUSTIFOLIA. This does not prove causation, but indicates an association observed in post-market surveillance data.
ACUTE RESPIRATORY FAILURE accounts for approximately 0.8% of all adverse event reports for ECHINACEA ANGUSTIFOLIA, making it a notable side effect.
If you experience acute respiratory failure while taking ECHINACEA ANGUSTIFOLIA, 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.