1,281 reports of this reaction
4.7% of all ACLIDINIUM BROMIDE reports
#2 most reported adverse reaction
DEVICE MALFUNCTION is the #2 most commonly reported adverse reaction for ACLIDINIUM BROMIDE, manufactured by Covis Pharma US, Inc. There are 1,281 FDA adverse event reports linking ACLIDINIUM BROMIDE to DEVICE MALFUNCTION. This represents approximately 4.7% of all 27,417 adverse event reports for this drug.
Patients taking ACLIDINIUM BROMIDE who experience device malfunction should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEVICE MALFUNCTION is moderately reported among ACLIDINIUM BROMIDE users, representing a notable but not dominant share of adverse events.
In addition to device malfunction, the following adverse reactions have been reported for ACLIDINIUM BROMIDE:
The following drugs have also been linked to device malfunction in FDA adverse event reports:
DEVICE MALFUNCTION has been reported as an adverse event in 1,281 FDA reports for ACLIDINIUM BROMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEVICE MALFUNCTION accounts for approximately 4.7% of all adverse event reports for ACLIDINIUM BROMIDE, making it one of the most commonly reported side effect.
If you experience device malfunction while taking ACLIDINIUM BROMIDE, 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.