520 reports of this reaction
2.9% of all UMECLIDINIUM reports
#5 most reported adverse reaction
WRONG TECHNIQUE IN DEVICE USAGE PROCESS is the #5 most commonly reported adverse reaction for UMECLIDINIUM, manufactured by GlaxoSmithKline LLC. There are 520 FDA adverse event reports linking UMECLIDINIUM to WRONG TECHNIQUE IN DEVICE USAGE PROCESS. This represents approximately 2.9% of all 18,218 adverse event reports for this drug.
Patients taking UMECLIDINIUM who experience wrong technique in device usage process should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
WRONG TECHNIQUE IN DEVICE USAGE PROCESS is a less commonly reported adverse event for UMECLIDINIUM, but still significant enough to appear in the safety profile.
In addition to wrong technique in device usage process, the following adverse reactions have been reported for UMECLIDINIUM:
The following drugs have also been linked to wrong technique in device usage process in FDA adverse event reports:
WRONG TECHNIQUE IN DEVICE USAGE PROCESS has been reported as an adverse event in 520 FDA reports for UMECLIDINIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
WRONG TECHNIQUE IN DEVICE USAGE PROCESS accounts for approximately 2.9% of all adverse event reports for UMECLIDINIUM, making it a notable side effect.
If you experience wrong technique in device usage process while taking UMECLIDINIUM, 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.