10,174 reports of this reaction
1.5% of all ALBUTEROL SULFATE reports
#15 most reported adverse reaction
DEVICE DELIVERY SYSTEM ISSUE is the #15 most commonly reported adverse reaction for ALBUTEROL SULFATE, manufactured by Aurobindo Pharma Limited. There are 10,174 FDA adverse event reports linking ALBUTEROL SULFATE to DEVICE DELIVERY SYSTEM ISSUE. This represents approximately 1.5% of all 683,072 adverse event reports for this drug.
Patients taking ALBUTEROL SULFATE who experience device delivery system issue 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 DELIVERY SYSTEM ISSUE is a less commonly reported adverse event for ALBUTEROL SULFATE, but still significant enough to appear in the safety profile.
In addition to device delivery system issue, the following adverse reactions have been reported for ALBUTEROL SULFATE:
The following drugs have also been linked to device delivery system issue in FDA adverse event reports:
DEVICE DELIVERY SYSTEM ISSUE has been reported as an adverse event in 10,174 FDA reports for ALBUTEROL SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEVICE DELIVERY SYSTEM ISSUE accounts for approximately 1.5% of all adverse event reports for ALBUTEROL SULFATE, making it a notable side effect.
If you experience device delivery system issue while taking ALBUTEROL SULFATE, 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.