67 reports of this reaction
1.8% of all IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE reports
#9 most reported adverse reaction
DIZZINESS is the #9 most commonly reported adverse reaction for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE, manufactured by American Health Packaging. There are 67 FDA adverse event reports linking IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE to DIZZINESS. This represents approximately 1.8% of all 3,750 adverse event reports for this drug.
Patients taking IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE who experience dizziness should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIZZINESS is a less commonly reported adverse event for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE, but still significant enough to appear in the safety profile.
In addition to dizziness, the following adverse reactions have been reported for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE:
The following drugs have also been linked to dizziness in FDA adverse event reports:
DIZZINESS has been reported as an adverse event in 67 FDA reports for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIZZINESS accounts for approximately 1.8% of all adverse event reports for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE, making it a notable side effect.
If you experience dizziness while taking IPRATROPIUM BROMIDE AND 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.