COUGH is the #4 most commonly reported adverse reaction for ALBUTEROL, manufactured by Amneal Pharmaceuticals NY LLC. There are 7,339 FDA adverse event reports linking ALBUTEROL to COUGH. This represents approximately 2.6% of all 283,047 adverse event reports for this drug.
Patients taking ALBUTEROL who experience cough should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
COUGH7,339 of 283,047 reports
COUGH is a less commonly reported adverse event for ALBUTEROL, but still significant enough to appear in the safety profile.
Other Side Effects of ALBUTEROL
In addition to cough, the following adverse reactions have been reported for ALBUTEROL:
COUGH has been reported as an adverse event in 7,339 FDA reports for ALBUTEROL. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is COUGH with ALBUTEROL?
COUGH accounts for approximately 2.6% of all adverse event reports for ALBUTEROL, making it a notable side effect.
What should I do if I experience COUGH while taking ALBUTEROL?
If you experience cough while taking ALBUTEROL, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.