298 reports of this reaction
1.6% of all ACETYLCYSTEINE reports
#12 most reported adverse reaction
DEATH is the #12 most commonly reported adverse reaction for ACETYLCYSTEINE, manufactured by Cumberland Pharmaceuticals Inc.. There are 298 FDA adverse event reports linking ACETYLCYSTEINE to DEATH. This represents approximately 1.6% of all 18,714 adverse event reports for this drug.
Patients taking ACETYLCYSTEINE who experience death should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEATH is a less commonly reported adverse event for ACETYLCYSTEINE, but still significant enough to appear in the safety profile.
In addition to death, the following adverse reactions have been reported for ACETYLCYSTEINE:
The following drugs have also been linked to death in FDA adverse event reports:
DEATH has been reported as an adverse event in 298 FDA reports for ACETYLCYSTEINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEATH accounts for approximately 1.6% of all adverse event reports for ACETYLCYSTEINE, making it a notable side effect.
If you experience death while taking ACETYLCYSTEINE, 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.