1 reports of this reaction
0.8% of all CHEWABLE ASPIRIN reports
#19 most reported adverse reaction
ANAPHYLACTIC SHOCK is the #19 most commonly reported adverse reaction for CHEWABLE ASPIRIN, manufactured by Chain Drug Marketing Association, Inc.. There are 1 FDA adverse event reports linking CHEWABLE ASPIRIN to ANAPHYLACTIC SHOCK. This represents approximately 0.8% of all 121 adverse event reports for this drug.
Patients taking CHEWABLE ASPIRIN who experience anaphylactic shock should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ANAPHYLACTIC SHOCK is a less commonly reported adverse event for CHEWABLE ASPIRIN, but still significant enough to appear in the safety profile.
In addition to anaphylactic shock, the following adverse reactions have been reported for CHEWABLE ASPIRIN:
The following drugs have also been linked to anaphylactic shock in FDA adverse event reports:
ANAPHYLACTIC SHOCK has been reported as an adverse event in 1 FDA reports for CHEWABLE ASPIRIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
ANAPHYLACTIC SHOCK accounts for approximately 0.8% of all adverse event reports for CHEWABLE ASPIRIN, making it a notable side effect.
If you experience anaphylactic shock while taking CHEWABLE ASPIRIN, 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.