287 reports of this reaction
1.9% of all IOHEXOL reports
#11 most reported adverse reaction
ANAPHYLACTIC REACTION is the #11 most commonly reported adverse reaction for IOHEXOL, manufactured by GE Healthcare. There are 287 FDA adverse event reports linking IOHEXOL to ANAPHYLACTIC REACTION. This represents approximately 1.9% of all 15,311 adverse event reports for this drug.
Patients taking IOHEXOL who experience anaphylactic reaction 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 REACTION is a less commonly reported adverse event for IOHEXOL, but still significant enough to appear in the safety profile.
In addition to anaphylactic reaction, the following adverse reactions have been reported for IOHEXOL:
The following drugs have also been linked to anaphylactic reaction in FDA adverse event reports:
ANAPHYLACTIC REACTION has been reported as an adverse event in 287 FDA reports for IOHEXOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ANAPHYLACTIC REACTION accounts for approximately 1.9% of all adverse event reports for IOHEXOL, making it a notable side effect.
If you experience anaphylactic reaction while taking IOHEXOL, 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.