281 reports of this reaction
2.8% of all KETOROLAC TROMETHAMINE reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for KETOROLAC TROMETHAMINE, manufactured by Allergan, Inc.. There are 281 FDA adverse event reports linking KETOROLAC TROMETHAMINE to NAUSEA. This represents approximately 2.8% of all 10,197 adverse event reports for this drug.
Patients taking KETOROLAC TROMETHAMINE who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is a less commonly reported adverse event for KETOROLAC TROMETHAMINE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for KETOROLAC TROMETHAMINE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 281 FDA reports for KETOROLAC TROMETHAMINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.8% of all adverse event reports for KETOROLAC TROMETHAMINE, making it one of the most commonly reported side effect.
If you experience nausea while taking KETOROLAC TROMETHAMINE, 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.