9,549 reports of this reaction
1.7% of all HYDROXYCHLOROQUINE SULFATE reports
#10 most reported adverse reaction
ABDOMINAL DISCOMFORT is the #10 most commonly reported adverse reaction for HYDROXYCHLOROQUINE SULFATE, manufactured by Advanz Pharma (US) Corp.. There are 9,549 FDA adverse event reports linking HYDROXYCHLOROQUINE SULFATE to ABDOMINAL DISCOMFORT. This represents approximately 1.7% of all 558,480 adverse event reports for this drug.
Patients taking HYDROXYCHLOROQUINE SULFATE who experience abdominal discomfort should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL DISCOMFORT is a less commonly reported adverse event for HYDROXYCHLOROQUINE SULFATE, but still significant enough to appear in the safety profile.
In addition to abdominal discomfort, the following adverse reactions have been reported for HYDROXYCHLOROQUINE SULFATE:
The following drugs have also been linked to abdominal discomfort in FDA adverse event reports:
ABDOMINAL DISCOMFORT has been reported as an adverse event in 9,549 FDA reports for HYDROXYCHLOROQUINE SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISCOMFORT accounts for approximately 1.7% of all adverse event reports for HYDROXYCHLOROQUINE SULFATE, making it a notable side effect.
If you experience abdominal discomfort while taking HYDROXYCHLOROQUINE SULFATE, 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.