269 reports of this reaction
1.8% of all PYRIDOXINE HYDROCHLORIDE reports
#7 most reported adverse reaction
ABDOMINAL DISTENSION is the #7 most commonly reported adverse reaction for PYRIDOXINE HYDROCHLORIDE, manufactured by Fresenius Kabi USA, LLC. There are 269 FDA adverse event reports linking PYRIDOXINE HYDROCHLORIDE to ABDOMINAL DISTENSION. This represents approximately 1.8% of all 14,601 adverse event reports for this drug.
Patients taking PYRIDOXINE HYDROCHLORIDE who experience abdominal distension 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 DISTENSION is a less commonly reported adverse event for PYRIDOXINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to abdominal distension, the following adverse reactions have been reported for PYRIDOXINE HYDROCHLORIDE:
The following drugs have also been linked to abdominal distension in FDA adverse event reports:
ABDOMINAL DISTENSION has been reported as an adverse event in 269 FDA reports for PYRIDOXINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISTENSION accounts for approximately 1.8% of all adverse event reports for PYRIDOXINE HYDROCHLORIDE, making it a notable side effect.
If you experience abdominal distension while taking PYRIDOXINE HYDROCHLORIDE, 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.