728 reports of this reaction
2.0% of all DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE reports
#9 most reported adverse reaction
ABDOMINAL PAIN is the #9 most commonly reported adverse reaction for DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 728 FDA adverse event reports linking DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE to ABDOMINAL PAIN. This represents approximately 2.0% of all 35,651 adverse event reports for this drug.
Patients taking DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE who experience abdominal pain 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 PAIN is a less commonly reported adverse event for DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE, but still significant enough to appear in the safety profile.
In addition to abdominal pain, the following adverse reactions have been reported for DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE:
The following drugs have also been linked to abdominal pain in FDA adverse event reports:
ABDOMINAL PAIN has been reported as an adverse event in 728 FDA reports for DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL PAIN accounts for approximately 2.0% of all adverse event reports for DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE, making it a notable side effect.
If you experience abdominal pain while taking DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE 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.