VOMITING is the #9 most commonly reported adverse reaction for METOCLOPRAMIDE, manufactured by ANI Pharmaceuticals, Inc.. There are 3,129 FDA adverse event reports linking METOCLOPRAMIDE to VOMITING. This represents approximately 2.0% of all 156,854 adverse event reports for this drug.
Patients taking METOCLOPRAMIDE who experience vomiting should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
Reporting Frequency
VOMITING3,129 of 156,854 reports
VOMITING is a less commonly reported adverse event for METOCLOPRAMIDE, but still significant enough to appear in the safety profile.
Other Side Effects of METOCLOPRAMIDE
In addition to vomiting, the following adverse reactions have been reported for METOCLOPRAMIDE:
VOMITING has been reported as an adverse event in 3,129 FDA reports for METOCLOPRAMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is VOMITING with METOCLOPRAMIDE?
VOMITING accounts for approximately 2.0% of all adverse event reports for METOCLOPRAMIDE, making it a notable side effect.
What should I do if I experience VOMITING while taking METOCLOPRAMIDE?
If you experience vomiting while taking METOCLOPRAMIDE, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.