3,372 reports of this reaction
1.3% of all HYDROMORPHONE HYDROCHLORIDE reports
#11 most reported adverse reaction
VOMITING is the #11 most commonly reported adverse reaction for HYDROMORPHONE HYDROCHLORIDE, manufactured by Fresenius Kabi USA, LLC. There are 3,372 FDA adverse event reports linking HYDROMORPHONE HYDROCHLORIDE to VOMITING. This represents approximately 1.3% of all 268,941 adverse event reports for this drug.
Patients taking HYDROMORPHONE HYDROCHLORIDE 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.
VOMITING is a less commonly reported adverse event for HYDROMORPHONE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to vomiting, the following adverse reactions have been reported for HYDROMORPHONE HYDROCHLORIDE:
The following drugs have also been linked to vomiting in FDA adverse event reports:
VOMITING has been reported as an adverse event in 3,372 FDA reports for HYDROMORPHONE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
VOMITING accounts for approximately 1.3% of all adverse event reports for HYDROMORPHONE HYDROCHLORIDE, making it a notable side effect.
If you experience vomiting while taking HYDROMORPHONE 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.