1,535 reports of this reaction
2.6% of all HYDRALAZINE HYDROCHLORIDE reports
#6 most reported adverse reaction
DYSPNOEA is the #6 most commonly reported adverse reaction for HYDRALAZINE HYDROCHLORIDE, manufactured by Nivagen Pharmaceuticals, Inc.. There are 1,535 FDA adverse event reports linking HYDRALAZINE HYDROCHLORIDE to DYSPNOEA. This represents approximately 2.6% of all 59,065 adverse event reports for this drug.
Patients taking HYDRALAZINE HYDROCHLORIDE who experience dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSPNOEA is a less commonly reported adverse event for HYDRALAZINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to dyspnoea, the following adverse reactions have been reported for HYDRALAZINE HYDROCHLORIDE:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 1,535 FDA reports for HYDRALAZINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 2.6% of all adverse event reports for HYDRALAZINE HYDROCHLORIDE, making it a notable side effect.
If you experience dyspnoea while taking HYDRALAZINE 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.