57 reports of this reaction
1.7% of all NICARDIPINE HYDROCHLORIDE reports
#10 most reported adverse reaction
HEPATIC CYTOLYSIS is the #10 most commonly reported adverse reaction for NICARDIPINE HYDROCHLORIDE, manufactured by Baxter Healthcare Corporation. There are 57 FDA adverse event reports linking NICARDIPINE HYDROCHLORIDE to HEPATIC CYTOLYSIS. This represents approximately 1.7% of all 3,434 adverse event reports for this drug.
Patients taking NICARDIPINE HYDROCHLORIDE who experience hepatic cytolysis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HEPATIC CYTOLYSIS is a less commonly reported adverse event for NICARDIPINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to hepatic cytolysis, the following adverse reactions have been reported for NICARDIPINE HYDROCHLORIDE:
HEPATIC CYTOLYSIS has been reported as an adverse event in 57 FDA reports for NICARDIPINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HEPATIC CYTOLYSIS accounts for approximately 1.7% of all adverse event reports for NICARDIPINE HYDROCHLORIDE, making it a notable side effect.
If you experience hepatic cytolysis while taking NICARDIPINE 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.