401 reports of this reaction
2.7% of all TERBINAFINE HYDROCHLORIDE reports
#3 most reported adverse reaction
PRURITUS is the #3 most commonly reported adverse reaction for TERBINAFINE HYDROCHLORIDE, manufactured by Aurobindo Pharma Limited. There are 401 FDA adverse event reports linking TERBINAFINE HYDROCHLORIDE to PRURITUS. This represents approximately 2.7% of all 14,851 adverse event reports for this drug.
Patients taking TERBINAFINE HYDROCHLORIDE who experience pruritus should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRURITUS is a less commonly reported adverse event for TERBINAFINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to pruritus, the following adverse reactions have been reported for TERBINAFINE HYDROCHLORIDE:
The following drugs have also been linked to pruritus in FDA adverse event reports:
PRURITUS has been reported as an adverse event in 401 FDA reports for TERBINAFINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRURITUS accounts for approximately 2.7% of all adverse event reports for TERBINAFINE HYDROCHLORIDE, making it one of the most commonly reported side effect.
If you experience pruritus while taking TERBINAFINE 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.