485 reports of this reaction
2.1% of all NORTRIPTYLINE HYDROCHLORIDE reports
#7 most reported adverse reaction
HYPERHIDROSIS is the #7 most commonly reported adverse reaction for NORTRIPTYLINE HYDROCHLORIDE, manufactured by SpecGx LLC. There are 485 FDA adverse event reports linking NORTRIPTYLINE HYDROCHLORIDE to HYPERHIDROSIS. This represents approximately 2.1% of all 23,339 adverse event reports for this drug.
Patients taking NORTRIPTYLINE HYDROCHLORIDE who experience hyperhidrosis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPERHIDROSIS is a less commonly reported adverse event for NORTRIPTYLINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to hyperhidrosis, the following adverse reactions have been reported for NORTRIPTYLINE HYDROCHLORIDE:
The following drugs have also been linked to hyperhidrosis in FDA adverse event reports:
HYPERHIDROSIS has been reported as an adverse event in 485 FDA reports for NORTRIPTYLINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERHIDROSIS accounts for approximately 2.1% of all adverse event reports for NORTRIPTYLINE HYDROCHLORIDE, making it a notable side effect.
If you experience hyperhidrosis while taking NORTRIPTYLINE 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.