1,011 reports of this reaction
4.1% of all NOREPINEPHRINE reports
#3 most reported adverse reaction
HYPOTENSION is the #3 most commonly reported adverse reaction for NOREPINEPHRINE, manufactured by Professional Complementary Health Formulas. There are 1,011 FDA adverse event reports linking NOREPINEPHRINE to HYPOTENSION. This represents approximately 4.1% of all 24,944 adverse event reports for this drug.
Patients taking NOREPINEPHRINE who experience hypotension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPOTENSION is moderately reported among NOREPINEPHRINE users, representing a notable but not dominant share of adverse events.
In addition to hypotension, the following adverse reactions have been reported for NOREPINEPHRINE:
The following drugs have also been linked to hypotension in FDA adverse event reports:
HYPOTENSION has been reported as an adverse event in 1,011 FDA reports for NOREPINEPHRINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOTENSION accounts for approximately 4.1% of all adverse event reports for NOREPINEPHRINE, making it one of the most commonly reported side effect.
If you experience hypotension while taking NOREPINEPHRINE, 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.