487 reports of this reaction
2.9% of all ATROPINE reports
#4 most reported adverse reaction
HYPOTENSION is the #4 most commonly reported adverse reaction for ATROPINE, manufactured by Meridian Medical Technologies LLC. There are 487 FDA adverse event reports linking ATROPINE to HYPOTENSION. This represents approximately 2.9% of all 16,519 adverse event reports for this drug.
Patients taking ATROPINE 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 a less commonly reported adverse event for ATROPINE, but still significant enough to appear in the safety profile.
In addition to hypotension, the following adverse reactions have been reported for ATROPINE:
The following drugs have also been linked to hypotension in FDA adverse event reports:
HYPOTENSION has been reported as an adverse event in 487 FDA reports for ATROPINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPOTENSION accounts for approximately 2.9% of all adverse event reports for ATROPINE, making it a notable side effect.
If you experience hypotension while taking ATROPINE, 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.