7,761 reports of this reaction
1.6% of all AMLODIPINE reports
#17 most reported adverse reaction
HYPERTENSION is the #17 most commonly reported adverse reaction for AMLODIPINE, manufactured by Azurity Pharmaceuticals, Inc.. There are 7,761 FDA adverse event reports linking AMLODIPINE to HYPERTENSION. This represents approximately 1.6% of all 472,892 adverse event reports for this drug.
Patients taking AMLODIPINE who experience hypertension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPERTENSION is a less commonly reported adverse event for AMLODIPINE, but still significant enough to appear in the safety profile.
In addition to hypertension, the following adverse reactions have been reported for AMLODIPINE:
The following drugs have also been linked to hypertension in FDA adverse event reports:
HYPERTENSION has been reported as an adverse event in 7,761 FDA reports for AMLODIPINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERTENSION accounts for approximately 1.6% of all adverse event reports for AMLODIPINE, making it a notable side effect.
If you experience hypertension while taking AMLODIPINE, 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.