353 reports of this reaction
1.9% of all AMLODIPINE BESYLATE AND VALSARTAN reports
#11 most reported adverse reaction
OEDEMA PERIPHERAL is the #11 most commonly reported adverse reaction for AMLODIPINE BESYLATE AND VALSARTAN, manufactured by Novartis Pharmaceuticals Corporation. There are 353 FDA adverse event reports linking AMLODIPINE BESYLATE AND VALSARTAN to OEDEMA PERIPHERAL. This represents approximately 1.9% of all 18,550 adverse event reports for this drug.
Patients taking AMLODIPINE BESYLATE AND VALSARTAN who experience oedema peripheral should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OEDEMA PERIPHERAL is a less commonly reported adverse event for AMLODIPINE BESYLATE AND VALSARTAN, but still significant enough to appear in the safety profile.
In addition to oedema peripheral, the following adverse reactions have been reported for AMLODIPINE BESYLATE AND VALSARTAN:
The following drugs have also been linked to oedema peripheral in FDA adverse event reports:
OEDEMA PERIPHERAL has been reported as an adverse event in 353 FDA reports for AMLODIPINE BESYLATE AND VALSARTAN. This does not prove causation, but indicates an association observed in post-market surveillance data.
OEDEMA PERIPHERAL accounts for approximately 1.9% of all adverse event reports for AMLODIPINE BESYLATE AND VALSARTAN, making it a notable side effect.
If you experience oedema peripheral while taking AMLODIPINE BESYLATE AND VALSARTAN, 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.