1 reports of this reaction
2.1% of all AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE reports
#6 most reported adverse reaction
ADRENOCORTICAL INSUFFICIENCY ACUTE is the #6 most commonly reported adverse reaction for AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE, manufactured by Aurobindo Pharma Limited. There are 1 FDA adverse event reports linking AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE to ADRENOCORTICAL INSUFFICIENCY ACUTE. This represents approximately 2.1% of all 48 adverse event reports for this drug.
Patients taking AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE who experience adrenocortical insufficiency acute should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ADRENOCORTICAL INSUFFICIENCY ACUTE is a less commonly reported adverse event for AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to adrenocortical insufficiency acute, the following adverse reactions have been reported for AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE:
ADRENOCORTICAL INSUFFICIENCY ACUTE has been reported as an adverse event in 1 FDA reports for AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ADRENOCORTICAL INSUFFICIENCY ACUTE accounts for approximately 2.1% of all adverse event reports for AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE, making it a notable side effect.
If you experience adrenocortical insufficiency acute while taking AMLODIPINE AND BENAZEPRIL 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.