79 reports of this reaction
2.0% of all ACYCLOVIR SODIUM reports
#6 most reported adverse reaction
HYPERTENSION is the #6 most commonly reported adverse reaction for ACYCLOVIR SODIUM, manufactured by AuroMedics Pharma LLC. There are 79 FDA adverse event reports linking ACYCLOVIR SODIUM to HYPERTENSION. This represents approximately 2.0% of all 4,002 adverse event reports for this drug.
Patients taking ACYCLOVIR SODIUM 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 ACYCLOVIR SODIUM, but still significant enough to appear in the safety profile.
In addition to hypertension, the following adverse reactions have been reported for ACYCLOVIR SODIUM:
The following drugs have also been linked to hypertension in FDA adverse event reports:
HYPERTENSION has been reported as an adverse event in 79 FDA reports for ACYCLOVIR SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERTENSION accounts for approximately 2.0% of all adverse event reports for ACYCLOVIR SODIUM, making it a notable side effect.
If you experience hypertension while taking ACYCLOVIR SODIUM, 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.