7,611 reports of this reaction
4.1% of all ACYCLOVIR reports
#1 most reported adverse reaction
FATIGUE is the #1 most commonly reported adverse reaction for ACYCLOVIR, manufactured by Bausch Health US, LLC. There are 7,611 FDA adverse event reports linking ACYCLOVIR to FATIGUE. This represents approximately 4.1% of all 186,079 adverse event reports for this drug.
Patients taking ACYCLOVIR who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is moderately reported among ACYCLOVIR users, representing a notable but not dominant share of adverse events.
In addition to fatigue, the following adverse reactions have been reported for ACYCLOVIR:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 7,611 FDA reports for ACYCLOVIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 4.1% of all adverse event reports for ACYCLOVIR, making it one of the most commonly reported side effect.
If you experience fatigue while taking ACYCLOVIR, 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.