3,194 reports of this reaction
1.7% of all ACYCLOVIR reports
#11 most reported adverse reaction
ASTHENIA is the #11 most commonly reported adverse reaction for ACYCLOVIR, manufactured by Bausch Health US, LLC. There are 3,194 FDA adverse event reports linking ACYCLOVIR to ASTHENIA. This represents approximately 1.7% of all 186,079 adverse event reports for this drug.
Patients taking ACYCLOVIR who experience asthenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ASTHENIA is a less commonly reported adverse event for ACYCLOVIR, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for ACYCLOVIR:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 3,194 FDA reports for ACYCLOVIR. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 1.7% of all adverse event reports for ACYCLOVIR, making it a notable side effect.
If you experience asthenia 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.