3,613 reports of this reaction
2.3% of all RIBAVIRIN reports
#9 most reported adverse reaction
ASTHENIA is the #9 most commonly reported adverse reaction for RIBAVIRIN, manufactured by Bausch Health US, LLC. There are 3,613 FDA adverse event reports linking RIBAVIRIN to ASTHENIA. This represents approximately 2.3% of all 157,291 adverse event reports for this drug.
RIBAVIRIN has an overall safety score of 85 out of 100. Patients taking RIBAVIRIN 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 RIBAVIRIN, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for RIBAVIRIN:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 3,613 FDA reports for RIBAVIRIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 2.3% of all adverse event reports for RIBAVIRIN, making it a notable side effect.
If you experience asthenia while taking RIBAVIRIN, 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.