1,473 reports of this reaction
1.8% of all OFATUMUMAB reports
#10 most reported adverse reaction
ASTHENIA is the #10 most commonly reported adverse reaction for OFATUMUMAB, manufactured by Novartis Pharmaceuticals Corporation. There are 1,473 FDA adverse event reports linking OFATUMUMAB to ASTHENIA. This represents approximately 1.8% of all 82,579 adverse event reports for this drug.
OFATUMUMAB has an overall safety score of 78 out of 100. Patients taking OFATUMUMAB 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 OFATUMUMAB, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for OFATUMUMAB:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 1,473 FDA reports for OFATUMUMAB. This does not prove causation, but indicates an association observed in post-market surveillance data.
ASTHENIA accounts for approximately 1.8% of all adverse event reports for OFATUMUMAB, making it a notable side effect.
If you experience asthenia while taking OFATUMUMAB, 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.