3 reports of this reaction
1.8% of all ARTHRITIS PAIN RELIEF reports
#8 most reported adverse reaction
ASTHENIA is the #8 most commonly reported adverse reaction for ARTHRITIS PAIN RELIEF, manufactured by CVS Health. There are 3 FDA adverse event reports linking ARTHRITIS PAIN RELIEF to ASTHENIA. This represents approximately 1.8% of all 170 adverse event reports for this drug.
Patients taking ARTHRITIS PAIN RELIEF 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 ARTHRITIS PAIN RELIEF, but still significant enough to appear in the safety profile.
In addition to asthenia, the following adverse reactions have been reported for ARTHRITIS PAIN RELIEF:
The following drugs have also been linked to asthenia in FDA adverse event reports:
ASTHENIA has been reported as an adverse event in 3 FDA reports for ARTHRITIS PAIN RELIEF. 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 ARTHRITIS PAIN RELIEF, making it a notable side effect.
If you experience asthenia while taking ARTHRITIS PAIN RELIEF, 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.