1,414 reports of this reaction
2.4% of all ABALOPARATIDE reports
#8 most reported adverse reaction
BONE PAIN is the #8 most commonly reported adverse reaction for ABALOPARATIDE, manufactured by Radius Health, Inc.. There are 1,414 FDA adverse event reports linking ABALOPARATIDE to BONE PAIN. This represents approximately 2.4% of all 58,437 adverse event reports for this drug.
Patients taking ABALOPARATIDE who experience bone pain should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BONE PAIN is a less commonly reported adverse event for ABALOPARATIDE, but still significant enough to appear in the safety profile.
In addition to bone pain, the following adverse reactions have been reported for ABALOPARATIDE:
The following drugs have also been linked to bone pain in FDA adverse event reports:
BONE PAIN has been reported as an adverse event in 1,414 FDA reports for ABALOPARATIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
BONE PAIN accounts for approximately 2.4% of all adverse event reports for ABALOPARATIDE, making it a notable side effect.
If you experience bone pain while taking ABALOPARATIDE, 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.