1,196 reports of this reaction
1.5% of all CALCIUM GLUCONATE reports
#10 most reported adverse reaction
ARTHROPATHY is the #10 most commonly reported adverse reaction for CALCIUM GLUCONATE, manufactured by WG Critical Care, LLC. There are 1,196 FDA adverse event reports linking CALCIUM GLUCONATE to ARTHROPATHY. This represents approximately 1.5% of all 80,205 adverse event reports for this drug.
Patients taking CALCIUM GLUCONATE who experience arthropathy should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ARTHROPATHY is a less commonly reported adverse event for CALCIUM GLUCONATE, but still significant enough to appear in the safety profile.
In addition to arthropathy, the following adverse reactions have been reported for CALCIUM GLUCONATE:
The following drugs have also been linked to arthropathy in FDA adverse event reports:
ARTHROPATHY has been reported as an adverse event in 1,196 FDA reports for CALCIUM GLUCONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ARTHROPATHY accounts for approximately 1.5% of all adverse event reports for CALCIUM GLUCONATE, making it a notable side effect.
If you experience arthropathy while taking CALCIUM GLUCONATE, 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.