29 reports of this reaction
2.8% of all CALCIUM FLUORIDE reports
#4 most reported adverse reaction
FATIGUE is the #4 most commonly reported adverse reaction for CALCIUM FLUORIDE, manufactured by DNA Labs, Inc.. There are 29 FDA adverse event reports linking CALCIUM FLUORIDE to FATIGUE. This represents approximately 2.8% of all 1,044 adverse event reports for this drug.
Patients taking CALCIUM FLUORIDE who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is a less commonly reported adverse event for CALCIUM FLUORIDE, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for CALCIUM FLUORIDE:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 29 FDA reports for CALCIUM FLUORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 2.8% of all adverse event reports for CALCIUM FLUORIDE, making it a notable side effect.
If you experience fatigue while taking CALCIUM FLUORIDE, 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.