1,076 reports of this reaction
3.0% of all LITHIUM CARBONATE reports
#3 most reported adverse reaction
TREMOR is the #3 most commonly reported adverse reaction for LITHIUM CARBONATE, manufactured by ANI Pharmaceuticals, Inc.. There are 1,076 FDA adverse event reports linking LITHIUM CARBONATE to TREMOR. This represents approximately 3.0% of all 35,528 adverse event reports for this drug.
Patients taking LITHIUM CARBONATE who experience tremor should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
TREMOR is a less commonly reported adverse event for LITHIUM CARBONATE, but still significant enough to appear in the safety profile.
In addition to tremor, the following adverse reactions have been reported for LITHIUM CARBONATE:
The following drugs have also been linked to tremor in FDA adverse event reports:
TREMOR has been reported as an adverse event in 1,076 FDA reports for LITHIUM CARBONATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
TREMOR accounts for approximately 3.0% of all adverse event reports for LITHIUM CARBONATE, making it one of the most commonly reported side effect.
If you experience tremor while taking LITHIUM CARBONATE, 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.