2 reports of this reaction
10.5% of all LIQUID BANDAGE reports
#1 most reported adverse reaction
MUSCLE SPASMS is the #1 most commonly reported adverse reaction for LIQUID BANDAGE, manufactured by AmerisourceBergen Drug Corporation. There are 2 FDA adverse event reports linking LIQUID BANDAGE to MUSCLE SPASMS. This represents approximately 10.5% of all 19 adverse event reports for this drug.
Patients taking LIQUID BANDAGE who experience muscle spasms should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MUSCLE SPASMS is a frequently reported adverse event for LIQUID BANDAGE, accounting for a significant proportion of all reports.
In addition to muscle spasms, the following adverse reactions have been reported for LIQUID BANDAGE:
The following drugs have also been linked to muscle spasms in FDA adverse event reports:
MUSCLE SPASMS has been reported as an adverse event in 2 FDA reports for LIQUID BANDAGE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MUSCLE SPASMS accounts for approximately 10.5% of all adverse event reports for LIQUID BANDAGE, making it one of the most commonly reported side effect.
If you experience muscle spasms while taking LIQUID BANDAGE, 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.