1 reports of this reaction
11.1% of all LYTTA VESICATORIA reports
#2 most reported adverse reaction
DEVICE RELATED INFECTION is the #2 most commonly reported adverse reaction for LYTTA VESICATORIA, manufactured by SEVENE USA. There are 1 FDA adverse event reports linking LYTTA VESICATORIA to DEVICE RELATED INFECTION. This represents approximately 11.1% of all 9 adverse event reports for this drug.
Patients taking LYTTA VESICATORIA who experience device related infection should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEVICE RELATED INFECTION is a frequently reported adverse event for LYTTA VESICATORIA, accounting for a significant proportion of all reports.
In addition to device related infection, the following adverse reactions have been reported for LYTTA VESICATORIA:
The following drugs have also been linked to device related infection in FDA adverse event reports:
DEVICE RELATED INFECTION has been reported as an adverse event in 1 FDA reports for LYTTA VESICATORIA. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEVICE RELATED INFECTION accounts for approximately 11.1% of all adverse event reports for LYTTA VESICATORIA, making it one of the most commonly reported side effect.
If you experience device related infection while taking LYTTA VESICATORIA, 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.