975 reports of this reaction
2.7% of all INTERFERON BETA 1B reports
#6 most reported adverse reaction
INJECTION SITE ERYTHEMA is the #6 most commonly reported adverse reaction for INTERFERON BETA 1B, manufactured by Bayer HealthCare Pharmaceuticals Inc.. There are 975 FDA adverse event reports linking INTERFERON BETA 1B to INJECTION SITE ERYTHEMA. This represents approximately 2.7% of all 36,175 adverse event reports for this drug.
Patients taking INTERFERON BETA 1B who experience injection site erythema should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INJECTION SITE ERYTHEMA is a less commonly reported adverse event for INTERFERON BETA 1B, but still significant enough to appear in the safety profile.
In addition to injection site erythema, the following adverse reactions have been reported for INTERFERON BETA 1B:
The following drugs have also been linked to injection site erythema in FDA adverse event reports:
INJECTION SITE ERYTHEMA has been reported as an adverse event in 975 FDA reports for INTERFERON BETA 1B. This does not prove causation, but indicates an association observed in post-market surveillance data.
INJECTION SITE ERYTHEMA accounts for approximately 2.7% of all adverse event reports for INTERFERON BETA 1B, making it a notable side effect.
If you experience injection site erythema while taking INTERFERON BETA 1B, 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.