4,135 reports of this reaction
6.8% of all ANAKINRA reports
#2 most reported adverse reaction
DRUG INEFFECTIVE is the #2 most commonly reported adverse reaction for ANAKINRA, manufactured by Swedish Orphan Biovitrum AB (publ). There are 4,135 FDA adverse event reports linking ANAKINRA to DRUG INEFFECTIVE. This represents approximately 6.8% of all 60,861 adverse event reports for this drug.
Patients taking ANAKINRA who experience drug ineffective should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRUG INEFFECTIVE is moderately reported among ANAKINRA users, representing a notable but not dominant share of adverse events.
In addition to drug ineffective, the following adverse reactions have been reported for ANAKINRA:
The following drugs have also been linked to drug ineffective in FDA adverse event reports:
DRUG INEFFECTIVE has been reported as an adverse event in 4,135 FDA reports for ANAKINRA. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG INEFFECTIVE accounts for approximately 6.8% of all adverse event reports for ANAKINRA, making it one of the most commonly reported side effect.
If you experience drug ineffective while taking ANAKINRA, 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.