782 reports of this reaction
4.2% of all THIOTEPA reports
#2 most reported adverse reaction
FEBRILE NEUTROPENIA is the #2 most commonly reported adverse reaction for THIOTEPA, manufactured by Amneal Pharmaceuticals LLC. There are 782 FDA adverse event reports linking THIOTEPA to FEBRILE NEUTROPENIA. This represents approximately 4.2% of all 18,516 adverse event reports for this drug.
Patients taking THIOTEPA who experience febrile neutropenia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FEBRILE NEUTROPENIA is moderately reported among THIOTEPA users, representing a notable but not dominant share of adverse events.
In addition to febrile neutropenia, the following adverse reactions have been reported for THIOTEPA:
The following drugs have also been linked to febrile neutropenia in FDA adverse event reports:
FEBRILE NEUTROPENIA has been reported as an adverse event in 782 FDA reports for THIOTEPA. This does not prove causation, but indicates an association observed in post-market surveillance data.
FEBRILE NEUTROPENIA accounts for approximately 4.2% of all adverse event reports for THIOTEPA, making it one of the most commonly reported side effect.
If you experience febrile neutropenia while taking THIOTEPA, 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.