3,874 reports of this reaction
2.8% of all CISPLATIN reports
#7 most reported adverse reaction
ANAEMIA is the #7 most commonly reported adverse reaction for CISPLATIN, manufactured by Accord Healthcare Inc.. There are 3,874 FDA adverse event reports linking CISPLATIN to ANAEMIA. This represents approximately 2.8% of all 137,577 adverse event reports for this drug.
Patients taking CISPLATIN who experience anaemia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ANAEMIA is a less commonly reported adverse event for CISPLATIN, but still significant enough to appear in the safety profile.
In addition to anaemia, the following adverse reactions have been reported for CISPLATIN:
The following drugs have also been linked to anaemia in FDA adverse event reports:
ANAEMIA has been reported as an adverse event in 3,874 FDA reports for CISPLATIN. This does not prove causation, but indicates an association observed in post-market surveillance data.
ANAEMIA accounts for approximately 2.8% of all adverse event reports for CISPLATIN, making it a notable side effect.
If you experience anaemia while taking CISPLATIN, 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.