519 reports of this reaction
2.4% of all GRANISETRON HYDROCHLORIDE reports
#9 most reported adverse reaction
ANAEMIA is the #9 most commonly reported adverse reaction for GRANISETRON HYDROCHLORIDE, manufactured by Fresenius Kabi USA, LLC. There are 519 FDA adverse event reports linking GRANISETRON HYDROCHLORIDE to ANAEMIA. This represents approximately 2.4% of all 22,079 adverse event reports for this drug.
Patients taking GRANISETRON HYDROCHLORIDE 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 GRANISETRON HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to anaemia, the following adverse reactions have been reported for GRANISETRON HYDROCHLORIDE:
The following drugs have also been linked to anaemia in FDA adverse event reports:
ANAEMIA has been reported as an adverse event in 519 FDA reports for GRANISETRON HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ANAEMIA accounts for approximately 2.4% of all adverse event reports for GRANISETRON HYDROCHLORIDE, making it a notable side effect.
If you experience anaemia while taking GRANISETRON HYDROCHLORIDE, 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.