Does ROMIPLOSTIM Cause Post procedural haemorrhage? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Post procedural haemorrhage have been filed in association with ROMIPLOSTIM (Nplate). This represents 0.2% of all adverse event reports for ROMIPLOSTIM.
15
Reports of Post procedural haemorrhage with ROMIPLOSTIM
0.2%
of all ROMIPLOSTIM reports
1
Deaths
3
Hospitalizations
How Dangerous Is Post procedural haemorrhage From ROMIPLOSTIM?
Of the 15 reports, 1 (6.7%) resulted in death, 3 (20.0%) required hospitalization.
Is Post procedural haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROMIPLOSTIM. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does ROMIPLOSTIM Cause?
Off label use (1,027)
Platelet count decreased (892)
Platelet count abnormal (703)
Drug ineffective (513)
Thrombocytopenia (369)
Headache (359)
Death (356)
Product storage error (344)
Fatigue (251)
Circumstance or information capable of leading to medication error (238)
What Other Drugs Cause Post procedural haemorrhage?
LEVONORGESTREL (1,106)
RIVAROXABAN (930)
ASPIRIN (618)
APIXABAN (539)
ADALIMUMAB (476)
IBRUTINIB (269)
CLOPIDOGREL BISULFATE (235)
HEPARIN (174)
WARFARIN (170)
DABIGATRAN ETEXILATE (121)
Which ROMIPLOSTIM Alternatives Have Lower Post procedural haemorrhage Risk?
ROMIPLOSTIM vs ROMOSOZUMAB
ROMIPLOSTIM vs ROMOSOZUMAB-AQQG
ROMIPLOSTIM vs ROPEGINTERFERON ALFA-2B-NJFT
ROMIPLOSTIM vs ROPINIROLE
ROMIPLOSTIM vs ROPIVACAINE