Does ROMIPLOSTIM Cause Product storage error? 344 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 344 reports of Product storage error have been filed in association with ROMIPLOSTIM (Nplate). This represents 4.6% of all adverse event reports for ROMIPLOSTIM.
344
Reports of Product storage error with ROMIPLOSTIM
4.6%
of all ROMIPLOSTIM reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product storage error From ROMIPLOSTIM?
Of the 344 reports, 3 (0.9%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROMIPLOSTIM. However, 344 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)
Fatigue (251)
Circumstance or information capable of leading to medication error (238)
Thrombocytosis (234)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ROMIPLOSTIM Alternatives Have Lower Product storage error Risk?
ROMIPLOSTIM vs ROMOSOZUMAB
ROMIPLOSTIM vs ROMOSOZUMAB-AQQG
ROMIPLOSTIM vs ROPEGINTERFERON ALFA-2B-NJFT
ROMIPLOSTIM vs ROPINIROLE
ROMIPLOSTIM vs ROPIVACAINE