Does ROMIPLOSTIM Cause Condition aggravated? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Condition aggravated have been filed in association with ROMIPLOSTIM (Nplate). This represents 0.6% of all adverse event reports for ROMIPLOSTIM.
45
Reports of Condition aggravated with ROMIPLOSTIM
0.6%
of all ROMIPLOSTIM reports
7
Deaths
23
Hospitalizations
How Dangerous Is Condition aggravated From ROMIPLOSTIM?
Of the 45 reports, 7 (15.6%) resulted in death, 23 (51.1%) required hospitalization, and 3 (6.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROMIPLOSTIM. However, 45 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ROMIPLOSTIM Alternatives Have Lower Condition aggravated Risk?
ROMIPLOSTIM vs ROMOSOZUMAB
ROMIPLOSTIM vs ROMOSOZUMAB-AQQG
ROMIPLOSTIM vs ROPEGINTERFERON ALFA-2B-NJFT
ROMIPLOSTIM vs ROPINIROLE
ROMIPLOSTIM vs ROPIVACAINE