Does ROMOSOZUMAB-AQQG Cause Adverse event? 106 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Adverse event have been filed in association with ROMOSOZUMAB-AQQG. This represents 0.9% of all adverse event reports for ROMOSOZUMAB-AQQG.
106
Reports of Adverse event with ROMOSOZUMAB-AQQG
0.9%
of all ROMOSOZUMAB-AQQG reports
4
Deaths
27
Hospitalizations
How Dangerous Is Adverse event From ROMOSOZUMAB-AQQG?
Of the 106 reports, 4 (3.8%) resulted in death, 27 (25.5%) required hospitalization.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROMOSOZUMAB-AQQG. However, 106 reports have been filed with the FAERS database.
What Other Side Effects Does ROMOSOZUMAB-AQQG Cause?
Fall (646)
Fracture (612)
Arthralgia (517)
Injection site pain (490)
Bone density abnormal (454)
Off label use (419)
Hospitalisation (381)
Headache (360)
Product storage error (348)
Death (263)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which ROMOSOZUMAB-AQQG Alternatives Have Lower Adverse event Risk?
ROMOSOZUMAB-AQQG vs ROPEGINTERFERON ALFA-2B-NJFT
ROMOSOZUMAB-AQQG vs ROPINIROLE
ROMOSOZUMAB-AQQG vs ROPIVACAINE
ROMOSOZUMAB-AQQG vs ROSIGLITAZONE
ROMOSOZUMAB-AQQG vs ROSUVASTATIN