Does ROMOSOZUMAB-AQQG Cause Intercepted product administration error? 115 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Intercepted product administration error have been filed in association with ROMOSOZUMAB-AQQG. This represents 1.0% of all adverse event reports for ROMOSOZUMAB-AQQG.
115
Reports of Intercepted product administration error with ROMOSOZUMAB-AQQG
1.0%
of all ROMOSOZUMAB-AQQG reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intercepted product administration error From ROMOSOZUMAB-AQQG?
Of the 115 reports, 1 (0.9%) required hospitalization.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROMOSOZUMAB-AQQG. However, 115 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 Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ERENUMAB-AOOE (1,015)
ETANERCEPT (574)
DARBEPOETIN ALFA (385)
PEGFILGRASTIM (356)
LEUPROLIDE (307)
ERYTHROPOIETIN (301)
BENZYL ALCOHOL\ETANERCEPT (112)
CARFILZOMIB (102)
Which ROMOSOZUMAB-AQQG Alternatives Have Lower Intercepted product administration error Risk?
ROMOSOZUMAB-AQQG vs ROPEGINTERFERON ALFA-2B-NJFT
ROMOSOZUMAB-AQQG vs ROPINIROLE
ROMOSOZUMAB-AQQG vs ROPIVACAINE
ROMOSOZUMAB-AQQG vs ROSIGLITAZONE
ROMOSOZUMAB-AQQG vs ROSUVASTATIN