Does ROMOSOZUMAB-AQQG Cause Product storage error? 348 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 348 reports of Product storage error have been filed in association with ROMOSOZUMAB-AQQG. This represents 3.1% of all adverse event reports for ROMOSOZUMAB-AQQG.
348
Reports of Product storage error with ROMOSOZUMAB-AQQG
3.1%
of all ROMOSOZUMAB-AQQG reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product storage error From ROMOSOZUMAB-AQQG?
Of the 348 reports, 2 (0.6%) 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 ROMOSOZUMAB-AQQG. However, 348 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)
Death (263)
Spinal fracture (256)
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 ROMOSOZUMAB-AQQG Alternatives Have Lower Product storage 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