Does ROMOSOZUMAB-AQQG Cause Wrong technique in product usage process? 109 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 109 reports of Wrong technique in product usage process have been filed in association with ROMOSOZUMAB-AQQG. This represents 1.0% of all adverse event reports for ROMOSOZUMAB-AQQG.
109
Reports of Wrong technique in product usage process with ROMOSOZUMAB-AQQG
1.0%
of all ROMOSOZUMAB-AQQG reports
0
Deaths
3
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ROMOSOZUMAB-AQQG?
Of the 109 reports, 3 (2.8%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROMOSOZUMAB-AQQG. However, 109 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ROMOSOZUMAB-AQQG Alternatives Have Lower Wrong technique in product usage process Risk?
ROMOSOZUMAB-AQQG vs ROPEGINTERFERON ALFA-2B-NJFT
ROMOSOZUMAB-AQQG vs ROPINIROLE
ROMOSOZUMAB-AQQG vs ROPIVACAINE
ROMOSOZUMAB-AQQG vs ROSIGLITAZONE
ROMOSOZUMAB-AQQG vs ROSUVASTATIN