Does FREMANEZUMAB-VFRM Cause Device defective? 115 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Device defective have been filed in association with FREMANEZUMAB-VFRM. This represents 1.3% of all adverse event reports for FREMANEZUMAB-VFRM.
115
Reports of Device defective with FREMANEZUMAB-VFRM
1.3%
of all FREMANEZUMAB-VFRM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device defective From FREMANEZUMAB-VFRM?
Of the 115 reports, 1 (0.9%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FREMANEZUMAB-VFRM. However, 115 reports have been filed with the FAERS database.
What Other Side Effects Does FREMANEZUMAB-VFRM Cause?
Accidental exposure to product (1,346)
Injection site pain (1,153)
Migraine (740)
Drug ineffective (707)
Injection site erythema (596)
Device leakage (528)
Headache (528)
Injection site pruritus (462)
Device malfunction (431)
Injection site swelling (398)
What Other Drugs Cause Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which FREMANEZUMAB-VFRM Alternatives Have Lower Device defective Risk?
FREMANEZUMAB-VFRM vs FROVATRIPTAN
FREMANEZUMAB-VFRM vs FRUCTOSE
FREMANEZUMAB-VFRM vs FRUQUINTINIB
FREMANEZUMAB-VFRM vs FULVESTRANT
FREMANEZUMAB-VFRM vs FURAZOLIDONE