Does FREMANEZUMAB-VFRM Cause Device issue? 270 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 270 reports of Device issue have been filed in association with FREMANEZUMAB-VFRM. This represents 3.0% of all adverse event reports for FREMANEZUMAB-VFRM.
270
Reports of Device issue with FREMANEZUMAB-VFRM
3.0%
of all FREMANEZUMAB-VFRM reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device issue From FREMANEZUMAB-VFRM?
Of the 270 reports, 2 (0.7%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FREMANEZUMAB-VFRM. However, 270 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which FREMANEZUMAB-VFRM Alternatives Have Lower Device issue Risk?
FREMANEZUMAB-VFRM vs FROVATRIPTAN
FREMANEZUMAB-VFRM vs FRUCTOSE
FREMANEZUMAB-VFRM vs FRUQUINTINIB
FREMANEZUMAB-VFRM vs FULVESTRANT
FREMANEZUMAB-VFRM vs FURAZOLIDONE