Does FREMANEZUMAB-VFRM Cause Device malfunction? 431 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 431 reports of Device malfunction have been filed in association with FREMANEZUMAB-VFRM. This represents 4.7% of all adverse event reports for FREMANEZUMAB-VFRM.
431
Reports of Device malfunction with FREMANEZUMAB-VFRM
4.7%
of all FREMANEZUMAB-VFRM reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device malfunction From FREMANEZUMAB-VFRM?
Of the 431 reports, 1 (0.2%) required hospitalization.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FREMANEZUMAB-VFRM. However, 431 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)
Injection site swelling (398)
Incorrect dose administered by device (369)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which FREMANEZUMAB-VFRM Alternatives Have Lower Device malfunction Risk?
FREMANEZUMAB-VFRM vs FROVATRIPTAN
FREMANEZUMAB-VFRM vs FRUCTOSE
FREMANEZUMAB-VFRM vs FRUQUINTINIB
FREMANEZUMAB-VFRM vs FULVESTRANT
FREMANEZUMAB-VFRM vs FURAZOLIDONE