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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FREMANEZUMAB-VFRM Cause Device leakage? 528 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 528 reports of Device leakage have been filed in association with FREMANEZUMAB-VFRM. This represents 5.8% of all adverse event reports for FREMANEZUMAB-VFRM.

528
Reports of Device leakage with FREMANEZUMAB-VFRM
5.8%
of all FREMANEZUMAB-VFRM reports
0
Deaths
4
Hospitalizations

How Dangerous Is Device leakage From FREMANEZUMAB-VFRM?

Of the 528 reports, 4 (0.8%) required hospitalization.

Is Device leakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FREMANEZUMAB-VFRM. However, 528 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) Headache (528) Injection site pruritus (462) Device malfunction (431) Injection site swelling (398) Incorrect dose administered by device (369)

What Other Drugs Cause Device leakage?

SOMATROPIN (9,113) LEUPROLIDE (5,861) EXENATIDE (5,115) PEGFILGRASTIM (1,380) ALBIGLUTIDE (1,195) SECUKINUMAB (910) RISPERIDONE (878) TREPROSTINIL (874) DEVICE (795) GUSELKUMAB (712)

Which FREMANEZUMAB-VFRM Alternatives Have Lower Device leakage Risk?

FREMANEZUMAB-VFRM vs FROVATRIPTAN FREMANEZUMAB-VFRM vs FRUCTOSE FREMANEZUMAB-VFRM vs FRUQUINTINIB FREMANEZUMAB-VFRM vs FULVESTRANT FREMANEZUMAB-VFRM vs FURAZOLIDONE

Related Pages

FREMANEZUMAB-VFRM Full Profile All Device leakage Reports All Drugs Causing Device leakage FREMANEZUMAB-VFRM Demographics