Does FREMANEZUMAB-VFRM Cause Device delivery system issue? 221 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 221 reports of Device delivery system issue have been filed in association with FREMANEZUMAB-VFRM. This represents 2.4% of all adverse event reports for FREMANEZUMAB-VFRM.
221
Reports of Device delivery system issue with FREMANEZUMAB-VFRM
2.4%
of all FREMANEZUMAB-VFRM reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device delivery system issue From FREMANEZUMAB-VFRM?
Of the 221 reports, 2 (0.9%) required hospitalization.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FREMANEZUMAB-VFRM. However, 221 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 delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which FREMANEZUMAB-VFRM Alternatives Have Lower Device delivery system issue Risk?
FREMANEZUMAB-VFRM vs FROVATRIPTAN
FREMANEZUMAB-VFRM vs FRUCTOSE
FREMANEZUMAB-VFRM vs FRUQUINTINIB
FREMANEZUMAB-VFRM vs FULVESTRANT
FREMANEZUMAB-VFRM vs FURAZOLIDONE