Does FREMANEZUMAB-VFRM Cause Wrong technique in product usage process? 181 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 181 reports of Wrong technique in product usage process have been filed in association with FREMANEZUMAB-VFRM. This represents 2.0% of all adverse event reports for FREMANEZUMAB-VFRM.
181
Reports of Wrong technique in product usage process with FREMANEZUMAB-VFRM
2.0%
of all FREMANEZUMAB-VFRM reports
0
Deaths
5
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FREMANEZUMAB-VFRM?
Of the 181 reports, 5 (2.8%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FREMANEZUMAB-VFRM. However, 181 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which FREMANEZUMAB-VFRM Alternatives Have Lower Wrong technique in product usage process Risk?
FREMANEZUMAB-VFRM vs FROVATRIPTAN
FREMANEZUMAB-VFRM vs FRUCTOSE
FREMANEZUMAB-VFRM vs FRUQUINTINIB
FREMANEZUMAB-VFRM vs FULVESTRANT
FREMANEZUMAB-VFRM vs FURAZOLIDONE