Does LANADELUMAB-FLYO Cause Wrong technique in product usage process? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Wrong technique in product usage process have been filed in association with LANADELUMAB-FLYO. This represents 0.5% of all adverse event reports for LANADELUMAB-FLYO.
7
Reports of Wrong technique in product usage process with LANADELUMAB-FLYO
0.5%
of all LANADELUMAB-FLYO reports
0
Deaths
5
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LANADELUMAB-FLYO?
Of the 7 reports, 5 (71.4%) 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 LANADELUMAB-FLYO. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does LANADELUMAB-FLYO Cause?
Hereditary angioedema (794)
Product dose omission issue (177)
Inappropriate schedule of product administration (144)
Drug ineffective (137)
Headache (126)
Weight decreased (125)
Weight increased (120)
Injection site pain (119)
Product use issue (114)
Malaise (90)
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 LANADELUMAB-FLYO Alternatives Have Lower Wrong technique in product usage process Risk?
LANADELUMAB-FLYO vs LANREOTIDE
LANADELUMAB-FLYO vs LANSOPRAZOLE
LANADELUMAB-FLYO vs LANTHANUM
LANADELUMAB-FLYO vs LANTUS
LANADELUMAB-FLYO vs LANTUS SOLOSTAR