Does LANADELUMAB-FLYO Cause Product prescribing error? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product prescribing error have been filed in association with LANADELUMAB-FLYO. This represents 2.3% of all adverse event reports for LANADELUMAB-FLYO.
35
Reports of Product prescribing error with LANADELUMAB-FLYO
2.3%
of all LANADELUMAB-FLYO reports
1
Deaths
11
Hospitalizations
How Dangerous Is Product prescribing error From LANADELUMAB-FLYO?
Of the 35 reports, 1 (2.9%) resulted in death, 11 (31.4%) required hospitalization, and 9 (25.7%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LANADELUMAB-FLYO. However, 35 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which LANADELUMAB-FLYO Alternatives Have Lower Product prescribing error Risk?
LANADELUMAB-FLYO vs LANREOTIDE
LANADELUMAB-FLYO vs LANSOPRAZOLE
LANADELUMAB-FLYO vs LANTHANUM
LANADELUMAB-FLYO vs LANTUS
LANADELUMAB-FLYO vs LANTUS SOLOSTAR