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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 LANADELUMAB Cause Intentional product use issue? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional product use issue have been filed in association with LANADELUMAB (TAKHZYRO). This represents 0.4% of all adverse event reports for LANADELUMAB.

8
Reports of Intentional product use issue with LANADELUMAB
0.4%
of all LANADELUMAB reports
1
Deaths
5
Hospitalizations

How Dangerous Is Intentional product use issue From LANADELUMAB?

Of the 8 reports, 1 (12.5%) resulted in death, 5 (62.5%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LANADELUMAB. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does LANADELUMAB Cause?

Hereditary angioedema (1,343) Product dose omission issue (555) Weight decreased (361) Weight increased (353) Inappropriate schedule of product administration (318) Product use issue (229) Covid-19 (225) Injection site pain (201) Insurance issue (172) Drug ineffective (142)

What Other Drugs Cause Intentional product use issue?

INFLIXIMAB (11,028) RITUXIMAB (9,602) INFLIXIMAB-DYYB (7,549) TOCILIZUMAB (5,078) METHOTREXATE (4,087) PREDNISONE (3,961) ABATACEPT (3,693) ADALIMUMAB (3,557) NIVOLUMAB (3,297) LEFLUNOMIDE (3,280)

Which LANADELUMAB Alternatives Have Lower Intentional product use issue Risk?

LANADELUMAB vs LANADELUMAB-FLYO LANADELUMAB vs LANREOTIDE LANADELUMAB vs LANSOPRAZOLE LANADELUMAB vs LANTHANUM LANADELUMAB vs LANTUS

Related Pages

LANADELUMAB Full Profile All Intentional product use issue Reports All Drugs Causing Intentional product use issue LANADELUMAB Demographics