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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 BRODALUMAB Cause Intentional product use issue? 136 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 136 reports of Intentional product use issue have been filed in association with BRODALUMAB (Siliq). This represents 6.5% of all adverse event reports for BRODALUMAB.

136
Reports of Intentional product use issue with BRODALUMAB
6.5%
of all BRODALUMAB reports
7
Deaths
40
Hospitalizations

How Dangerous Is Intentional product use issue From BRODALUMAB?

Of the 136 reports, 7 (5.1%) resulted in death, 40 (29.4%) required hospitalization.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRODALUMAB. However, 136 reports have been filed with the FAERS database.

What Other Side Effects Does BRODALUMAB Cause?

Psoriasis (418) Drug ineffective (177) Arthralgia (175) Fatigue (152) Psoriatic arthropathy (141) Headache (126) Therapy interrupted (126) Product dose omission issue (124) Disease recurrence (118) Inappropriate schedule of product administration (108)

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 BRODALUMAB Alternatives Have Lower Intentional product use issue Risk?

BRODALUMAB vs BROLUCIZUMAB BRODALUMAB vs BROLUCIZUMAB-DBLL BRODALUMAB vs BROMAZEPAM BRODALUMAB vs BROMFENAC BRODALUMAB vs BROMHEXINE

Related Pages

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