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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 Product storage error? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product storage error have been filed in association with BRODALUMAB (Siliq). This represents 0.4% of all adverse event reports for BRODALUMAB.

8
Reports of Product storage error with BRODALUMAB
0.4%
of all BRODALUMAB reports
1
Deaths
2
Hospitalizations

How Dangerous Is Product storage error From BRODALUMAB?

Of the 8 reports, 1 (12.5%) resulted in death, 2 (25.0%) required hospitalization.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BRODALUMAB. However, 8 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) Intentional product use issue (136) Headache (126) Therapy interrupted (126) Product dose omission issue (124) Disease recurrence (118)

What Other Drugs Cause Product storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which BRODALUMAB Alternatives Have Lower Product storage error Risk?

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

Related Pages

BRODALUMAB Full Profile All Product storage error Reports All Drugs Causing Product storage error BRODALUMAB Demographics