Does LECANEMAB-IRMB Cause Condition aggravated? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with LECANEMAB-IRMB (LECANEMAB AUTOINJECTOR). This represents 0.2% of all adverse event reports for LECANEMAB-IRMB.
5
Reports of Condition aggravated with LECANEMAB-IRMB
0.2%
of all LECANEMAB-IRMB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Condition aggravated From LECANEMAB-IRMB?
Of the 5 reports, 1 (20.0%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LECANEMAB-IRMB. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does LECANEMAB-IRMB Cause?
Headache (399)
Amyloid related imaging abnormality-oedema/effusion (307)
Amyloid related imaging abnormality-microhaemorrhages and haemosiderin deposits (298)
Infusion related reaction (219)
Chills (205)
Fatigue (178)
Pyrexia (135)
Confusional state (132)
Dizziness (126)
Nausea (119)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which LECANEMAB-IRMB Alternatives Have Lower Condition aggravated Risk?
LECANEMAB-IRMB vs LECITHIN\POLOXAMER 407
LECANEMAB-IRMB vs LEDIPASVIR
LECANEMAB-IRMB vs LEDIPASVIR\SOFOSBUVIR
LECANEMAB-IRMB vs LEFLUNOMIDE
LECANEMAB-IRMB vs LEMBOREXANT