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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 NATALIZUMAB Cause Condition aggravated? 218 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 218 reports of Condition aggravated have been filed in association with NATALIZUMAB (TYRUKO). This represents 0.3% of all adverse event reports for NATALIZUMAB.

218
Reports of Condition aggravated with NATALIZUMAB
0.3%
of all NATALIZUMAB reports
9
Deaths
62
Hospitalizations

How Dangerous Is Condition aggravated From NATALIZUMAB?

Of the 218 reports, 9 (4.1%) resulted in death, 62 (28.4%) required hospitalization, and 5 (2.3%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NATALIZUMAB. However, 218 reports have been filed with the FAERS database.

What Other Side Effects Does NATALIZUMAB Cause?

Multiple sclerosis relapse (6,478) Fatigue (4,456) Multiple sclerosis (4,078) Memory impairment (3,024) Malaise (2,523) Fall (2,481) Headache (2,476) Gait disturbance (2,427) Prescribed underdose (2,162) Maternal exposure during pregnancy (1,948)

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 NATALIZUMAB Alternatives Have Lower Condition aggravated Risk?

NATALIZUMAB vs NATALIZUMAB-SZTN NATALIZUMAB vs NATAMYCIN NATALIZUMAB vs NATEGLINIDE NATALIZUMAB vs NAVITOCLAX NATALIZUMAB vs NAXITAMAB-GQGK

Related Pages

NATALIZUMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated NATALIZUMAB Demographics