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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 SATRALIZUMAB-MWGE 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 SATRALIZUMAB-MWGE. This represents 0.5% of all adverse event reports for SATRALIZUMAB-MWGE.

5
Reports of Condition aggravated with SATRALIZUMAB-MWGE
0.5%
of all SATRALIZUMAB-MWGE reports
0
Deaths
3
Hospitalizations

How Dangerous Is Condition aggravated From SATRALIZUMAB-MWGE?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SATRALIZUMAB-MWGE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does SATRALIZUMAB-MWGE Cause?

Neuromyelitis optica spectrum disorder (181) Off label use (87) Urinary tract infection (87) Pneumonia (64) Covid-19 (47) No adverse event (47) Fatigue (41) Headache (36) Pain (36) Arthralgia (31)

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 SATRALIZUMAB-MWGE Alternatives Have Lower Condition aggravated Risk?

SATRALIZUMAB-MWGE vs SAXAGLIPTIN SATRALIZUMAB-MWGE vs SCHOLL'S INGROWN TOENAIL PAIN RELIEVER SATRALIZUMAB-MWGE vs SCOPOLAMINE SATRALIZUMAB-MWGE vs SCOPOLAMINE HYDROBROMIDE SATRALIZUMAB-MWGE vs SEBELIPASE ALFA

Related Pages

SATRALIZUMAB-MWGE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated SATRALIZUMAB-MWGE Demographics