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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 Device issue? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device issue have been filed in association with SATRALIZUMAB-MWGE. This represents 0.8% of all adverse event reports for SATRALIZUMAB-MWGE.

9
Reports of Device issue with SATRALIZUMAB-MWGE
0.8%
of all SATRALIZUMAB-MWGE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device issue From SATRALIZUMAB-MWGE?

Of the 9 reports, 1 (11.1%) required hospitalization.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SATRALIZUMAB-MWGE. However, 9 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 Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which SATRALIZUMAB-MWGE Alternatives Have Lower Device issue 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 Device issue Reports All Drugs Causing Device issue SATRALIZUMAB-MWGE Demographics