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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 TYSABRI 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 TYSABRI. This represents 0.1% of all adverse event reports for TYSABRI.

9
Reports of Device issue with TYSABRI
0.1%
of all TYSABRI reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device issue From TYSABRI?

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 TYSABRI. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does TYSABRI Cause?

Multiple sclerosis relapse (811) Fatigue (759) Malaise (523) Gait disturbance (445) Multiple sclerosis (443) Memory impairment (422) Headache (368) Drug ineffective (329) Asthenia (328) Fall (324)

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 TYSABRI Alternatives Have Lower Device issue Risk?

TYSABRI vs TYVASO TYSABRI vs UBIDECARENONE TYSABRI vs UBLITUXIMAB TYSABRI vs UBLITUXIMAB-XIIY TYSABRI vs UBROGEPANT

Related Pages

TYSABRI Full Profile All Device issue Reports All Drugs Causing Device issue TYSABRI Demographics