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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 GLATIRAMER Cause Device issue? 385 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 385 reports of Device issue have been filed in association with GLATIRAMER (GLATIRAMER ACETATE). This represents 0.8% of all adverse event reports for GLATIRAMER.

385
Reports of Device issue with GLATIRAMER
0.8%
of all GLATIRAMER reports
0
Deaths
14
Hospitalizations

How Dangerous Is Device issue From GLATIRAMER?

Of the 385 reports, 14 (3.6%) required hospitalization.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GLATIRAMER. However, 385 reports have been filed with the FAERS database.

What Other Side Effects Does GLATIRAMER Cause?

Injection site pain (5,003) Multiple sclerosis relapse (3,695) Drug ineffective (3,321) Injection site reaction (3,317) Multiple sclerosis (2,596) Injection site erythema (2,560) Fatigue (2,408) Dyspnoea (2,364) Injection site mass (2,172) Injection site swelling (1,836)

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 GLATIRAMER Alternatives Have Lower Device issue Risk?

GLATIRAMER vs GLECAPREVIR\PIBRENTASVIR GLATIRAMER vs GLEEVEC GLATIRAMER vs GLICLAZIDE GLATIRAMER vs GLIMEPIRIDE GLATIRAMER vs GLIMEPIRIDE\ROSIGLITAZONE

Related Pages

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