Does GLATIRAMER Cause Condition aggravated? 499 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 499 reports of Condition aggravated have been filed in association with GLATIRAMER (GLATIRAMER ACETATE). This represents 1.1% of all adverse event reports for GLATIRAMER.
499
Reports of Condition aggravated with GLATIRAMER
1.1%
of all GLATIRAMER reports
0
Deaths
88
Hospitalizations
How Dangerous Is Condition aggravated From GLATIRAMER?
Of the 499 reports, 88 (17.6%) required hospitalization, and 2 (0.4%) 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 GLATIRAMER. However, 499 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 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 GLATIRAMER Alternatives Have Lower Condition aggravated Risk?
GLATIRAMER vs GLECAPREVIR\PIBRENTASVIR
GLATIRAMER vs GLEEVEC
GLATIRAMER vs GLICLAZIDE
GLATIRAMER vs GLIMEPIRIDE
GLATIRAMER vs GLIMEPIRIDE\ROSIGLITAZONE