Does GLATIRAMER Cause Wrong technique in product usage process? 427 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 427 reports of Wrong technique in product usage process have been filed in association with GLATIRAMER (GLATIRAMER ACETATE). This represents 0.9% of all adverse event reports for GLATIRAMER.
427
Reports of Wrong technique in product usage process with GLATIRAMER
0.9%
of all GLATIRAMER reports
0
Deaths
35
Hospitalizations
How Dangerous Is Wrong technique in product usage process From GLATIRAMER?
Of the 427 reports, 35 (8.2%) required hospitalization, and 4 (0.9%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLATIRAMER. However, 427 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which GLATIRAMER Alternatives Have Lower Wrong technique in product usage process Risk?
GLATIRAMER vs GLECAPREVIR\PIBRENTASVIR
GLATIRAMER vs GLEEVEC
GLATIRAMER vs GLICLAZIDE
GLATIRAMER vs GLIMEPIRIDE
GLATIRAMER vs GLIMEPIRIDE\ROSIGLITAZONE