Does GLATIRAMER Cause Maternal exposure timing unspecified? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Maternal exposure timing unspecified have been filed in association with GLATIRAMER (GLATIRAMER ACETATE). This represents 0.0% of all adverse event reports for GLATIRAMER.
16
Reports of Maternal exposure timing unspecified with GLATIRAMER
0.0%
of all GLATIRAMER reports
0
Deaths
3
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From GLATIRAMER?
Of the 16 reports, 3 (18.8%) required hospitalization.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLATIRAMER. However, 16 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which GLATIRAMER Alternatives Have Lower Maternal exposure timing unspecified Risk?
GLATIRAMER vs GLECAPREVIR\PIBRENTASVIR
GLATIRAMER vs GLEEVEC
GLATIRAMER vs GLICLAZIDE
GLATIRAMER vs GLIMEPIRIDE
GLATIRAMER vs GLIMEPIRIDE\ROSIGLITAZONE