Does FINGOLIMOD Cause Product dose omission? 658 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 658 reports of Product dose omission have been filed in association with FINGOLIMOD (Fingolimod). This represents 0.9% of all adverse event reports for FINGOLIMOD.
658
Reports of Product dose omission with FINGOLIMOD
0.9%
of all FINGOLIMOD reports
0
Deaths
20
Hospitalizations
How Dangerous Is Product dose omission From FINGOLIMOD?
Of the 658 reports, 20 (3.0%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FINGOLIMOD. However, 658 reports have been filed with the FAERS database.
What Other Side Effects Does FINGOLIMOD Cause?
Fatigue (8,901)
Multiple sclerosis relapse (6,728)
Headache (5,993)
Dizziness (4,317)
White blood cell count decreased (3,597)
Lymphocyte count decreased (3,232)
Hypoaesthesia (3,180)
Gait disturbance (3,007)
Fall (2,715)
Memory impairment (2,623)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which FINGOLIMOD Alternatives Have Lower Product dose omission Risk?
FINGOLIMOD vs FINGOLIMOD LAURYL
FINGOLIMOD vs FISH OIL
FINGOLIMOD vs FISH OIL\MEDIUM-CHAIN TRIGLYCERIDES\OLIVE OIL\SOYBEAN OIL
FINGOLIMOD vs FLAGYL
FINGOLIMOD vs FLECAINIDE