Does DALFAMPRIDINE Cause Intentional product use issue? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Intentional product use issue have been filed in association with DALFAMPRIDINE (Dalfampridine). This represents 0.1% of all adverse event reports for DALFAMPRIDINE.
27
Reports of Intentional product use issue with DALFAMPRIDINE
0.1%
of all DALFAMPRIDINE reports
2
Deaths
8
Hospitalizations
How Dangerous Is Intentional product use issue From DALFAMPRIDINE?
Of the 27 reports, 2 (7.4%) resulted in death, 8 (29.6%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DALFAMPRIDINE. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does DALFAMPRIDINE Cause?
Gait disturbance (8,780)
Drug ineffective (6,794)
Fall (5,554)
Therapy cessation (4,580)
Fatigue (3,778)
Balance disorder (3,753)
Multiple sclerosis relapse (3,322)
Condition aggravated (3,240)
Dizziness (2,959)
Urinary tract infection (2,757)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DALFAMPRIDINE Alternatives Have Lower Intentional product use issue Risk?
DALFAMPRIDINE vs DALTEPARIN
DALFAMPRIDINE vs DAMOCTOCOG ALFA PEGOL
DALFAMPRIDINE vs DANAPAROID
DALFAMPRIDINE vs DANAZOL
DALFAMPRIDINE vs DANICOPAN