Does DALFAMPRIDINE Cause Product dose omission? 786 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 786 reports of Product dose omission have been filed in association with DALFAMPRIDINE (Dalfampridine). This represents 1.4% of all adverse event reports for DALFAMPRIDINE.
786
Reports of Product dose omission with DALFAMPRIDINE
1.4%
of all DALFAMPRIDINE reports
1
Deaths
81
Hospitalizations
How Dangerous Is Product dose omission From DALFAMPRIDINE?
Of the 786 reports, 1 (0.1%) resulted in death, 81 (10.3%) required hospitalization, and 1 (0.1%) 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 DALFAMPRIDINE. However, 786 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 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 DALFAMPRIDINE Alternatives Have Lower Product dose omission Risk?
DALFAMPRIDINE vs DALTEPARIN
DALFAMPRIDINE vs DAMOCTOCOG ALFA PEGOL
DALFAMPRIDINE vs DANAPAROID
DALFAMPRIDINE vs DANAZOL
DALFAMPRIDINE vs DANICOPAN