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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DALFAMPRIDINE Cause Incorrect product storage? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect product storage have been filed in association with DALFAMPRIDINE (Dalfampridine). This represents 0.0% of all adverse event reports for DALFAMPRIDINE.

7
Reports of Incorrect product storage with DALFAMPRIDINE
0.0%
of all DALFAMPRIDINE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Incorrect product storage From DALFAMPRIDINE?

Of the 7 reports, 1 (14.3%) required hospitalization.

Is Incorrect product storage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DALFAMPRIDINE. However, 7 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 Incorrect product storage?

ETANERCEPT (2,149) INSULIN LISPRO (1,114) ABATACEPT (583) TERIPARATIDE (573) ADALIMUMAB (476) GOLIMUMAB (392) INSULIN GLARGINE (341) INSULIN HUMAN (336) USTEKINUMAB (299) ERYTHROPOIETIN (268)

Which DALFAMPRIDINE Alternatives Have Lower Incorrect product storage Risk?

DALFAMPRIDINE vs DALTEPARIN DALFAMPRIDINE vs DAMOCTOCOG ALFA PEGOL DALFAMPRIDINE vs DANAPAROID DALFAMPRIDINE vs DANAZOL DALFAMPRIDINE vs DANICOPAN

Related Pages

DALFAMPRIDINE Full Profile All Incorrect product storage Reports All Drugs Causing Incorrect product storage DALFAMPRIDINE Demographics