Dalfampridine side effects: what 71,315 FDA adverse event reports show
Drug class
Potassium Channel Blocker
Who reports
71,315 reports · 28% serious · 1,759 with death outcome · 74% female
Used for
Dalfampridine extended-release tablets are indicated as a treatment to improve walking in adult patients with multiple sclerosis (MS). This was demonstrated by an increase in walking speed . Dalfampridine is a potassium channel blocker indicated to improve walking in adult patients with multiple sclerosis (MS). This was demonstrated by an increase in walking speed ( 1 , 14 ).
What it is
Dalfampridine is a potassium channel blocker, available in a 10 mg tablet strength.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
Strongest disproportionality signals
Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,142 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Gait spastic | 123 | 161.7 129.7–201.6ROR 161.9 · calibrated p 4e-9 ✓ | 102.4 EB05 88.1 · IC025 +5.9 3/3 methods agree | Not in label — unassessed | serious n=102 · ♀ 28% (drug 74%) | not reported in cached trials |
| Needle fatigue | 87 | 68.9 54.6–87.1ROR 69.0 · calibrated p 2e-6 ✓ | 55.2 EB05 46.1 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=76 · ♀ 17% (drug 74%) | not reported in cached trials |
| Social problem | 687 | 58.4 53.8–63.4ROR 59.0 · calibrated p 5e-6 ✓ | 48.7 EB05 45.7 · IC025 +5.4 3/3 methods agree | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Relapsing-remitting multiple sclerosis | 132 | 53.0 44.0–63.8ROR 53.1 · calibrated p 1e-5 ✓ | 44.7 EB05 38.6 · IC025 +5.0 3/3 methods agree | Labeled (related wording) related wording | serious n=118 · ♀ 32% (drug 74%) | not reported in cached trials |
| Jc virus test positive | 124 | 49.9 41.3–60.4ROR 50.0 · calibrated p 2e-5 ✓ | 42.5 EB05 36.6 · IC025 +4.9 3/3 methods agree | Lab value / disease marker | serious n=52 · 76% consumer | not reported in cached trials |
| Secondary progressive multiple sclerosis | 222 | 38.9 33.8–44.8ROR 39.0 · calibrated p 6e-5 ✓ | 34.3 EB05 30.7 · IC025 +4.8 3/3 methods agree | Labeled (related wording) related wording | serious n=118 · 75% consumer | not reported in cached trials |
| Peroneal nerve palsy | 641 | 37.3 34.4–40.5ROR 37.6 · calibrated p 8e-5 ✓ | 33.1 EB05 31.0 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=279 · 79% consumer | not reported in cached trials |
| Upper motor neurone lesion | 25 | 37.3 24.6–56.5ROR 37.3 · calibrated p 1e-4 ✓ | 32.4 EB05 23.1 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=20 | not reported in cached trials |
| T-lymphocyte count increased | 21 | 37.0 23.5–58.3ROR 37.0 · calibrated p 2e-4 ✓ | 32.1 EB05 22.1 · IC025 +3.5 3/3 methods agree | Lab value / disease marker | 100% clinician | not reported in cached trials |
| Primary progressive multiple sclerosis | 54 | 36.8 27.7–48.9ROR 36.9 · calibrated p 1e-4 ✓ | 32.4 EB05 25.8 · IC025 +4.2 3/3 methods agree | Labeled (related wording) related wording | serious n=28 · 72% consumer | not reported in cached trials |
| Cd8 lymphocytes decreased | 22 | 35.9 23.1–56.0ROR 36.0 · calibrated p 2e-4 ✓ | 31.3 EB05 21.8 · IC025 +3.5 3/3 methods agree | Lab value / disease marker | – | not reported in cached trials |
| Progressive multiple sclerosis | 116 | 32.3 26.6–39.1ROR 32.3 · calibrated p 2e-4 ✓ | 29.0 EB05 24.8 · IC025 +4.4 3/3 methods agree | Labeled (related wording) related wording | serious n=57 | not reported in cached trials |
| Haemoglobin urine present | 20 | 31.8 20.0–50.4ROR 31.8 · calibrated p 4e-4 ✓ | 28.0 EB05 19.2 · IC025 +3.3 3/3 methods agree | Lab value / disease marker | – | not reported in cached trials |
| Cd4 lymphocytes increased | 22 | 30.1 19.4–46.8ROR 30.2 · calibrated p 5e-4 ✓ | 26.8 EB05 18.7 · IC025 +3.4 3/3 methods agree | Lab value / disease marker | 100% clinician | not reported in cached trials |
| Therapeutic product ineffective for unapproved indication | 42 | 29.5 21.5–40.6ROR 29.6 · calibrated p 4e-4 ✓ | 26.6 EB05 20.5 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | – | not reported in cached trials |
| Walking aid user | 602 | 29.3 27.0–31.9ROR 29.6 · calibrated p 3e-4 ✓ | 26.7 EB05 25.0 · IC025 +4.6 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=219 · 89% consumer | not reported in cached trials |
| Therapy cessation | 4,510 | 28.4 27.6–29.3ROR 30.3 · calibrated p 2e-4 ✓ | 26.0 EB05 25.3 · IC025 +4.6 3/3 methods agree | Reporting / coding artifact | serious PRR 28.9 · 93% consumer | not reported in cached trials |
| Urine leukocyte esterase positive | 61 | 27.6 21.3–35.9ROR 27.7 · calibrated p 5e-4 ✓ | 25.1 EB05 20.3 · IC025 +4.0 3/3 methods agree | Lab value / disease marker | serious n=18 · 100% clinician | not reported in cached trials |
| Orthosis user | 24 | 27.3 18.0–41.5ROR 27.3 · calibrated p 7e-4 ✓ | 24.6 EB05 17.4 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | – | not reported in cached trials |
| B-lymphocyte count decreased | 110 | 26.1 21.5–31.7ROR 26.1 · calibrated p 6e-4 ✓ | 23.9 EB05 20.4 · IC025 +4.1 3/3 methods agree | Lab value / disease marker | serious n=41 | not reported in cached trials |
| Urine analysis abnormal | 232 | 24.5 21.4–28.0ROR 24.6 · calibrated p 8e-4 ✓ | 22.6 EB05 20.3 · IC025 +4.2 3/3 methods agree | Reporting / coding artifact | serious n=59 | not reported in cached trials |
| Wheelchair user | 339 | 24.1 21.6–26.9ROR 24.2 · calibrated p 8e-4 ✓ | 22.3 EB05 20.4 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=230 · 88% consumer | not reported in cached trials |
| Muscle spasticity | 877 | 22.3 20.8–23.9ROR 22.6 · calibrated p 0.001 ✓ | 20.8 EB05 19.7 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious PRR 31.4 | not reported in cached trials |
| Multiple sclerosis relapse | 4,774 | 21.8 21.1–22.4ROR 23.2 · calibrated p 1e-3 ✓ | 20.3 EB05 19.8 · IC025 +4.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 32.5 · 77% consumer | not reported in cached trials |
| Multiple sclerosis pseudo relapse | 22 | 20.9 13.6–32.3ROR 20.9 · calibrated p 0.003 ✓ | 19.2 EB05 13.3 · IC025 +3.1 3/3 methods agree | Labeled (related wording) related wording | serious n=19 | not reported in cached trials |
| Sars-cov-2 antibody test negative | 32 | 20.9 14.6–29.9ROR 20.9 · calibrated p 0.002 ✓ | 19.3 EB05 14.3 · IC025 +3.3 3/3 methods agree | Reporting / coding artifact | serious n=23 · 100% consumer | not reported in cached trials |
| Jc polyomavirus test positive | 77 | 20.5 16.3–25.9ROR 20.5 · calibrated p 0.002 ✓ | 19.1 EB05 15.8 · IC025 +3.7 3/3 methods agree | Lab value / disease marker | serious n=43 | not reported in cached trials |
| Multiple sclerosis | 3,127 | 20.4 19.7–21.1ROR 21.3 · calibrated p 0.001 ✓ | 19.1 EB05 18.6 · IC025 +4.2 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 27.9 · 77% consumer | not reported in cached trials |
| Neurogenic bladder | 132 | 19.5 16.3–23.2ROR 19.5 · calibrated p 0.002 ✓ | 18.3 EB05 15.8 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=97 | not reported in cached trials |
| Decreased vibratory sense | 20 | 18.4 11.7–28.9ROR 18.4 · calibrated p 0.004 ✓ | 16.9 EB05 11.3 · IC025 +2.9 3/3 methods agree | Not in label — unassessed | serious n=19 | not reported in cached trials |
| Gait disturbance | 10,976 | 17.8 17.5–18.1ROR 20.8 · calibrated p 0.002 ✓ | 16.8 EB05 16.6 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious PRR 11.8 · 84% consumer | NCT02271217: 1/126 (0.8%) on Dalfampridine (serious AE) |
| Balance disorder | 4,900 | 17.6 17.1–18.1ROR 18.8 · calibrated p 0.003 ✓ | 16.6 EB05 16.3 · IC025 +4.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 14.1 · 82% consumer | NCT01328379: 2/142 (1.4%) on Dalfampridine; 6/143 (4.2%) control |
| T-lymphocyte count decreased | 38 | 17.3 12.5–24.0ROR 17.3 · calibrated p 0.005 ✓ | 16.2 EB05 12.2 · IC025 +3.2 3/3 methods agree | Lab value / disease marker | 100% clinician | not reported in cached trials |
| Vitamin b12 increased | 43 | 16.8 12.4–22.9ROR 16.9 · calibrated p 0.005 ✓ | 15.8 EB05 12.1 · IC025 +3.3 3/3 methods agree | Lab value / disease marker | serious n=15 | not reported in cached trials |
| Central nervous system lesion | 726 | 16.2 15.1–17.5ROR 16.4 · calibrated p 0.005 ✓ | 15.4 EB05 14.5 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious PRR 24.7 · 76% consumer | not reported in cached trials |
| Bladder dysfunction | 51 | 15.3 11.5–20.3ROR 15.3 · calibrated p 0.007 ✓ | 14.4 EB05 11.3 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=33 | not reported in cached trials |
| Trigeminal neuralgia | 197 | 15.1 13.1–17.4ROR 15.1 · calibrated p 0.007 ✓ | 14.4 EB05 12.7 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious n=112 | not reported in cached trials |
| Culture urine positive | 68 | 14.8 11.6–18.9ROR 14.8 · calibrated p 0.008 ✓ | 14.0 EB05 11.4 · IC025 +3.3 3/3 methods agree | Lab value / disease marker | serious n=14 · 100% clinician | not reported in cached trials |
| Hypertonic bladder | 136 | 14.5 12.2–17.3ROR 14.6 · calibrated p 0.008 ✓ | 13.8 EB05 12.0 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=103 · ♀ 44% (drug 74%) | not reported in cached trials |
| Monoparesis | 84 | 14.2 11.4–17.6ROR 14.2 · calibrated p 0.010 ✓ | 13.5 EB05 11.2 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=81 · ♀ 0% (drug 74%) | not reported in cached trials |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Dalfampridine as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (2 of 40 signal terms matched).
- NCT01328379 — Study of Fampridine-ER Tablets in Patients With Multiple Sclerosis (N=430, PHASE3; 23 AE terms posted; arms: Placebo; Dalfampridine-ER 5mg; Dalfampridine-ER 10mg)
- NCT02271217 — A Study to Evaluate the Efficacy and Safety of Two Dose Strengths of Dalfampridine Extended Release Tablets. (N=377, PHASE3; 49 AE terms posted; arms: Placebo; Dalfampridine-ER 7.5 mg; Dalfampridine-ER 10mg)
Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.
Most frequently reported reactions
By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Gait disturbance | 10,976 | 17.8 17.5–18.1ROR 20.8 · calibrated p 0.002 ✓ | 16.8 EB05 16.6 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious PRR 11.8 · 84% consumer | NCT02271217: 1/126 (0.8%) on Dalfampridine (serious AE) |
| Drug ineffective (drug did not work) | 8,309 | 1.9 1.8–1.9ROR 2.0 · calibrated p 0.930 | 1.9 EB05 1.8 · IC025 +0.9 | Reporting / coding artifact | serious PRR 1.5 · 79% consumer | not reported in cached trials |
| Fall | 7,335 | 6.6 6.5–6.8ROR 7.3 · calibrated p 0.089 | 6.5 EB05 6.4 · IC025 +2.7 3/3 methods agree | Not in label — unassessed | serious PRR 7.2 · 81% consumer | NCT01328379: 3/142 (2.1%) on Dalfampridine; 7/143 (4.9%) control |
| Fatigue (tiredness) | 5,527 | 2.1 2.0–2.2ROR 2.2 · calibrated p 0.955 | 2.1 EB05 2.0 · IC025 +1.0 3/3 methods agree | Labeled (related wording) related wording | serious PRR 2.4 · 82% consumer | NCT01328379: 4/142 (2.8%) on Dalfampridine; 3/143 (2.1%) control |
| Balance disorder | 4,900 | 17.6 17.1–18.1ROR 18.8 · calibrated p 0.003 ✓ | 16.6 EB05 16.3 · IC025 +4.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 14.1 · 82% consumer | NCT01328379: 2/142 (1.4%) on Dalfampridine; 6/143 (4.2%) control |
| Multiple sclerosis relapse | 4,774 | 21.8 21.1–22.4ROR 23.2 · calibrated p 1e-3 ✓ | 20.3 EB05 19.8 · IC025 +4.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 32.5 · 77% consumer | not reported in cached trials |
| Therapy cessation | 4,510 | 28.4 27.6–29.3ROR 30.3 · calibrated p 2e-4 ✓ | 26.0 EB05 25.3 · IC025 +4.6 3/3 methods agree | Reporting / coding artifact | serious PRR 28.9 · 93% consumer | not reported in cached trials |
| Dizziness | 3,989 | 2.4 2.3–2.4ROR 2.4 · calibrated p 0.836 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.2 · 79% consumer | NCT01328379: 15/142 (10.6%) on Dalfampridine; 3/143 (2.1%) control |
| Urinary tract infection (bladder infection) | 3,741 | 6.6 6.4–6.8ROR 6.9 · calibrated p 0.103 | 6.5 EB05 6.3 · IC025 +2.6 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 8.8 | NCT01328379: 14/142 (9.9%) on Dalfampridine; 8/143 (5.6%) control |
| Condition aggravated | 3,484 | 3.4 3.3–3.5ROR 3.5 · calibrated p 0.474 | 3.4 EB05 3.3 · IC025 +1.7 3/3 methods agree | Reporting / coding artifact | serious PRR 3.0 · 88% consumer | not reported in cached trials |
| Asthenia (weakness) | 3,461 | 2.7 2.6–2.8ROR 2.8 · calibrated p 0.691 | 2.7 EB05 2.6 · IC025 +1.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.2 · 79% consumer | NCT02271217: 4/126 (3.2%) on Dalfampridine |
| Insomnia (trouble sleeping) | 3,306 | 3.7 3.6–3.8ROR 3.8 · calibrated p 0.415 | 3.6 EB05 3.5 · IC025 +1.8 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.9 · 80% consumer | NCT01328379: 11/142 (7.7%) on Dalfampridine; 6/143 (4.2%) control |
| Headache | 3,266 | 1.5 1.5–1.6ROR 1.6 · calibrated p 0.682 | 1.5 EB05 1.5 · IC025 +0.6 | Labeled adverse reaction exact term | serious PRR 1.7 · 80% consumer | NCT01328379: 18/142 (12.7%) on Dalfampridine; 16/143 (11.2%) control |
| Multiple sclerosis | 3,127 | 20.4 19.7–21.1ROR 21.3 · calibrated p 0.001 ✓ | 19.1 EB05 18.6 · IC025 +4.2 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 27.9 · 77% consumer | not reported in cached trials |
| Mobility decreased | 2,998 | 12.8 12.4–13.3ROR 13.3 · calibrated p 0.011 ✓ | 12.3 EB05 11.9 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious PRR 7.5 · 86% consumer | not reported in cached trials |
Unlabeled candidate signals
These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.
- Gait spastic — n=123, PRR 161.7
- Needle fatigue — n=87, PRR 68.9
- Peroneal nerve palsy — n=641, PRR 37.3
- Upper motor neurone lesion — n=25, PRR 37.3
- Orthosis user — n=24, PRR 27.3
- Wheelchair user — n=339, PRR 24.1
- Muscle spasticity — n=877, PRR 22.3
- Neurogenic bladder — n=132, PRR 19.5
- Decreased vibratory sense — n=20, PRR 18.4
- Gait disturbance — n=10,976, PRR 17.8 (also seen in trial arm)
Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.
Common questions
What are the most reported side effects of Dalfampridine?
In FDA FAERS, the most frequently co-reported reaction terms for Dalfampridine are gait disturbance, fall, fatigue, balance disorder, multiple sclerosis relapse, dizziness. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.
Does Dalfampridine have an FDA boxed warning?
No. The FDA label retrieved for Dalfampridine has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Dalfampridine causes these side effects?
No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.
Sources & methods
- FDA label via openFDA (set ID 1134ac0f-59c1-a20b-e063-6294a90affcc, effective 20260728; matched on
openfda.generic_name.exact:"DALFAMPRIDINE") - Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,182 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
DALFAMPRIDINE, results-bearing studies sorted by enrollment)
Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.