Drug lookup
Drug reference

edaravone

Free-radical scavenger / antioxidant · Anti-ALS

START
60 mg IV over 60 min daily, cycle schedule (or 105 mg oral)
TYPICAL MAX
60 mg IV/day (105 mg oral/day)
STOP IF
Anaphylaxis, significant AKI/hepatotoxicity, or DIC
WATCH
Renal function, LFTs, infusion reactions, sulfite allergy history
CDSCO approvedATC N07XX14
Dose laddermg/d
60IV daily105oral/day
Renal dose adjustmenteGFR mL/min/1.73m²
CAUTIONUsual cycle30AVOIDAvoid — limited safety data90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
6minONSET1hPEAK7h1dDURATION
ONSET
6min · infusion start
PEAK
1h · end infusion
7h ·
DURATION
1d · daily dose
EXCRETION
Renal — metabolites; some unchanged
route + CYP
INTERACTIONS
none in our sources
PREGNANCY
Limited data; use only if clearly needed.
FDA category + note

Mechanism

Pyrazolone free-radical scavenger that quenches hydroxyl radicals and lipid peroxyl radicals, reducing oxidative neuronal injury; mechanism in ALS attributed to slowing motor-neuron oxidative damage.

Indications

Amyotrophic lateral sclerosis (selected patients meeting trial inclusion criteria)Acute ischaemic stroke (selected use in Japan/China — adjunct)

Dosing

Adult
IV: 60 mg IV over 60 min once daily on days 1–14 of an initial 28-day cycle, then 60 mg once daily on 10 of 14 days in subsequent 28-day cycles. Oral suspension 105 mg once daily fasting (approved alternative formulation).
Pediatric
Not established.
Renal adjustment
Caution / not recommended in severe renal impairment.
Hepatic adjustment
Caution in significant hepatic impairment.
Geriatric
No specific adjustment.
Max dose
60 mg IV/day (or 105 mg oral suspension/day)

Pharmacokinetics

Onset
Neuroprotective effect requires chronic dosing
Peak effect
End of infusion (IV)
Duration
Cycle-based dosing schedule
Half-life
Terminal ~5–9 h
Bioavailability
IV 100%; oral suspension reasonable fasting
Protein binding
~92%
Metabolism
Hepatic conjugation
Excretion
Renal (metabolites; some unchanged)

Contraindications

  • Severe renal impairment (caution / avoid IV)
  • Hypersensitivity / sulfite hypersensitivity (asthmatic)
  • Caution: chronic respiratory failure (oral suspension excipient)

Side effects

Common
Bruising/contusionGait disturbanceHeadacheDermatitisEczema
Serious
  • Anaphylaxis / serious hypersensitivity
  • Acute kidney injury (rare)
  • Hepatotoxicity (rare)
  • Disseminated intravascular coagulation (reported, stroke use)

Pregnancy & lactation

Pregnancy

Limited data; use only if clearly needed.

Lactation

Limited data; weigh benefit/risk.

Drug interactions

Antiplatelets
Moderate
Database

Bleeding risk in stroke context

Per stroke protocol monitoring

Source: Kimi deep-research + Cla

Hepatotoxic Drugs
Moderate
Database

Additive hepatic effect

Monitor LFTs

Source: Kimi deep-research + Cla

Nephrotoxic Drugs
Moderate
Database

Additive renal stress

Monitor renal function

Source: Kimi deep-research + Cla

Sulfites
Moderate
Database

Cross-hypersensitivity (formulation excipient)

Avoid in sulfite-sensitive patients

Source: Kimi deep-research + Cla

Other Cns Depressants
Mild
Database

Possible additive sedation (oral suspension)

Counsel

Source: Kimi deep-research + Cla

Related guidelines

Ask House about edaravone

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: Goodman & Gilman 14e·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20