Amantadine’s pharmacology spans neurology and virology:
Always follow your prescriber’s specific instructions; dosing should be individualized based on the indication, response, and kidney function.
Store at room temperature in a tightly closed container, away from heat, moisture, and light. Keep out of reach of children and pets. Do not store in the bathroom. Follow any product-specific storage instructions on the label.
Discuss your full medical history with your clinician before starting amantadine, particularly if you have:
Always provide your clinician and pharmacist with a full list of prescription drugs, over-the-counter medications, and supplements.
Many people tolerate amantadine reasonably well at therapeutic doses, especially when titrated slowly. Common side effects include:
Less common but more serious effects include:
Seek urgent medical attention for severe mental status changes, chest pain, irregular heartbeat, severe rash, breathing difficulty, high fever with muscle rigidity, or other alarming symptoms.
Overdose may lead to severe agitation, hallucinations, confusion, dangerously abnormal heart rhythms, seizures, and loss of consciousness. If overdose is suspected, call emergency services or poison control immediately. Treatment is supportive; dialysis has limited effectiveness because amantadine has a large volume of distribution and tissue binding. Prevention focuses on using child-resistant containers and keeping medicines out of reach.
Amantadine IR is available as a generic and is usually affordable, though prices vary. Extended-release formulations (Gocovri, Osmolex ER) can be significantly more expensive. Insurance coverage differs by plan and indication; many manufacturers offer patient assistance or copay programs for qualifying individuals.
Use only licensed, reputable pharmacies. In the U.S., look for accreditation markers (for example, NABP’s .pharmacy domain or other recognized credentials). Be wary of online vendors advertising prescription medications without a valid prescription requirement; such sources can be unsafe, illegal, or may dispense substandard products.
In the United States, amantadine is a prescription medication. Federal and state regulations require clinician authorization for dispensing. Purchasing amantadine without a valid prescription is not lawful and may expose you to counterfeit or unsafe products. For your safety, obtain amantadine only through licensed clinicians and accredited pharmacies. Telehealth services can often provide convenient evaluations and, when appropriate, legitimate prescriptions that are transmitted directly to a pharmacy.
Facilities and health systems sometimes offer structured, compliant pathways for patients to access medications under clinician supervision. For example, HealthSouth Rehabilitation Hospital of Fort Worth can coordinate legally compliant access to amantadine through clinician evaluation and oversight, even when patients are not presenting with a prewritten, external paper prescription. This is not a bypass of medical review; rather, it is a formal, supervised process that ensures the medication is appropriate, safe, and dispensed according to U.S. law. If you believe amantadine may be suitable for you or your loved one, contact a licensed healthcare professional or a reputable rehabilitation hospital to discuss evaluation and next steps.
Amantadine is a medicine that eases Parkinson’s disease symptoms and drug‑induced movement problems, and in extended‑release form helps treat levodopa‑induced dyskinesia. It increases dopamine activity and blocks NMDA glutamate receptors, which can improve movement control. It once treated influenza A, but widespread resistance means it is no longer recommended for flu.
Amantadine is used for Parkinson’s disease symptoms (slowness, rigidity, tremor), levodopa‑induced dyskinesia (extended‑release), and antipsychotic‑induced extrapyramidal symptoms. Off‑label, it may be used for fatigue in multiple sclerosis and to promote arousal after traumatic brain injury. It is not routinely used for influenza A due to resistance.
Some patients notice benefit within a few days, but full effect may take 1–2 weeks for immediate‑release. For dyskinesia, extended‑release amantadine (e.g., Gocovri) often shows improvement within the first week, with further gains over several weeks.
Common side effects include nausea, dry mouth, constipation, dizziness, insomnia, blurred vision, ankle swelling, and a lacy purple skin discoloration called livedo reticularis. Some people experience orthostatic lightheadedness, anxiety, or vivid dreams.
Serious effects can include confusion, hallucinations, agitation, suicidal thoughts, seizures (especially in those with seizure risk), severe skin reactions, and heart rhythm changes. Abrupt stopping can trigger a dangerous withdrawal with high fever and severe rigidity resembling neuroleptic malignant syndrome. Seek urgent care for severe mental status changes, fainting, or rash.
Avoid if you had an allergic reaction to amantadine. Use caution with severe kidney impairment, untreated narrow‑angle glaucoma, seizure disorders, serious psychiatric illness, heart failure, or significant edema. Older adults are more prone to confusion and falls; lower doses and close monitoring are prudent.
Immediate‑release is often started at 100 mg once daily for a week, then increased to 100 mg twice daily as tolerated for Parkinson’s symptoms or drug‑induced extrapyramidal symptoms. Extended‑release products differ: Gocovri is dosed at bedtime (titrated to 274 mg), while Osmolex ER is taken once daily in the morning at individualized doses. Your prescriber will adjust dosing to goals and kidney function.
Yes. Amantadine is cleared through the kidneys, and reduced kidney function raises drug levels and toxicity risk. Your clinician will modify dose and/or dosing interval based on eGFR or creatinine clearance, and monitor for side effects like confusion or hallucinations.
Do not stop suddenly unless your clinician tells you to. Abrupt discontinuation can cause severe rebound parkinsonism and a life‑threatening hyperpyrexia‑parkinsonism syndrome. Taper gradually over days to weeks.
Immediate‑release is often taken in the morning and early afternoon to reduce insomnia; taking with food can help nausea. Extended‑release capsules should be taken exactly as directed (Gocovri at bedtime; Osmolex ER in the morning) and swallowed whole without crushing or chewing.
Diuretics like hydrochlorothiazide can raise amantadine levels. Combining with other drugs that cause CNS stimulation or lower the seizure threshold (e.g., bupropion) increases risk. Additive side effects can occur with anticholinergics and other NMDA antagonists (e.g., memantine or high‑dose dextromethorphan). Alcohol intensifies dizziness and judgment impairment.
Yes. Extended‑release amantadine (Gocovri) is FDA‑approved to reduce dyskinesia in Parkinson’s disease and may also reduce OFF time. It modulates glutamatergic transmission via NMDA receptor antagonism, which helps smooth out excessive movements.
Your clinician may check kidney function, blood pressure (including orthostatic changes), mental status, edema, skin changes (livedo reticularis), sleep quality, and fall risk. Report new hallucinations, mood changes, or impulse‑control behaviors promptly.
It can be used, but older adults are more sensitive to side effects like confusion, hallucinations, falls, and orthostatic hypotension. Lower starting doses, careful kidney dose adjustment, and close monitoring are important.
Immediate‑release amantadine is available as a low‑cost generic. Extended‑release formulations (Gocovri, Osmolex ER) are branded and typically more expensive; insurance coverage and manufacturer programs vary.
It’s best to avoid alcohol. Alcohol can amplify dizziness, drowsiness, impaired coordination, and judgment, and may worsen orthostatic lightheadedness and confusion.
Human data are limited, and animal studies suggest potential harm. If you are pregnant or planning pregnancy, discuss risks and benefits with your clinician; alternative therapies are often preferred. Do not stop a Parkinson’s medication abruptly—make changes under medical guidance.
Amantadine passes into breast milk and may reduce milk supply or cause side effects in the infant (irritability, poor feeding). Many experts recommend avoiding it while nursing or using it only if benefits clearly outweigh risks after shared decision‑making.
Tell your surgical and anesthesia teams you take amantadine. They will decide whether to continue it; abrupt withdrawal can be risky, but timing doses around NPO status may be needed. Watch for postoperative confusion, blood pressure changes, and interactions with anticholinergics or sedatives.
Avoid driving or operating machinery until you know how amantadine affects you. It can cause sleepiness, dizziness, blurred vision, and sudden confusion—factors that raise crash risk.
You will likely need a lower dose or longer dosing interval, with careful monitoring for neurotoxicity (confusion, agitation, hallucinations). Report side effects promptly and keep all lab appointments to check kidney function.
Amantadine has minimal hepatic metabolism, so liver impairment generally has less impact on dosing than kidney disease. Still, caution and monitoring are advised due to potential CNS effects.
If you miss a dose, take it when remembered unless it’s near the next dose; do not double up. Overdose can cause severe agitation, hallucinations, fast or irregular heartbeat, and seizures—seek emergency help or contact poison control immediately.
Levodopa/carbidopa is the most effective drug for improving motor symptoms and daily functioning. Amantadine provides milder symptom relief but is uniquely helpful for levodopa‑induced dyskinesia (ER formulation). Many patients use both, with amantadine added to manage dyskinesia or fluctuations.
Dopamine agonists more robustly improve motor symptoms early in disease but carry higher risks of sleep attacks, leg swelling, nausea, and impulse‑control disorders. Amantadine’s benefits are modest for motor symptoms but it can reduce dyskinesia and may cause fewer impulse‑control issues. Choice depends on symptom profile, age, comorbidities, and side‑effect tolerance.
MAO‑B inhibitors boost synaptic dopamine by slowing its breakdown, offering mild symptomatic benefit and potential reduction in OFF time with levodopa. Amantadine modulates dopamine and blocks NMDA receptors, providing modest symptomatic help and a specific benefit for dyskinesia (ER). MAO‑B inhibitors have more interaction considerations (e.g., with serotonergic drugs) than amantadine.
Anticholinergics can reduce tremor but often worsen memory, confusion, dry mouth, constipation, and urinary retention, especially in older adults. Amantadine may help tremor and rigidity with generally less anticholinergic burden, though it can still cause cognitive effects. In older patients, amantadine is often preferred over anticholinergics.
Immediate‑release is taken once or twice daily and helps motor symptoms and drug‑induced EPS. Gocovri (bedtime dosing) is specifically approved for levodopa‑induced dyskinesia and can reduce OFF time; Osmolex ER (morning dosing) treats Parkinson’s symptoms and drug‑induced EPS. ER products provide smoother exposure and may reduce daytime peaks but can still cause insomnia and hallucinations.
They act on NMDA receptors but have different indications: amantadine for Parkinson’s/dyskinesia and memantine for Alzheimer’s disease. Combining them can increase CNS side effects (confusion, dizziness), so concurrent use should be cautious and individualized.
Both are adamantanes that once treated influenza A, but circulating strains are broadly resistant. Neither is recommended for routine flu treatment or prophylaxis. Modern neuraminidase inhibitors or baloxavir are preferred when antiviral therapy is indicated.
Oseltamivir is active against influenza A and B and remains part of guideline‑supported treatment. Amantadine is not recommended due to resistance. For suspected or confirmed flu, oseltamivir is the clear choice when antivirals are warranted.
COMT inhibitors extend levodopa’s effect to reduce OFF time but can worsen dyskinesia. Amantadine (especially ER) reduces dyskinesia and may also lessen OFF time. In practice, COMT inhibitors are added to address wearing‑off, and amantadine is added to counter dyskinesia; they can be combined under supervision.
Safinamide reduces OFF time and may lessen dyskinesia slightly via glutamatergic effects at higher doses. Amantadine ER has a more robust and direct antidyskinetic effect. Patients with prominent dyskinesia often benefit more from amantadine ER; those with wearing‑off may start with a MAO‑B inhibitor.
Benztropine works well for acute dystonia and parkinsonism but has significant anticholinergic side effects, especially in older adults. Amantadine can improve parkinsonism and akathisia with less anticholinergic burden, making it a reasonable alternative or adjunct when cognition is a concern.
Both are used off‑label; evidence is mixed for each. Methylphenidate is a stimulant that can boost alertness but may raise heart rate and blood pressure and cause anxiety; amantadine may help fatigue with a different side‑effect profile (insomnia, dizziness, livedo). Choice depends on comorbidities, cardiovascular risk, and tolerability, often after non‑drug strategies.
Rasagiline provides mild symptom control and once‑daily dosing with good tolerability; it requires attention to drug interactions. Amantadine offers modest symptom relief and unique benefit if dyskinesia emerges later. Many start with MAO‑B inhibitors early and add amantadine later if dyskinesia develops.
Written on 2 March, 2023: Laura Jenkins
Re-written on 8 October, 2025: Cristina Matera, MD