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Indications: Where Amantadine Fits in Today

  • Parkinson’s disease (PD): Amantadine helps reduce tremor, rigidity, and bradykinesia in some patients and can improve overall motor function as an adjunct to other PD therapies.
  • Levodopa-induced dyskinesia (LID): Extended-release (ER) formulations, notably Gocovri, are approved to decrease dyskinesia in patients receiving levodopa-based therapy with or without concomitant dopaminergic medications. Many clinicians consider amantadine ER a go-to option for troublesome dyskinesias.
  • Drug-induced extrapyramidal symptoms (EPS): Immediate-release (IR) amantadine or the ER product Osmolex ER may be used off-label or as labeled (per product) to reduce EPS caused by certain antipsychotics and other agents.
  • Influenza A (historical/limited role): Amantadine’s antiviral action targets the M2 protein of influenza A only. Due to widespread resistance, major guidelines in the U.S. and many other countries no longer recommend amantadine for prevention or treatment of seasonal influenza. It does not work for influenza B.

How Amantadine Works

Amantadine’s pharmacology spans neurology and virology:

  • NMDA receptor antagonism: In the central nervous system, amantadine acts as a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist. By dampening glutamatergic overactivity, it can reduce dyskinesias and modulate motor circuitry implicated in PD.
  • Dopaminergic effects: Amantadine may enhance dopamine release and inhibit dopamine reuptake, contributing to symptomatic relief in PD.
  • Anticholinergic-like effects: Mild anticholinergic properties may further reduce tremor in some individuals.
  • Antiviral action (influenza A): Amantadine blocks the M2 ion channel of influenza A, inhibiting viral uncoating. This mechanism is largely obsolete in practice because contemporary influenza A strains are typically resistant.

Dosage and Administration

Always follow your prescriber’s specific instructions; dosing should be individualized based on the indication, response, and kidney function.

  • Immediate-release (IR) amantadine capsules/tablets:
    • Parkinson’s disease and EPS: Common starting dose is 100 mg once daily for several days, then 100 mg twice daily. Some patients may require 300 mg daily in divided doses. Doses above 300 mg/day are uncommon and increase the risk of side effects.
    • Tapering: To discontinue or reduce dose, taper gradually to avoid withdrawal symptoms or a neuroleptic malignant syndrome (NMS)-like reaction.
  • Gocovri (amantadine ER) for dyskinesia:
    • Typical regimen: 137 mg by mouth at bedtime for 1 week, then increase to 274 mg at bedtime as tolerated.
    • Do not crush, chew, or split capsules. If swallowing is difficult, some capsules may be opened and sprinkled on soft food per product labeling; confirm with your pharmacist.
  • Osmolex ER (amantadine ER) for PD/EPS:
    • Morning dosing: Taken once daily in the morning. Dosing is individualized (commonly 129 mg to 322 mg daily). Follow the titration schedule provided by your prescriber.
    • Swallow whole; do not crush, chew, or split.
  • Renal impairment:
    • Amantadine is primarily renally eliminated. Reduced kidney function significantly prolongs half-life and raises exposure.
    • Dose adjustments are critical. Depending on creatinine clearance, dosing frequency may be reduced (e.g., every 24–72 hours for IR, or lower nightly doses/extended intervals for ER). Your prescriber will tailor a regimen based on renal function and the specific product used.

Instructions for Use

  • Take with or without food. If stomach upset occurs, taking with food can help.
  • Be consistent with timing to maintain steady symptom control, especially with ER formulations.
  • Missed dose:
    • IR: If you miss a dose, take it when remembered unless it’s close to the next dose; do not double up.
    • ER: If a bedtime dose (Gocovri) or morning dose (Osmolex ER) is missed and you are close to the next scheduled dose, skip the missed dose and resume your usual schedule.
  • Do not abruptly stop amantadine without prescriber guidance. Gradual taper helps avoid withdrawal symptoms such as agitation, hallucinations, paranoia, anxiety, depression, confusion, or slurred speech. Rarely, sudden withdrawal can precipitate an NMS-like syndrome.
  • If amantadine is being used for influenza A in special circumstances per a clinician’s judgment, complete the entire prescribed course.

Storage and Handling

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.

Who Should Not Use Amantadine

  • Hypersensitivity to amantadine or product components.
  • Untreated narrow-angle (angle-closure) glaucoma.
  • Severe renal impairment without the ability to appropriately adjust dose; certain ER products may be contraindicated or require substantial modification in advanced kidney disease.

Discuss your full medical history with your clinician before starting amantadine, particularly if you have:

  • Kidney disease; any condition affecting urination or fluid balance.
  • History of seizures, significant psychiatric conditions (e.g., psychosis, depression, suicidality), or cognitive impairment.
  • Cardiovascular disease, congestive heart failure, or prone to edema.
  • Low blood pressure or orthostatic hypotension.
  • Ocular issues, including glaucoma risk.
  • Dermatologic conditions or a history of livedo reticularis (mottled skin).
  • Liver disease (though renal function is the main concern), or a history of severe skin reactions or drug allergies.

Warnings and Precautions

  • Central nervous system effects: Drowsiness, dizziness, blurred vision, confusion, hallucinations, agitation, and insomnia may occur. Caution with driving or operating machinery until you know how you respond.
  • Impulse control disorders: Gambling, hypersexuality, or compulsive spending/eating can emerge or worsen. Report new or escalating urges promptly.
  • Suicidal ideation and mood changes: Monitor for depression, anxiety, or suicidal thoughts, especially during dose changes.
  • Orthostatic hypotension and syncope: Rise slowly from sitting or lying positions. Hydration and compression stockings may help if recommended by your clinician.
  • Peripheral edema: Swelling of ankles/legs is not uncommon; notify your clinician if significant.
  • Livedo reticularis: A lace-like purplish skin discoloration on the legs or trunk can occur; it is usually benign but may be bothersome cosmetically.
  • Heat intolerance: Amantadine can impair heat dissipation; avoid overheating and maintain hydration, especially in hot weather or during exercise.
  • Withdrawal and NMS-like reactions: Taper gradually under guidance. Seek urgent care if high fever, rigidity, altered mental status, or autonomic instability develops.
  • Falls risk: Dizziness, sedation, or orthostatic changes can increase falls; review home safety measures if needed.

Drug and Vaccine Interactions

  • Anticholinergics (e.g., benztropine, trihexyphenidyl, scopolamine): Additive side effects such as dry mouth, constipation, blurred vision, confusion.
  • Diuretics, especially hydrochlorothiazide (HCTZ) and combinations with triamterene: May increase amantadine levels and side effects via reduced renal clearance.
  • Quinidine and quinine: Potential to increase amantadine toxicity; use with caution.
  • Memantine: Both are NMDA antagonists. Co-administration can increase CNS effects; avoid or use with careful monitoring.
  • Stimulants and sympathomimetics (e.g., caffeine in high doses, methylphenidate, amphetamines, pseudoephedrine): May heighten nervousness, insomnia, or cardiovascular effects.
  • Alcohol and CNS depressants: Additive sedation and impaired coordination; limit or avoid alcohol.
  • Live attenuated influenza vaccine (LAIV, intranasal): Amantadine can decrease LAIV effectiveness. Avoid LAIV use within 48 hours before starting amantadine and for 2 weeks after stopping it. Inactivated influenza vaccines (injection) are not affected.
  • Other dopaminergic therapy (levodopa, dopamine agonists): Combined effects may increase dyskinesia or psychiatric symptoms; prescribers often adjust regimens together.

Always provide your clinician and pharmacist with a full list of prescription drugs, over-the-counter medications, and supplements.

Side Effects: What to Expect and When to Call

Many people tolerate amantadine reasonably well at therapeutic doses, especially when titrated slowly. Common side effects include:

  • Dizziness, lightheadedness, and fatigue.
  • Insomnia or vivid/strange dreams.
  • Nausea, decreased appetite, dry mouth, constipation.
  • Blurred vision or dry eyes.
  • Headache.
  • Peripheral edema and livedo reticularis.

Less common but more serious effects include:

  • Confusion, hallucinations, agitation, or paranoia.
  • Severe orthostatic hypotension or fainting.
  • Seizures.
  • Allergic reactions, including rash, itching, swelling, or difficulty breathing.
  • Worsening depression or emergence of suicidal thoughts.

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 and Emergency Information

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.

Special Populations

  • Elderly: Higher susceptibility to confusion, falls, hallucinations, and orthostatic hypotension. Lower starting doses and cautious titration are recommended.
  • Renal impairment: Meticulous dose adjustment is essential. Your care team should check kidney function before and during therapy in at-risk patients.
  • Hepatic impairment: No formal dose adjustments are typically required, but comorbid hepatic disease may still influence overall tolerability and drug handling; use clinical judgment.
  • Pregnancy: Data are limited. Use only if potential benefits justify potential risks. Discuss family planning and pregnancy intentions with your clinician.
  • Lactation: Amantadine is present in breast milk. Potential infant exposure may cause adverse effects; avoid or use only if benefits outweigh risks under clinician guidance.
  • Pediatrics: Safety and efficacy for PD are not established in children. For influenza A, historical pediatric use existed but is largely obsolete due to resistance and updated guidelines.

Clinical Evidence and Place in Therapy

  • Parkinson’s disease: Small and moderate-sized studies have demonstrated symptomatic improvement of motor features with IR amantadine as adjunct therapy. Its benefit can wane over time in some patients, yet many maintain a clinically meaningful response.
  • Dyskinesia: Randomized controlled trials of amantadine ER (Gocovri) showed significant reductions in dyskinesia scores and improved “OFF” time versus placebo. These data support its use in patients whose quality of life is impacted by LID.
  • EPS: Amantadine can alleviate antipsychotic-induced EPS in some cases, potentially offering an alternative to anticholinergics that are poorly tolerated in older adults. Prescribers weigh cognitive side effects and individual response when choosing among options.
  • Influenza A: Although the antiviral mechanism is well characterized, widespread resistance has rendered amantadine largely ineffective in routine clinical settings. Contemporary seasonal influenza management relies on neuraminidase inhibitors (e.g., oseltamivir) and other agents per current guidelines.

Practical Tips for Patients and Caregivers

  • Start low, go slow: Gradual titration can limit dizziness, insomnia, and confusion.
  • Hydration and salt balance: Especially in older adults, adequate hydration can reduce orthostatic symptoms. Discuss individualized fluid and salt guidance with your clinician if you have heart or kidney disease.
  • Sleep hygiene: If insomnia or vivid dreams occur, earlier daytime dosing of IR amantadine may help. For ER products, discuss timing adjustments with your prescriber.
  • Skin and circulation: Livedo reticularis is typically benign. If it’s concerning, report it; dose adjustment may help.
  • Fall prevention: Stand up slowly, use support rails if needed, ensure good lighting at night, and review medications that increase falls risk.
  • Driving and machinery: Do not drive until you know how amantadine affects alertness and vision.
  • Medication reconciliation: Bring a complete list of medications and supplements to every appointment.

Cost, Coverage, and Availability

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.

Key Differences Among Formulations

  • Immediate-release amantadine:
    • Often dosed once or twice daily.
    • Useful for PD symptom control and EPS.
    • Requires careful renal dose adjustments.
  • Gocovri (ER amantadine):
    • Once nightly dosing designed to decrease dyskinesia.
    • Evidence-based dyskinesia reduction; may also reduce “OFF” time in some patients.
    • Renal dosing is critical; not appropriate for severe renal impairment.
  • Osmolex ER:
    • Once-daily morning dosing for PD/EPS.
    • May provide smoother plasma levels than IR; avoid crushing or splitting.
    • Adjust for renal impairment; consult the specific product guidance.

Vaccinations and Amantadine

  • Amantadine may reduce the effectiveness of the live attenuated influenza vaccine (intranasal). Time vaccination and amantadine therapy appropriately under clinician guidance (generally avoid LAIV 48 hours before starting and for 2 weeks after stopping amantadine).
  • Inactivated (injectable) influenza vaccines are not affected by amantadine and remain recommended per seasonal public health guidance.

Monitoring and Follow-Up

  • Symptom tracking: Record motor symptoms, dyskinesia severity, sleep patterns, and mood/behavior changes. Share these with your clinician to fine-tune therapy.
  • Blood pressure: Check for orthostatic changes during dose titration or when adding other medications that affect blood pressure.
  • Renal function: Baseline and periodic assessment in older adults or those with kidney disease.
  • Adverse effects: Promptly report hallucinations, paranoia, compulsive behaviors, severe edema, rash, or signs of infection or fever with rigidity.

Patient Counseling Summary

  • Use exactly as prescribed; do not adjust your dose on your own.
  • Do not stop suddenly; a proper taper is important to avoid withdrawal or NMS-like symptoms.
  • Limit alcohol and discuss sedating medications with your clinician.
  • Be alert to mood or behavior changes and report them quickly.
  • Maintain hydration and avoid overheating.
  • Store safely and keep out of reach of children and pets.

Amantadine U.S. Sale and Prescription Policy

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 FAQ

What is Amantadine and how does it work?

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.

What conditions is Amantadine used to treat?

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.

How quickly does Amantadine start working for Parkinson’s symptoms?

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.

What are the common side effects of Amantadine?

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.

What serious side effects can occur with Amantadine?

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.

Who should avoid or use caution with Amantadine?

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.

How is Amantadine typically dosed?

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.

Do I need a kidney dose adjustment with Amantadine?

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.

Can I stop Amantadine abruptly?

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.

What is the best time to take Amantadine, and should I take it with food?

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.

Which medications interact with Amantadine?

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.

Does Amantadine help levodopa‑induced dyskinesia?

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.

What monitoring is recommended while on Amantadine?

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.

Is Amantadine safe for older adults?

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.

Is there a generic for Amantadine and how does cost compare?

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.

Can I drink alcohol while taking Amantadine?

It’s best to avoid alcohol. Alcohol can amplify dizziness, drowsiness, impaired coordination, and judgment, and may worsen orthostatic lightheadedness and confusion.

Is Amantadine safe in pregnancy?

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.

Can I use Amantadine while breastfeeding?

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.

What should I know about Amantadine before surgery or anesthesia?

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.

Is it safe to drive while taking Amantadine?

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.

What should patients with kidney disease know about Amantadine?

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.

Does liver disease affect Amantadine use?

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.

What should I do if I miss a dose of Amantadine or take too much?

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.

How does Amantadine compare with levodopa/carbidopa for Parkinson’s disease?

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.

Amantadine vs dopamine agonists (pramipexole, ropinirole): which is better?

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.

Amantadine vs MAO‑B inhibitors (rasagiline, selegiline): how do they differ?

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.

Amantadine vs anticholinergics (benztropine, trihexyphenidyl) for tremor?

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.

Amantadine immediate‑release vs extended‑release (Gocovri, Osmolex ER): what’s the difference?

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.

Amantadine vs memantine: both are NMDA antagonists—can they be used together?

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.

Amantadine vs rimantadine for influenza A: is either still useful?

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.

Amantadine vs oseltamivir (Tamiflu) for flu?

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.

Amantadine vs entacapone or opicapone (COMT inhibitors): when to choose which?

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.

Amantadine vs safinamide (MAO‑B inhibitor) for fluctuations?

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.

Amantadine vs benztropine for antipsychotic‑induced extrapyramidal symptoms?

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.

Amantadine vs methylphenidate for fatigue in MS or after TBI?

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.

Amantadine vs rasagiline for early Parkinson’s disease?

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