Amantadine is a dopaminergic and antiviral medicine used to treat Parkinson’s disease symptoms, reduce levodopa‑induced dyskinesia, and, less commonly today, for influenza A. Available as immediate‑release tablets/capsules and extended‑release formulations (Gocovri, Osmolex ER), it can ease tremor, rigidity, fatigue, and gait freezing in select patients. Because amantadine affects the brain and is renally cleared, dosing must be individualized, especially in older adults and people with kidney impairment. Common side effects include insomnia, dizziness, dry mouth, and livedo reticularis; hallucinations can occur. In the U.S., amantadine is prescription‑only; use should follow evaluation by a licensed clinician and regular monitoring for safety.
Amantadine is a unique medicine with both dopaminergic and antiglutamatergic (NMDA receptor–blocking) activity. In neurology, it is used to treat motor symptoms of Parkinson’s disease (PD), such as bradykinesia, rigidity, tremor, and gait freezing, and to reduce levodopa‑induced dyskinesia. Its dual mechanisms can improve movement while smoothing out troublesome involuntary movements in patients on levodopa.
Extended‑release amantadine (Gocovri, Osmolex ER) is FDA‑approved for PD‑related dyskinesia and as an adjunct to manage “off” episodes. Immediate‑release amantadine is also used for drug‑induced extrapyramidal symptoms caused by antipsychotics. Off‑label, clinicians may consider it for fatigue in multiple sclerosis, apathy or arousal improvement after traumatic brain injury, and gait disorders in PD, though evidence and dosing vary and careful monitoring is required.
Historically, amantadine had a role against influenza A via M2 protein blockade. Due to widespread resistance, U.S. public health guidance does not recommend amantadine for influenza treatment or prophylaxis. Today, its clinical value is principally neurological, where individualized selection of formulation and dose can meaningfully improve quality of life for selected patients under specialist care.
Dosing must be tailored to indication, formulation, age, and kidney function. For Parkinson’s disease with immediate‑release (IR) amantadine, a common starting regimen is 100 mg once daily for one week, then 100 mg twice daily if tolerated. Some patients may respond to 100 mg twice daily as a maintenance dose; others may require adjustments. Doses above 200 mg per day increase adverse effects and are typically reserved for select cases under specialist supervision.
For levodopa‑induced dyskinesia, extended‑release (ER) options are often preferred. Gocovri ER capsules are taken once nightly: start 137 mg at bedtime for one week, then increase to 274 mg at bedtime. Osmolex ER is taken once each morning, generally 129–322 mg daily, titrated based on response and tolerability. Do not substitute ER and IR formulations on a milligram‑for‑milligram basis; they have different pharmacokinetics and titration schedules.
Renal function is critical. Amantadine is primarily renally eliminated, so dose reductions are required in chronic kidney disease to prevent toxicity (e.g., confusion, hallucinations, myoclonus). In severe renal impairment or end‑stage renal disease, certain ER products (including Gocovri and Osmolex ER) are contraindicated. Elderly patients often need lower starting doses and slower titration due to both renal decline and increased CNS sensitivity.
Take IR amantadine with or without food; if stomach upset occurs, a light snack can help. ER capsules should be taken exactly as directed (Gocovri at bedtime; Osmolex ER in the morning). Swallow capsules whole unless the specific product allows sprinkling contents on applesauce; always check the package insert. To discontinue, taper gradually to lower the risk of withdrawal‑like symptoms or sudden worsening of PD features. Follow your clinician’s schedule rather than stopping abruptly.
Amantadine can cause central nervous system effects, including insomnia, agitation, confusion, hallucinations, and, rarely, psychosis—risks that rise with higher doses, older age, cognitive impairment, or concomitant psychoactive medications. Screen for baseline cognitive status and psychiatric history and monitor closely after dose changes, especially in patients with Parkinson’s disease dementia or Lewy body disease.
Orthostatic hypotension, edema, and livedo reticularis (a mottled, lace‑like skin discoloration) are possible. Patients with heart failure or significant peripheral edema need careful assessment. Because amantadine may lower seizure threshold, those with seizure disorders warrant cautious dosing and avoidance of interacting pro‑convulsant drugs where possible. Visual disturbances and precipitation of angle‑closure glaucoma have been reported; patients with narrow angles require ophthalmic evaluation if symptoms arise.
Renal function should be checked at baseline and periodically, especially in older adults. Counsel patients to report mood changes, suicidal ideation, new impulse‑control problems (such as compulsive gambling or shopping), or sudden sleep episodes. If influenza vaccination with the live attenuated intranasal vaccine is planned, coordinate timing to avoid interference. Alcohol and sedatives can worsen CNS adverse effects; advise moderation or avoidance.
Do not use amantadine in patients with known hypersensitivity to amantadine or any component of the formulation. Extended‑release products such as Gocovri and Osmolex ER are contraindicated in end‑stage renal disease due to markedly reduced clearance and risk of toxicity. Severe untreated angle‑closure glaucoma is a practical contraindication given potential for increased intraocular pressure.
Relative contraindications and situations requiring extra caution include severe psychiatric illness (particularly active psychosis), poorly controlled seizure disorders, decompensated heart failure with edema, and significant renal impairment without dose adjustment. Pregnancy and lactation require individualized risk–benefit assessment; data are limited, and nonpharmacologic strategies or alternative therapies may be preferred depending on the indication.
Common adverse effects include insomnia, vivid dreams, dizziness, lightheadedness, nausea, dry mouth, constipation, and livedo reticularis. Livedo reticularis is usually benign but can be cosmetically bothersome; it often improves after dose reduction or discontinuation. Mild ankle swelling may occur. Some patients experience blurred vision or difficulty with concentration.
Neuropsychiatric reactions can be more concerning: agitation, anxiety, confusion, hallucinations, paranoia, and, rarely, frank psychosis. These risks are greatest in older adults, in those with cognitive impairment, and when amantadine is combined with other dopaminergic agents or anticholinergics. Daytime sleepiness and sudden sleep episodes have been reported; driving and operating machinery should be avoided if these occur. Impulse‑control disorders (e.g., compulsive gambling, hypersexuality) have been observed with dopaminergic therapies and can emerge with amantadine; prompt medical review is warranted if behaviors change.
Cardiovascular effects include orthostatic hypotension and, less commonly, arrhythmias. Dermatologic reactions beyond livedo reticularis are uncommon but possible. Rare but serious events include neuroleptic malignant syndrome–like symptoms with abrupt withdrawal (rigidity, fever, autonomic instability), seizures, and severe hypersensitivity. Any rapid mental status change, high fever, severe rigidity, chest pain, or suicidal thoughts requires urgent evaluation.
Most side effects are dose‑related and improve by lowering the dose, switching formulations, or spacing doses earlier in the day to reduce insomnia. Keeping well hydrated, standing up slowly, and minimizing alcohol can reduce dizziness and hypotension. Never adjust your dose without consulting your prescriber, especially if you take other medications that affect the central nervous system.
Amantadine’s CNS effects can be amplified by other psychoactive drugs. Combining with anticholinergics (e.g., benztropine, trihexyphenidyl) may intensify confusion, blurred vision, constipation, and urinary retention. Concomitant dopaminergic therapies (levodopa, dopamine agonists) increase risks of hallucinations and impulse‑control issues, necessitating careful titration and monitoring.
Drugs that reduce seizure threshold (such as bupropion, tramadol, certain antidepressants, or fluoroquinolone antibiotics) may raise seizure risk when taken with amantadine. Alcohol, benzodiazepines, sedative‑hypnotics, and cannabis can potentiate dizziness and somnolence. Memantine, another NMDA antagonist, may produce additive neuropsychiatric toxicity if combined; avoid coadministration unless a specialist deems it necessary.
Renal elimination creates interactions with agents that alter kidney handling. Triamterene/hydrochlorothiazide and some other diuretics have been reported to increase amantadine concentrations; dose adjustment and monitoring may be required. Cimetidine can reduce renal tubular secretion of certain cationic drugs and has been implicated in raising amantadine levels; consider alternatives or closer observation.
Because amantadine is no longer recommended for influenza, vaccine interactions are uncommon, but timing conflicts can occur with the live attenuated intranasal influenza vaccine; avoid administering the vaccine within 48 hours of stopping amantadine or starting it within two weeks after vaccination to preserve vaccine efficacy. Always provide your clinician and pharmacist a complete, updated medication list, including over‑the‑counter products and supplements.
If you miss a dose of immediate‑release amantadine, take it as soon as you remember unless it is close to your next scheduled dose; if so, skip the missed dose and resume your usual schedule. Do not double up to “catch up.” For extended‑release products, follow the specific instructions in the package insert: generally, take the missed dose the same day if there is sufficient time before the next scheduled dose (for Gocovri, avoid taking late doses near bedtime if it will cause daytime sedation). When in doubt, call your pharmacist or prescriber for guidance.
Amantadine overdose can be serious, particularly in older adults or those with renal impairment. Symptoms may include severe agitation, confusion, hallucinations, myoclonus, tremor, dilated pupils, rapid or irregular heartbeat, marked dizziness, fainting, seizures, and, in extreme cases, respiratory depression or cardiac arrest. Because amantadine is renally cleared, toxicity can persist if kidney function is reduced.
If an overdose is suspected, call emergency services or your regional poison control center immediately (in the U.S., 1‑800‑222‑1222). Do not attempt to self‑induce vomiting. Supportive care in a medical setting may include cardiac monitoring, airway protection, seizure management, and measures to enhance elimination. Bring a list of all medications and the amantadine bottle to help clinicians assess the ingested dose and formulation.
Store amantadine at controlled room temperature, typically 20–25°C (68–77°F), in a tightly closed container protected from moisture and excessive heat. Keep out of reach of children and pets. Do not store in a bathroom where humidity fluctuates. Check expiration dates regularly, and do not use expired medication. If your product is a sprinkle or ER formulation, follow the label for any specific storage nuances and handling instructions.
In the United States, amantadine is a prescription‑only medication. Buying amantadine without a prescription is not legal and may be unsafe due to risks of counterfeit products, wrong dosing, and dangerous interactions. The lawful path is to obtain an evaluation by a licensed clinician who can confirm the indication (for example, Parkinson’s disease symptoms or dyskinesia), review your medical history, check kidney function, and then prescribe an appropriate formulation and dose if it is right for you.
HealthSouth Rehabilitation Hospital of Tallahassee offers a legal, structured care pathway that can help eligible patients access amantadine appropriately—without requiring a prior in‑person prescription in hand—by arranging legitimate clinical assessment, diagnosis confirmation, and prescription management through its care team or affiliated providers. This means you are not “skipping” the prescription; you are obtaining one through proper channels, potentially via streamlined or telehealth‑enabled evaluation, with follow‑up and monitoring built in.
If you are exploring how to buy amantadine without prescription online, reconsider and choose safety: schedule a consultation, verify pharmacy licensure, and use U.S. FDA‑regulated dispensing. The hospital’s team can coordinate insurance checks, discuss brand versus generic options (IR vs ER, including Gocovri or Osmolex ER), and set up lab monitoring and dose titration. Avoid overseas or unverified websites that promise prescription‑free amantadine; they may expose you to legal risk and significant health harms.
Amantadine is a medication used for Parkinson’s disease symptoms and levodopa-induced dyskinesia. It blocks NMDA receptors (reducing glutamate-mediated overactivity) and has dopaminergic effects by promoting dopamine release and inhibiting its reuptake. Historically it had antiviral activity against influenza A, but resistance has made that use largely obsolete.
It is used to improve Parkinson’s disease symptoms such as tremor, rigidity, and bradykinesia, and to reduce levodopa-induced dyskinesia. Extended-release amantadine (Gocovri) is approved for dyskinesia and to reduce OFF episodes in Parkinson’s. Osmolex ER and immediate-release amantadine are used for Parkinson’s symptoms and certain drug-induced movement disorders.
Some patients notice improvement in mobility or reduction in dyskinesia within several days, with fuller effects typically seen over 1–2 weeks. If no meaningful benefit is observed after a few weeks at an appropriate dose, clinicians may reassess therapy.
Common effects include dizziness, insomnia, nausea, dry mouth, constipation, ankle swelling, livedo reticularis (mottled skin discoloration), blurred vision, and orthostatic lightheadedness. Confusion and hallucinations can occur, especially in older adults or at higher doses.
Seek medical attention for new or worsening confusion, agitation, hallucinations, suicidal thoughts, severe rash, shortness of breath or swelling suggestive of heart issues, seizures, urinary retention, or a sudden high fever and severe stiffness (rare, can occur with abrupt withdrawal).
Dosing is individualized. Many start with immediate-release 100 mg daily and titrate to 100 mg twice daily; some require higher doses if tolerated. Gocovri (ER) is typically taken once nightly with a gradual titration. Osmolex ER is taken once daily in the morning. Always follow your prescriber’s instructions, and do not crush ER tablets.
Yes. Amantadine is cleared by the kidneys. Reduced kidney function requires lower doses or extended dosing intervals to avoid toxicity such as confusion, hallucinations, and arrhythmias. People on dialysis need careful specialist dosing. Your clinician will adjust based on your eGFR.
Do not stop suddenly unless directed by your clinician. Abrupt discontinuation can cause rapid worsening of Parkinson’s symptoms and, rarely, a neuroleptic malignant syndrome–like reaction (fever, rigidity). Tapering over days to weeks is recommended.
Yes. Notable interactions include anticholinergics (increased confusion, dry mouth, constipation), CNS stimulants or other dopaminergic drugs (agitation, insomnia), and diuretics like triamterene/HCTZ (can raise amantadine levels). Combining with other NMDA antagonists (e.g., memantine) may increase CNS side effects. Always share your medication list with your clinician.
Yes. It is commonly used alongside levodopa to reduce dyskinesia and may smooth motor fluctuations. Your prescriber may adjust levodopa or other Parkinson’s medicines to balance benefits and side effects.
Avoid if you’ve had a serious allergic reaction to amantadine. Use caution in people with severe kidney impairment, seizure disorders, untreated narrow-angle glaucoma, significant psychiatric illness, orthostatic hypotension, or heart failure. Older adults are more sensitive to cognitive side effects.
Data in pregnancy are limited; risks and benefits must be weighed with your obstetric and neurology teams. Amantadine is excreted in breast milk, and adverse effects in infants are possible. Discuss alternatives and monitoring if treatment is necessary.
Rise slowly to prevent dizziness, limit alcohol, stay well hydrated, and be cautious with driving or operating machinery until you know how it affects you. Report new confusion, hallucinations, or swelling promptly. Protect skin if you develop livedo reticularis; it is usually cosmetic and reversible.
Take it when you remember unless it’s close to the next dose. Do not double up. For once-nightly Gocovri, skip the missed dose if it’s nearly time for the next, and resume your usual schedule.
It’s typically a benign, net-like purplish skin discoloration, often on the legs, that improves with dose reduction or discontinuation. If accompanied by pain, ulcers, or other concerning symptoms, seek medical evaluation.
Levodopa is the most effective drug for core motor symptoms and is first-line for many patients. Amantadine is less potent for bradykinesia and rigidity but can help tremor and is uniquely useful for levodopa-induced dyskinesia. Many patients use both, with amantadine as an adjunct.
MAO-B inhibitors modestly boost dopamine by slowing breakdown and are often used early for symptom control and fluctuation smoothing. Amantadine is chosen when dyskinesia emerges or when tremor persists. Side effects differ: MAO-B inhibitors may cause insomnia or interactions with certain antidepressants; amantadine more often causes edema, livedo reticularis, and confusion in older adults.
Dopamine agonists directly stimulate dopamine receptors and can improve motor symptoms and reduce OFF time but carry risks of sleep attacks, impulse-control disorders, leg edema, and hallucinations. Amantadine is generally less effective for core symptoms but better for dyskinesia. In older patients, amantadine may be better tolerated than dopamine agonists regarding impulse-control issues.
Anticholinergics can reduce tremor, particularly in younger patients, but often worsen cognition, constipation, and urinary retention, especially in older adults. Amantadine may help tremor without as much anticholinergic burden, though it can still cause confusion. Choice depends on age, cognitive status, and symptom profile.
COMT inhibitors extend levodopa’s effect to reduce wearing-off but can increase dyskinesia. Amantadine reduces dyskinesia and can modestly reduce OFF time (especially with Gocovri). They are often combined: a COMT inhibitor to lengthen levodopa benefit and amantadine to control dyskinesia.
Immediate-release is typically taken once or twice daily for symptom relief. Gocovri is once nightly and is specifically indicated for dyskinesia and reducing OFF time; it provides higher nighttime levels to improve next-day motor control. Osmolex ER is taken in the morning for Parkinson’s symptoms and drug-induced movement disorders. ER forms may have steadier levels and different side effect profiles.
Both were M2 inhibitors active against influenza A, but widespread resistance has rendered them ineffective for routine flu treatment. Current flu therapy relies on neuraminidase inhibitors (e.g., oseltamivir) or baloxavir. Amantadine’s modern role is neurologic, not antiviral.
No. Both affect NMDA receptors, but memantine is used for Alzheimer’s disease, while amantadine targets Parkinson’s symptoms and dyskinesia. Using them together may increase CNS side effects (confusion, dizziness) and requires careful monitoring.
Apomorphine is a rapid-acting rescue dopamine agonist that reverses sudden OFF episodes within minutes but can cause nausea, low blood pressure, and requires premedication and training. Gocovri (amantadine ER) reduces the frequency and severity of OFF over time but does not provide instant rescue.
Safinamide is a MAO-B inhibitor with additional glutamatergic effects; it reduces OFF time and may modestly lessen dyskinesia as a secondary effect. Amantadine is the only oral agent with a primary indication for dyskinesia (Gocovri). If dyskinesia is prominent, amantadine is typically preferred; safinamide is useful mainly for OFF time.
In older adults, MAO-B inhibitors are often better tolerated than dopamine agonists, but can still cause insomnia and interactions. Amantadine can help tremor and dyskinesia but carries risks of confusion, hallucinations, and edema—especially with reduced kidney function. Renal dosing makes amantadine use more complex in this group.
Both can help medication-induced parkinsonism. Anticholinergics like benztropine are effective but often poorly tolerated due to cognitive and anticholinergic side effects, particularly in older patients. Amantadine may be a preferable option when cognition is a concern, provided renal function allows safe dosing.