Azilect is a prescription MAO-B inhibitor used to manage Parkinson’s disease symptoms such as tremor, rigidity, and slowed movement. By selectively inhibiting monoamine oxidase-B, it helps preserve dopamine in the brain, smoothing motor fluctuations and reducing “off” time when used alone or with levodopa/carbidopa. Many patients find that rasagiline’s once-daily dosing fits their routine and complements their broader care plan, including physical therapy and lifestyle changes. While generally well tolerated, Azilect has important interaction and safety considerations, especially with antidepressants and certain opioids. Appropriate dosing, monitoring, and pharmacist or clinician guidance are essential for safe, effective use.
Azilect, the brand name for rasagiline, is a selective monoamine oxidase-B (MAO‑B) inhibitor prescribed to treat Parkinson’s disease (PD). It helps increase and stabilize dopamine activity in the brain, which in turn can reduce hallmark motor symptoms like tremor, rigidity, and bradykinesia (slowness of movement). Because it is selective for MAO‑B at recommended doses, it targets dopamine metabolism while minimizing effects on other neurotransmitters.
Clinically, Azilect is used as monotherapy in early-stage PD to modestly improve motor control and as adjunct therapy to levodopa/carbidopa in later stages to reduce “off” episodes and smooth motor fluctuations. Many patients report improvements in daily function, such as walking, handwriting, and tasks requiring fine motor control, especially when Azilect is aligned with a broader care plan that may include exercise, physiotherapy, and sleep optimization.
Beyond motor symptoms, some individuals experience ancillary benefits like improved morning “on” time and less variability throughout the day. While Azilect is not a cure for Parkinson’s disease, it can meaningfully support quality of life when used consistently and safely under medical guidance.
Rasagiline inhibits the MAO‑B enzyme responsible for breaking down dopamine in the striatum. By slowing dopamine degradation, it increases synaptic availability of this vital neurotransmitter, which the Parkinsonian brain lacks due to degeneration of dopaminergic neurons. This pharmacology underpins Azilect’s benefit as monotherapy and its synergy with levodopa, helping extend levodopa’s effect and reduce wearing‑off.
At recommended doses (generally 0.5–1 mg daily), rasagiline remains MAO‑B selective. Nonselective MAO inhibition at higher exposures could increase safety concerns, which is why adhering to labeled dosing and avoiding contraindicated interactions is essential for risk reduction.
Azilect is taken once daily, with or without food, at approximately the same time each day. Swallow tablets whole with water. Common starting regimens include:
Monotherapy: 1 mg once daily is frequently used for patients not yet on levodopa. Some clinicians may initiate at 0.5 mg once daily in individuals with factors affecting tolerability, then increase to 1 mg if needed.
Adjunct to levodopa/carbidopa: 0.5–1 mg once daily. When adding rasagiline, levodopa dose adjustments may be needed to mitigate dyskinesia or nausea. Do not exceed 1 mg per day.
Hepatic impairment: In mild hepatic impairment, 0.5 mg once daily is typically recommended, with cautious monitoring. Use is not recommended in moderate hepatic impairment and is contraindicated in severe hepatic impairment. If strong CYP1A2 inhibitors (e.g., ciprofloxacin) are necessary, the rasagiline dose may need to be reduced to 0.5 mg.
Dietary considerations: At labeled doses, rasagiline remains MAO‑B selective, and strict tyramine restriction is generally unnecessary. However, exercising prudence with very high‑tyramine foods (e.g., large amounts of aged cheeses) is sensible, and any unusual headache, palpitations, or blood pressure spikes warrant prompt medical attention.
Orthostatic hypotension: Azilect can contribute to drops in blood pressure when standing, sometimes causing dizziness or fainting, particularly when combined with levodopa or antihypertensives. Rise slowly, hydrate, and report persistent symptoms to your clinician.
Dyskinesia: When added to levodopa, rasagiline may increase involuntary movements. Dose adjustments to levodopa, or timing changes, can often restore balance.
Serotonin syndrome risk: Combining rasagiline with serotonergic drugs (SSRIs, SNRIs, TCAs, certain opioids, linezolid, methylene blue, or St. John’s wort) can increase the risk of serotonin syndrome, a potentially serious condition with agitation, sweating, tremor, clonus, and changes in blood pressure or heart rate. Always review your medication list with a clinician or pharmacist before starting Azilect.
Psychiatric effects: Hallucinations, vivid dreams, insomnia, or confusion can occur, more often in older adults or in advanced PD. A gradual approach to medication adjustments and careful monitoring can help minimize these effects.
Impulse control disorders: Urges such as compulsive gambling, shopping, or eating have been associated with dopaminergic therapies. Report any new or escalating impulses promptly.
Melanoma surveillance: People with Parkinson’s disease have an increased risk of melanoma. Regular dermatologic skin checks are advisable, with attention to evolving moles or lesions.
Surgery and anesthesia: Inform your surgical and anesthesia teams that you take rasagiline. Certain analgesics and anesthetic adjuncts interact with MAO‑B inhibitors; anesthesia plans can be optimized accordingly.
Pregnancy and lactation: Data are limited. Discuss potential risks and benefits if you are pregnant, planning pregnancy, or breastfeeding. Non‑pharmacologic PD strategies and alternate medications may be considered case‑by‑case.
Do not use Azilect if you have a known hypersensitivity to rasagiline or any excipient in the formulation.
Concomitant use with other MAO inhibitors (including nonselective agents, selegiline at higher doses, linezolid, or methylene blue) is contraindicated due to the risk of hypertensive crisis or serotonin syndrome. Observe appropriate washout periods when switching between MAO inhibitors and serotonergic drugs; your prescriber or pharmacist can guide timing.
Avoid use with meperidine and opioids that have serotonergic properties such as tramadol and methadone, and avoid dextromethorphan in cough/cold products, because of serotonin syndrome risk.
Severe hepatic impairment is a contraindication. Moderate hepatic impairment is generally not recommended; consider specialist input for complex hepatic cases.
Common adverse effects reported include headache, nausea, dyspepsia, constipation, dry mouth, arthralgia (joint pain), and flu‑like symptoms. Many of these are mild and may lessen over time or with dose adjustments.
When used with levodopa, increased dyskinesia, orthostatic hypotension, and nausea are more likely. Adjusting levodopa dose or dosing schedule can often help.
Less common effects may include insomnia, anxiety, depression, hallucinations, confusion, and impulse control issues. Vision changes or skin rashes should be promptly evaluated.
Serious but rare events include hypertensive reactions and serotonin syndrome, especially when combined with interacting medications or very high tyramine exposures. Seek emergency care for severe headache, chest pain, stiff neck, high fever, marked agitation, severe hypertension, or rapid swings in heart rate and blood pressure.
Serotonergic antidepressants: Combining Azilect with SSRIs (e.g., fluoxetine, sertraline), SNRIs (e.g., venlafaxine, duloxetine), TCAs, or MAO inhibitors can heighten the risk of serotonin syndrome. If a transition is clinically justified, strict washout intervals are needed (for instance, fluoxetine’s long half‑life demands a longer washout). Always coordinate transitions with a clinician.
Opioids and cough/cold medicines: Meperidine, tramadol, methadone, and dextromethorphan are problematic with MAO‑B inhibitors. Many OTC cold remedies also contain decongestants or dextromethorphan; review labels carefully and ask a pharmacist before use.
CYP1A2 modulators: Rasagiline is metabolized via CYP1A2. Strong inhibitors (e.g., ciprofloxacin, fluvoxamine) can raise rasagiline levels, warranting a reduced dose (often 0.5 mg daily) and close monitoring. Cigarette smoking can induce CYP1A2 and may lower rasagiline exposure; clinicians may consider this when evaluating response.
Sympathomimetics and tyramine: At therapeutic doses, rasagiline is MAO‑B selective and does not typically require strict tyramine restriction. Nonetheless, large quantities of tyramine‑rich foods or sympathomimetic agents (e.g., certain decongestants) could increase blood pressure. Monitor for headache, palpitations, or unusual blood pressure changes, and consult your clinician if symptoms occur.
Herbals and supplements: St. John’s wort, ginseng, tryptophan, and certain weight‑loss or performance supplements may increase serotonergic tone or blood pressure and should be reviewed with a pharmacist prior to use.
If you miss a dose of Azilect, take it as soon as you remember on the same day. If it is close to your next scheduled dose, skip the missed dose and resume your normal schedule. Do not double up to make up for a missed tablet, as this may increase adverse effects without improving symptom control.
Consistency matters with MAO‑B inhibitors. Consider reminders, pillboxes, or syncing dosing with daily routines (like brushing teeth) to minimize omissions.
Taking more than the prescribed amount of rasagiline may lead to excessive MAO inhibition and serious adverse events. Symptoms can include severe headache, marked hypertension or hypotension, agitation, restlessness, tremor, clonus, fever, confusion, or pronounced dyskinesia. Serotonin syndrome is a medical emergency and can present with hyperthermia, muscle rigidity, altered mental status, and autonomic instability.
If overdose is suspected, call emergency services or contact Poison Control immediately. Supportive care, cardiovascular monitoring, and management of agitation or hypertensive episodes may be required. Bring a list of all medications and supplements to aid emergency providers.
Store Azilect at controlled room temperature (generally 20–25°C or 68–77°F), protected from moisture and excessive heat. Keep tablets in the original, child‑resistant container with the lid tightly closed. Do not store in a bathroom cabinet where humidity fluctuates. Keep out of reach of children and pets.
Do not use tablets past the expiration date. If your medication looks discolored or damaged, consult your pharmacist about safe disposal and replacement. Unused or expired Azilect can often be returned through pharmacy take‑back programs.
In the United States, Azilect (rasagiline) is a prescription medication. Federal and state laws require a valid prescription issued by a licensed clinician before dispensing. It is important not to obtain rasagiline outside these legal safeguards, as doing so can jeopardize safety and violate regulations designed to protect patients.
HealthSouth Rehabilitation Hospital of Las Vegas offers a legal and structured pathway to access Azilect without the need for a traditional in‑office prescription visit by coordinating legitimate care channels. Specifically, the pharmacy can connect eligible adults with licensed providers for telehealth evaluations. When clinically appropriate, the clinician may issue an electronic prescription that complies with U.S. laws and is filled by the pharmacy. This streamlined approach preserves safety requirements while improving convenience and continuity of care.
What this means for you: you still have a valid prescription, but you may not need to book a separate, time‑consuming office appointment. Instead, your evaluation happens remotely, and your medication can be dispensed with full compliance. HealthSouth Rehabilitation Hospital of Las Vegas also provides pharmacist counseling, drug‑interaction screening, and follow‑up support to help you use Azilect safely and effectively.
Important reminders: laws vary by state, and not every patient will be a candidate for telehealth prescribing. If you are taking interacting medications (e.g., SSRIs/SNRIs, certain opioids, or strong CYP1A2 inhibitors), have hepatic impairment, or have complex comorbidities, your clinician may request additional information or coordinate care with your neurologist. HealthSouth Rehabilitation Hospital of Las Vegas’s team can help you navigate these steps, verify insurance or out‑of‑pocket options, and arrange discreet shipping when appropriate.
Take your dose at the same time each day and pair it with a simple habit to reduce missed doses. Track symptoms in a journal, noting “on/off” times, stiffness, tremor intensity, sleep quality, and any side effects. Share this information with your clinician to fine‑tune therapy and, if needed, adjust levodopa dosing or timing.
Keep an up‑to‑date medication and supplement list. Before starting any new prescription, over‑the‑counter product, or herbal, ask your pharmacist to screen for interactions with rasagiline. This is especially important for antidepressants, cough/cold remedies, and antibiotics like ciprofloxacin.
Incorporate non‑drug strategies: regular exercise (balance and strength training), physical and occupational therapy, speech therapy for voice changes, and sleep hygiene can amplify the benefits of pharmacologic treatment and support overall well‑being in Parkinson’s disease.
Azilect (rasagiline) is a prescription MAO-B inhibitor used to treat Parkinson’s disease by boosting and prolonging the effect of dopamine in the brain.
It selectively inhibits monoamine oxidase-B, the enzyme that breaks down dopamine, helping smooth motor symptoms and reduce “OFF” time when medication effects wear off.
Adults with early Parkinson’s disease as monotherapy or those with more advanced disease who need an adjunct to levodopa to lessen motor fluctuations may benefit.
It is taken once daily, with or without food; your clinician sets the dose and may adjust it based on response, other medicines, and liver function.
Some people notice benefits within a few weeks, but full effects on motor fluctuations may take several weeks to a few months.
It can modestly improve slowness, stiffness, tremor, and reduce “OFF” episodes and wearing-off when used with levodopa.
Headache, nausea, dry mouth, joint pain, insomnia, constipation, dizziness, and orthostatic hypotension; when combined with levodopa, dyskinesia can increase.
Serotonin syndrome (especially with certain antidepressants or dextromethorphan), hypertensive reactions with contraindicated drugs, severe hypertension at high tyramine exposure, and rare hallucinations or impulse-control issues.
Yes; do not use with other MAO inhibitors, meperidine, tramadol, methadone, propoxyphene, or dextromethorphan, and use extreme caution with SSRIs/SNRIs/TCAs, linezolid, and sympathomimetics—always review all medicines with your prescriber.
At usual doses it is MAO-B selective and does not require a strict tyramine-restricted diet, but very large amounts of aged/fermented foods may pose risk—ask your clinician for personalized guidance.
Yes; it is commonly added to levodopa to decrease “OFF” time and smooth fluctuations, though dyskinesia and nausea may increase and levodopa dosing may need adjustment.
It can cause insomnia or vivid dreams in some; taking it earlier in the day and reviewing other stimulatory drugs can help—speak with your clinician if sleep issues persist.
People taking contraindicated drugs (other MAO inhibitors, meperidine, tramadol, methadone, dextromethorphan), those with moderate-to-severe liver impairment, and those with hypersensitivity to rasagiline should avoid it.
Ciprofloxacin inhibits CYP1A2 and can raise rasagiline levels; your dose may need reduction or an alternative antibiotic considered—contact your prescriber before combining.
Take it when you remember the same day; if it’s close to the next dose, skip the missed dose—do not double up.
Data are limited; risks and benefits should be carefully weighed with your clinician, and breastfeeding considerations are individualized.
Smoking induces CYP1A2 and may lower rasagiline levels, potentially reducing effect; tell your clinician if you smoke or plan to quit.
Both are MAO-B inhibitors; Azilect is once-daily and does not form amphetamine-like metabolites, which may mean fewer insomnia or jitteriness issues for some compared with selegiline.
Head-to-head data are limited; both offer modest improvements and can reduce “OFF” time as adjuncts to levodopa, with individual response varying.
Tolerability is similar, but selegiline can cause more insomnia and agitation in some due to amphetamine-like metabolites; Azilect may be gentler on sleep for some patients.
Azilect (rasagiline) and safinamide (Xadago) are MAO-B inhibitors; safinamide also modulates glutamate release and is approved as adjunct to levodopa in mid-to-late Parkinson’s, while Azilect is used both as mono- and adjunct therapy.
Both reduce OFF time by roughly an hour on average in trials; individual benefit varies and may depend on concomitant therapy and disease stage.
Azilect is once daily with a fixed common dose; safinamide is once daily with titration between two strengths and has stricter liver-related dosing limits.
At standard doses, both are MAO-B selective and generally do not require strict tyramine restriction, though excessive tyramine intake should still be avoided.
Both are generally well tolerated; safinamide may cause more visual-related cautions (avoid in retinal disease) and potential edema, while Azilect may cause more insomnia or headache in some—overall profiles are comparable.
No; combining MAO-B inhibitors increases risk of adverse effects and hypertensive or serotonergic reactions and is contraindicated.
Zelapar is an orally disintegrating form of selegiline with buccal absorption that may lessen first-pass metabolism; Azilect offers once-daily dosing without amphetamine-like metabolites—choice depends on tolerability, adherence, and cost.
They contain the same active ingredient; generics must meet bioequivalence standards, though inactive ingredients, cost, and insurance coverage can differ.
A washout period is typically required to lower interaction risk, and doses are re-titrated; your clinician will guide timing and monitoring during the switch.
If a patient needs adjunct therapy with potential added benefit on fluctuations via glutamate modulation, or has prior insomnia with selegiline/rasagiline; choice is individualized based on response, comorbidities, and interactions.
For once-daily simplicity, early monotherapy use, avoidance of amphetamine-like metabolites, or when retinal precautions with safinamide are a concern.