Dilantin is a long-established antiepileptic medicine that helps prevent and control seizures by stabilizing overactive electrical activity in the brain. Also known by its generic name, phenytoin, it comes in capsules, chewable tablets, and liquid forms. Because Dilantin has narrow therapeutic levels and complex, non‑linear pharmacokinetics, dosing is individualized and often guided by blood tests. Common effects include dizziness and gum changes; rare but serious reactions such as severe rash can occur. Dilantin is prescription-only in the United States. This guide explains uses, dosage principles, precautions, side effects, interactions, and legal access so you can discuss options with your clinician.
Dilantin is an anticonvulsant used to prevent and control certain types of seizures, especially focal (partial-onset) seizures and generalized tonic-clonic seizures. It works by stabilizing neuronal membranes and reducing repetitive firing of action potentials, helping to keep abnormal bursts of brain activity from spreading. In emergency settings, closely related formulations are used for status epilepticus, but long-term maintenance is typically with oral Dilantin or generic phenytoin. Some clinicians may also use phenytoin off-label for seizure prevention after severe head injury or neurosurgery, though practice varies and duration is usually short.
Because seizure disorders are diverse, Dilantin is not a one-size-fits-all therapy. It may be used alone (monotherapy) or alongside other antiseizure medications. Response depends on seizure type, age, coexisting medical conditions, and genetics. When effective and well tolerated, Dilantin can help reduce seizure frequency, maintain driving eligibility under local regulations, and improve day-to-day safety and independence.
Dosing is individualized and guided by clinical response and blood levels. Many adults start around 300 mg per day in divided doses (for example, 100 mg three times daily), though some will need dose adjustments over time. In certain situations, a loading dose may be used to reach therapeutic levels more quickly. Because phenytoin follows non-linear (Michaelis–Menten) kinetics, small dose changes can cause disproportionate shifts in blood concentration. Therapeutic drug monitoring is common, with typical total serum targets of about 10–20 mcg/mL (free level 1–2 mcg/mL), interpreted in context of albumin, renal function, and clinical status.
Take Dilantin exactly as prescribed, at consistent times each day. Swallow extended-release capsules whole; chew chewable tablets thoroughly; and shake liquid suspensions well before measuring with an oral syringe or dosing spoon. Food can help with stomach upset, but separate doses from antacids or calcium/magnesium supplements, which may interfere with absorption. Tube feedings can significantly reduce phenytoin levels; clinicians often adjust timing or dosing and monitor levels more closely in patients on enteral nutrition.
Avoid abrupt discontinuation, which can trigger breakthrough seizures. If a change in brand, formulation, or manufacturer is necessary, levels and symptoms should be watched closely because bioavailability can vary. Keep all lab and follow-up appointments so your prescriber can fine-tune therapy and minimize adverse effects.
Serious skin reactions, including Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), though rare, can occur—most often within the first weeks to months. Seek urgent care for rash, blistering, mouth sores, or fever. People of certain Asian ancestries with HLA-B*1502 may face higher SJS/TEN risk; genetic testing may be considered. Another rare but severe reaction is DRESS (Drug Reaction with Eosinophilia and Systemic Symptoms), characterized by fever, rash, swollen lymph nodes, and organ involvement—this requires immediate medical attention.
Phenytoin can affect the liver and blood. Report unusual fatigue, dark urine, jaundice, easy bruising, persistent fever, or signs of infection. Over time, Dilantin may reduce bone density; your clinician may recommend vitamin D and calcium, bone health monitoring, and lifestyle measures. Gingival hyperplasia (gum overgrowth) is common—excellent dental hygiene, regular cleanings, and folic acid as advised can help. Neurologic effects such as nystagmus, ataxia, tremor, and cognitive slowing may occur, especially at higher levels.
Use during pregnancy requires careful risk–benefit discussion. Uncontrolled seizures are dangerous for mother and fetus, yet phenytoin is associated with fetal hydantoin syndrome and other risks. If pregnancy is possible, discuss contraception—Dilantin can decrease the effectiveness of estrogen/progestin contraceptives—and preconception planning, including folic acid. Do not start or stop therapy without clinician guidance. Use caution with driving or operating machinery until you know how Dilantin affects you and your seizure control. Avoid heavy alcohol use; acute intake can raise levels, while chronic intake may lower them.
Do not use Dilantin if you have a known hypersensitivity to phenytoin or other hydantoins, or a history of severe skin reactions related to aromatic anticonvulsants. For intravenous forms, sinus bradycardia, sinoatrial block, second- or third-degree heart block, and Adams–Stokes syndrome are contraindications due to arrhythmia risk. Use extreme caution in severe hepatic impairment, porphyria, or in known CYP2C9 poor metabolizers, as toxicity risk is increased.
Common effects include dizziness, drowsiness, headache, slurred speech, blurred or double vision, tremor, and balance problems. Gum overgrowth, coarsening of facial features, unwanted hair growth, acne, and folate deficiency may develop with longer-term use. Gastrointestinal upset can occur, especially early in therapy. Many effects correlate with serum levels and may improve with dose adjustment.
Serious reactions are uncommon but require immediate care: severe rash or blistering, mouth/eye sores, fever, swollen glands, unexplained bruising or bleeding, persistent vomiting, abdominal pain, dark urine or jaundice, chest pain, fainting, or signs of confusion and severe unsteadiness. Rare hematologic disorders (agranulocytosis, aplastic anemia), hepatic injury, pancreatitis, and neurologic toxicity can occur. Suicidal thoughts and mood changes have been reported with antiepileptic drugs; seek help promptly for concerning behavioral changes.
Phenytoin is a potent inducer of hepatic enzymes (notably CYP3A4, CYP2C9, CYP2C19, and UGT), which can lower blood levels and effectiveness of many medications, including oral contraceptives, some anticoagulants (certain direct oral anticoagulants), antiretrovirals, azole antifungals, immunosuppressants, and other antiseizure drugs. Conversely, inhibitors such as amiodarone, some azoles (e.g., fluconazole, voriconazole), metronidazole, certain macrolides, cimetidine, isoniazid, and fluoxetine can raise phenytoin levels and toxicity risk. Valproate uniquely both displaces protein binding and inhibits metabolism, increasing free phenytoin levels.
Warfarin has a complex, bidirectional interaction; close INR and drug-level monitoring is essential. Herbs and supplements—St. John’s wort, ginkgo, high-dose folate—may alter seizure threshold or drug metabolism. Antacids and calcium/magnesium/iron products can reduce absorption; separate administration times. Enteral feedings significantly reduce phenytoin bioavailability; clinicians often pause feeds around dosing or adjust therapy. Always provide a complete medication and supplement list to your healthcare team, and never start new medicines without checking for interactions.
If you miss a dose, 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 regular schedule. Do not double up. Because steady levels matter for seizure prevention, consider alarms, pillboxes, or smartphone reminders. If you miss more than one dose or have a seizure, contact your clinician for guidance and do not make unapproved dose changes.
Overdose can cause profound dizziness, nystagmus, confusion, slurred speech, severe ataxia, vomiting, low blood pressure, cardiac rhythm changes, respiratory depression, or coma. Call emergency services or Poison Control (1-800-222-1222 in the U.S.) immediately. Do not induce vomiting. Treatment is supportive in a medical setting, with cardiac and respiratory monitoring, airway protection if needed, and consideration of activated charcoal if appropriate. Bring medication bottles so clinicians can verify the product and dose.
Store Dilantin at room temperature (generally 20–25°C/68–77°F), in a dry place away from excess heat and light, and out of reach of children and pets. Keep tablets and capsules in the original, tightly closed container; shake suspensions well and measure doses accurately. Do not use past the expiration date. Dispose of unused medicine through take-back programs or pharmacist guidance—avoid flushing unless specifically instructed.
In the United States, Dilantin (phenytoin) is an FDA-approved prescription medication. By law, a valid prescription from a licensed clinician is required for dispensing, whether you use a local pharmacy, hospital pharmacy, or a legitimate mail-order/telepharmacy. Websites that promise you can buy Dilantin without prescription are unsafe and often illegal; products may be counterfeit, subtherapeutic, or contaminated, and bypassing medical supervision increases the risk of toxicity, interactions, and uncontrolled seizures. To access Dilantin legally and conveniently, consider scheduling an in-person or telehealth visit, asking about generic phenytoin, and using pharmacy price comparison tools. Verify online pharmacies through NABP or LegitScript to ensure safety.
If you receive inpatient or rehabilitative care at a hospital, medications are provided under physician orders as part of your treatment plan—this is not “without a prescription,” but rather within the supervised medical record and pharmacy system. We cannot assist with or endorse obtaining Dilantin without a prescription. If affordability or transportation is a barrier, talk with your care team about community clinics, sliding-scale services, manufacturer or foundation patient assistance programs, and prescription discount resources. Your clinician and pharmacist can help build a legal, structured pathway to therapy that maintains monitoring, minimizes side effects, and supports reliable seizure control.
Dilantin is the brand name for phenytoin, an antiepileptic medication used primarily to prevent and control focal seizures and generalized tonic–clonic seizures. It’s also used in the hospital to manage status epilepticus and to prevent seizures after certain neurosurgical injuries.
Phenytoin stabilizes hyperexcitable neurons by blocking voltage-gated sodium channels, reducing repetitive firing. This dampens abnormal electrical activity in the brain that can trigger seizures.
Dilantin is effective for focal seizures and generalized tonic–clonic seizures. It is not effective for absence (petit mal) seizures and can potentially worsen them; other agents like ethosuximide or valproate are preferred for absence seizures.
Take Dilantin consistently with regard to meals. If you use tube feeds, they can significantly reduce absorption—your clinician may advise holding enteral nutrition 1–2 hours before and after a dose. Swallow extended-release capsules whole and avoid switching between formulations without guidance.
The usual total phenytoin therapeutic range is about 10–20 mcg/mL (free level 1–2 mcg/mL). Blood level monitoring helps ensure effectiveness and safety, because levels that are too low may allow seizures and levels that are too high increase toxicity risk.
Phenytoin has nonlinear (saturable) metabolism. Once enzymes are near capacity, small dose increases can cause disproportionate rises in blood levels. That’s why dose adjustments are usually small and guided by levels and symptoms.
Common effects include dizziness, drowsiness, unsteady gait, coordination problems, slurred speech, tremor, and nausea. Long-term use may cause gum overgrowth, hair growth, acne, coarse facial features, and reduced bone mineral density.
Seek urgent care for rash or blistering (possible Stevens–Johnson syndrome or TEN), fever with swollen lymph nodes and organ issues (possible DRESS), severe confusion, jaundice, persistent vomiting, suicidal thoughts, or signs of toxicity like severe ataxia or nystagmus.
Yes. Gingival hyperplasia (gum overgrowth) is a known effect, especially in younger patients and with poor oral hygiene. Regular dental care, meticulous brushing/flossing, and professional cleanings can reduce risk; folate optimization may help.
Phenytoin is a strong liver enzyme inducer (CYP3A4, CYP2C, UGT), which can lower levels of many drugs including hormonal contraceptives, warfarin, certain antivirals, antifungals, and antibiotics. Use a nonhormonal or higher-dose contraceptive method and review all meds with your prescriber.
Alcohol can unpredictably alter phenytoin levels—acute use may increase levels, while chronic heavy use induces enzymes and can lower levels. Alcohol also raises seizure risk and impairs judgment, so avoidance or careful limitation is advised after discussing with your clinician.
Phenytoin carries teratogenic risk (e.g., fetal hydantoin syndrome) and can lower folate. If pregnancy is possible, discuss safer alternatives and effective contraception. If continued in pregnancy, high-dose folic acid before conception and during pregnancy is typically recommended, along with close monitoring.
Phenytoin passes into breast milk in low amounts, and many guidelines consider breastfeeding compatible if the infant is healthy and monitored. Watch for excessive sleepiness, poor feeding, or rash in the baby and discuss with your pediatrician.
If you miss a dose, take it when remembered unless it’s close to the next one—don’t double up without advice. Overdose symptoms include severe drowsiness, confusion, nystagmus, vomiting, ataxia, and in severe cases coma or arrhythmias; seek emergency care immediately.
Phenytoin is highly protein-bound. Low albumin (or displacement by drugs like valproate) increases the free, active drug. In such cases, the total level can be misleading, so a corrected or free level better reflects clinical effect.
People of Asian ancestry with HLA-B*1502 may have higher risk of severe skin reactions with aromatic anticonvulsants, including phenytoin. Genetic testing may be considered before starting therapy in high-risk groups.
Long-term enzyme induction can increase vitamin D metabolism, contributing to osteopenia or osteoporosis. Calcium/vitamin D optimization, weight-bearing exercise, and periodic bone health assessments are advisable.
Because phenytoin has a narrow therapeutic index, switching manufacturers can alter blood levels for some people. If a switch is necessary, monitoring for symptoms and checking levels is prudent; many clinicians prefer staying with one manufacturer.
IV phenytoin contains propylene glycol and can cause hypotension and arrhythmias if infused too fast. Extravasation may cause severe tissue injury known as purple glove syndrome. Fosphenytoin (an IV prodrug) reduces these risks and is often preferred in acute care.
Until seizures are controlled and side effects like dizziness and blurred vision are settled, driving and operating machinery may be unsafe. Follow local laws on seizure-free intervals and your clinician’s guidance.
Fosphenytoin is a water-soluble prodrug that’s converted to phenytoin. It can be infused faster with less risk of hypotension, arrhythmias, and tissue injury, making it preferred IV/IM for status epilepticus. Oral use isn’t typical; for maintenance, both result in phenytoin exposure.
Both are effective for focal-onset seizures. Carbamazepine may be better tolerated long term for some patients but also induces enzymes and has its own risks (hyponatremia, rash). Phenytoin is often used acutely or when carbamazepine isn’t tolerated. Choice depends on comorbidities, interactions, and patient factors.
Efficacy for focal seizures is comparable. Oxcarbazepine tends to have fewer drug–drug interactions and less hematologic toxicity but more hyponatremia. Phenytoin has gum overgrowth, cosmetic effects, and bone loss over time. Many clinicians prefer oxcarbazepine for chronic therapy.
Valproate covers a broad spectrum, including generalized epilepsies and absence seizures; it also treats migraine and bipolar disorder. However, it’s highly teratogenic and can cause weight gain and liver issues. Phenytoin is not useful for absence seizures but is effective for focal and tonic–clonic seizures and in acute settings.
Levetiracetam has minimal interactions, no routine level monitoring, and is easy to dose, making it a first-line choice for many. Behavioral side effects (irritability, mood changes) can occur. Phenytoin requires levels, has many interactions, and more chronic adverse effects, but is potent and useful in emergencies.
Lamotrigine is favored for long-term maintenance due to cognitive neutrality and broad-spectrum efficacy, but it requires slow titration to avoid rash. Phenytoin works quickly and is useful acutely but is less favored for chronic use because of cosmetic, bone, and interaction burdens.
Both treat focal and generalized tonic–clonic seizures. Topiramate can cause cognitive slowing, paresthesias, kidney stones, and weight loss. Phenytoin causes ataxia and cosmetic effects and contributes to bone loss. Neither is ideal in pregnancy; selection depends on individual risk profiles.
Both are strong enzyme inducers with long histories in epilepsy. Phenobarbital is very sedating and can impair cognition and mood; it’s still used where cost and availability matter. Phenytoin is less sedating but has cosmetic and bone effects. Neither is usually first-line for long-term therapy in high-resource settings.
Both act on sodium channels, but lacosamide enhances slow inactivation and is often better tolerated with fewer interactions. Lacosamide can prolong PR interval and cause dizziness. Phenytoin requires level monitoring and has more chronic adverse effects but is widely available and inexpensive.
Gabapentin and pregabalin are not strong antiseizure options for focal epilepsy and are primarily used for neuropathic pain and anxiety. Phenytoin is much more effective for focal and tonic–clonic seizures. For epilepsy, if gabapentin fails, escalation to agents like levetiracetam or lamotrigine is common.
Benzodiazepines (lorazepam, diazepam, midazolam) are first-line for stopping an active seizure. Phenytoin is a second-line agent to prevent seizure recurrence. Benzodiazepines work rapidly but cause sedation and respiratory depression; phenytoin maintains control but is slower to load.
Newer agents like levetiracetam, lacosamide, brivaracetam, and perampanel often have simpler dosing and fewer interactions, making them easier for long-term use. Phenytoin’s need for blood levels, interaction profile, and chronic adverse effects limit its role mainly to specific situations.
Valproate has a high risk of birth defects and neurodevelopmental problems and is generally avoided if pregnancy is possible. Phenytoin also carries teratogenic risk but is typically considered less severe than valproate. In this group, options like levetiracetam or lamotrigine are often preferred.
All three can reduce bone mineral density over time via enzyme induction (oxcarbazepine to a lesser extent). Vitamin D supplementation and bone monitoring are prudent with any long-term enzyme-inducing antiseizure medication.
Both deliver phenytoin exposure, but fosphenytoin allows faster, safer infusion with fewer local reactions and cardiac events. When available, fosphenytoin is usually chosen for rapid IV loading; phenytoin may be used where cost or access is limiting.