NURSING MOTHERS SECTION.

In Nursing Mothers. There is evidence in mothers treated with primidone, the drug appears in the milk in substantial quantities. Since tests for the presence of primidone in biological fluids are too complex to be carried out in the average clinical laboratory, it is suggested that the presence of undue somnolence and drowsiness in nursing newborns of primidone-treated mothers be taken as an indication that nursing should be discontinued.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.

Package/Label Display Panel PRIMIDONE TABLETS, USP50 mg100 Tablets. Bottle label.

MECHANISM OF ACTION SECTION.

ACTIONS. Primidone raises electro- or chemoshock seizure thresholds or alters seizure patterns in experimental animals. The mechanism(s) of primidones antiepileptic action is not known.Primidone per se has anticonvulsant activity as do its two metabolites, phenobarbital and phenylethylmalonamide (PEMA). In addition to its anticonvulsant activity, PEMA potentiates the anticonvulsant activity of phenobarbital in experimental animals.

ADVERSE REACTIONS SECTION.

ADVERSE REACTIONS. The most frequently occurring early side effects are ataxia and vertigo. These tend to disappear with continued therapy, or with reduction of initial dosage. Occasionally, the following have been reported: nausea, anorexia, vomiting, fatigue, hyperirritability, emotional disturbances, sexual impotency, diplopia, nystagmus, drowsiness, and morbilliform skin eruptions. Granulocytopenia, agranulocytosis, and red-cell hypoplasia and aplasia, have been reported rarely. These and, occasionally, other persistent or severe side effects may necessitate withdrawal of the drug. Megaloblastic anemia may occur as rare idiosyncrasy to primidone and to other anticonvulsants. The anemia responds to folic acid without necessity of discontinuing medication.

CONTRAINDICATIONS SECTION.

CONTRAINDICATIONS. Primidone is contraindicated in: 1) patients with porphyria and 2) patients who are hypersensitive to phenobarbital (see ACTIONS).

DESCRIPTION SECTION.

DESCRIPTION. AnticonvulsantChemical name: 5-ethyldihydro-5-phenyl-4,6 (1H,5H)-pyrimidinedione. Structural formula:Primidone is white, crystalline, highly stable substance, M.P. 279 -284C. It is poorly soluble in water (60 mg per 100 mL at 37C) and in most organic solvents. It possesses no acidic properties, in contrast to its barbiturate analog.Each tablet, for oral administration, contains either 50 mg or 250 mg of primidone. In addition, each tablet contains the following inactive ingredients: lactose monohydrate, acacia, methylcellulose, magnesium stearate, and sodium starch glycolate.. primidone-molecular-structure.

DOSAGE & ADMINISTRATION SECTION.

DOSAGE AND ADMINISTRATION. Adult DosagePatients years of age and older who have received no previous treatment may be started on primidone according to the following regimen using either 50 mg or scored 250 mg primidone tablets.Days to 3: 100 to 125 mg at bedtimeDays to 6: 100 to 125 mg b.i.d.Days to 9: 100 to 125 mg t.i.d.Day 10 to maintenance: 250 mg t.i.d.For most adults and children years of age and over, the usual maintenance dosage is three to four 250 mg primidone tablets in divided doses (250 mg t.i.d. or q.i.d.). If required, an increase to five or six 250 mg tablets daily may be made but daily doses should not exceed 500 mg q.i.d.INITIAL: ADULTS AND CHILDREN OVER KEY: 50 mg tablet; = 250 mg tablet DAY 2 4 6 AM NOON PM DAY 8 10 11 12 AM Adjust to Maintenance NOON PM oDosage should be individualized to provide maximum benefit. In some cases, serum blood level determinations of primidone may be necessary for optimal dosage adjustment. The clinically effective serum level for primidone is between to 12 mcg/mL.In Patients Already Receiving Other AnticonvulsantsPrimidone should be started at 100 to 125 mg at bedtime and gradually increased to maintenance level as the other drug is gradually decreased. This regimen should be continued until satisfactory dosage level is achieved for the combination, or the other medication is completely withdrawn. When therapy with primidone alone is the objective, the transition from concomitant therapy should not be completed in less than two weeks.Pediatric DosageFor children under years of age, the following regimen may be used:Days to 3: 50 mg at bedtimeDays to 6: 50 mg b.i.d.Days to 9: 100 mg b.i.d.Day 10 to maintenance: 125 mg t.i.d. to 250 mg t.i.d.For children under years of age, the usual maintenance dosage is 125 to 250 mg three times daily or, 10 to 25 mg/kg/day in divided doses.

HOW SUPPLIED SECTION.

HOW SUPPLIED. Primidone Tablets USP, 50 mg are available as white, round, flat faced, beveled edge, scored tablets debossed LAN over 1301, supplied in bottles of 100 and 500 tablets.100 Tablets NDC 0904-5559-60500 Tablets NDC 0904-5559-40Store at 20 to 25C (68 to 77F)[see USP Controlled Room Temperature].Dispense in well-closed container as defined in the USP with child-resistant closure.Distributed by:Lannett Company, Inc.Philadelphia, PA 19154Distributed by:Major PharmaceuticalsLivonia, MI 48150 USACIB70303CRev. 08/18.

INDICATIONS & USAGE SECTION.

INDICATIONS AND USAGE. Primidone, used alone or concomitantly with other anticonvulsants, is indicated in the control of grand mal, psychomotor, and focal epileptic seizures. It may control grand mal seizures refractory to other anticonvulsant therapy.

INFORMATION FOR PATIENTS SECTION.

Information for Patients. Suicidal Thinking and Behavior Patients, their caregivers, and families should be counseled that AEDs, including primidone, may increase the risk of suicidal thoughts and behavior and should be advised of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts about self-harm. Behaviors of concern should be reported immediately to healthcare providers.Patients should be encouraged to enroll in the NAAED Pregnancy Registry if they become pregnant. This registry is collecting information about the safety of antiepileptic drugs during pregnancy. To enroll, patients can call the toll free number 1-888-233-2334 (see Usage in Pregnancy section).Please refer to the Primidone Tablets, USP Medication Guide provided with the product for more information.

PRECAUTIONS SECTION.

PRECAUTIONS. The total daily dosage should not exceed g. Since primidone therapy generally extends over prolonged periods, complete blood count and sequential multiple analysis-12 (SMA-12) test should be made every six months.. In Nursing Mothers. There is evidence in mothers treated with primidone, the drug appears in the milk in substantial quantities. Since tests for the presence of primidone in biological fluids are too complex to be carried out in the average clinical laboratory, it is suggested that the presence of undue somnolence and drowsiness in nursing newborns of primidone-treated mothers be taken as an indication that nursing should be discontinued.. Information for Patients. Suicidal Thinking and Behavior Patients, their caregivers, and families should be counseled that AEDs, including primidone, may increase the risk of suicidal thoughts and behavior and should be advised of the need to be alert for the emergence or worsening of symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts about self-harm. Behaviors of concern should be reported immediately to healthcare providers.Patients should be encouraged to enroll in the NAAED Pregnancy Registry if they become pregnant. This registry is collecting information about the safety of antiepileptic drugs during pregnancy. To enroll, patients can call the toll free number 1-888-233-2334 (see Usage in Pregnancy section).Please refer to the Primidone Tablets, USP Medication Guide provided with the product for more information.

PREGNANCY SECTION.

Usage in Pregnancy. To provide information regarding the effects of in utero exposure to primidone, physicians are advised to recommend that pregnant patients taking primidone enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry. This can be done by calling the toll free number 1-888-233-2334, and must be done by patients themselves. Information on the registry can also be found at the website http://www.aedpregnancyregistry.org/. The effects of primidone in human pregnancy and nursing infants are unknown.Recent reports suggest an association between the use of anticonvulsant drugs by women with epilepsy and an elevated incidence of birth defects in children born to these women. Data are more extensive with respect to diphenylhydantoin and phenobarbital, but these are also the most commonly prescribed anticonvulsants; less systematic or anecdotal reports suggest possible similar association with the use of all known anticonvulsant drugs.The reports suggesting an elevated incidence of birth defects in children of drug-treated epileptic women cannot be regarded as adequate to prove definite cause and effect relationship.There are intrinsic methodologic problems in obtaining adequate data on drug teratogenicity in humans; the possibility also exists that other factors leading to birth defects, e.g., genetic factors or the epileptic condition itself, may be more important than drug therapy. The great majority of mothers on anticonvulsant medication deliver normal infants. It is important to note that anticonvulsant drugs should not be discontinued in patients in whom the drug is administered to prevent major seizures because of the strong possibility of precipitating status epilepticus with attendant hypoxia and threat to life. In individual cases where the severity and frequency of the seizure disorders are such that the removal of medication does not pose serious threat to the patient, discontinuation of the drug may be considered prior to and during pregnancy, although it cannot be said with any confidence that even minor seizures do not pose some hazard to the developing embryo or fetus.The prescribing physician will wish to weigh these considerations in treating or counseling epileptic women of childbearing potential. Neonatal hemorrhage, with coagulation defect resembling vitamin deficiency, has been described in newborns whose mothers were taking primidone and other anticonvulsants. Pregnant women under anticonvulsant therapy should receive prophylactic vitamin K1 therapy for one month prior to, and during, delivery.

SPL MEDGUIDE SECTION.

MEDICATION GUIDE. Primidone Tablets, USPRead this Medication Guide before you start taking primidone tablets, USP and each time you get refill. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or treatment.What is the most important information should know about Primidone Tablets, USPDo not stop taking primidone tablets, USP without first talking to your healthcare provider.Stopping primidone tablets, USP suddenly can cause serious problems.Primidone tablets, USP can cause serious side effects, including:1. Like other antiepileptic drugs, primidone tablets, USP may cause suicidal thoughts or actions in very small number of people, about in 500.Call healthcare provider right away if you have any of these symptoms, especially if they are new, worse, or worry you:othoughts about suicide or dyingoattempts to commit suicideonew or worse depressiononew or worse anxietyofeeling agitated or restlessopanic attacksotrouble sleeping (insomnia)onew or worse irritabilityoacting aggressive, being angry, or violentoacting on dangerous impulsesoan extreme increase in activity and talking (mania)oother unusual changes in behavior or moodHow can watch for early symptoms of suicidal thoughts and actionsoPay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.oKeep all follow-up visits with your healthcare provider as scheduled.Call your healthcare provider between visits as needed, especially if you are worried about symptoms.Do not stop primidone tablets, USP without first talking to healthcare provider.oStopping primidone tablets, USP suddenly can cause serious problems. Stopping seizure medicine suddenly in patient who has epilepsy can cause seizures that will not stop (status epilepticus).Suicidal thoughts or actions can be caused by things other than medicines. If you have suicidal thoughts or actions, your healthcare provider may check for other causes.What is Primidone Tablets, USPPrimidone tablets, USP is prescription medicine used alone or with other medicines to treat people with:ogeneralized tonic-clonic (grand mal) seizuresocomplex partial (psychomotor) seizuresopartial (focal) epileptic seizures.Who should not take Primidone Tablets, USPDo not take primidone tablets, USP if you:ohave genetic disorder called porphyriaoare allergic to phenobarbitalWhat should tell my healthcare provider before taking Primidone Tablets, USPBefore you take primidone tablets, USP, tell your healthcare provider if you:ohave or have had depression, mood problems or suicidal thoughts or behaviorohave any other medical conditionsoare pregnant or planning to become pregnant. Primidone tablets, USP may harm your unborn baby. Tell your healthcare provider right away if you become pregnant while taking primidone tablets, USP. You and your healthcare provider will decide if you should take primidone tablets, USP while you are pregnant.oIf you become pregnant while taking primidone tablets, USP, talk to your healthcare provider about registering with the North American Antiepileptic Drug (NAAED) Pregnancy Registry. You can enroll in this registry by calling 1-888-233-2334. The purpose of this registry is to collect information about the safety of antiepileptic drugs during pregnancy.oare breastfeeding or plan to breastfeed. Primidone tablets, USP can pass into breast milk. Talk to your healthcare provider about the best way to feed your baby if you take primidone tablets, USP.Tell your healthcare provider about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. Taking primidone tablets, USP with certain other medicines can cause side effects or affect how well they work. Do not start or stop other medicines without talking to your healthcare provider.Know the medicines you take. Keep list of them and show it to your healthcare provider and pharmacist each time you get new medicine.How should take Primidone Tablets, USPTake primidone tablets, USP exactly as prescribed. Your healthcare provider will tell you how much primidone tablets, USP to take and when to take it.oYour healthcare provider may change your dose. Do not change your dose without talking to your healthcare provider.oDo not stop taking primidone tablets, USP without first talking to your healthcare provider. Stopping primidone tablets, USP suddenly can cause serious problems.oIf you take too much primidone tablets, USP, call your healthcare provider or local Poison Control Center right away.What should avoid while taking Primidone Tablets, USPoPrimidone tablets, USP can make you sleepy or dizzy. Do not drink alcohol or take other drugs that make you sleepy or dizzy while taking primidone tablets, USP without first discussing this with your healthcare provider. Taking primidone tablets, USP with alcohol or drugs that cause sleepiness or dizziness may make your sleepiness or dizziness worse.oDo not drive, operate heavy machinery, or do other dangerous activities until you know how primidone tablets, USP affects you. Primidone tablets, USP can slow your thinking and motor skills.What are the possible side effects of Primidone Tablets, USPSee What is the most important information should know about Primidone Tablets, USP.Primidone tablets, USP may cause other serious side effects including:oSleepiness that can be severe, especially when you first start taking primidone tablets, USP.oPrimidone tablets, USP may rarely cause blood problems. Symptoms may include:ofever, swollen glands, or sore throat that come and go or do not go awayoFrequent infections or an infection that does not go awayotirednessoshortness of breathoPrimidone tablets, USP may rarely cause allergic reactions. Symptoms may include:oskin rashohivesosores in your mouthoblistering or peeling skinThe most common side effects of primidone tablets, USP include:oproblems with walking and movingofeelings of dizziness, spinning, or swaying (vertigo)These are not all the possible side effects of primidone tablets, USP. For more information, ask your healthcare provider or pharmacist.Tell your healthcare provider if you have any side effect that bothers you or that does not go away.Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.How should store Primidone Tablets, USPStore primidone tablets, USP at room temperature between 68F to 77F (20C to 25C) in well-closed container.Keep primidone tablets, USP and all medicines out of the reach of children.General Information about Primidone Tablets, USPMedicines are sometimes prescribed for purposes other than those listed in Medication Guide. Do not use primidone tablets, USP for condition for which it was not prescribed. Do not give primidone tablets, USP to other people, even if they have the same symptoms that you have. It may harm them.This Medication Guide summarizes the most important information about primidone tablets, USP. If you would like more information, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about primidone tablets, USP that is written for health professionals. For more information, call Lannett Company, Inc. at 1-844-834-0530.What are the ingredients in Primidone Tablets, USPActive Ingredient: primidoneInactive ingredients: lactose monohydrate, acacia, methylcellulose, magnesium stearate, and sodium starch glycolateDistributed by:Lannett Company, Inc.Philadelphia, PA 19154Distributed by:Major PharmaceuticalsLivonia, MI 48150 USAThis Medication Guide has been approved by the U.S. Food and Drug AdministrationCIB70304CRev. 08/18. othoughts about suicide or dying. oattempts to commit suicide. onew or worse depression. onew or worse anxiety. ofeeling agitated or restless. opanic attacks. otrouble sleeping (insomnia). onew or worse irritability. oacting aggressive, being angry, or violent. oacting on dangerous impulses. oan extreme increase in activity and talking (mania). oother unusual changes in behavior or mood. oPay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.. oKeep all follow-up visits with your healthcare provider as scheduled.. oStopping primidone tablets, USP suddenly can cause serious problems. Stopping seizure medicine suddenly in patient who has epilepsy can cause seizures that will not stop (status epilepticus).. ogeneralized tonic-clonic (grand mal) seizures. ocomplex partial (psychomotor) seizures. opartial (focal) epileptic seizures.. ohave genetic disorder called porphyria. oare allergic to phenobarbital. ohave or have had depression, mood problems or suicidal thoughts or behavior. ohave any other medical conditions. oare pregnant or planning to become pregnant. Primidone tablets, USP may harm your unborn baby. Tell your healthcare provider right away if you become pregnant while taking primidone tablets, USP. You and your healthcare provider will decide if you should take primidone tablets, USP while you are pregnant.oIf you become pregnant while taking primidone tablets, USP, talk to your healthcare provider about registering with the North American Antiepileptic Drug (NAAED) Pregnancy Registry. You can enroll in this registry by calling 1-888-233-2334. The purpose of this registry is to collect information about the safety of antiepileptic drugs during pregnancy.. oIf you become pregnant while taking primidone tablets, USP, talk to your healthcare provider about registering with the North American Antiepileptic Drug (NAAED) Pregnancy Registry. You can enroll in this registry by calling 1-888-233-2334. The purpose of this registry is to collect information about the safety of antiepileptic drugs during pregnancy.. oare breastfeeding or plan to breastfeed. Primidone tablets, USP can pass into breast milk. Talk to your healthcare provider about the best way to feed your baby if you take primidone tablets, USP.. oYour healthcare provider may change your dose. Do not change your dose without talking to your healthcare provider.. oDo not stop taking primidone tablets, USP without first talking to your healthcare provider. Stopping primidone tablets, USP suddenly can cause serious problems.. oIf you take too much primidone tablets, USP, call your healthcare provider or local Poison Control Center right away.. oPrimidone tablets, USP can make you sleepy or dizzy. Do not drink alcohol or take other drugs that make you sleepy or dizzy while taking primidone tablets, USP without first discussing this with your healthcare provider. Taking primidone tablets, USP with alcohol or drugs that cause sleepiness or dizziness may make your sleepiness or dizziness worse.. oDo not drive, operate heavy machinery, or do other dangerous activities until you know how primidone tablets, USP affects you. Primidone tablets, USP can slow your thinking and motor skills.. oSleepiness that can be severe, especially when you first start taking primidone tablets, USP.. oPrimidone tablets, USP may rarely cause blood problems. Symptoms may include:ofever, swollen glands, or sore throat that come and go or do not go awayoFrequent infections or an infection that does not go awayotirednessoshortness of breath. ofever, swollen glands, or sore throat that come and go or do not go away. oFrequent infections or an infection that does not go away. otiredness. oshortness of breath. oPrimidone tablets, USP may rarely cause allergic reactions. Symptoms may include:oskin rashohivesosores in your mouthoblistering or peeling skin. oskin rash. ohives. osores in your mouth. oblistering or peeling skin. oproblems with walking and moving. ofeelings of dizziness, spinning, or swaying (vertigo).

WARNINGS SECTION.

WARNINGS. The abrupt withdrawal of antiepileptic medication may precipitate status epilepticus. The therapeutic efficacy of dosage regimen takes several weeks before it can be assessed.. Suicidal Behavior and Ideation. Antiepileptic drugs (AEDs), including primidone, increase the risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Patients treated with any AED for any indication should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior.Pooled analyses of 199 placebo-controlled clinical trials (mono- and adjunctive therapy) of 11 different AEDs showed that patients randomized to one of the AEDs had approximately twice the risk (adjusted Relative Risk 1.8, 95% CI:1.2, 2.7) of suicidal thinking or behavior compared to patients randomized to placebo. In these trials, which had median treatment duration of 12 weeks, the estimated incidence rate of suicidal behavior or ideation among 27,863 AED-treated patients was 0.43%, compared to 0.24% among 16,029 placebo-treated patients, representing an increase of approximately one case of suicidal thinking or behavior for every 530 patients treated. There were four suicides in drug-treated patients in the trials and none in placebo-treated patients, but the number is too small to allow any conclusion about drug effect on suicide.The increased risk of suicidal thoughts or behavior with AEDs was observed as early as one week after starting drug treatment with AEDs and persisted for the duration of treatment assessed. Because most trials included in the analysis did not extend beyond 24 weeks, the risk of suicidal thoughts or behavior beyond 24 weeks could not be assessed. The risk of suicidal thoughts or behavior was generally consistent among drugs in the data analyzed. The finding of increased risk with AEDs of varying mechanisms of action and across range of indications suggests that the risk applies to all AEDs used for any indication. The risk did not vary substantially by age (5-100 years) in the clinical trials analyzed.Table shows absolute and relative risk by indication for all evaluated AEDs.Table Risk by indication for antiepileptic drugs in the pooled analysisIndicationPlacebo Patients with Events Per 1000 PatientsDrug Patients with Events Per 1000 PatientsRelative Risk: Incidence of Events in Drug Patients/Incidence in Placebo PatientsRisk Difference: Additional Drug Patients with Events Per 1000 Patients Epilepsy 1.0 3.4 3.5 2.4 Psychiatric 5.7 8.5 1.5 2.9 Other 1.0 1.8 1.9 0.9 Total 2.4 4.3 1.8 1.9The relative risk for suicidal thoughts or behavior was higher in clinical trials for epilepsy than in clinical trials for psychiatric or other conditions, but the absolute risk differences were similar for the epilepsy and psychiatric indications.Anyone considering prescribing primidone or any other AED must balance the risk of suicidal thoughts or behavior with the risk of untreated illness. Epilepsy and many other illnesses for which AEDs are prescribed are themselves associated with morbidity and mortality and an increased risk of suicidal thoughts and behavior. Should suicidal thoughts and behavior emerge during treatment, the prescriber needs to consider whether the emergence of these symptoms in any given patient may be related to the illness being treated.Patients, their caregivers, and families should be informed that AEDs increase the risk of suicidal thoughts and behavior and should be advised of the need to be alert for the emergence or worsening of the signs and symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts about self-harm. Behaviors of concern should be reported immediately to healthcare providers.. Usage in Pregnancy. To provide information regarding the effects of in utero exposure to primidone, physicians are advised to recommend that pregnant patients taking primidone enroll in the North American Antiepileptic Drug (NAAED) Pregnancy Registry. This can be done by calling the toll free number 1-888-233-2334, and must be done by patients themselves. Information on the registry can also be found at the website http://www.aedpregnancyregistry.org/. The effects of primidone in human pregnancy and nursing infants are unknown.Recent reports suggest an association between the use of anticonvulsant drugs by women with epilepsy and an elevated incidence of birth defects in children born to these women. Data are more extensive with respect to diphenylhydantoin and phenobarbital, but these are also the most commonly prescribed anticonvulsants; less systematic or anecdotal reports suggest possible similar association with the use of all known anticonvulsant drugs.The reports suggesting an elevated incidence of birth defects in children of drug-treated epileptic women cannot be regarded as adequate to prove definite cause and effect relationship.There are intrinsic methodologic problems in obtaining adequate data on drug teratogenicity in humans; the possibility also exists that other factors leading to birth defects, e.g., genetic factors or the epileptic condition itself, may be more important than drug therapy. The great majority of mothers on anticonvulsant medication deliver normal infants. It is important to note that anticonvulsant drugs should not be discontinued in patients in whom the drug is administered to prevent major seizures because of the strong possibility of precipitating status epilepticus with attendant hypoxia and threat to life. In individual cases where the severity and frequency of the seizure disorders are such that the removal of medication does not pose serious threat to the patient, discontinuation of the drug may be considered prior to and during pregnancy, although it cannot be said with any confidence that even minor seizures do not pose some hazard to the developing embryo or fetus.The prescribing physician will wish to weigh these considerations in treating or counseling epileptic women of childbearing potential. Neonatal hemorrhage, with coagulation defect resembling vitamin deficiency, has been described in newborns whose mothers were taking primidone and other anticonvulsants. Pregnant women under anticonvulsant therapy should receive prophylactic vitamin K1 therapy for one month prior to, and during, delivery.