ADVERSE REACTIONS SECTION.

ADVERSE REACTIONS. The prescriber should be aware that the adverse event incidence figures in the following tables, obtained when levetiracetam was added to concurrent AED therapy, cannot be used to predict the frequency of adverse experiences in the course of usual medical practice where patient characteristics and other factors may differ from those prevailing during clinical studies. Similarly, the cited frequencies cannot be directly compared with figures obtained from other clinical investigations involving different treatments, uses, or investigators. An inspection of these frequencies, however, does provide the prescriber with one basis to estimate the relative contribution of drug and non-drug factors to the adverse event incidences in the population studied.. Partial Onset Seizures. In well-controlled clinical studies in adults with partial onset seizures, the most frequently reported adverse events associated with the use of levetiracetam in combination with other AEDs, not seen at an equivalent frequency among placebo-treated patients, were somnolence, asthenia, infection and dizziness. In the well-controlled pediatric clinical study in children to 16 years of age with partial onset seizures, the adverse events most frequently reported with the use of levetiracetam in combination with other AEDs, not seen at an equivalent frequency among placebo-treated patients, were somnolence, accidental injury, hostility, nervousness, and asthenia.Table lists treatment-emergent adverse events that occurred in at least 1% of adult epilepsy patients treated with levetiracetam participating in placebo-controlled studies and were numerically more common than in patients treated with placebo. Table lists treatment-emergent adverse events that occurred in at least 2% of pediatric epilepsy patients (ages to 16 years) treated with levetiracetam participating in the placebo-controlled study and were numerically more common than in pediatric patients treated with placebo. In these studies, either levetiracetam or placebo was added to concurrent AED therapy. Adverse events were usually mild to moderate in intensity.Table 7: Incidence (%) Of Treatment-Emergent Adverse Events In Placebo-Controlled, Add-On Studies In Adults Experiencing Partial Onset Seizures By Body System (Adverse Events Occurred In At Least 1% Of Levetiracetam-Treated Patients And Occurred More Frequently Than Placebo-Treated Patients)Body System/ Adverse EventLevetiracetam(N=769)%Placebo(N=439)%Body as Whole Asthenia159 Headache1413 Infection138 Pain76Digestive System Anorexia32Nervous System Somnolence158 Dizziness94 Depression42 Nervousness42 Ataxia31 Vertigo31 Amnesia21 Anxiety21 Hostility21 Paresthesia21 Emotional Lability20Respiratory System Pharyngitis64 Rhinitis43 Cough Increased21 Sinusitis21Special Senses Diplopia21Other events reported by at least 1% of adult levetiracetam-treated patients but as or more frequent in the placebo group were the following: abdominal pain, accidental injury, amblyopia, arthralgia, back pain, bronchitis, chest pain, confusion, constipation, convulsion, diarrhea, drug level increased, dyspepsia, ecchymosis, fever, flu syndrome, fungal infection, gastroenteritis, gingivitis, grand mal convulsion, insomnia, nausea, otitis media, rash, thinking abnormal, tremor, urinary tract infection, vomiting and weight gain.Table 8: Incidence (%) Of Treatment-Emergent Adverse Events In Placebo-Controlled, Add-On Study In Pediatric Patients Ages to 16 Years Experiencing Partial Onset Seizures By Body System (Adverse Events Occurred In At Least 2% Of Levetiracetam-Treated Patients And Occurred More Frequently Than Placebo-Treated Patients)Body System/ Adverse EventLevetiracetam(N=101)%Placebo(N=97)%Body as Whole Accidental Injury1710 Asthenia93 Pain63 Flu Syndrome32 Face Edema21 Neck Pain21 Viral Infection21Digestive System Vomiting1513 Anorexia138 Diarrhea87 Gastroenteritis42 Constipation31Hemic and Lymphatic System Ecchymosis41Metabolic and Nutritional Dehydration21Nervous System Somnolence2311 Hostility126 Nervousness102 Personality Disorder87 Dizziness72 Emotional Lability64 Agitation61 Depression31 Vertigo31 Reflexes Increased21 Confusion20Respiratory System Rhinitis138 Cough Increased117 Pharyngitis108 Asthma21Skin and Appendages Pruritus20 Skin Discoloration20 Vesiculobullous Rash20Special Senses Conjunctivitis32 Amblyopia20 Ear Pain20Urogenital System Albuminuria40 Urine Abnormality21Other events occurring in at least 2% of pediatric levetiracetam-treated patients but as or more frequent in the placebo group were the following: abdominal pain, allergic reaction, ataxia, convulsion, epistaxis, fever, headache, hyperkinesia, infection, insomnia, nausea, otitis media, rash, sinusitis, status epilepticus (not otherwise specified), thinking abnormal, tremor, and urinary incontinence.. Myoclonic Seizures. Although the pattern of adverse events in this study seems somewhat different from that seen in patients with partial seizures, this is likely due to the much smaller number of patients in this study compared to partial seizure studies. The adverse event pattern for patients with JME is expected to be essentially the same as for patients with partial seizures.In the well-controlled clinical study that included both adolescent (12 to 16 years of age) and adult patients with myoclonic seizures, the most frequently reported adverse events associated with the use of levetiracetam in combination with other AEDs, not seen at an equivalent frequency among placebo-treated patients, were somnolence, neck pain, and pharyngitis.Table lists treatment-emergent adverse events that occurred in at least 5% of juvenile myoclonic epilepsy patients experiencing myoclonic seizures treated with levetiracetam and were numerically more common than in patients treated with placebo. In this study, either levetiracetam or placebo was added to concurrent AED therapy. Adverse events were usually mild to moderate in intensity.Table 9: Incidence (%) Of Treatment-Emergent Adverse Events In Placebo-Controlled, Add-On Study In Patients 12 Years Of Age And Older With Myoclonic Seizures By Body System (Adverse Events Occurred In At Least 5% Of Levetiracetam-Treated Patients And Occurred More Frequently Than Placebo-Treated Patients)Body System/ MedDRA preferred termLevetiracetam(N=60)%Placebo(N=60)%Ear and labyrinth disorders Vertigo53Infections and infestations Pharyngitis70 Influenza52Musculoskeletal and connective tissue disorders Neck pain82Nervous system disorders Somnolence122Psychiatric disorders Depression52Other events occurring in at least 5% of levetiracetam-treated patients with myoclonic seizures but as or more frequent in the placebo group were the following: fatigue and headache.. Time Course Of Onset Of Adverse Events For Partial Onset Seizures. Of the most frequently reported adverse events in adults experiencing partial onset seizures, asthenia, somnolence and dizziness appeared to occur predominantly during the first weeks of treatment with levetiracetam.. Discontinuation Or Dose Reduction In Well-Controlled Clinical Studies. Partial Onset Seizures. In well-controlled adult clinical studies, 15.0% of patients receiving levetiracetam and 11.6% receiving placebo either discontinued or had dose reduction as result of an adverse event. Table 10 lists the most common (>1%) adverse events that resulted in discontinuation or dose reduction.Table 10: Adverse Events That Most Commonly Resulted In Discontinuation Or Dose Reduction In Placebo-Controlled Studies In Adult Patients Experiencing Partial Onset SeizuresNumber (%)Levetiracetam(N=769)Placebo(N=439)Asthenia10 (1.3%)3 (0.7%)Convulsion23 (3.0%)15 (3.4%)Dizziness11 (1.4%)0Rash05 (1.1%)Somnolence34 (4.4%)7 (1.6%)In the well-controlled pediatric clinical study, 16.8% of patients receiving levetiracetam and 20.6% receiving placebo either discontinued or had dose reduction as result of an adverse event. The adverse events most commonly associated (>=3% in patients receiving levetiracetam) with discontinuation or dose reduction in the well-controlled study are presented in Table 11.Table 11: Adverse Events Most Commonly Associated With Discontinuation Or Dose Reduction In The Placebo-Controlled Study In Pediatric Patients Ages to 16 Years Experiencing Onset SeizuresNumber (%)Levetiracetam(N=101)Placebo(N=97)Asthenia3 (3.0%)0Hostility7 (6.9%)2 (2.1%)Somnolence3 (3.0%)3 (3.1%). Myoclonic Seizures. In the placebo-controlled study, 8.3% of patients receiving levetiracetam and 1.7% receiving placebo either discontinued or had dose reduction as result of an adverse event. The adverse events that led to discontinuation or dose reduction in the well-controlled study are presented in Table 12.Table 12: Adverse Events That Resulted In Discontinuation Or Dose Reduction In The Placebo-Controlled Study In Patients With Juvenile Myoclonic EpilepsyBody System/ MedDRA preferred term Levetiracetam(N=60)n %Placebo(N=60)n %Anxiety2 (3.3%)1 (1.7%)Depressed mood1 (1.7%)0Depression1 (1.7%)0Diplopia1 (1.7%)0Hypersomnia1 (1.7%)0Insomnia1 (1.7%)0Irritability1 (1.7%)0Nervousness1 (1.7%)0Somnolence1 (1.7%)0. Comparison Of Gender, Age And Race. The overall adverse experience profile of levetiracetam was similar between females and males. There are in-sufficient data to support statement regarding the distribution of adverse experience reports by age and race.. Postmarketing Experience. The following adverse events have been identified during postapproval use of levetiracetam. Because these events are reported voluntarily from population of uncertain size, it is not always possible to reliably estimate their frequency or establish casual relationship to drug exposure.In addition to the adverse experiences listed above, the following have been reported in patients receiving marketed levetiracetam worldwide. The listing is alphabetized: abnormal liver function test, hepatic failure, hepatitis, leukopenia, neutropenia, pancreatitis, pancytopenia (with bone marrow suppression identified in some of these cases), thrombocytopenia, and weight loss. Alopecia has been reported with levetiracetam use; recovery was observed in majority of cases where levetiracetam was discontinued. These adverse experiences have not been listed above, and data are insufficient to support an estimate of their incidence or to establish causation.

CLINICAL PHARMACOLOGY SECTION.

CLINICAL PHARMACOLOGY. Mechanism Of Action. The precise mechanism(s) by which levetiracetam exerts its antiepileptic effect is unknown. The antiepileptic activity of levetiracetam was assessed in number of animal models of epileptic seizures. Levetiracetam did not inhibit single seizures induced by maximal stimulation with electrical current or different chemoconvulsants and showed only minimal activity in submaximal stimulation and in threshold tests. Protection was observed, however, against secondarily generalized activity from focal seizures induced by pilocarpine and kainic acid, two chemoconvulsants that induce seizures that mimic some features of human complex partial seizures with secondary generalization. Levetiracetam also displayed inhibitory properties in the kindling model in rats, another model of human complex partial seizures, both during kindling development and in the fully kindled state. The predictive value of these animal models for specific types of human epilepsy is uncertain.In vitro and in vivo recordings of epileptiform activity from the hippocampus have shown that levetiracetam inhibits burst firing without affecting normal neuronal excitability, suggesting that levetiracetam may selectively prevent hypersynchronization of epileptiform burst firing and propagation of seizure activity.Levetiracetam at concentrations of up to 10 uM did not demonstrate binding affinity for variety of known receptors, such as those associated with benzodiazepines, GABA (gamma-aminobutyric acid), glycine, NMDA (N-methyl-D-aspartate), re-uptake sites, and second messenger systems. Furthermore, in vitro studies have failed to find an effect of levetiracetam on neuronal voltage-gated sodium or T-type calcium currents and levetiracetam does not appear to directly facilitate GABAergic neurotransmission. However, in vitro studies have demonstrated that levetiracetam opposes the activity of negative modulators of GABA- and glycine-gated currents and partially inhibits N-type calcium currents in neuronal cells.A saturable and stereoselective neuronal binding site in rat brain tissue has been described for levetiracetam. Experimental data indicate that this binding site is the synaptic vesicle protein SV2A, thought to be involved in the regulation of vesicle exocytosis. Although the molecular significance of levetiracetam binding to synaptic vesicle protein SV2A is not understood, levetiracetam and related analogs showed rank order of affinity for SV2A which correlated with the potency of their antiseizure activity in audiogenic seizure-prone mice. These findings suggest that the interaction of levetiracetam with the SV2A protein may contribute to the antiepileptic mechanism of action of the drug.. Pharmacokinetics. The pharmacokinetics of levetiracetam have been studied in healthy adult subjects, adults and pediatric patients with epilepsy, elderly subjects and subjects with renal and hepatic impairment.. Overview. Levetiracetam is rapidly and almost completely absorbed after oral administration. Levetiracetam tablets and oral solution are bioequivalent. The pharmacokinetics are linear and time-invariant, with low intra- and inter-subject variability. The extent of bioavailability of levetiracetam is not affected by food. Levetiracetam is not significantly protein-bound (<10% bound) and its volume of distribution is close to the volume of intracellular and extracellular water. Sixty-six percent (66%) of the dose is renally excreted unchanged. The major metabolic pathway of levetiracetam (24% of dose) is an enzymatic hydrolysis of the acetamide group. It is not liver cytochrome P450 dependent. The metabolites have no known pharmacological activity and are renally excreted. Plasma half-life of levetiracetam across studies is approximately to hours. It is increased in the elderly (primarily due to impaired renal clearance) and in subjects with renal impairment.. Absorption And Distribution. Absorption of levetiracetam is rapid, with peak plasma concentrations occurring in about an hour following oral administration in fasted subjects. The oral bioavailability of levetiracetam tablets is 100% and the tablets and oral solution are bioequivalent in rate and extent of absorption. Food does not affect the extent of absorption of levetiracetam but it decreases Cmax by 20% and delays Tmax by 1.5 hours. The pharmacokinetics of levetiracetam are linear over the dose range of 500 to 5000 mg. Steady state is achieved after days of multiple twice-daily dosing. Levetiracetam and its major metabolite are less than 10% bound to plasma proteins; clinically significant interactions with other drugs through competition for protein binding sites are therefore unlikely.. Metabolism. Levetiracetam is not extensively metabolized in humans. The major metabolic pathway is the enzymatic hydrolysis of the acetamide group, which produces the carboxylic acid metabolite, ucb L057 (24% of dose) and is not dependent on any liver cytochrome P450 isoenzymes. The major metabolite is inactive in animal seizure models. Two minor metabolites were identified as the product of hydroxylation of the 2-oxo-pyrrolidine ring (2% of dose) and opening of the 2-oxo-pyrrolidine ring in position (1% of dose). There is no enantiomeric interconversion of levetiracetam or its major metabolite.. Elimination. Levetiracetam plasma half-life in adults is +- hour and is unaffected by either dose or repeated administration. Levetiracetam is eliminated from the systemic circulation by renal excretion as unchanged drug which represents 66% of administered dose. The total body clearance is 0.96 mL/min/kg and the renal clearance is 0.6 mL/min/kg. The mechanism of excretion is glomerular filtration with subsequent partial tubular reabsorption. The metabolite ucb L057 is excreted by glomerular filtration and active tubular secretion with renal clearance of mL/min/kg. Levetiracetam elimination is correlated to creatinine clearance. Levetiracetam clearance is reduced in patients with impaired renal function (see Special Populations, Renal Impairment and DOSAGE AND ADMINISTRATION, Adult Patients with Impaired Renal Function).. Pharmacokinetic Interactions. In vitro data on metabolic interactions indicate that levetiracetam is unlikely to produce, or be subject to, pharmacokinetic interactions. Levetiracetam and its major metabolite, at concentrations well above Cmax levels achieved within the therapeutic dose range, are neither inhibitors of, nor high affinity substrates for, human liver cytochrome P450 isoforms, epoxide hydrolase or UDP-glucuronidation enzymes. In addition, levetiracetam does not affect the in vitro glucuronidation of valproic acid.Potential pharmacokinetic interactions of or with levetiracetam were assessed in clinical pharmacokinetic studies (phenytoin, valproate, warfarin, digoxin, oral contraceptive, probenecid) and through pharmacokinetic screening in the placebo-controlled clinical studies in epilepsy patients (see PRECAUTIONS, Drug Interactions).. Special Populations. Elderly. Pharmacokinetics of levetiracetam were evaluated in 16 elderly subjects (age 61 to 88 years) with creatinine clearance ranging from 30 to 74 mL/min. Following oral administration of twice-daily dosing for 10 days, total body clearance decreased by 38% and the half-life was 2.5 hours longer in the elderly compared to healthy adults. This is most likely due to the decrease in renal function in these subjects.. Pediatric Patients. Pharmacokinetics of levetiracetam were evaluated in 24 pediatric patients (age to 12 years) after single dose (20 mg/kg). The body weight adjusted apparent clearance of levetiracetam was approximately 40% higher than in adults.A repeat dose pharmacokinetic study was conducted in pediatric patients (age to 12 years) at doses of 20 mg/kg/day, 40 mg/kg/day, and 60 mg/kg/day. The evaluation of the pharmacokinetic profile of levetiracetam and its metabolite (ucb L057) in 14 pediatric patients demonstrated rapid absorption of levetiracetam at all doses with Tmax of about hour and t1/2 of hours across the three dosing levels. The pharmacokinetics of levetiracetam in children was linear between 20 to 60 mg/kg/day. The potential interaction of levetiracetam with other AEDs was also evaluated in these patients (see PRECAUTIONS, Drug Interactions). Levetiracetam had no significant effect on the plasma concentrations of carbamazepine, valproic acid, topiramate or lamotrigine. However, there was about 22% increase of apparent clearance of levetiracetam when it was coadministered with an enzyme-inducing AED (e.g. carbamazepine). Population pharmacokinetic analysis showed that body weight was significantly correlated to clearance of levetiracetam in pediatric patients; clearance increased with an increase in body weight.. Gender. Levetiracetam Cmax and AUC were 20% higher in women (N=11) compared to men (N=12). However, clearances adjusted for body weight were comparable.. Race. Formal pharmacokinetic studies of the effects of race have not been conducted. Cross study comparisons involving Caucasians (N=12) and Asians (N=12), however, show that pharmacokinetics of levetiracetam were comparable between the two races. Because levetiracetam is primarily renally excreted and there are no important racial differences in creatinine clearance, pharmacokinetic differences due to race are not expected.. Renal Impairment. The disposition of levetiracetam was studied in adult subjects with varying degrees of renal function. Total body clearance of levetiracetam is reduced in patients with impaired renal function by 40% in the mild group (CLcr 50 to 80 mL/min), 50% in the moderate group (CLcr 30 to 50 mL/min) and 60% in the severe renal impairment group (CLcr <30 mL/min). Clearance of levetiracetam is correlated with creatinine clearance.In anuric (end stage renal disease) patients, the total body clearance decreased 70% compared to normal subjects (CLcr >80 mL/min). Approximately 50% of the pool of levetiracetam in the body is removed during standard 4-hour hemodialysis procedure.Dosage should be reduced in patients with impaired renal function receiving levetiracetam, and supplemental doses should be given to patients after dialysis (see PRECAUTIONS and DOSAGE AND ADMINISTRATION, Adult Patients with Impaired Renal Function).. Hepatic Impairment. In subjects with mild (Child-Pugh A) to moderate (Child-Pugh B) hepatic impairment, the pharmacokinetics of levetiracetam were unchanged. In patients with severe hepatic impairment (Child-Pugh C), total body clearance was 50% that of normal subjects, but decreased renal clearance accounted for most of the decrease. No dose adjustment is needed for patients with hepatic impairment.

CLINICAL STUDIES SECTION.

CLINICAL STUDIES. In the following studies, statistical significance versus placebo indicates p value <0.05.. Effectiveness In Partial Onset Seizures In Adults With Epilepsy. The effectiveness of levetiracetam as adjunctive therapy (added to other antiepileptic drugs) in adults was established in three multicenter, randomized, double-blind, placebo-controlled clinical studies in patients who had refractory partial onset seizures with or without secondary generalization. The tablet formulation was used in all these studies. In these studies, 904 patients were randomized to placebo, 1000 mg, 2000 mg, or 3000 mg/day. Patients enrolled in Study or Study had refractory partial onset seizures for at least two years and had taken two or more classical AEDs. Patients enrolled in Study had refractory partial onset seizures for at least year and had taken one classical AED. At the time of the study, patients were taking stable dose regimen of at least one and could take maximum of two AEDs. During the baseline period, patients had to have experienced at least two partial onset seizures during each 4-week period.. Study 1. Study was double-blind, placebo-controlled, parallel-group study conducted at 41 sites in the United States comparing levetiracetam 1000 mg/day (N=97), levetiracetam 3000 mg/day (N=101), and placebo (N=95) given in equally divided doses twice daily. After prospective baseline period of 12 weeks, patients were randomized to one of the three treatment groups described above. The 18-week treatment period consisted of 6-week titration period, followed by 12-week fixed dose evaluation period, during which concomitant AED regimens were held constant. The primary measure of effectiveness was between group comparison of the percent reduction in weekly partial seizure frequency relative to placebo over the entire randomized treatment period (titration evaluation period). Secondary outcome variables included the responder rate (incidence of patients with >=50% reduction from baseline in partial onset seizure frequency). The results of the analysis of Study are displayed in Table 1.Table 1: Reduction In Mean Over Placebo In Weekly Frequency Of Partial Onset Seizures In Study 1Placebo(N=95)Levetiracetam1000 mg/day(N=97)Levetiracetam3000 mg/day(N=101)Percent reduction in partial seizure frequency over placebo--26.1%statistically significant versus placebo 30.1% The percentage of patients (y-axis) who achieved >=50% reduction in weekly seizure rates from baseline in partial onset seizure frequency over the entire randomized treatment period (titration evaluation period) within the three treatment groups (x-axis) is presented in Figure 1.Figure 1: Responder Rate (>=50% Reduction From Baseline) In Study 1statistically significant versus placebo. Figure 1. Study 2. Study was double-blind, placebo-controlled, crossover study conducted at 62 centers in Europe comparing levetiracetam 1000 mg/day (N=106), levetiracetam 2000 mg/day (N=105), and placebo (N=111) given in equally divided doses twice daily.The first period of the study (Period A) was designed to be analyzed as parallel-group study. After prospective baseline period of up to 12 weeks, patients were randomized to one of the three treatment groups described above. The 16-week treatment period consisted of the 4-week titration period followed by 12-week fixed dose evaluation period, during which concomitant AED regimens were held constant. The primary measure of effectiveness was between group comparison of the percent reduction in weekly partial seizure frequency relative to placebo over the entire randomized treatment period (titration evaluation period). Secondary outcome variables included the responder rate (incidence of patients with >=50% reduction from baseline in partial onset seizure frequency). The results of the analysis of Period are displayed in Table 2.Table 2: Reduction In Mean Over Placebo In Weekly Frequency Of Partial Onset Seizures In Study 2: Period APlacebo(N=111)Levetiracetam1000 mg/day(N=106)Levetiracetam2000 mg/day(N=105)Percent reduction in partial seizure frequency over placebo--17.1%statistically significant versus placebo 21.4% The percentage of patients (y-axis) who achieved >=50% reduction in weekly seizure rates from baseline in partial onset seizure frequency over the entire randomized treatment period (titration evaluation period) within the three treatment groups (x-axis) is presented in Figure 2.Figure 2: Responder Rate (>=50% Reduction From Baseline) In Study 2: Period Astatistically significant versus placeboThe comparison of levetiracetam 2000 mg/day to levetiracetam 1000 mg/day for responder rate was statistically significant (P=0.02). Analysis of the trial as cross-over yielded similar results.. Figure 2. Study 3. Study was double-blind, placebo-controlled, parallel-group study conducted at 47 centers in Europe comparing levetiracetam 3000 mg/day (N=180) and placebo (N=104) in patients with refractory partial onset seizures, with or without secondary generalization, receiving only one concomitant AED. Study drug was given in two divided doses. After prospective baseline period of 12 weeks, patients were randomized to one of two treatment groups described above. The 16-week treatment period consisted of 4-week titration period, followed by 12-week fixed dose evaluation period, during which concomitant AED doses were held constant. The primary measure of effectiveness was between group comparison of the percent reduction in weekly seizure frequency relative to placebo over the entire randomized treatment period (titration evaluation period). Secondary outcome variables included the responder rate (incidence of patients with >=50% reduction from baseline in partial onset seizure frequency). Table displays the results of the analysis of Study 3.Table 3: Reduction In Mean Over Placebo In Weekly Frequency Of Partial Onset Seizures In Study 3Placebo(N=104)Levetiracetam3000 mg/day(N=180)Percent reduction in partial seizure frequency over placebo--23.0%statistically significant versus placebo The percentage of patients (y-axis) who achieved >=50% reduction in weekly seizure rates from baseline in partial onset seizure frequency over the entire randomized treatment period (titration evaluation period) within the two treatment groups (x-axis) is presented in Figure 3.Figure 3: Responder Rate (>=50% Reduction From Baseline) In Study statistically significant versus placebo. Figure 3. Effectiveness In Partial Onset Seizures In Pediatric Patients With Epilepsy. The effectiveness of levetiracetam as adjunctive therapy (added to other antiepileptic drugs) in pediatric patients was established in one multicenter, randomized double-blind, placebo-controlled study, conducted at 60 sites in North America, in children to 16 years of age with partial seizures uncontrolled by standard antiepileptic drugs (AEDs). Eligible patients on stable dose of to AEDs, who still experienced at least partial onset seizures during the weeks prior to screening, as well as at least partial onset seizures in each of the two 4-week baseline periods, were randomized to receive either levetiracetam or placebo. The enrolled population included 198 patients (levetiracetam N=101, placebo N=97) with refractory partial onset seizures, whether or not secondarily generalized. The study consisted of an 8-week baseline period and 4-week titration period followed by 10-week evaluation period. Dosing was initiated at dose of 20 mg/kg/day in two divided doses. During the treatment period, levetiracetam doses were adjusted in 20 mg/kg/day increments, at 2-week intervals to the target dose of 60 mg/kg/day. The primary measure of effectiveness was between group comparison of the percent reduction in weekly partial seizure frequency relative to placebo over the entire 14-week randomized treatment period (titration evaluation period). Secondary outcome variables included the responder rate (incidence of patients with >=50% reduction from baseline in partial onset seizure frequency per week). Table displays the results of this study.Table 4: Reduction In Mean Over Placebo In Weekly Frequency Of Partial Onset SeizuresPlacebo(N=97)Levetiracetam(N=101)Percent reduction in partial seizure frequency over placebo--26.8%statistically significant versus placebo The percentage of patients (y-axis) who achieved >=50% reduction in weekly seizure rates from baseline in partial onset seizure frequency over the entire randomized treatment period (titration evaluation period) within the two treatment groups (x-axis) is presented in Figure 4.Figure 4: Responder Rate (>=50% Reduction From Baseline)statistically significant versus placebo. Figure 4. Effectiveness In Myoclonic Seizures In Patients >=12 Years Of Age With Juvenile Myoclonic Epilepsy (JME). The effectiveness of levetiracetam as adjunctive therapy (added to other antiepileptic drugs) in patients 12 years of age and older with juvenile myoclonic epilepsy (JME) experiencing myoclonic seizures was established in one multicenter, randomized, double-blind, placebo-controlled study, conducted at 37 sites in 14 countries. Of the 120 patients enrolled, 113 had diagnosis of confirmed or suspected JME. Eligible patients on stable dose of antiepileptic drug (AED) experiencing one or more myoclonic seizures per day for at least days during the prospective 8-week baseline period were randomized to either levetiracetam or placebo (levetiracetam N=60, placebo N=60). Patients were titrated over weeks to target dose of 3000 mg/day and treated at stable dose of 3000 mg/day over 12 weeks (evaluation period). Study drug was given in divided doses.The primary measure of effectiveness was the proportion of patients with at least 50% reduction in the number of days per week with one or more myoclonic seizures during the treatment period (titration evaluation periods) as compared to baseline. Table displays the results for the 113 patients with JME in this study.Table 5: Responder Rate (>=50% Reduction From Baseline) in Myoclonic Seizure Days Per Week for Patients with JMEPlacebo(N=59)Levetiracetam(N=54)Percentage of responders23.760.4%statistically significant versus placebo.

DOSAGE & ADMINISTRATION SECTION.

DOSAGE AND ADMINISTRATION. Levetiracetam oral solution is indicated as adjunctive treatment of partial onset seizures in adults and children years of age and older with epilepsy.Levetiracetam oral solution is indicated as adjunctive therapy in the treatment of myoclonic seizures in adults and adolescents 12 years of age and older with juvenile myoclonic epilepsy.. Partial Onset Seizures. Adults 16 Years And Older. In clinical trials, daily doses of 1000 mg, 2000 mg, and 3000 mg, given as twice-daily dosing, were shown to be effective. Although in some studies there was tendency toward greater response with higher dose (see CLINICAL STUDIES), consistent increase in response with increased dose has not been shown.Treatment should be initiated with daily dose of 1000 mg/day, given as twice-daily dosing (500 mg BID). Additional dosing increments may be given (1000 mg/day additional every weeks) to maximum recommended daily dose of 3000 mg. Doses greater than 3000 mg/day have been used in open-label studies for periods of months and longer. There is no evidence that doses greater than 3000 mg/day confer additional benefit.. Pediatric Patients Ages To <16 Years. Treatment should be initiated with daily dose of 20 mg/kg in divided doses (10 mg/kg BID). The daily dose should be increased every weeks by increments of 20 mg/kg to the recommended daily dose of 60 mg/kg (30 mg/kg BID). If patient cannot tolerate daily dose of 60 mg/kg, the daily dose may be reduced. In the clinical trial, the mean daily dose was 52 mg/kg. Patients with body weight <=20 kg should be dosed with oral solution. Patients with body weight above 20 kg can be dosed with either tablets or oral solution. Table 13 below provides guideline for dosing based on weight during titration to 60 mg/kg/day.Levetiracetam is given orally with or without food.Table 13: Levetiracetam Oral Solution Weight-Based Dosing Guide For ChildrenPatient WeightDaily Dose20 mg/kg/day(BID dosing)40 mg/kg/day(BID dosing)60 mg/kg/day(BID dosing)20.1-40 kg500 mg/day2.5 mLBID1000 mg/day5 mLBID1500 mg/day7.5 mLBID>40 kg1000 mg/day5 mLBID2000 mg/day10 mLBID3000 mg/day15 mLBIDThe following calculation should be used to determine the appropriate daily dose of oral solution for pediatric patients based on daily dose of 20 mg/kg/day, 40 mg/kg/day or 60 mg/kg/day:Total daily dose (mL/day) =Daily dose (mg/kg/day) patient weight (kg)100 mg/mLA household teaspoon or tablespoon is not an adequate measuring device. It is recommended that calibrated measuring device be obtained and used. Healthcare providers should recommend device that can measure and deliver the prescribed dose accurately, and provide instructions for measuring the dosage.. Myoclonic Seizures In Patients 12 Years Of Age And Older With Juvenile Myoclonic Epilepsy. Treatment should be initiated with dose of 1000 mg/day, given as twice-daily dosing (500 mg BID). Dosage should be increased by 1000 mg/day every weeks to the recommended daily dose of 3000 mg. The effectiveness of doses lower than 3000 mg/day has not been studied.. Adult Patients With Impaired Renal Function. Levetiracetam dosing must be individualized according to the patients renal function status. Recommended doses and adjustment for dose for adults are shown in Table 14. To use this dosing table, an estimate of the patients creatinine clearance (CLcr) in mL/min is needed. CLcr in mL/min may be estimated from serum creatinine (mg/dL) determination using the following formula:CLcr [140-age (years)] weight (kg)(x 0.85 for female patients)72 serum creatinine (mg/dL)Table 14: Dosing Adjustment Regimen For Adult Patients With Impaired Renal FunctionGroupCreatinine Clearance(mL/min)Dosage(mg)FrequencyNormal>80500 to 1,500Every 12 hMild50 to 80500 to 1,000Every 12 hModerate30 to 50250 to 750Every 12 hSevere<30250 to 500Every 12 hESRD patients using dialysis----500 to 1,000Following dialysis, 250 to 500 mg supplemental dose is recommended.Every 24 h.

DRUG INTERACTIONS SECTION.

Drug Interactions. In vitro data on metabolic interactions indicate that levetiracetam is unlikely to produce, or be subject to, pharmacokinetic interactions. Levetiracetam and its major metabolite, at concentrations well above Cmax levels achieved within the therapeutic dose range, are neither inhibitors of nor high affinity substrates for human liver cytochrome P450 isoforms, epoxide hydrolase or UDP-glucuronidation enzymes. In addition, levetiracetam does not affect the in vitro glucuronidation of valproic acid.Levetiracetam circulates largely unbound (<10% bound) to plasma proteins; clinically significant interactions with other drugs through competition for protein binding sites are therefore unlikely.Potential pharmacokinetic interactions were assessed in clinical pharmacokinetic studies (phenytoin, valproate, oral contraceptive, digoxin, warfarin, probenecid) and through pharmacokinetic screening in the placebo-controlled clinical studies in epilepsy patients.. Drug-Drug Interactions Between Levetiracetam And Other Antiepileptic Drugs (AEDs). Phenytoin. Levetiracetam (3000 mg daily) had no effect on the pharmacokinetic disposition of phenytoin in patients with refractory epilepsy. Pharmacokinetics of levetiracetam were also not affected by phenytoin.. Valproate. Levetiracetam (1500 mg twice daily) did not alter the pharmacokinetics of valproate in healthy volunteers. Valproate 500 mg twice daily did not modify the rate or extent of levetiracetam absorption or its plasma clearance or urinary excretion. There also was no effect on exposure to and the excretion of the primary metabolite, ucb L057.Potential drug interactions between levetiracetam and other AEDs (carbamazepine, gabapentin, lamotrigine, phenobarbital, phenytoin, primidone and valproate) were also assessed by evaluating the serum concentrations of levetiracetam and these AEDs during placebo-controlled clinical studies. These data indicate that levetiracetam does not influence the plasma concentration of other AEDs and that these AEDs do not influence the pharmacokinetics of levetiracetam.. Effect Of AEDs In Pediatric Patients. There was about 22% increase of apparent total body clearance of levetiracetam when it was co-administered with enzyme-inducing AEDs. Dose adjustment is not recommended. Levetiracetam had no effect on plasma concentrations of carbamazepine, valproate, topiramate, or lamotrigine.. Other Drug Interactions. Oral Contraceptives. Levetiracetam (500 mg twice daily) did not influence the pharmacokinetics of an oral contraceptive containing 0.03 mg ethinyl estradiol and 0.15 mg levonorgestrel, or of the luteinizing hormone and progesterone levels, indicating that impairment of contraceptive efficacy is unlikely. Coadministration of this oral contraceptive did not influence the pharmacokinetics of levetiracetam.. Digoxin. Levetiracetam (1000 mg twice daily) did not influence the pharmacokinetics and pharmacodynamics (ECG) of digoxin given as 0.25 mg dose every day. Coadministration of digoxin did not influence the pharmacokinetics of levetiracetam.. Warfarin. Levetiracetam (1000 mg twice daily) did not influence the pharmacokinetics of and warfarin. Prothrombin time was not affected by levetiracetam. Coadministration of warfarin did not affect the pharmacokinetics of levetiracetam.. Probenecid. Probenecid, renal tubular secretion blocking agent, administered at dose of 500 mg four times day, did not change the pharmacokinetics of levetiracetam 1000 mg twice daily. CSS max of the metabolite, ucb L057, was approximately doubled in the presence of probenecid while the fraction of drug excreted unchanged in the urine remained the same. Renal clearance of ucb L057 in the presence of probenecid decreased 60%, probably related to competitive inhibition of tubular secretion of ucb L057. The effect of levetiracetam on probenecid was not studied.

PHARMACOKINETICS SECTION.

Pharmacokinetics. The pharmacokinetics of levetiracetam have been studied in healthy adult subjects, adults and pediatric patients with epilepsy, elderly subjects and subjects with renal and hepatic impairment.. Overview. Levetiracetam is rapidly and almost completely absorbed after oral administration. Levetiracetam tablets and oral solution are bioequivalent. The pharmacokinetics are linear and time-invariant, with low intra- and inter-subject variability. The extent of bioavailability of levetiracetam is not affected by food. Levetiracetam is not significantly protein-bound (<10% bound) and its volume of distribution is close to the volume of intracellular and extracellular water. Sixty-six percent (66%) of the dose is renally excreted unchanged. The major metabolic pathway of levetiracetam (24% of dose) is an enzymatic hydrolysis of the acetamide group. It is not liver cytochrome P450 dependent. The metabolites have no known pharmacological activity and are renally excreted. Plasma half-life of levetiracetam across studies is approximately to hours. It is increased in the elderly (primarily due to impaired renal clearance) and in subjects with renal impairment.. Absorption And Distribution. Absorption of levetiracetam is rapid, with peak plasma concentrations occurring in about an hour following oral administration in fasted subjects. The oral bioavailability of levetiracetam tablets is 100% and the tablets and oral solution are bioequivalent in rate and extent of absorption. Food does not affect the extent of absorption of levetiracetam but it decreases Cmax by 20% and delays Tmax by 1.5 hours. The pharmacokinetics of levetiracetam are linear over the dose range of 500 to 5000 mg. Steady state is achieved after days of multiple twice-daily dosing. Levetiracetam and its major metabolite are less than 10% bound to plasma proteins; clinically significant interactions with other drugs through competition for protein binding sites are therefore unlikely.. Metabolism. Levetiracetam is not extensively metabolized in humans. The major metabolic pathway is the enzymatic hydrolysis of the acetamide group, which produces the carboxylic acid metabolite, ucb L057 (24% of dose) and is not dependent on any liver cytochrome P450 isoenzymes. The major metabolite is inactive in animal seizure models. Two minor metabolites were identified as the product of hydroxylation of the 2-oxo-pyrrolidine ring (2% of dose) and opening of the 2-oxo-pyrrolidine ring in position (1% of dose). There is no enantiomeric interconversion of levetiracetam or its major metabolite.. Elimination. Levetiracetam plasma half-life in adults is +- hour and is unaffected by either dose or repeated administration. Levetiracetam is eliminated from the systemic circulation by renal excretion as unchanged drug which represents 66% of administered dose. The total body clearance is 0.96 mL/min/kg and the renal clearance is 0.6 mL/min/kg. The mechanism of excretion is glomerular filtration with subsequent partial tubular reabsorption. The metabolite ucb L057 is excreted by glomerular filtration and active tubular secretion with renal clearance of mL/min/kg. Levetiracetam elimination is correlated to creatinine clearance. Levetiracetam clearance is reduced in patients with impaired renal function (see Special Populations, Renal Impairment and DOSAGE AND ADMINISTRATION, Adult Patients with Impaired Renal Function).. Pharmacokinetic Interactions. In vitro data on metabolic interactions indicate that levetiracetam is unlikely to produce, or be subject to, pharmacokinetic interactions. Levetiracetam and its major metabolite, at concentrations well above Cmax levels achieved within the therapeutic dose range, are neither inhibitors of, nor high affinity substrates for, human liver cytochrome P450 isoforms, epoxide hydrolase or UDP-glucuronidation enzymes. In addition, levetiracetam does not affect the in vitro glucuronidation of valproic acid.Potential pharmacokinetic interactions of or with levetiracetam were assessed in clinical pharmacokinetic studies (phenytoin, valproate, warfarin, digoxin, oral contraceptive, probenecid) and through pharmacokinetic screening in the placebo-controlled clinical studies in epilepsy patients (see PRECAUTIONS, Drug Interactions).. Special Populations. Elderly. Pharmacokinetics of levetiracetam were evaluated in 16 elderly subjects (age 61 to 88 years) with creatinine clearance ranging from 30 to 74 mL/min. Following oral administration of twice-daily dosing for 10 days, total body clearance decreased by 38% and the half-life was 2.5 hours longer in the elderly compared to healthy adults. This is most likely due to the decrease in renal function in these subjects.. Pediatric Patients. Pharmacokinetics of levetiracetam were evaluated in 24 pediatric patients (age to 12 years) after single dose (20 mg/kg). The body weight adjusted apparent clearance of levetiracetam was approximately 40% higher than in adults.A repeat dose pharmacokinetic study was conducted in pediatric patients (age to 12 years) at doses of 20 mg/kg/day, 40 mg/kg/day, and 60 mg/kg/day. The evaluation of the pharmacokinetic profile of levetiracetam and its metabolite (ucb L057) in 14 pediatric patients demonstrated rapid absorption of levetiracetam at all doses with Tmax of about hour and t1/2 of hours across the three dosing levels. The pharmacokinetics of levetiracetam in children was linear between 20 to 60 mg/kg/day. The potential interaction of levetiracetam with other AEDs was also evaluated in these patients (see PRECAUTIONS, Drug Interactions). Levetiracetam had no significant effect on the plasma concentrations of carbamazepine, valproic acid, topiramate or lamotrigine. However, there was about 22% increase of apparent clearance of levetiracetam when it was coadministered with an enzyme-inducing AED (e.g. carbamazepine). Population pharmacokinetic analysis showed that body weight was significantly correlated to clearance of levetiracetam in pediatric patients; clearance increased with an increase in body weight.. Gender. Levetiracetam Cmax and AUC were 20% higher in women (N=11) compared to men (N=12). However, clearances adjusted for body weight were comparable.. Race. Formal pharmacokinetic studies of the effects of race have not been conducted. Cross study comparisons involving Caucasians (N=12) and Asians (N=12), however, show that pharmacokinetics of levetiracetam were comparable between the two races. Because levetiracetam is primarily renally excreted and there are no important racial differences in creatinine clearance, pharmacokinetic differences due to race are not expected.. Renal Impairment. The disposition of levetiracetam was studied in adult subjects with varying degrees of renal function. Total body clearance of levetiracetam is reduced in patients with impaired renal function by 40% in the mild group (CLcr 50 to 80 mL/min), 50% in the moderate group (CLcr 30 to 50 mL/min) and 60% in the severe renal impairment group (CLcr <30 mL/min). Clearance of levetiracetam is correlated with creatinine clearance.In anuric (end stage renal disease) patients, the total body clearance decreased 70% compared to normal subjects (CLcr >80 mL/min). Approximately 50% of the pool of levetiracetam in the body is removed during standard 4-hour hemodialysis procedure.Dosage should be reduced in patients with impaired renal function receiving levetiracetam, and supplemental doses should be given to patients after dialysis (see PRECAUTIONS and DOSAGE AND ADMINISTRATION, Adult Patients with Impaired Renal Function).. Hepatic Impairment. In subjects with mild (Child-Pugh A) to moderate (Child-Pugh B) hepatic impairment, the pharmacokinetics of levetiracetam were unchanged. In patients with severe hepatic impairment (Child-Pugh C), total body clearance was 50% that of normal subjects, but decreased renal clearance accounted for most of the decrease. No dose adjustment is needed for patients with hepatic impairment.

PRECAUTIONS SECTION.

PRECAUTIONS. Hematologic Abnormalities. Partial Onset Seizures. Adults. Minor, but statistically significant, decreases compared to placebo in total mean RBC count (0.03 106/mm3), mean hemoglobin (0.09 g/dL), and mean hematocrit (0.38%), were seen in levetiracetam-treated patients in controlled trials.A total of 3.2% of treated and 1.8% of placebo patients had at least one possibly significant (<=2.8 109/L) decreased WBC, and 2.4% of treated and 1.4% of placebo patients had at least one possibly significant (<=1.0 109/L) decreased neutrophil count. Of the treated patients with low neutrophil count, all but one rose towards or to baseline with continued treatment. No patient was discontinued secondary to low neutrophil counts.. Pediatric Patients. Minor, but statistically significant, decreases in WBC and neutrophil counts were seen in levetiracetam-treated patients as compared to placebo. The mean decreases from baseline in the levetiracetam-treated group were -0.4 109/L and -0.3 109/L, respectively, whereas there were small increases in the placebo group. Mean relative lymphocyte counts increased by 1.7% in levetiracetam-treated patients, compared to decrease of 4% in placebo patients (statistically significant).In the well-controlled trial, more levetiracetam-treated patients had possibly clinically significant abnormally low WBC value (3.0% levetiracetam-treated versus 0% placebo), however, there was no apparent difference between treatment groups with respect to neutrophil count (5.0% levetiracetam-treated versus 4.2% placebo). No patient was discontinued secondary to low WBC or neutrophil counts.. Juvenile Myoclonic Epilepsy. Although there were no obvious hematologic abnormalities observed in patients with JME, the limited number of patients makes any conclusion tentative. The data from the partial seizure patients should be considered to be relevant for JME patients.. Hepatic Abnormalities. There were no meaningful changes in mean liver function tests (LFT) in controlled trials in adult or pediatric patients; lesser LFT abnormalities were similar in drug and placebo treated patients in controlled trials (1.4%). No adult or pediatric patients were discontinued from controlled trials for LFT abnormalities except for (0.07%) adult epilepsy patient receiving open treatment.. Information For Patients. Patients and caregivers should be informed of the availability of Medication Guide, and they should be instructed to read the Medication Guide prior to taking levetiracetam. The Medication Guide may also be found posted on www.paipharma.com or by calling 1-800-845-8210. Patients should be instructed to take levetiracetam only as prescribed.Patients, their caregivers, and families should be counseled that AEDs, including levetiracetam, 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 advised that levetiracetam may cause changes in behavior (e.g. aggression, agitation, anger, anxiety, apathy, depression, hostility, and irritability) and in rare cases patients may experience psychotic symptoms.Patients should be advised to notify their physician if they become pregnant or intend to become pregnant during therapy. Patients should be encouraged to enroll in the North American Antiepileptic Drug (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.Patients should be advised that levetiracetam may cause dizziness and somnolence. Accordingly, patients should be advised not to drive or operate machinery or engage in other hazardous activities until they have gained sufficient experience on levetiracetam to gauge whether it adversely affects their performance of these activities.. Laboratory Tests. Although most laboratory tests are not systematically altered with levetiracetam treatment, there have been relatively infrequent abnormalities seen in hematologic parameters and liver function tests.. Drug Interactions. In vitro data on metabolic interactions indicate that levetiracetam is unlikely to produce, or be subject to, pharmacokinetic interactions. Levetiracetam and its major metabolite, at concentrations well above Cmax levels achieved within the therapeutic dose range, are neither inhibitors of nor high affinity substrates for human liver cytochrome P450 isoforms, epoxide hydrolase or UDP-glucuronidation enzymes. In addition, levetiracetam does not affect the in vitro glucuronidation of valproic acid.Levetiracetam circulates largely unbound (<10% bound) to plasma proteins; clinically significant interactions with other drugs through competition for protein binding sites are therefore unlikely.Potential pharmacokinetic interactions were assessed in clinical pharmacokinetic studies (phenytoin, valproate, oral contraceptive, digoxin, warfarin, probenecid) and through pharmacokinetic screening in the placebo-controlled clinical studies in epilepsy patients.. Drug-Drug Interactions Between Levetiracetam And Other Antiepileptic Drugs (AEDs). Phenytoin. Levetiracetam (3000 mg daily) had no effect on the pharmacokinetic disposition of phenytoin in patients with refractory epilepsy. Pharmacokinetics of levetiracetam were also not affected by phenytoin.. Valproate. Levetiracetam (1500 mg twice daily) did not alter the pharmacokinetics of valproate in healthy volunteers. Valproate 500 mg twice daily did not modify the rate or extent of levetiracetam absorption or its plasma clearance or urinary excretion. There also was no effect on exposure to and the excretion of the primary metabolite, ucb L057.Potential drug interactions between levetiracetam and other AEDs (carbamazepine, gabapentin, lamotrigine, phenobarbital, phenytoin, primidone and valproate) were also assessed by evaluating the serum concentrations of levetiracetam and these AEDs during placebo-controlled clinical studies. These data indicate that levetiracetam does not influence the plasma concentration of other AEDs and that these AEDs do not influence the pharmacokinetics of levetiracetam.. Effect Of AEDs In Pediatric Patients. There was about 22% increase of apparent total body clearance of levetiracetam when it was co-administered with enzyme-inducing AEDs. Dose adjustment is not recommended. Levetiracetam had no effect on plasma concentrations of carbamazepine, valproate, topiramate, or lamotrigine.. Other Drug Interactions. Oral Contraceptives. Levetiracetam (500 mg twice daily) did not influence the pharmacokinetics of an oral contraceptive containing 0.03 mg ethinyl estradiol and 0.15 mg levonorgestrel, or of the luteinizing hormone and progesterone levels, indicating that impairment of contraceptive efficacy is unlikely. Coadministration of this oral contraceptive did not influence the pharmacokinetics of levetiracetam.. Digoxin. Levetiracetam (1000 mg twice daily) did not influence the pharmacokinetics and pharmacodynamics (ECG) of digoxin given as 0.25 mg dose every day. Coadministration of digoxin did not influence the pharmacokinetics of levetiracetam.. Warfarin. Levetiracetam (1000 mg twice daily) did not influence the pharmacokinetics of and warfarin. Prothrombin time was not affected by levetiracetam. Coadministration of warfarin did not affect the pharmacokinetics of levetiracetam.. Probenecid. Probenecid, renal tubular secretion blocking agent, administered at dose of 500 mg four times day, did not change the pharmacokinetics of levetiracetam 1000 mg twice daily. CSS max of the metabolite, ucb L057, was approximately doubled in the presence of probenecid while the fraction of drug excreted unchanged in the urine remained the same. Renal clearance of ucb L057 in the presence of probenecid decreased 60%, probably related to competitive inhibition of tubular secretion of ucb L057. The effect of levetiracetam on probenecid was not studied.. Carcinogenesis, Mutagenesis, Impairment Of Fertility. Carcinogenesis. Rats were dosed with levetiracetam in the diet for 104 weeks at doses of 50, 300 and 1800 mg/kg/day. The highest dose corresponds to times the maximum recommended daily human dose (MRHD) of 3000 mg on mg/m2 basis and it also provided systemic exposure (AUC) approximately times that achieved in humans receiving the MRHD. There was no evidence of carcinogenicity. study was conducted in which mice received levetiracetam in the diet for 80 weeks at doses of 60, 240 and 960 mg/kg/day (high dose is equivalent to times the MRHD on mg/m2 or exposure basis). Although no evidence for carcinogenicity was seen, the potential for carcinogenic response has not been fully evaluated in that species because adequate doses have not been studied.. Mutagenesis. Levetiracetam was not mutagenic in the Ames test or in mammalian cells in vitro in the Chinese hamster ovary/HGPRT locus assay. It was not clastogenic in an in vitro analysis of metaphase chromosomes obtained from Chinese hamster ovary cells or in an in vivo mouse micronucleus assay. The hydrolysis product and major human metabolite of levetiracetam (ucb L057) was not mutagenic in the Ames test or the in vitro mouse lymphoma assay.. Impairment Of Fertility. No adverse effects on male or female fertility or reproductive performance were observed in rats at doses up to 1800 mg/kg/day (approximately times the maximum recommended human dose on mg/m2 or exposure basis).. Pregnancy. Pregnancy Category C. In animal studies, levetiracetam produced evidence of developmental toxicity at doses similar to or greater than human therapeutic doses.Administration to female rats throughout pregnancy and lactation was associated with increased incidences of minor fetal skeletal abnormalities and retarded offspring growth pre- and/or postnatally at doses >=350 mg/kg/day (approximately equivalent to the maximum recommended human dose of 3000 mg [MRHD] on mg/m2 basis) and with increased pup mortality and offspring behavioral alterations at dose of 1800 mg/kg/day (6 times the MRHD on mg/m2 basis). The developmental no effect dose was 70 mg/kg/day (0.2 times the MRHD on mg/m2 basis). There was no overt maternal toxicity at the doses used in this study.Treatment of pregnant rabbits during the period of organogenesis resulted in increased embryofetal mortality and increased incidences of minor fetal skeletal abnormalities at doses >=600 mg/kg/day (approximately times MRHD on mg/m2 basis) and in decreased fetal weights and increased incidences of fetal malformations at dose of 1800 mg/kg/day (12 times the MRHD on mg/m2 basis). The developmental no effect dose was 200 mg/kg/day (1.3 times the MRHD on mg/m2 basis). Maternal toxicity was also observed at 1800 mg/kg/day.When pregnant rats were treated during the period of organogenesis, fetal weights were decreased and the incidence of fetal skeletal variations was increased at dose of 3600 mg/kg/day (12 times the MRHD). 1200 mg/kg/day (4 times the MRHD) was developmental no effect dose. There was no evidence of maternal toxicity in this study.Treatment of rats during the last third of gestation and throughout lactation produced no adverse developmental or maternal effects at doses of up to 1800 mg/kg/day (6 times the MRHD on mg/m2 basis).There are no adequate and well-controlled studies in pregnant women. Levetiracetam should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.. Pregnancy Registry. To provide information regarding the effects of in utero exposure to levetiracetam, physicians are advised to recommend that pregnant patients taking levetiracetam 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 the patients themselves. Information on the registry can also be found at the website http://www.aedpregnancyregistry.org/.. Labor And Delivery. The effect of levetiracetam on labor and delivery in humans is unknown.. Nursing Mothers. Levetiracetam is excreted in breast milk. Because of the potential for serious adverse reactions in nursing infants from levetiracetam, decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother.. Pediatric Use. Safety and effectiveness in patients below years of age have not been established.Studies of levetiracetam in juvenile rats (dosing from day through day 52 of age) and dogs (dosing from week through week of age) at doses of up to 1800 mg/kg/day (approximately and 24 times, respectively, the maximum recommended pediatric dose of 60 mg/kg/day on mg/m2 basis) did not indicate potential for age-specific toxicity.. Geriatric Use. Of the total number of subjects in clinical studies of levetiracetam, 347 were 65 and over. No overall differences in safety were observed between these subjects and younger subjects. There were insufficient numbers of elderly subjects in controlled trials of epilepsy to adequately assess the effectiveness of levetiracetam in these patients.A study in 16 elderly subjects (age 61 to 88 years) with oral administration of single dose and multiple twice-daily doses for 10 days showed no pharmacokinetic differences related to age alone.Levetiracetam is known to be substantially excreted by the kidney, and the risk of adverse reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.. Use In Patients With Impaired Renal Function. Clearance of levetiracetam is decreased in patients with renal impairment and is correlated with creatinine clearance. Caution should be taken in dosing patients with moderate and severe renal impairment and in patients under-going hemodialysis. The dosage should be reduced in patients with impaired renal function receiving levetiracetam and supplemental doses should be given to patients after dialysis (see CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION, Adult Patients with Impaired Renal Function).

SPL MEDGUIDE SECTION.

MEDICATION GUIDE. Levetiracetam Oral Solution, 100 mg/mLRead this Medication Guide before you start taking Levetiracetam Oral Solution 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 Levetiracetam Oral SolutionLike other antiepileptic drugs, Levetiracetam Oral Solution may cause suicidal thoughts or actions in very small number of people, about in 500 people taking it.Call healthcare provider right away if you have any of these symptoms, especially if they are new, worse, or worry you:thoughts about suicide or dyingattempts to commit suicidenew or worse depressionnew or worse anxietyfeeling agitated or restlesspanic attackstrouble sleeping (insomnia)new or worse irritabilityacting aggressive, being angry, or violentacting on dangerous impulsesan extreme increase in activity and talking (mania)other unusual changes in behavior or moodDo not stop Levetiracetam Oral Solution without first talking to healthcare provider.Stopping levetiracetam suddenly can cause serious problems. Stopping seizure medicine suddenly 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.How can watch for early symptoms of suicidal thoughts and actionsPay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.Keep 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.What is Levetiracetam Oral SolutionLevetiracetam is prescription medicine taken by mouth that is used with other medicines to treat:partial onset seizures in people years of age and older with epilepsymyoclonic seizures in people 12 years of age and older with juvenile myoclonic epilepsyIt is not known if levetiracetam is safe or effective in children under years of age.Before taking your medicine, make sure you have received the correct medicine. Compare the name above with the name on your bottle and the appearance of your medicine with the description of levetiracetam provided below. Contact your pharmacist immediately if you believe dispensing error may have occurred.Levetiracetam oral solution is clear, colorless to slightly yellowish, grape-flavored liquid.What should tell my healthcare provider before starting Levetiracetam Oral SolutionBefore taking levetiracetam, tell your healthcare provider about all of your medical conditions, including if you:have or have had depression, mood problems or suicidal thoughts or behaviorhave kidney problemsare pregnant or planning to become pregnant. It is not known if levetiracetam will harm your unborn baby. You and your healthcare provider will have to decide if you should take levetiracetam while you are pregnant. If you become pregnant while taking levetiracetam, talk to your healthcare provider about registering with the North American Antiepileptic Drug Pregnancy Registry. You can enroll in this registry by calling 1-888-233-2334.are breast feeding. Levetiracetam can pass into your milk and may harm your baby. You and your healthcare provider should discuss whether you should take levetiracetam or breast-feed; you should not do both.Tell your healthcare provider about all the medicines you take, including prescription and nonprescription medicines, vitamins, and herbal supplements. Do not start new medicine without first talking with your healthcare provider.Know the medicines you take. Keep list of them to show your healthcare provider and pharmacist each time you get new medicine.How should take Levetiracetam Oral SolutionTake levetiracetam exactly as prescribed.Your healthcare provider will tell you how much levetiracetam to take and when to take it. Levetiracetam is usually taken twice day. Take levetiracetam at the same times each day.Your healthcare provider may change your dose. Do not change your dose without talking to your healthcare provider.Take levetiracetam with or without food.If your healthcare provider has prescribed levetiracetam oral solution, be sure to ask your pharmacist for medicine dropper or medicine cup to help you measure the correct amount of levetiracetam oral solution. Do not use household teaspoon. Ask your pharmacist for instructions on how to use the measuring device the right way.If you miss dose of levetiracetam, take it as soon as you remember. If it is almost time for your next dose, just skip the missed dose. Take the next dose at your regular time. Do not take two doses at the same time. If you take too much levetiracetam, call your local Poison Control Center or go to the nearest emergency room right away.What should avoid while taking Levetiracetam Oral SolutionDo not drive, operate machinery or do other dangerous activities until you know how levetiracetam affects you. Levetiracetam may make you dizzy or sleepy.What are the possible side effects of Levetiracetam Oral SolutionSee What is the most important information should know about Levetiracetam Oral SolutionLevetiracetam can cause serious side effects.Call your healthcare provider right away if you have any of these symptoms:mood and behavior changes such as aggression, agitation, anger, anxiety, apathy, mood swings, depression, hostility, and irritability. few people may get psychotic symptoms such as hallucinations (seeing or hearing things that are really not there), delusions (false or strange thoughts or beliefs) and unusual behavior.extreme sleepiness, tiredness, and weaknessproblems with muscle coordination (problems walking and moving)The most common side effects seen in people who take levetiracetam include:sleepinessweaknessdizzinessinfectionThe most common side effects seen in children who take levetiracetam include, in addition to those listed above:accidental injuryirritabilityhostilityThese side effects can happen at any time but happen more often within the first weeks of treatment except for infection.Tell your healthcare provider if you have any side effect that bothers you or that does not go away.These are not all the possible side effects of levetiracetam. For more information, ask your healthcare provider or pharmacist.Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.How should store Levetiracetam Oral SolutionStore Levetiracetam at room temperature, 59F to 86F (15C to 30C) away from heat and light.Keep levetiracetam and all medicines out of the reach of children.General information about Levetiracetam Oral Solution.Medicines are sometimes prescribed for purposes other than those listed in Medication Guide. Do not use levetiracetam for condition for which it was not prescribed. Do not give levetiracetam 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 levetiracetam. If you would like more information, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about levetiracetam that is written for health professionals. You can also call 1-800-845-8210.What are the ingredients of Levetiracetam Oral SolutionLevetiracetam oral solution active ingredient: levetiracetamInactive ingredients: ammonium glycyrrhizinate, citric acid, glycerin, maltitol solution, methylparaben, potassium acesulfame, propylparaben, purified water, sodium citrate dihydrate and natural and artificial flavor.Levetiracetam does not contain lactose or gluten. Levetiracetam oral solution does contain carbohydrates. The liquid is dye-free.Rx OnlyThis Medication Guide has been approved by the US Food and Drug Administration.Manufactured by:Morton Grove Pharmaceuticals, Inc.Morton Grove, IL 60053Packaged by:Pharmaceutical Associates, Inc.Greenville, SC 29605MGAE100R11/10. thoughts about suicide or dying. attempts to commit suicide. new or worse depression. new or worse anxiety. feeling agitated or restless. panic attacks. trouble sleeping (insomnia). new or worse irritability. acting aggressive, being angry, or violent. acting on dangerous impulses. an extreme increase in activity and talking (mania). other unusual changes in behavior or mood. Stopping levetiracetam suddenly can cause serious problems. Stopping seizure medicine suddenly 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.. Pay attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings.. Keep 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.. partial onset seizures in people years of age and older with epilepsy. myoclonic seizures in people 12 years of age and older with juvenile myoclonic epilepsy. have or have had depression, mood problems or suicidal thoughts or behavior. have kidney problems. are pregnant or planning to become pregnant. It is not known if levetiracetam will harm your unborn baby. You and your healthcare provider will have to decide if you should take levetiracetam while you are pregnant. If you become pregnant while taking levetiracetam, talk to your healthcare provider about registering with the North American Antiepileptic Drug Pregnancy Registry. You can enroll in this registry by calling 1-888-233-2334.. are breast feeding. Levetiracetam can pass into your milk and may harm your baby. You and your healthcare provider should discuss whether you should take levetiracetam or breast-feed; you should not do both.. Your healthcare provider will tell you how much levetiracetam to take and when to take it. Levetiracetam is usually taken twice day. Take levetiracetam at the same times each day.. Your healthcare provider may change your dose. Do not change your dose without talking to your healthcare provider.. Take levetiracetam with or without food.. If your healthcare provider has prescribed levetiracetam oral solution, be sure to ask your pharmacist for medicine dropper or medicine cup to help you measure the correct amount of levetiracetam oral solution. Do not use household teaspoon. Ask your pharmacist for instructions on how to use the measuring device the right way.. If you miss dose of levetiracetam, take it as soon as you remember. If it is almost time for your next dose, just skip the missed dose. Take the next dose at your regular time. Do not take two doses at the same time. If you take too much levetiracetam, call your local Poison Control Center or go to the nearest emergency room right away.. See What is the most important information should know about Levetiracetam Oral Solution. mood and behavior changes such as aggression, agitation, anger, anxiety, apathy, mood swings, depression, hostility, and irritability. few people may get psychotic symptoms such as hallucinations (seeing or hearing things that are really not there), delusions (false or strange thoughts or beliefs) and unusual behavior.. extreme sleepiness, tiredness, and weakness. problems with muscle coordination (problems walking and moving). sleepiness. weakness. dizziness. infection. accidental injury. irritability. hostility. Store Levetiracetam at room temperature, 59F to 86F (15C to 30C) away from heat and light.. Keep levetiracetam and all medicines out of the reach of children.

WARNINGS SECTION.

WARNINGS. Suicidal Behavior and Ideation. Antiepileptic drugs (AEDs), including levetiracetam, 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 to 100 years) in the clinical trials analyzed. Table shows absolute and relative risk by indication for all evaluated AEDs.Table 6: 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 Incidence in Placebo PatientsRisk Difference:Additional Drug Patients with Events Per 1000 PatientsEpilepsy1.03.43.52.4Psychiatric5.78.51.52.9Other1.01.81.90.9Total2.44.31.81.9The 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 levetiracetam or any other AED must balance the risk of suicidal thoughts or behaviors 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.. Neuropsychiatric Adverse Events. Partial Onset Seizures. Adults. In adults experiencing partial onset seizures, levetiracetam use is associated with the occurrence of central nervous system adverse events that can be classified into the following categories: 1) somnolence and fatigue, 2) coordination difficulties, and 3) behavioral abnormalities.In controlled trials of adult patients with epilepsy experiencing partial onset seizures, 14.8% of levetiracetam-treated patients reported somnolence, compared to 8.4% of placebo patients. There was no clear dose response up to 3000 mg/day. In study where there was no titration, about 45% of patients receiving 4000 mg/day reported somnolence. The somnolence was considered serious in 0.3% of the treated patients, compared to 0% in the placebo group. About 3% of levetiracetam-treated patients discontinued treatment due to somnolence, compared to 0.7% of placebo patients. In 1.4% of treated patients and in 0.9% of placebo patients the dose was reduced, while 0.3% of the treated patients were hospitalized due to somnolence.In controlled trials of adult patients with epilepsy experiencing partial onset seizures, 14.7% of treated patients reported asthenia, compared to 9.1% of placebo patients. Treatment was discontinued in 0.8% of treated patients as compared to 0.5% of placebo patients. In 0.5% of treated patients and in 0.2% of placebo patients the dose was reduced.A total of 3.4% of levetiracetam-treated patients experienced coordination difficulties, (reported as either ataxia, abnormal gait, or incoordination) compared to 1.6% of placebo patients. total of 0.4% of patients in controlled trials discontinued levetiracetam treatment due to ataxia, compared to 0% of placebo patients. In 0.7% of treated patients and in 0.2% of placebo patients the dose was reduced due to coordination difficulties, while one of the treated patients was hospitalized due to worsening of pre-existing ataxia.Somnolence, asthenia and coordination difficulties occurred most frequently within the first weeks of treatment.In controlled trials of patients with epilepsy experiencing partial onset seizures, (0.7%) of levetiracetam-treated patients experienced psychotic symptoms compared to (0.2%) placebo patient. Two (0.3%) levetiracetam-treated patients were hospitalized and their treatment was discontinued. Both events, reported as psychosis, developed within the first week of treatment and resolved within to weeks following treatment discontinuation. Two other events, reported as hallucinations, occurred after to months and resolved within to days while the patients remained on treatment. In one patient experiencing psychotic depression occurring within month, symptoms resolved within 45 days while the patient continued treatment. total of 13.3% of levetiracetam patients experienced other behavioral symptoms (reported as aggression, agitation, anger, anxiety, apathy, depersonalization, depression, emotional lability, hostility, irritability, etc.) compared to 6.2% of placebo patients. Approximately half of these patients reported these events within the first weeks. total of 1.7% of treated patients discontinued treatment due to these events, compared to 0.2% of placebo patients. The treatment dose was reduced in 0.8% of treated patients and in 0.5% of placebo patients. total of 0.8% of treated patients had serious behavioral event (compared to 0.2% of placebo patients) and were hospitalized.. Pediatric Patients. In pediatric patients experiencing partial onset seizures, levetiracetam is associated with somnolence, fatigue, and behavioral abnormalities.In the double-blind, controlled trial in children with epilepsy experiencing partial onset seizures, 22.8% of levetiracetam-treated patients experienced somnolence, compared to 11.3% of placebo patients. The design of the study prevented accurately assessing dose-response effects. No patient discontinued treatment for somnolence. In about 3.0% of levetiracetam-treated patients and in 3.1% of placebo patients the dose was reduced as result of somnolence.Asthenia was reported in 8.9% of levetiracetam-treated patients, compared to 3.1% of placebo patients. No patient discontinued treatment for asthenia, but asthenia led to dose reduction in 3.0% of levetiracetam-treated patients compared to 0% of placebo patients.A total of 37.6% of the levetiracetam-treated patients experienced behavioral symptoms (reported as agitation, anxiety, apathy, depersonalization, depression, emotional lability, hostility, hyperkinesia, nervousness, neurosis, and personality disorder), compared to 18.6% of placebo patients. Hostility was reported in 11.9% of levetiracetam-treated patients, compared to 6.2% of placebo patients. Nervousness was reported in 9.9% of levetiracetam-treated patients, compared to 2.1% of placebo patients. Depression was reported in 3.0% of levetiracetam-treated patients, compared to 1.0% of placebo patients.A total of 3.0% of levetiracetam-treated patients discontinued treatment due to psychotic and nonpsychotic adverse events, compared to 4.1% of placebo patients. Overall, 10.9% of levetiracetam-treated patients experienced behavioral symptoms associated with discontinuation or dose reduction, compared to 6.2% of placebo patients.. Myoclonic Seizures. During clinical development, the number of patients with myoclonic seizures exposed to levetiracetam was considerably smaller than the number with partial seizures. Therefore, under-reporting of certain adverse events was more likely to occur in the myoclonic seizure population. In adult and adolescent patients experiencing myoclonic seizures, levetiracetam is associated with somnolence and behavioral abnormalities. It is expected that the events seen in partial seizure patients would occur in patients with JME.In the double-blind, controlled trial in adults and adolescents with juvenile myoclonic epilepsy experiencing myoclonic seizures, 11.7% of levetiracetam-treated patients experienced somnolence compared to 1.7% of placebo patients. No patient discontinued treatment as result of somnolence. In 1.7% of levetiracetam-treated patients and in 0% of placebo patients the dose was reduced as result of somnolence.Non-psychotic behavioral disorders (reported as aggression and irritability) occurred in 5% of the levetiracetam-treated patients compared to 0% of placebo patients. Non-psychotic mood disorders (reported as depressed mood, depression, and mood swings) occurred in 6.7% of levetiracetam-treated patients compared to 3.3% of placebo patients. total of 5.0% of levetiracetam-treated patients had reduction in dose or discontinued treatment due to behavioral or psychiatric events (reported as anxiety, depressed mood, depression, irritability, and nervousness), compared to 1.7% of placebo patients.. Withdrawal Seizures. Antiepileptic drugs, including levetiracetam, should be withdrawn gradually to minimize the potential of increased seizure frequency.