Trileptal, 600 mg 50 pcs

How to take, the dosage

It is taken orally.

The initial dose is 8-10 mg/kg body weight/day. Then the dose is adjusted depending on the treatment regimen, patient’s age, treatment efficacy, and renal function.

In patients with impaired renal function (CKG less than 30 ml/min), the initial dose and dosage regimen need to be adjusted.

Trileptal® may be used both as monotherapy and in combination with other antiepileptic drugs. In both cases, the course of treatment begins with a clinically effective dose, the frequency of administration is 2 times per day. The dose may be increased depending on the response to therapy. In case of replacement of another antiepileptic drug with Trileptal® at the beginning of taking Trileptal®, the dose of the replaced drug should be gradually reduced. When using Trileptal® in combination therapy, it may be necessary to decrease the dose of concomitant antiepileptic drugs and/or to increase the dose of Trileptal® more slowly due to increase in the total dose of antiepileptic drugs.

Trileptal® may be taken regardless of meals (during, after or between meals).

Table of Dose Conversion Table for Trileptal® from mg to ml.

Dose in milligrams (mg)Dose in milliliters (ml)10 mg0.2 ml20 mg0.3 ml30 mg0.5 ml40 mg0.7 ml50 mg0.8 ml60 mg1.0 ml70 mg1.2 ml80 mg1.3 ml90 mg1.5 ml100 mg1.7 ml200 mg3.3 ml300 mg5.0 ml400 mg6.7 ml500 mg8.3 ml600 mg10.0 ml700 mg11.7 ml800 mg13.3 ml900 mg15.0 ml1000 mg16.7 ml

Before taking the oral suspension, the bottle should be shaken thoroughly and the desired amount of suspension should be measured immediately. The desired dose (ml) is taken from the bottle using the syringe supplied. If the 10 ml syringe (supplied with the 250 ml bottle for adults and older children) is used, the amount of suspension should be rounded up to 0.5 ml. When using a 1 ml syringe (supplied with a 100 ml bottle for younger children) the amount of suspension should be rounded up to 0.1 ml. After each use the vial should be closed tightly and the syringe should be wiped with a clean dry cloth. The suspension can be taken directly from the syringe or diluted with a little water before intake. Keep the bottle open for no more than 7 weeks.

The oral suspension and tablets are bioequivalent and interchangeable in equivalent doses.

The therapeutic effect of Trileptal® (oxcarbazepine) is due primarily to the action of its metabolite, MGP.

The routine determination of plasma concentrations of oxcarbazepine or MND is not warranted. However, control of plasma concentrations of MND can be used to clarify adherence to the drug by the patient (compliance), or in situations where there may be changes in MND clearance, such as changes in renal function, pregnancy, concomitant use with drugs that increase activity of “liver” enzymes. In the above-mentioned situations, the dose of Trileptal® should be adjusted with regard to plasma concentrations of MND (measured 2-4 h after administration), which should be maintained at the level

Adult patients

Monotherapy:and combination therapy

The initial dose is 600 mg/day (8-10 mg/kg body weight/day) divided into 2 doses. Gradual increase of the dose is possible if necessary. The dose is increased by no more than 600 mg/day at intervals of about 1 week, until the desired therapeutic response is achieved. A good therapeutic response is seen in the dose range of 600-2400 mg/day, with most patients having good clinical effect at a dose of 900 mg/day.

In patients who have not previously received therapy with antiepileptic agents the effective dose is 1200 mg/day, in patients who previously received but poorly responded to therapy with other antiepileptic agents – 2400 mg/day.

The use of Trileptal® in a daily dose of 2400 mg in combination therapy without reducing the dose of another antiepileptic agent was accompanied by poor tolerability in most patients mainly due to the development of adverse events in the nervous system. The use of Trileptal® in daily dose higher than 2400 mg has not been studied.

In children

In monotherapy with Trileptal® and in combination therapy, the recommended starting dose of 8-10 mg/kg body weight per day is divided into 2 doses.

In combination therapy, the target dose of Trileptal® of 30-46 mg/kg/day should not be reached before 2 weeks from the start of therapy.

If necessary to achieve the desired therapeutic effect, the dose may be gradually increased – at an interval of about 1 week the dose is increased – by maximum 10 mg/kg/day, up to maximum daily dose of 60 mg/kg of body weight.

When using Trileptal® in monotherapy and as part of combination therapy, the apparent clearance of MND in children decreases significantly with increasing age. Children aged 1 month to 4 years may require a dose of the drug that is 2 times the adult dose when adjusted by body weight; children aged 4 to 12 years may require a dose that is 50% higher than the adult dose when adjusted by body weight.

In children aged 1 month to 4 years, the effect of antiepileptic drugs – hepatic enzyme inducers on their apparent clearance is more pronounced than in children of older age groups (when adjusted by body weight). When using Trileptal® in children aged 1 month to 4 years in combination with antiepileptic drugs – inducers of liver enzymes, a 60% higher dose of oxcarbazepine may be required (when adjusted by body weight) than when using Trileptal® alone or in combination with antiepileptic drugs that do not induce enzymes. For children of older age groups, combination therapy with Trileptal® with liver enzyme inducers may require a slight increase in the drug dose compared to monotherapy.

In children younger than 3 years of age the drug should be used in the syrup form due to difficulties in using solid dosage forms in this age group.

Patients aged ≥65 years

Special dosing adjustment in this category of patients is necessary if renal function is impaired (CKR less than 30 ml/min). If there is a risk of hyponaremia, careful monitoring of plasma sodium is necessary.

Patients with hepatic impairment

There is no need for dosing adjustment in patients with mild to moderate hepatic impairment. Caution should be used in patients with severe hepatic impairment.

Patients with renal impairment

For patients with renal impairment (CKR less than 30 ml/min), the recommended starting dose is 300 mg/day; the dose should be increased slowly, at intervals of at least 1 week, until the desired therapeutic response is achieved. Patients should be closely monitored during dose adjustment.

Interaction

Enzyme inhibition

Occarbazepine and its pharmacologically active metabolite MND are inhibitors of cytochrome CYP2C19. Thus, simultaneous use of Trileptal® in high doses and preparations that are metabolized with participation of CYP2C19 isoenzyme (e.g., phenobarbital, phenytoin) may lead to their interaction. For some patients it may be necessary to reduce the dose of drugs – substrates of CYP2C19. Oxcarbazepine and MND have been shown to interact weakly or not at all with the following microsomal isoenzymes: CYP1A2, CYP2A6, CYP2C9, CYP2D9, CYP2E1, CYP4A4 and CYP4C11.

Induction of enzymes

As they are weak inducers of cytochrome CYP3A4 and CYP3A5, they decrease plasma concentrations of drugs metabolized by these enzymes: dihydropyridine calcium antagonists, oral contraceptives and antiepileptic drugs (e.g. carbamazepine). In concomitant use of Trileptal® preparation it is also possible decrease of plasma concentration of other drugs, which are substrates of CYP3A4 and CYP3A5 isoenzymes (for example, drugs from immunosuppressants group – cyclosporine).

As in vitro oxcarbazepine and MNP are weak inducers of uridine diphosphate-glucuronyl transferase, it is unlikely that in vivo they can have a clinically significant effect on the metabolism of drugs excreted as glucuronic acid conjugates (for example, valproic acid and lamotrigine). But, taking into account even weak inducing ability of oxcarbazepine and MND, it may be necessary to increase doses of concomitantly used drugs that are metabolized with participation of CYP3A4 isoenzyme or uridine diphosphate-glucourene transferase. In case of withdrawal of Trileptal® , a dose reduction of these drugs may be required based on clinical and laboratory monitoring. In vitro studies have confirmed weak inducing ability of oxcarbazepine and MND with regard to isoenzymes of CYP2B and CYP3A4 enzyme subsystems. The inducing effect of oxcarbazepine and MND on other CYP isoenzymes is unknown.

Antiepileptic drugs (PEDs)

Possible interactions between Trileptal® and other antiepileptic drugs have been evaluated in clinical studies. The data on the effect of these interactions on AUC and minimum Cmin concentration are summarized in the table:

PEPThe effect of Trileptal® on PEP
CminThe effect of PEP on MPG
AUCCarbamazepine0-22% decrease (30% increase in carbamazepine-10,11-epoxide)40% decreaseClobazamNot studiedNo effectFelbamateNot studiedNo effectPhenobarbital14-15% increase30-31% decreasePhenytoin0-40% increase29-35% decreaseValproic acidNo effect0-18% decrease

Phenytoin plasma concentrations are increased up to 40% with concomitant administration of Trileptal® at a dose of 1200 mg/day or higher. Therefore, when using Trileptal® in the above doses, it may be necessary to reduce the dose of phenytoin.

The increase in plasma concentrations of phenobarbital when concomitantly used with Trileptal® is negligible (15%).

Concomitant use of strong cytochrome P450 inducers (i.e., carbamazepine, phenytoin and phenobarbital) decreases plasma concentrations of MND (by 29-40%). Thus it is necessary to monitor plasma concentrations of MND and if necessary to adjust the dose of the drug in case of concomitant use of oxcarbazepine with one or more of the above mentioned drugs.

Trileptal® has not shown any autoinduction phenomena.

Hormonal contraceptives

Trileptal® has been shown to interact with oral contraceptive components: ethinylestradiol and levonorgestrel. Mean AUC values for them were decreased by 48-52% and 32-52%, respectively. No studies of interaction of Trileptal® with other oral or implantable contraceptives have been conducted. Thus, the simultaneous use of Trileptal® and hormonal contraceptives may reduce the effectiveness of the latter, and in this connection, it is recommended that patients treated with Trileptal® should make additional use of reliable non-hormonal contraceptive methods.

Calcium channel blockers

Combined use of Trileptal® and felodipine may decrease AUC of felodipine by 28%, although plasma concentrations remain within the therapeutic range.

On the other hand, concomitant use with verapamil may decrease plasma concentrations of MPG by 20%. This decrease in plasma concentrations is not clinically relevant.

Interaction with other medicinal products

Cimetidine, erythromycin, dextropropoxyphene do not influence pharmacokinetic parameters of MND; viloxazine slightly influences plasma concentration of MND (concentration of MND is increased by 10% after reuse together). No interaction with warfarin was noted when taking both single and multiple doses of Trileptal®.

No interactions with warfarin have been observed with both single concomitant and repeated doses of Trileptal®.

Trileptal® may increase the sedative effect of ethanol.

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Special Instructions

There are reports of a risk of worsening of the course of epileptic seizures when using Trileptal®. An increased risk of seizure worsening has been observed mainly in children, but may also occur in adults. If during the use of Trileptal® worsening of the course of epileptic seizures is observed, the drug should be discontinued.

Hypersensitivity reactions

In clinical use of Trileptal® there have been individual cases (post-marketing reports) of immediate hypersensitivity reactions (type I) including rash, pruritus, urticaria, angioedema and anaphylactic reactions. Hypersensitivity reactions may cause disorders of the skin, liver, blood and lymphatic system and other organs both individually and as part of a systemic reaction. Angioneurotic edema and anaphylactic reactions with lesions of the larynx, vocal folds (vocal cleft area), tongue, lips, eyelids have developed both during the first and repeated use of Trileptal®. If immediate-onset hypersensitivity develops, Trileptal® should be immediately discontinued and an alternative therapy should be prescribed.

The drug should be used with caution in patients with known hypersensitivity to carbamazepine because hypersensitivity reactions to oxcarbazepine may develop in about 25-30% of cases in this group of patients. Patients with no history of hypersensitivity to carbamazepine may also develop hypersensitivity reactions to the drug, including multiple organ disorders. If signs and symptoms of hypersensitivity reactions occur, the drug Trileptal® should be discontinued immediately.

Hyponatremia

In 2.7% of patients receiving Trileptal®, hyponatremia (serum sodium less than 125 mmol/L) was observed, which usually was not accompanied by clinical manifestations and did not require therapy correction. Sodium content is normalized in case of withdrawal (dose reduction) of Trileptal® or conservative treatment (restriction of fluid intake). Patients with renal dysfunction in anamnesis and low serum sodium content (for example, patients with inadequate secretion of antidiuretic hormone syndrome), or patients receiving concurrent treatment with agents that promote sodium excretion from the body (diuretics, drugs that influence on antidiuretic hormone secretion), sodium content in serum should be determined before starting the therapy with Trileptal® preparation. Thereafter sodium content in serum should be controlled in 2 weeks after the therapy start and further monthly during 3 months or as per necessity. Elderly patients should be treated with particular attention to these risk factors. If it is necessary to use diuretics and other drugs that reduce sodium content in blood serum, the same recommendations should be followed in patients receiving the therapy with Trileptal®. If clinical symptoms of hyponatremia appear, serum sodium content should be determined. For other patients, determination of serum sodium may be performed during routine blood tests.

Body weight control should be performed in all patients with heart failure for timely diagnosis of fluid retention. In case of fluid retention or in case of progression of heart failure symptoms serum sodium content should be determined. In case of hyponatremia the amount of fluid intake should be limited. As far as in very rare cases of oxcarbazepine use cardiac conduction disorders may occur, the patients with previous conduction disorders (atrioventricular blockade, arrhythmia) treated with Trileptal® should be closely monitored.

Hematologic changes

According to post-marketing reports, agranulocytosis, aplastic anemia and pancytopenia have been reported in very rare cases in patients treated with Trileptal®. Taking into account the low incidence of agranulocytosis, aplastic anemia and pancytopenia, as well as concomitant factors (e.g., concomitant use of other drugs, presence of concomitant diseases), a causal relationship between the development of these adverse events and the use of the drug cannot be established. If symptoms of marked suppression of medullary hematopoiesis develop, it is necessary to consider discontinuation of the drug.

Suicidal thoughts and behavior

Patients receiving anticonvulsants have had episodes of suicidal behavior and suicidal thoughts. Results of a meta-analysis of randomized placebo-controlled trials showed a small increase in the risk of suicidal behavior in patients receiving anticonvulsants. The mechanism for the increased risk of suicide in this patient population has not been established. Therefore, close monitoring of patients treated with the drug is necessary at all stages of treatment. Patients and medical personnel should be alerted to the risk of suicidal ideation and episodes in patients treated with Trileptal®.

Dermatological reactions

The development of serious dermatological reactions such as: Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell’s syndrome), erythema exudative multiforme have very rarely been reported with the use of Trileptal®. Patients with the above dermatological reactions may require hospitalization due to the development of life-threatening conditions; very rarely lethal outcomes are possible. When using Trileptal®, dermatological reactions have been observed in both children and adults, and developed on average 19 days after the start of the drug. There have been isolated reports of cases of recurrence of serious skin reactions upon resumption of Trileptal® administration. If skin reactions develop during the use of Trileptal® , discontinuation of the drug and use of another antiepileptic agent should be considered.

Correlation with HLA-B*1502

There is considerable evidence to support the role of human leukocyte antigen (HLA) alleles in the development of serious skin reactions in patients with predisposition to these conditions. Because of the similarity in chemical structure between oxcarbamazepine and carbamazepine, there is a possibility of developing Stevens-Johnson syndrome and Lyell’s syndrome in patients with the HLA-B*1502 allele in the genome who take oxcarbamazepine.

In Chinese and Thai patients, there was a clear association between the development of Stevens-Johnson syndrome and Lyell’s syndrome when using carbamazepine and the presence of the HLA-B*1502 human leukocyte antigen allele in their genome.

The incidence of this allele in Chinese patients is 2-12%, in Thai patients it is about 8%, and in some Malaysian populations it is more than 15%. The frequency of the HLA-B*1502 allele in Korea and India is 2% and 6%, respectively. The prevalence of this allele in individuals of Caucasoid, Negroid, Hispanic, Native American, and Japanese races is insignificant (

The frequencies of these alleles represent the percentage of chromosomes in certain populations that carry the allele. This means that the percentage of patients carrying a copy of the allele in at least one of their two chromosomes is almost twice the frequency of the allele. Thus, the percentage of patients at risk is almost twice the frequency of the allele.

When using Trileptal® in possible carriers of the HLA-B*1502 allele, genotyping for this allele is recommended. The drug should be used in carriers of this allele only if the expected benefit of therapy outweighs the possible risk. The presence of this allele in Chinese people taking other antiepileptic drugs increases the risk of severe dermatological reactions. Patients with the HLA-B*1502 allele should avoid the use of drugs leading to Stevens-Johnson syndrome or Lyell syndrome, with possible substitution with alternative drugs. Genotyping for HLA-B*1502 allele before using Trileptal® is not necessary in patients belonging to populations with low frequency of this allele and also in patients already treated with this drug, because severe skin reactions were observed in most cases in first months of treatment (regardless of HLA-B*1502 presence).

Correlation with HLA-B*3101

The presence of HLA-A*3101 allele may be a risk factor for severe skin lesions (Stevens-Johnson syndrome, Lyell syndrome, drug rash with eosinophilia and systemic manifestations, acute generalized exanthematous pustulosis and spot-nodule rash) when using carbamazepine. The frequency of the HLA-A*3101 allele of the human leukocyte antigen (HLA) gene may vary in different ethnic groups: about 2-5% in the European population, about 10% in the Japanese population, about 6.7% in the population of Western Europe, depending on the geographic region. The frequency of the allele is less than 5% in the populations of Australia, Asia, Africa and North America, with exceptions ranging from 5% to 12%. Frequencies higher than 15% are found in some ethnic groups in South America (Argentina and Brazil), indigenous people in North America (Navajo and Siocs tribes, in Mexico – Sanora Ceri), South India (Tamil Nadu), and 10-15% among other indigenous people in these regions.

The frequencies of these alleles represent the percentage of chromosomes in certain populations that carry the allele. This means that the percentage of patients carrying a copy of the allele in at least one of their two chromosomes is almost twice the frequency of the allele. Thus, the percentage of patients who might be at risk is almost twice the frequency of the allele.

There is insufficient evidence to recommend genotyping for this allele in patients before starting oxcarbazepine therapy. Patients already receiving therapy with Trileptal® should not be genotyped for this allele because skin reactions were observed in most cases in the first months of therapy (regardless of the presence of HLA-A*3101).

However, the results of genotyping should not affect the degree of control of the patient and the physician’s alertness to severe skin reactions. The development of severe skin lesions is possible in patients negative for these alleles. Also in many cases patients positive for HLA-B*1502 or HLA-A*3101 alleles have not developed severe skin syndromes while using Trilertal®.

High resolution methodology should be preferred when genotyping for the HLA-B*1502 allele. The test is positive if at least one of the alleles is detected; it is negative if no alleles are detected. The same guidelines should be followed when genotyping for the HLA-A*3101 allele. The influence of other factors, such as anticonvulsant medication dosage, patient compliance, concomitant therapy with other drugs, comorbidities, or level of dermatologic reaction control, on the incidence and prevalence of severe skin reactions has not been established.

Liver dysfunction

There have been reports of very rare cases of hepatitis, which in most cases have resolved safely. If hepatitis is suspected, discontinuation of the drug should be considered.

Hypothyroidism

Hypothyroidism is an extremely rare adverse event with oxcabazepine. Taking into consideration the effect of thyroid hormones on the development of children, it is recommended to determine the thyroid hormone concentration before initiating therapy with the drug, and also to monitor this indicator during the use of Trileptal® in this category of patients, especially at the age of less than two years.

Concomitant use of oral contraceptives

Women of childbearing age taking oral contraceptives concomitantly with Trileptal® should be warned about possible decrease in effectiveness of oral contraceptives. Additional use of non-hormonal contraceptive methods is recommended for this category of patients receiving Trileptal®.

The withdrawal syndrome

As with other antiepileptic drugs, abrupt discontinuation of therapy with Trileptal® should be avoided because of the risk of increased seizure frequency.

Persons taking alcohol during therapy with Trileptal® should be warned about possible increased sedative effects.

Trileptal® in oral suspension form contains less than 100 mg of ethanol per dose. The suspension also contains parabens, which may cause allergic reactions (possibly delayed).

The oral suspension contains sorbitol, therefore Trileptal® in suspension form should not be used in patients with hereditary fructose tolerance disorder.

Impact on potentially hazardous activities requiring particular attention and quick reactions

. Patients should be cautious when driving or operating machinery with Trileptal® due to the possibility of adverse events, such as dizziness, somnolence, ataxia, diplopia, blurred vision, visual disturbances, hyponatremia, and depression of consciousness or other central nervous system disorders, especially at the start of treatment or during dose adjustment, during drug administration.

In case of the occurrence of the described adverse events, patients should refrain from performing the specified activities.

Contraindications

• children under 1 month;
• high sensitivity to oxcarbazepine or any other components of the drug.

Patients with known hypersensitivity to carbamazepine should be prescribed with caution because this group of patients may develop hypersensitivity reactions to oxcarbazepine in approximately 25-30% of cases. In patients with no history of hypersensitivity to carbamazepine it is also possible to develop hypersensitivity reactions to the drug, including multiple organ disorders.

The use of Trileptal® in patients with hepatic impairment has not been studied; therefore, the drug should be used with caution in this category of patients.

The use in hepatic impairment

There is no need for dosing adjustment in patients with mild to moderate hepatic impairment. Caution should be used in patients with severe hepatic impairment.

Perhaps with renal impairment

For patients with renal impairment (CKD less than 30 ml/min) the recommended initial dose is 300 mg/day; The dose should be increased slowly, at intervals of at least 1 week, until the desired therapeutic response is achieved. Patients should be closely monitored during dose adjustment.

Pediatric use

The use is possible according to the dosing regimen.

It is contraindicated in children under 1 month of age.

Performance in elderly patients

Particular dosage regimen correction in this category of patients is necessary if renal function is impaired (CKG less than 30 ml/min). If there is a risk of hyponaremia, careful monitoring of plasma sodium is necessary.

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Side effects

The following adverse reactions have been most commonly reported: somnolence, headache, dizziness, diplopia, nausea, vomiting, feeling of fatigue (in more than 10% of patients).

In clinical trials it has been shown that the undesirable effects are usually mild to moderate, transient, and occur mostly at the beginning of therapy.

The following data summarizes the information on adverse reactions (HP) reported in clinical trials, as well as data on the safety profile of the drug obtained during its use in clinical practice. HPs are grouped according to the MedDRA organ and system classification, and are listed in decreasing order of importance.

Criteria for evaluating the incidence of adverse events: very common (≥1/10), common (≥1/100,

Blood and lymphatic system disorders: infrequent – leukopenia; very rare – suppression of medullary hematopoiesis, agranulocytosis, aplastic anemia, neutropenia, pancytopenia, thrombocytopenia.

In immune system disorders: very rarely – anaphylactic reactions, hypersensitivity reactions (including multi-organ disorders), characterized by such phenomena as rash and increased body temperature. Blood and lymphatic systems may be affected (eosinophilia, thrombocytopenia, leukopenia, lymphadenopathy, splenomegaly), liver (hepatitis, changes in liver function parameters), muscles and joints (myalgia, edema in joints, arthralgia), nervous system (hepatic encephalopathy), kidneys (renal failure, interstitial nephritis, proteinuria), lungs (pulmonary edema, bronchospasm, bronchial asthma, interstitial inflammation, dyspnea), angioedema.

Endocrine system disorders: very rarely – hypothyroidism.

Metabolism and nutrition disorders: often – hyponatremia (more frequently in patients aged >65 years); very rarely – clinically significant hyponatremia (concentration of sodium®. This condition can lead to the development of such manifestations and symptoms as convulsive seizures, encephalopathy, decreased level of consciousness, confusion, visual disturbances (including blurred vision), hypothyroidism, vomiting, nausea, folic acid deficiency.

Psychiatric disorders: often – agitation (including nervousness), emotional lability, confusion, depression, apathy.

Nervous system disorders: very frequently – somnolence (22.5%), headache (14.6%), dizziness (22.6%); frequently – ataxia, tremor, nystagmus, disorder of attention, amnesia.

VIight: very common – diplopia (13.9%); common – blurred vision, visual disturbances.

Hearing organ and labyrinth disorders: often – systemic dizziness.

Heart: very rare – AV-blockade, arrhythmia.

Vascular disorders: very rarely – arterial hypertension.

Gastrointestinal system: very common – vomiting (11.1%), nausea (14.1%); common – diarrhea, abdominal pain, constipation; very rare – pancreatitis.

Liver and biliary tract: very rare – hepatitis.

Skin and subcutaneous tissue disorders: common – rash, alopecia, acne; infrequent – urticaria; very rare – Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell’s syndrome caused by taking medicinal products), angioedema, erythema multiforme, systemic lupus erythematosus.

General disorders and disorders at the site of administration: very often – feeling of fatigue (12%); often – asthenia.

Laboratory and instrumental data: infrequent – increased activity of liver enzymes, ALP; very rare – increased activity of amylase, lipase.

In clinical studies conducted in children aged 1 month to 4 years, the most frequently observed sleepiness was observed (in 11% of patients). With a frequency of >1%-

The undesirable reactions identified in the post-marketing period based on individual reports and cases described in the literature.

Because data on post-marketing adverse reactions were derived from voluntary reports from a population of unknown size, the incidence cannot be estimated (frequency is unknown). The adverse reactions are classified by organ system, and within each organ system, the adverse reactions are arranged in decreasing order of severity.

Germ and subcutaneous tissue disorders

Medicated rash with eosinophilia and systemic manifestations, acute generalized exanthematous pustulosis.

Skeletal, musculoskeletal and connective tissue disorders

There have been reports of decreased bone mineral density, osteopenia, osteoporosis and fractures in patients treated with Trileptal® for a long time. The mechanism of oxcarbazepine effect on bone metabolism is not known.

Metabolism and nutrition disorders

An inadequate antidiuretic hormone secretion syndrome manifested by lethargy, nausea, dizziness, decreased plasma osmolality, vomiting, headache, confusion and other nervous system symptoms.

Injuries, intoxications, and complications of manipulation

Fall.

Nervous system disorders

Speech disorders (including dysarthria), especially during dosage adjustment.

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Overdose

There have been isolated reports of drug overdose. The maximum dose reported was approximately 48,000 mg.

Symptoms:

Aqueous-electrolyte disturbances: hyponatremia.

Visually: diplopia, miosis, blurred vision.

Digestive system disorders: nausea, vomiting, hyperkinesia.

General disorders and disorders at the site of administration: fatigue.

Laboratory and instrumental findings: decreased respiratory rate, prolonged QTc interval .

Nervous system disorders: drowsiness, dizziness, ataxia, nystagmus, tremor, coordination disorders, convulsions, headache, coma, loss of consciousness, dyskinesia.

Mental disorders: aggression, agitation, confusion.

Vascular disorders: decreased BP.

Respiratory system, chest and mediastinal organs: dyspnea.

Treatment. There is no specific antidote. Symptomatic and supportive treatment is carried out. It should be borne in mind that to reduce absorption of oxcarbazepine gastric lavage may be conducted and intake of activated charcoal may be prescribed. Vital body functions should be monitored, with special attention paid to disorders of water-electrolyte balance, cardiac conduction and disorders of the respiratory system.

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Pregnancy use

Children of patients with epilepsy are more often predisposed to developmental disorders, including congenital defects.

The experience of using Trileptal® in pregnancy is limited. The available reports indicate a possible association of taking the drug during pregnancy with the development of congenital malformations (CHD). The most common malformations in children whose mothers received Trileptal® during pregnancy were: atrial septal defect, atrial-ventricular septal defect, cleft palate and upper lip, Down syndrome, hip dysplasia (both unilateral and bilateral), tuberous sclerosis and ear malformations.

According to the North American Pregnancy Registry, the incidence of gross malformations related to structural abnormalities requiring surgical, medical, or cosmetic correction diagnosed within 12 weeks of birth was 2.0% (95% confidence interval 0.6 to 5.1%) among pregnant women who received oxcarbazepine monotherapy in the first trimester. Compared with pregnant women who did not receive therapy with any antiepileptic drugs during pregnancy, the relative risk of malformations in children was 1.6 with a 95% confidence interval of 0.46 to 5.7.

Patients of childbearing age should use reliable contraception during therapy with Trileptal® (optimally, intrauterine contraceptives) because the effectiveness of these medications may decrease when used concomitantly with oral contraceptives containing ethinylestradiol or levonorgestrel.

If a patient is planning a pregnancy or a pregnancy is diagnosed during the use of the drug, or if there is a question about the use of Trileptal® during pregnancy, the expected benefits of therapy must be carefully weighed against the possible risk to the fetus, especially in the first trimester of pregnancy.

In pregnancy, the lowest effective dose of the drug should be used. If clinically effective in women of childbearing age, Trileptal® should be used in monotherapy.

The patient should be warned about possible fetal abnormalities and the need for antenatal diagnosis.

The effective antiepileptic treatment should not be interrupted during pregnancy, because the progression of the disease may have a negative impact on the mother and fetus. Folic acid deficiency is known to develop during pregnancy. Antiepileptic drugs can exacerbate this deficiency, which is one of the possible causes of fetal abnormalities, so additional folic acid medication is recommended.

When using the drug during pregnancy, it should be taken into account that physiological changes that occur in the body during pregnancy may lead to a gradual decrease in plasma levels of 10-monohydroxy derivative (MGD). To maximize symptom control in pregnant patients, regular assessment of the clinical effect of the drug and determination of plasma concentrations of MND should be performed.

The determination of plasma levels of MND is also recommended in the postpartum period, especially if the drug dose was increased during pregnancy.

There are reports that the use of antiepileptic drugs during pregnancy may lead to increased bleeding in the newborn. As a precautionary measure, the use of vitamin K1 in the last few weeks of pregnancy is recommended, as well as in newborns whose mothers have received the drug Trileptal®.

Occarbazepine and MND pass through the placental barrier. Oxcarbazepine and MND are excreted with the breast milk. The ratio of concentrations in milk to plasma was 0.5 for both substances. Since the effect of oxcarbazepine and MND excreted with breast milk on neonates is unknown, Trileptal® should not be used while breastfeeding.

Performance in children less than 1 month of age

There are no data on the safety and effectiveness of Trileptal® in children less than 1 month of age.

Impact on fertility

There are no data on the effect of the drug on fertility in humans. In animal studies, no effect of oxcarbazepine and MND on fertility was found in individuals of either sex at daily doses of 150 and 450 mg/kg, respectively. When maximum doses of MND were used in females, however, there was a disruption of the astral cycle, a decrease in the number of luteal bodies, a decrease in the number of implantations and the number of live embryos.