Topiramate-ALSI, 25 mg 30 pcs

Topiramate is an antiepileptic drug belonging to the class of sulfamate-substituted monosaccharides.

Topiramate blocks sodium channels and suppresses the occurrence of repetitive action potentials against the background of prolonged depolarization of the neuronal membrane. Topiramate increases the activity of gamma-aminobutyric acid (GABA) against several subtypes of GABA receptors (including GABA_A-receptors), and also models the activity of GABA_A-receptors, prevents kainat activation of kainat/AMPK (α-amino-3-hydroxy-5-methylisoxalol-4-propionic acid)-receptor subtype sensitivity to glutamate, and does not affect N-methyl-D-aspartate (NMDA) activity with respect to the NMDA-receptor subtype. These effects of topiramate are dose-dependent at plasma concentrations of 1 μmol to

200 μmol, with minimal activity ranging from 1 μmol to 10 μmol.

In addition, topiramate inhibits the activity of some carboanhydrase isoenzymes. Topiramate is significantly inferior to acetazolamide, a known carbo anhydrase inhibitor, in terms of the severity of this pharmacological effect; therefore, this activity of topiramate is not considered to be the main component of its antiepileptic activity.

Pharmacokinetics

Eabsorption

Topiramate is absorbed quickly and efficiently. Its bioavailability is 81%. Food intake has no clinically significant effect on the bioavailability of topiramate.

Distribution

13-17% of topiramate is bound to plasma proteins. After a single dose of up to 1200 mg the average volume of distribution is 0.55-0.8 l/kg. Distribution volume depends on sex: in women it is about 50% of that in men, which is associated with a higher content of adipose tissue in women.

Metabolism

After oral administration about 20% of the administered dose is metabolized. However, in patients receiving concomitant therapy with antiepileptic drugs that induce enzymes responsible for drug metabolism, the metabolism of topiramate is increased up to 50%.

Six virtually inactive metabolites have been isolated and identified from human plasma, urine, and feces. The main route of excretion of unchanged topiramate (70%) and its metabolites is the kidneys. After oral administration the plasma clearance of topiramate is 20-30 ml/min.

Linearity/non-linearity

The pharmacokinetics of topiramate are linear, plasma clearance remains constant, and the area under the concentration-time curve (AUC) in the dose range from

100 to 400 mg increases in proportion to the dose. In patients with normal renal function, it may take 4 to 8 days to reach stable plasma concentrations. The value of maximum concentration (C_max) after multiple oral doses of 100 mg twice daily averaged 6.76 mcg/ml. After multiple doses of 50 and 100 mg twice daily, the plasma half-life of topiramate averaged 21 hours.

Renal disorders

In patients with moderate to severe renal impairment, plasma and renal clearance of topiramate is decreased (creatinine clearance (K_k) ≤ 70 ml/min), as a consequence, the equilibrium plasma concentrations of topiramate may be higher compared to patients with normal renal function. In addition, patients with impaired renal function take longer to reach equilibrium blood concentrations of topiramate. For patients with moderate to severe renal impairment, half the recommended initial and maintenance doses are recommended.

Hemodialysis

Topiramate is effectively eliminated from plasma by hemodialysis. Prolonged hemodialysis may cause blood concentrations of topiramate to fall below the amount required to maintain anticonvulsant activity. An additional dose of topiramate may need to be administered to avoid a rapid drop in plasma concentrations during hemodialysis.

• The duration of hemodialysis;
• the clearance rate of the hemodialysis system used;
• the effective renal clearance of topiramate in a patient on dialysis should be taken into account when adjusting the dose.

Hepatic disorders

The plasma clearance of topiramate is reduced by an average of 26% in patients with moderate to severe hepatic impairment. Therefore, patients with hepatic impairment should use topiramate with caution.

Elderly patients

The plasma clearance of topiramate is not altered in elderly patients without renal disease.

Pharmacokinetics in children (children under 12 years of age)

The pharmacokinetic parameters of topiramate in children, as well as in adults receiving this drug as adjuvant therapy, are linear, with its clearance independent of dose, and equilibrium plasma concentrations increase in proportion to increasing dose. However, the fact that in children, topiramate clearance is higher and the elimination half-life is shorter should be taken into account. Therefore, at the same dose per 1 kg body weight, plasma concentrations of topiramate in children may be lower than in adults. In children, as in adults, antiepileptic drugs that induce microsomal liver enzymes cause lower plasma concentrations of topiramate.

Indications

Epilepsy

As a monotherapy:

In adults and children over 3 years of age with epilepsy (including patients with newly diagnosed epilepsy).

As part of complex therapy:

In adults and children over 3 years of age with partial or generalized tonic-clonic seizures, as well as for the treatment of seizures associated with Lennox-Gastaut syndrome.

Migraine

Prevention of migraine attacks in adults. The use of topiramate for the treatment of acute migraine attacks has not been studied.

Pharmacological effect

Topiramate is an antiepileptic drug belonging to the class of sulfamate-substituted monosaccharides.

Topiramate blocks sodium channels and suppresses the occurrence of repeated action potentials against the background of prolonged depolarization of the neuron membrane. Topiramate increases the activity of gamma-aminobutyric acid (GABA) in relation to certain subtypes of GABA receptors (including GABAA receptors), and also models the activity of GABAA receptors themselves, prevents activation by kainate of the sensitivity of the subtype kainate/AMPK (α-amino-3-hydroxy-5-methylisoxalol-4-propionic acid) receptors to glutamate, does not affect the activity N-methyl-D-aspartate (NMDA) in relation to the NMDA receptor subtype. These effects of topiramate are dose-dependent with plasma drug concentrations ranging from 1 µmol to

200 µmol, with minimal activity ranging from 1 µmol to 10 µmol.

In addition, topiramate inhibits the activity of some carbonic anhydrase isoenzymes. In terms of the severity of this pharmacological effect, topiramate is significantly inferior to acetazolamide, a known inhibitor of carbonic anhydrase, therefore this activity of topiramate is not considered the main component of its antiepileptic activity.

Pharmacokinetics

Suction

Topiramate is absorbed quickly and efficiently. Its bioavailability is 81%. Food intake does not have a clinically significant effect on the bioavailability of topiramate.

Distribution

13-17% of topiramate is bound to plasma proteins. After a single dose of up to 1200 mg, the average volume of distribution is 0.55-0.8 l/kg. The magnitude of the volume of distribution depends on gender: in women it is approximately 50% of the values ​​observed in men, which is associated with a higher content of adipose tissue in the body of women.

Metabolism

After oral administration, about 20% of the dose taken is metabolized. However, in patients receiving concomitant therapy with antiepileptic drugs that induce enzymes responsible for drug metabolism, the metabolism of topiramate increases up to 50%.

Removal

Six essentially inactive metabolites have been isolated and identified from human plasma, urine, and feces. The main route of elimination of unchanged topiramate (70%) and its metabolites is the kidneys. After oral administration, plasma clearance of topiramate is 20-30 ml/min.

Linearity/non-linearity

The pharmacokinetics of topiramate is linear, plasma clearance remains constant, and the area under the concentration-time curve (AUC) in the dose range from

100 to 400 mg increases proportionally to dose. In patients with normal renal function, it may take 4 to 8 days to achieve steady-state plasma concentrations. The maximum concentration (Cmax) after repeated oral administration of 100 mg of the drug twice a day averaged 6.76 mcg/ml. After multiple doses of 50 and 100 mg twice daily, the plasma half-life of topiramate averaged 21 hours.

Renal dysfunction

In patients with moderate to severe renal impairment, the plasma and renal clearance of topiramate is reduced (creatinine clearance (Kk) ≤ 70 ml/min), as a result, the equilibrium concentration of topiramate in the blood plasma may increase compared to patients with normal renal function. In addition, patients with impaired renal function require more time to achieve equilibrium concentrations of topiramate in the blood. In patients with moderate or severe renal impairment, half the recommended initial and maintenance dose is recommended.

Hemodialysis

Topiramate is effectively eliminated from plasma by hemodialysis. Long-term hemodialysis may result in a decrease in blood concentrations of topiramate below the amount required to maintain anticonvulsant activity. To avoid a rapid fall in plasma concentrations of topiramate during hemodialysis, an additional dose of topiramate may be required. When adjusting the dose, you should take into account:

duration of hemodialysis;

the clearance value of the hemodialysis system used;

effective renal clearance of topiramate in a patient on dialysis.

Liver dysfunction

Plasma clearance of topiramate is reduced by an average of 26% in patients with moderate or severe hepatic impairment. Therefore, patients with hepatic impairment should use topiramate with caution.

Elderly patients

In elderly patients without renal disease, the plasma clearance of topiramate does not change.

Pharmacokinetics in childhood (in children under 12 years of age)

The pharmacokinetic parameters of topiramate in children, as well as in adults receiving this drug as adjuvant therapy, are linear, while its clearance does not depend on the dose, and equilibrium plasma concentrations increase in proportion to the dose. However, it should be taken into account that in children the clearance of topiramate is increased and its half-life is shorter. Therefore, at the same dose per 1 kg of body weight, plasma concentrations of topiramate in children may be lower than in adults. In children, as in adults, antiepileptic drugs that induce liver microsomal enzymes cause a decrease in plasma concentrations of topiramate.

Special instructions

Antiepileptic drugs, including Topiramate-ALSI, should be discontinued gradually to minimize the possibility of an increase in the frequency of seizures. To reduce the dose by 25-50 mg, use the drug Topiramate-ALSI at a dosage of 25 mg. In clinical studies, doses were reduced by 50-100 mg at weekly intervals for adults treated for epilepsy and by 25-50 mg in adults receiving 100 mg of Topiramate-ALSI per day for migraine prophylaxis. If rapid discontinuation of topiramate is necessary for medical reasons, it is recommended that appropriate monitoring of the patient’s condition be carried out.

As with other antiepileptic drugs, some patients taking topiramate experience an increase in the frequency of seizures or new types of seizures. This phenomenon may be a consequence of an overdose, a decrease in the concentration of concomitantly used antiepileptic drugs, disease progression, or a paradoxical effect. The rate of excretion through the kidneys depends on renal function and is independent of age. In patients with moderate or severe renal impairment, it may take 10 to 15 days to achieve steady-state plasma concentrations, compared with 4 to 8 days in patients with normal renal function.

As with any disease, dose selection should be based on clinical effect (i.e., degree of seizure control, absence of side effects) and take into account that in patients with impaired renal function, a longer time may be required to establish stable plasma concentrations for each dose.

During therapy with topiramate, oligohidrosis (decreased sweating) and anhidrosis may occur. Decreased sweating and hyperthermia (increased body temperature) may occur in children exposed to high ambient temperatures. In this regard, when treating with topiramate, it is very important to adequately increase the volume of fluid intake, which can reduce the risk of developing nephrolithiasis, as well as side effects that may occur under the influence of physical activity or elevated temperatures.

Mood disorders/depression

An increased incidence of mood disorders and depression has been observed during treatment with topiramate.

Suicide attempts

When using antiepileptic drugs, including Topiramate-ALSI, the risk of suicidal thoughts and behavior increases in patients taking these drugs for any indication.

In double-blind clinical trials, the incidence of suicide-related events (suicidal ideation, suicide attempts, suicide) was 0.5% in patients receiving topiramate (46 of 8652 people), which is approximately 3 times higher than in patients receiving placebo (0.2%: 8 of 4045 people). One case of suicide was reported in a double-blind study of bipolar disorder in a patient receiving topiramate.

Thus, it is necessary to monitor patients for signs of suicidal ideation and prescribe appropriate treatment. Patients (and, if appropriate, caregivers) should be advised to seek immediate medical attention if signs of suicidal thoughts or behavior occur.

Nephrolithiasis

Some patients, especially those with a predisposition to nephrolithiasis, may have an increased risk of developing kidney stones and associated symptoms such as renal colic, kidney pain, or flank pain. To reduce this risk, an adequate increase in fluid intake is necessary. Risk factors for the development of nephrolithiasis are a history of nephrolithiasis (including family history), hypercalciuria, and concomitant therapy with drugs that contribute to the development of nephrolithiasis.

Renal dysfunction

Caution should be exercised when prescribing topiramate to patients with renal failure (creatinine clearance <70 ml/min). This is due to the fact that in such patients the clearance of the drug is reduced.

Liver dysfunction

In patients with impaired liver function, topiramate should be used with caution due to the possible decrease in clearance of this drug.

Myopia and secondary angle-closure glaucoma

When using topiramate, a syndrome has been described that includes acute myopia with concomitant secondary angle-closure glaucoma. Symptoms include acute loss of visual acuity and/or eye pain. An ophthalmological examination may reveal myopia, flattening of the anterior chamber of the eye, hyperemia (redness) of the eyeball, and increased intraocular pressure. Mydriasis may occur. This syndrome may be accompanied by fluid secretion, leading to forward displacement of the lens and iris with the development of secondary angle-closure glaucoma. Symptoms usually appear 1 month after starting use of Topiramate-ALSI. Unlike primary open-angle glaucoma, which is rarely observed in patients under 40 years of age, secondary angle-closure glaucoma is observed with the use of topiramate in both adults and children. If a syndrome involving myopia associated with angle-closure glaucoma occurs, treatment includes discontinuation of Topiramate-ALSI as soon as deemed possible by the attending physician and appropriate measures aimed at lowering intraocular pressure. Typically, these measures lead to normalization of intraocular pressure.

Increased intraocular pressure of any etiology in the absence of adequate treatment can lead to serious complications, including loss of vision.

When prescribing topiramate to patients with a history of eye diseases, it is necessary to assess the ratio of the expected benefit to the possible risk of use.

Visual field defects

Visual field defects have been observed in patients taking topiramate, regardless of whether they had elevated intraocular pressure. In clinical studies, most of these cases were reversible, and visual field defects disappeared after discontinuation of topiramate therapy. If vision problems occur while taking topiramate, discontinuation of therapy should be considered.

Metabolic acidosis

When using topiramate, hyperchloremic, not associated with anion deficiency, metabolic acidosis (for example, a decrease in plasma bicarbonate concentrations below normal levels in the absence of respiratory alkalosis) may occur. This decrease in serum bicarbonate concentrations is a consequence of the inhibitory effect of topiramate on renal carbonic anhydrase. In most cases, a decrease in the concentration of bicarbonates occurs at the beginning of taking the drug, although this effect can occur at any time during treatment with topiramate. The degree of reduction in concentrations is usually mild to moderate (average value is 4 mmol/L when used in adult patients at a dose higher than

100 mg per day and about 6 mg per day per kg of body weight when used in pediatric practice). In rare cases, patients experienced a decrease in bicarbonate concentrations below 10 mmol/l. Certain diseases or treatments that predispose to the development of acidosis (eg, kidney disease, severe respiratory disease, status epilepticus, diarrhea, surgery, ketogenic diet, certain medications) may be additional factors that enhance the bicarbonate-lowering effect of topiramate.

In children, chronic metabolic acidosis can lead to growth retardation. The effect of topiramate on growth and possible complications related to the skeletal system have not been systematically studied in children and adults.

In connection with the above, when treating with topiramate, it is recommended to carry out the necessary studies, including determination of the concentration of bicarbonates in the serum. If symptoms of metabolic acidosis occur (eg, deep Kussmaul breathing, dyspnea, anorexia, nausea, vomiting, fatigue, tachycardia or arrhythmia), determination of serum bicarbonate concentrations is recommended. If metabolic acidosis occurs and persists, it is recommended to reduce the dose or discontinue topiramate.

Cognitive impairment

Impairment of cognitive functions in epilepsy is multifactorial in nature and can be caused by the underlying cause of the disease, epilepsy itself or antiepileptic therapy. In adult patients taking topiramate, cases of cognitive impairment requiring dose reduction or discontinuation of therapy have been reported. Data on the effects of topiramate on cognitive function in children are insufficient, and its effects require further study.

Hyperammonemia and encephalopathy

When using topiramate, the development of hyperammonemia with or without encephalopathy was observed (see section “Side effects”). The risk of developing hyperammonemia with topiramate is dose-dependent. Hyperammonemia is more often observed with simultaneous use of topiramate and valproic acid (see section “Other drug interactions”).

Clinical symptoms of hyperammonemic encephalopathy often include severe impairment of consciousness and/or cognitive function and lethargy. In most cases, hyperammonemic encephalopathy regresses when therapy is discontinued. In patients with developed lethargy or unexplained changes in mental status receiving topiramate as monotherapy or as part of combination therapy, it is recommended to take into account the possibility of hyperammonemic encephalopathy and determine the level of ammonia in the blood.

Enhanced nutrition

If a patient loses weight during treatment with Topiramate-ALSI, then it is necessary to consider the advisability of enhanced nutrition.

Impact on the ability to drive vehicles and machinery

Topiramate-ALSI acts on the central nervous system and may cause drowsiness, dizziness and other symptoms. It can also cause vision problems. These adverse events may pose a danger to patients driving cars and moving machinery, especially during the period until the patient’s response to the drug is established.

Active ingredient

Topiramate

Composition

One film-coated tablet contains:

active ingredient: topiramate – 25.0 mg;

excipients: microcrystalline cellulose – 31.4 mg, pregelatinized starch – 23.0 mg, magnesium stearate – 0.4 mg, colloidal silicon dioxide (aerosil) – 0.2 mg,

tablet shell: opadry II yellow (85F32830) – 3.2 mg (polyvinyl alcohol – 1.28 mg, macrogol (polyethylene glycol) – 0.65 mg, talc – 0.47 mg, titanium dioxide – 0.23 mg, dye quinoline yellow aluminum varnish – 0.53 mg and dye sunset yellow aluminum varnish – 0.04 mg).

Contraindications

Hypersensitivity to the active substance and to other components of the drug;

Children under 3 years of age;

The use of topiramate for the prevention of migraine attacks is contraindicated during pregnancy, as well as in women with preserved childbearing potential who do not use reliable methods of contraception.

With caution

It should be used with caution in case of renal and liver failure, nephrourolithiasis (including in the past or family history), hypercalciuria.

Side Effects

Adverse reactions are given with a distribution by frequency and organ system. The frequency of adverse reactions was classified as follows: very often (≥1/10); often (from ≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (from ≥1/10,000 to <1/1,000); very rare (< 1/10,000, including isolated cases) and frequency unknown (frequency cannot be estimated from available data).

The most common adverse reactions (the frequency of which was more than 5% and exceeded that in the placebo group for at least one of the indications during controlled clinical trials of topiramate) are: anorexia, decreased appetite, slow thinking, depression, impaired free speech, insomnia, impaired motor coordination, impaired concentration, dizziness, dysarthria, dysgeusia, hypoesthesia, retardation, memory impairment, nystagmus, paresthesia, somnolence, tremor, diplopia, blurred vision, diarrhea, nausea, fatigue, irritability and weight loss.

Infectious and parasitic diseases: very often – nasopharyngitis*.

Disorders of the blood and lymphatic system: often – anemia; uncommon – leukopenia, lymphadenopathy, thrombocytopenia, eosinophilia; rarely – neutropenia*.

Immune system disorders: often – hypersensitivity; frequency unknown – allergic edema*, conjunctival edema*.

Metabolic and nutritional disorders: often – anorexia, decreased appetite; uncommon – metabolic acidosis, hypokalemia, increased appetite, polydipsia; rarely – hyperchloremic acidosis, hyperammonemia, hyperammonemic encephalopathy.

Mental disorders: very often – depression; often – slow thinking, insomnia, impaired speech, anxiety, confusion, disorientation, aggressive reactions, mood disorders, agitation, emotional lability, depressed mood, anger, behavioral disturbances; uncommon – suicidal thoughts, suicide attempts, hallucinations, psychotic disorders, auditory hallucinations, visual hallucinations, apathy, difficulty speaking, sleep disturbances, affective lability, decreased libido, agitation, crying, dysphemia, euphoric mood, paranoia, perseveration of thinking, panic attacks, tearfulness, impaired reading skills, difficulty falling asleep, flattening emotions, pathological thinking, loss of libido, lethargy, intrasomnic disorder, absent-mindedness, early morning awakenings, panic reactions, high spirits; rarely – mania, panic disorder, feelings of hopelessness*, hypomania.

Nervous system disorders: very often – paresthesia, drowsiness, dizziness; often – impaired concentration, memory impairment, amnesia, cognitive disorders, impaired thinking, psychomotor impairment, convulsions, incoordination, tremor, lethargy, hypoesthesia, nystagmus, dysgeusia, impaired sense of balance, dysarthria, intention tremor, sedation; uncommon – depressed consciousness, tonic-clonic seizures of the “grand mal” type, visual field impairment, complex partial seizures, speech impairment, psychomotor hyperactivity, fainting, sensory disturbances, drooling, hypersomnia, aphasia, repetitive speech, hypokinesia, dyskinesia, postural dizziness, poor quality of sleep, burning sensation, loss of sensitivity, parosmia, cerebral syndrome, dysesthesia, hypogeusia, stupor, clumsiness, aura, ageusia, dysgraphia, dysphasia, peripheral neuropathy, presyncope, dystonia, sensation of “pins and needles” throughout the body; rarely – apraxia, disturbance of the circadian rhythm of sleep, hyperesthesia, hyposmia, anosmia, essential tremor, akinesia, lack of reactions to stimuli.

Visual disturbances: often – blurred vision, diplopia, visual impairment; uncommon – decreased visual acuity, scotoma, myopia*, strange sensations in the eyes*, dry eyes, photophobia, blepharospasm, increased lacrimation, photopsia, mydriasis, presbyopia; rarely – one-sided blindness, transient blindness, glaucoma, impaired accommodation, impaired visual spatial perception, atrial scotoma, eyelid edema*, night blindness, amblyopia; frequency unknown – angle-closure glaucoma*, maculopathy*, eye mobility disorders*.

Hearing disorders and labyrinthine disorders: often – vertigo, tinnitus, ear pain; uncommon – deafness, one-sided deafness, sensorineural deafness, ear discomfort, hearing impairment.

Cardiac disorders: uncommon – bradycardia, sinus bradycardia, palpitations.

Vascular disorders: uncommon – hypotension, orthostatic hypotension, hot flashes, hot flushes; rarely – Raynaud’s phenomenon.

Disorders of the respiratory system, chest and mediastinal organs: often – shortness of breath, nosebleeds, nasal congestion, rhinorrhea, cough *; infrequently – shortness of breath on exertion, hypersecretion in the paranasal sinuses, dysphonia.

Gastrointestinal disorders: very often – nausea, diarrhea; often – vomiting, constipation, pain in the epigastric region, dyspepsia, abdominal pain, dry mouth, stomach discomfort, impaired sensitivity in the oral cavity, gastritis, abdominal discomfort; uncommon – pancreatitis, flatulence, gastroesophageal reflux, pain in the lower abdomen, decreased sensitivity in the oral cavity, bleeding gums, bloating, discomfort in the epigastric region, sensitivity in the abdominal area, hypersalivation, pain in the oral cavity, bad breath, glossodynia.

Disorders of the liver and biliary tract: rarely – hepatitis, liver failure.

Disorders of the skin and subcutaneous tissues: often – alopecia, rash, itching; infrequently – anhidrosis, impaired sensitivity in the facial area, urticaria, erythema, generalized itching, macular rash, skin pigmentation disorder, allergic dermatitis, facial swelling; uncommon – Stevens-Johnson syndrome*, erythema multiforme*, change in skin odor, periorbital edema*, localized urticaria; frequency unknown – toxic epidermal necrolysis*.

Musculoskeletal and connective tissue disorders: often – arthralgia, muscle spasms, myalgia, muscle cramps, muscle weakness, musculoskeletal chest pain; uncommon – joint swelling*, muscle stiffness, side pain, muscle fatigue; rarely – discomfort in the limbs*.

Renal and urinary tract disorders: often – nephrolithiasis, pollakiuria, dysuria; uncommon – exacerbation of urolithiasis (kidney stones), stress urinary incontinence, hematuria, urinary incontinence, frequent urge to urinate, renal colic, pain in the kidney area; rarely – exacerbation of urolithiasis (stones in the urethra), renal tubular acidosis*.

Disorders of the genital organs and breast: uncommon – erectile dysfunction, sexual dysfunction.

General disorders and disorders at the injection site: very often – fatigue; often – increased body temperature, asthenia, irritability, gait disturbances, poor health, anxiety; uncommon – hyperthermia, thirst, flu-like syndrome*, slowness, cold extremities, feeling of intoxication, feeling of restlessness; rarely – facial swelling, calcification.

Impact on the results of laboratory and instrumental studies: very often – loss of body weight; often – weight gain*; uncommon – crystalluria, abnormal tandem gait test result, leukopenia, increased activity of liver enzymes in the blood serum; rarely – a decrease in the content of bicarbonates in the blood.

Influence on social factors: infrequently – learning disability.

* – adverse reaction was registered in the post-registration period from spontaneous reports. Frequency calculated based on data from clinical studies.

Special groups:

Children:

Below is a list of adverse reactions that, during controlled clinical studies, were recorded in children 2 or more times more often than in adults: decreased appetite, increased appetite, hyperchloremic acidosis, hypokalemia, behavioral disturbances, aggressive reactions, apathy, difficulty falling asleep, suicidal ideation, impaired concentration, lethargy, disturbance of the circadian rhythm of sleep, poor quality of sleep, increased lacrimation, sinus bradycardia, poor health, gait disturbances.

The following is a list of adverse reactions that were reported only in children during controlled clinical trials: eosinophilia, psychosis

Interaction

Effect of topiramate on concentrations of other antiepileptic drugs (AEDs)

Concomitant use of topiramate with other AEDs (phenytoin, carbamazepine, valproic acid, phenobarbital, primidone) does not affect the values ​​of their equilibrium concentrations in plasma, with the exception of certain patients in whom the addition of topiramate to phenytoin may cause an increase in the concentration of phenytoin in plasma. This may be due to inhibition of a specific polymorphic isoform of the cytochrome P450 enzyme (CYP2C19 isoenzyme). Therefore, phenytoin plasma concentrations should be monitored in any patient taking phenytoin who develops clinical signs or symptoms of toxicity. In a pharmacokinetic study in patients with epilepsy, the addition of topiramate to lamotrigine did not affect the steady-state concentration of the latter at doses of topiramate 100-400 mg per day. During therapy and after discontinuation of lamotrigine (average dose 327 mg per day), the equilibrium concentration of topiramate did not change.

Effect of other antiepileptic drugs on topiramate concentrations

Phenytoin and carbamazepine reduce plasma concentrations of topiramate. The addition or removal of phenytoin or carbamazepine during treatment with Topiramate-ALSI may require a change in the dose of the latter. The dose should be selected based on achieving the desired clinical effect. The addition or removal of valproic acid does not cause clinically significant changes in plasma concentrations of topiramate and, therefore, does not require a change in the dose of Topiramate-ALSI.

Other drug interactions

Digoxin: In a single-dose study, the area under the plasma concentration-time curve (AUC) of digoxin was reduced by 12% during concomitant administration of topiramate. The clinical significance of this observation is unclear. When prescribing or discontinuing Topiramate-ALSI in patients taking digoxin, special attention should be paid to monitoring serum digoxin concentrations.

CNS depressants: The effects of concomitant use of topiramate with alcohol or other CNS depressants have not been studied in clinical trials. It is recommended not to take Topiramate-ALSI together with alcohol or other drugs that cause depression of central nervous system function.

St. John’s wort

When taking topiramate and drugs based on St. John’s wort (Hypericum perforatum L.) together, the plasma concentration of topiramate may decrease and, as a result, the effectiveness of the drug may also decrease. Clinical studies of the interaction of the drug Topiramate-ALSI and drugs based on St. John’s wort have not been conducted.

Oral contraceptives: In a drug interaction study with oral contraceptives that used a combination product containing norethisterone (1 mg) and ethinyl estradiol (35 mcg), topiramate at doses of 50-800 mg per day did not significantly affect the effectiveness of norethisterone and dosages

50-200 mg per day – for the effectiveness of ethinyl estradiol. A significant dose-dependent decrease in the effectiveness of ethinyl estradiol was observed at doses of topiramate

200-800 mg per day. The clinical significance of the described changes is unclear. The risk of decreased contraceptive effectiveness and increased breakthrough bleeding should be taken into account in patients taking oral contraceptives in combination with Topiramate-ALSI. Patients taking estrogen-containing contraceptives should be informed of any changes in the timing and nature of menstruation. The effectiveness of contraceptives may be reduced even in the absence of breakthrough bleeding.

Lithium: In healthy volunteers, a 18% reduction in lithium AUC was observed when co-administering topiramate 200 mg daily. In patients with manic-depressive psychosis, the use of topiramate in doses up to 200 mg per day did not affect the pharmacokinetics of lithium, however, at higher doses (up to 600 mg per day), the AUC of lithium was increased by 26%. When using topiramate and lithium simultaneously, the concentration of the latter in the blood plasma should be monitored.

Risperidone: Drug interaction studies conducted with single and multiple doses of topiramate in healthy volunteers and patients with bipolar disorder yielded similar results. When co-administered with topiramate at doses of 250 or 400 mg per day, the AUC of risperidone taken at doses of 1-6 mg per day is reduced by 16% and 33%, respectively. At the same time, pharmacokinetics

9-hydroxyrisperidone did not change, and the total pharmacokinetics of the active substances (risperidone and 9-hydroxyrisperidone) changed slightly. The change in systemic exposure of risperidone/9-hydroxyrisperidone and topiramate was not clinically significant and this interaction is unlikely to be of clinical significance.

Hydrochlorothiazide: Drug interactions were assessed in healthy volunteers with the separate and combined use of hydrochlorothiazide (25 mg) and topiramate (96 mg). Study results showed that when topiramate and hydrochlorothiazide were taken concomitantly, the maximum concentration of topiramate increased by 27% and the area under the AUC curve of topiramate increased by 29%.

The clinical significance of these studies has not been established. Prescribing hydrochlorothiazide to patients taking topiramate may require a dose adjustment of topiramate. The pharmacokinetic parameters of hydrochlorothiazide were not significantly altered by concomitant therapy with topiramate.

Metformin: Drug interactions were assessed in healthy volunteers receiving metformin or a combination of metformin and topiramate. Study results showed that when topiramate and metformin were co-administered, the maximum concentration and area under the AUC curve of metformin increased by 18% and 25%, respectively, while the clearance of metformin when used concomitantly with topiramate decreased by 20%.

Topiramate had no effect on the time to reach maximum metformin plasma concentrations. The clearance of topiramate is reduced when used concomitantly with metformin. The extent of the observed changes in clearance has not been studied. The clinical significance of the effect of metformin on the pharmacokinetics of topiramate is unclear. If Topiramate-ALSI is added or discontinued in patients receiving metformin, the patient’s condition should be carefully monitored to assess the course of diabetes mellitus.

Pioglitazone: Drug interactions were assessed in healthy volunteers with the separate and concomitant use of pioglitazone and topiramate. A decrease in the area under the AUC curve of pioglitazone by 15% was detected, without changing the maximum concentration of the drug. These changes were not statistically significant. The active hydroxymetabolite pioglitazone also showed a 13% and 16% decrease in maximum concentration and AUC, respectively, and the active ketometabolite showed a 60% decrease in maximum concentration and AUC. The clinical significance of these data is unclear. When patients use Topiramate-ALSI and pioglitazone simultaneously, the patient’s condition should be carefully monitored to assess the course of diabetes mellitus.

Glibenclamide: A drug interaction study was conducted to examine the pharmacokinetics of glibenclamide (5 mg daily) at steady state, administered alone or concomitantly with topiramate (150 mg daily) in patients with type 2 diabetes mellitus. When topiramate was used, the AUC of glibenclamide decreased by 25%. Systemic exposure to 4-trans-hydroxy-glibenclamide and 3-cis-hydroxy-glibenclamide was also reduced (by 13% and 15%, respectively). Glibenclamide did not affect the pharmacokinetics of topiramate at steady state. A statistically insignificant decrease in the AUC of pioglitazone by 15% was detected with no change in Cmax. When prescribing topiramate to patients receiving glibenclamide (or prescribing glibenclamide to patients receiving topiramate), the patient’s condition should be carefully monitored to assess the course of diabetes mellitus.

Other drugs: simultaneous use of Topiramate-ALSI with drugs that predispose to nephrolithiasis may increase the risk of kidney stones. During treatment with Topiramate-ALSI, the use of drugs that predispose to nephrolithiasis should be avoided, as they may cause physiological changes that contribute to nephrolithiasis.

Valproic acid: The combined use of topiramate and valproic acid in patients who tolerate each drug separately is accompanied by hyperammonemia with or without encephalopathy. In most cases, symptoms and signs disappear after stopping one of the medications. This adverse reaction is not due to a pharmacokinetic interaction.

When topiramate and valproic acid are taken together, hypothermia (an unintentional decrease in body temperature below 35°C) may occur in combination with hyperammonemia or independently. This phenomenon can occur both after the start of co-administration of valproic acid and topiramate, and with an increase in the daily dose of topiramate.

Additional drug interaction studies: A number of clinical studies have been conducted to evaluate potential drug interactions between topiramate and other drugs.

Overdose

Symptoms

Signs and symptoms of topiramate overdose: convulsions, drowsiness, speech and vision disturbances, diplopia, impaired thinking, impaired motor coordination, lethargy, stupor, hypotension, abdominal pain, dizziness, agitation and depression. In most cases, the clinical consequences were not severe, but deaths have been reported after overdose using a mixture of several drugs, including topiramate. An overdose of topiramate can cause severe metabolic acidosis (see section “Special Instructions”).

There is a known case of overdose when the patient took a dose of topiramate from 96 to 110 g, which resulted in a coma that lasted 20-24 hours. After 3-4 days, the patient’s condition returned to normal.

Treatment

In case of acute overdose of topiramate, if the patient has eaten shortly before, it is necessary to immediately rinse the stomach or induce vomiting. Activated carbon has been shown to adsorb topiramate in in vitro studies. If necessary, symptomatic therapy should be carried out. An effective way to remove topiramate from the body is hemodialysis. Patients are advised to adequately increase their fluid intake.

Storage conditions

In a place protected from light, at a temperature not exceeding 25 °C.
Keep out of the reach of children.

Shelf life

2 years.
Do not use after the expiration date stated on the package.

Manufacturer

ALSI Pharma, Russia