Encorate chrono, 300 mg 30 pcs

Valproate has anticonvulsant activity for various degrees of epilepsy in humans.

In addition, the drug has no pronounced hypnotic or sedative effects and does not have a depressant effect on the respiratory center.

Encorate Chrono has no negative effect on blood pressure, heart rate, renal function and body temperature.

Indications

Treatment of generalized or partial epilepsy, especially in the following types of seizures:

Partial epilepsy:

Specific syndromes (West, Lennox-Gastaud)

Active ingredient

Composition

Associates:

Hypromellose-K100M (metocel-K100M),

Hypromellose-K15M (metocel-K15M),

starch (dried),

Purified talc,

Magnesium stearate,

Silicon dioxide colloid.

Composition of the shell:

Methacrylate, dimethylaminoethyl methacrylate and butyl methacrylate copolymer (Eudragite E100), titanium dioxide, polyethylene glycol 6000, sodium lauryl sulfate, sunset yellow dye.

How to take, the dosage

The dosing regimen is adjusted individually according to the patient’s age and weight.

Monitherapy:

Adults: The initial dose is 600 mg/day. Increase the dosage by 200 mg every three days until optimal effect is achieved.

The tablets should be swallowed whole with a small amount of water. It should be taken 1 to 2 times a day. The maximum recommended dose is 1 to 2 g.

In children with a body weight over 20 kg: The initial dose is 400 mg/day. Increase gradually until optimal dosage is reached, usually 20-30 mg/kg once daily or in two separate doses.

Children with a body weight less than 20 kg. Enkorat Chrono should not be used in children in this category.

Elderly patients: it is characteristic that the volume of distribution increases and the plasma volume decreases. However, in normal hepatic and renal function this increase in free drug volume is not clinically significant. Dosing regimen of Encorate chrono in elderly patients is similar to that in adults and is chosen individually. In patients in whom the required therapeutic effect is achieved with Enkorat tablet therapy, Enkorat Chrono may be used in appropriate daily dosage regimen.

Interaction

Valproate alters plasma concentrations of phenytoin and lamotrigine.

In combination with anticoagulants and acetylsalicylic acid derivatives increases inhibition of platelet aggregation.

Valproate increases the effect of antipsychotic drugs, anticonvulsants and antidepressants.

Unlike other anticonvulsants, valproate does not cause induction of hepatic enzymes, so it does not decrease the effectiveness of oral contraceptives.

When valproate and warfarin are used together the percentage of plasma protein binding of the latter decreases.

Special Instructions

Caution should be exercised when operating machinery, because the drug weakens attention. Transaminases, bilirubin, blood platelets, amylase levels should be monitored regularly (every 3 months).

Valproic acid inhibits platelet aggregation, which increases the risk of increased clotting time in bleeding. The possibility of bleeding-related complications in operated patients receiving valproate should be considered. In patients taking valproate for a long time, spontaneous hematomas and bleeding may develop. If this occurs, the drug should be discontinued immediately.

Valproate may cause drug-induced pancreatitis and impaired liver function (usually in the first 6 months of use). In this regard, during the first 6 months of treatment it is necessary to monitor the condition of the pancreas, conduct hepatic tests, monitor prothrombin levels. Impairment of liver function, hepatic failure during valproate therapy is sometimes observed in children with epilepsy and combined metabolic and degenerative diseases, organic pathology of brain tissue and delayed mental development. In case of symptoms such as marked weakness, lethargy, edema, vomiting and jaundice, the drug should be stopped immediately, marked weakness, lethargy, edema, vomiting and jaundice, the drug should be stopped immediately. Use during pregnancy and lactation period:

The drug may be administered to pregnant women only when the anticipated benefit to the mother exceeds the potential risk to the fetus. In case the drug is administered during pregnancy, specialized prenatal fetal monitoring is mandatory. Valproate administration during breastfeeding is not recommended.

Contraindications

Perhaps with liver disorders

It is contraindicated in severe liver function, acute hepatitis.

Performance in elderly patients

Elderly patients: characteristically, the volume of distribution increases and the plasma volume decreases. However, with normal hepatic and renal function this increase in free drug volume is not clinically significant. Dosing regimen of Encorate chrono in elderly patients is similar to that in adults and is chosen individually. In patients in whom the required therapeutic effect is achieved with Enkorat tablet therapy, Enkorat Chrono may be used in appropriate daily dosage regimen.

Side effects

In rare cases, the following side effects have been reported:

Overdose

Rare cases of accidental or intentional overdose of the drug have been reported. Nausea, vomiting, dizziness, diarrhea, respiratory depression, hyporeflexia, coma have been observed.

First aid: gastric lavage, administration of activated charcoal. If necessary – inpatient treatment with symptomatic therapy, hemodialysis.

Pregnancy use

The drug may be administered to pregnant women only when the expected benefits to the mother exceed the potential risk to the fetus. In case of taking the drug during pregnancy, specialized prenatal monitoring of the fetus is obligatory.

The use of valproate during breastfeeding is not recommended.

Pediatric use

Encorate Chrono should not be used in children with a body weight less than 20 kg.

Similarities