Anafranil® sr
It is known that tricyclic antidepressants reduce the threshold for convulsive readiness, therefore Anafranil should be used with extreme caution in patients with epilepsy, as well as in the presence of other factors predisposing to the occurrence of convulsive syndrome, for example, brain damage of any etiology, while using antipsychotic drugs, during the period of withdrawal from alcohol or withdrawal from drugs that have anticonvulsant properties (for example, benzodiazepines). It is believed that the occurrence of seizures while taking Anafranil depends on the dose of the drug. In this regard, you should not exceed the recommended daily dose of Anafranil.
Anafranil should be prescribed with extreme caution to patients with cardiovascular diseases, especially cardiovascular failure, intracardiac conduction disorders (for example, AV block I-III degrees) or arrhythmias. In such patients, as well as in elderly patients, it is necessary to regularly monitor heart function and ECG.
Before starting Anafranil therapy, it is recommended to measure blood pressure, since patients with orthostatic hypotension or lability of the cardiovascular system may experience a sharp decrease in blood pressure.
Because the drug has anticholinergic properties, it should be used with extreme caution in patients with a history of increased intraocular pressure, angle-closure glaucoma, or urinary retention (for example, due to prostate disease).
Due to the anticholinergic action characteristic of tricyclic antidepressants, there may be a decrease in tear production and accumulation of mucous secretion, which can lead to damage to the corneal epithelium in patients using contact lenses.
Caution is necessary when treating patients with severe liver disease with tricyclic antidepressants, as well as in patients with tumors of the adrenal medulla (for example, pheochromocytoma, neuroblastoma), since in this case these drugs can provoke the development of a hypertensive crisis.
It is known that patients with cyclic affective disorders taking tricyclic antidepressants may develop manic or hypomanic states during the depressive phase. In such cases, it may be necessary to reduce the dose of Anafranil or discontinue it and prescribe antipsychotic therapy. After relief of these conditions, if indicated, treatment with Anafranil in low doses can be resumed.
In predisposed patients and elderly patients, tricyclic antidepressants can provoke the development of drug-induced delirious psychoses, mainly at night. After discontinuation of the drug, these disorders disappear within a few days.
Caution should be exercised when treating patients with hyperthyroidism or receiving thyroid hormone medications, which may have cardiotoxic effects.
Although changes in white blood cell levels during treatment with Anafranil have been reported only in isolated cases, periodic examination of peripheral blood composition and attention to symptoms such as fever and sore throat are recommended, especially in the first months of therapy or with long-term use of the drug.
Caution is required when using Anafranil in patients with chronic constipation. Tricyclic antidepressants can cause paralytic ileus, mainly in elderly patients or in patients who are forced to remain in bed.
When using Anafranil in doses exceeding the average therapeutic one, or if the concentration of clomipramine in plasma exceeds the average therapeutic one, there is a risk of prolongation of the QTc interval and the occurrence of bidirectional fusiform ventricular tachycardia (ventricular disturbances). This occurs when taken together with selective serotonin reuptake inhibitors or serotonin-norepinephrine reuptake inhibitors. In this regard, it is necessary to avoid co-administration of clomipramine and drugs that cause its accumulation. It is also necessary to avoid co-administration with drugs that cause prolongation of the QTc interval. The use of diuretics can lead to the development of hypokalemia. It has been established that hypokalemia is a risk factor for prolongation of the QTc interval and the occurrence of bidirectional fusiform ventricular tachycardia (ventricular disorders). Therefore, hypokalemia must be eliminated before starting Anafranil therapy. Anafranil should be used with caution concomitantly with selective serotonin reuptake inhibitors or serotonin-norepinephrine reuptake inhibitors, as well as with diuretics.
Due to the risk of serotonin toxicity, the recommended dosage should be adhered to and the dose should be increased with caution if Anafranil is used concomitantly with serotonergic drugs.
With simultaneous use of Anafranil with serotonergic drugs, such as selective serotonin reuptake inhibitors, serotonin and norepinephrine reuptake inhibitors, tricyclic antidepressants or lithium preparations, the development of serotonin syndrome with symptoms such as fever, myoclonus, agitation, convulsions, delirium and coma is possible. . If it is necessary to prescribe fluoxetine, it is recommended to take a two to three week break between the use of Anafranil and fluoxetine.
Many patients with panic disorders experience increased anxiety at the beginning of treatment with Anafranil. This paradoxical increase in anxiety is most pronounced in the first days of therapy and usually subsides within two weeks.
In patients with schizophrenia receiving tricyclic antidepressants, activation of psychosis is sometimes observed.
In patients with liver disease, periodic monitoring of liver enzyme activity is recommended.
Anafranil, like other tricyclic antidepressants, is prescribed in combination with electroconvulsive therapy only under close medical supervision.
Severe depression is characterized by a risk of suicidal actions, which can persist until reliable remission is achieved. Patients with depression, both adults and children, may experience increased depression and/or suicidal behavior or other psychiatric symptoms, whether or not they are receiving antidepressant therapy. Antidepressants increased the risk of suicidal ideation and behavior in short-term studies in children and adolescents with depression and other psychiatric illnesses.
All patients taking Anafranil for any indication should be monitored for worsening clinical symptoms, suicidal behavior and other psychiatric symptoms, especially during the initial phase of therapy or when the dose of the drug is changed. In such patients, changes in the treatment regimen, including possible discontinuation of the drug, should be considered, especially if such changes are pronounced, appeared suddenly, or were not observed in the patients initially.
Families and caregivers of patients (both children and adults) taking antidepressants for psychiatric or non-psychiatric indications should be warned to monitor patients due to the risk of other psychiatric symptoms, including and suicidal behavior, and immediately report such symptoms to your healthcare provider.
When writing a prescription for Anafranil, the minimum number of tablets should be specified to reduce the risk of overdose. In this case, it is necessary to follow an adequate treatment regimen.
There is evidence that while taking Anafranil, there is a lower number of deaths due to overdose than when taking other tricyclic antidepressants.
Before performing general or local anesthesia, the anesthesiologist should be warned that the patient is taking Anafranil.
An increased incidence of dental caries has been reported with long-term treatment with tricyclic antidepressants. Therefore, in case of long-term therapy with Anafranil, regular examination of the patient by a dentist is recommended.
The use of diuretics can lead to the development of hypokalemia, which increases the risk of prolongation of the QTc interval and the occurrence of bidirectional fusiform ventricular tachycardia (pirouette type). Before starting Anafranil therapy, hypokalemia must be corrected.
Abrupt withdrawal of Anafranil should be avoided, because this may lead to adverse reactions. If a decision is made to discontinue treatment, the drug should be withdrawn gradually, as quickly as the clinical situation allows. It should be borne in mind that abrupt withdrawal of the drug may be accompanied by the development of certain symptoms.
25 mg film-coated tablets contain lactose and sucrose. Patients with rare hereditary diseases such as galactose and fructose intolerance, severe lactase deficiency, sucrase-isomaltase deficiency or glucose-galactose malabsorption should not take Anafranil film-coated tablets.
It should be borne in mind that alcohol can increase adverse effects from the central nervous system, such as blurred vision and drowsiness.
Use in pediatrics
Experience of using Anafranil in children under 5 years of age
not available, therefore it is not recommended to use the drug in children of this age group.
Impact on the ability to drive vehicles and operate machinery
Patients who experience drowsiness and other central nervous system disorders (including blurred vision) while taking Anafranil should not drive a car, operate machinery, or engage in other activities that require increased attention and quick reaction.
Compound
The tablets contain 25 mg of clopyramide hydrochloride + corn starch, stearic acid, glycerol 85%, talc, copovidone, crystalline sucrose, dispersed yellow dye, microcrystalline cellulose, lactose monohydrate, colloidal silicon dioxide anhydrous, magnesium stearate, hypromellose, titanium dioxide, polyvinylpyrrolidone K30, polyethylene glycol 8000.
One ampoule of injection solution contains: 25 mg of clopyramide hydrochloride , water, glycerol.
Pharmacodynamics and pharmacokinetics
Anafranil is a tricyclic antidepressant . Its main action is to inhibit the reuptake of norepinephrine and serotonin . This process is carried out by changing the concentration of monoamines in the central nervous system and blocking n2-histamine receptors.
Clomipramine eliminates psychomotor retardation, anxiety, and bad mood. The active substance can eliminate nocturnal enuresis , which is not determined by physiological disorders, and reduces appetite. serotonin and adrenaline is being established . The therapeutic effect will be noticeable after the first week of taking the drug, reaching its effective maximum after 2-3 weeks.
When intramuscularly, the drug is well and completely absorbed. 97% of the product binds to blood plasma proteins.
The drug reaches its equilibrium maximum concentration after 2 weeks of systematic use. About 2% of the substance is found in the cerebrospinal fluid. The drug penetrates well into breast milk.
The drug is metabolized by demethylation , with the participation of the enzymes CYP3A4, CYP2C19, and CYP1A2 , the resulting metabolites are active. The period of elimination of the drug from the body is from 18 to 25 hours, depending on the method of administration.
Metabolites are excreted in urine and feces.
In elderly patients, plasma concentrations of the drug may vary significantly due to slow metabolism.
Anafranil price, where to buy
The price of Anafranil tablets is approximately 300 rubles for 30 pieces of 25 mg each.
The cost of the solution for injection is 640 rubles for 10 pieces of 2 ml.
- Online pharmacies in RussiaRussia
ZdravCity
- Anafranil tablets p.p.o.
25 mg 30 pcs Novartis Pharma S.р.A 294 RUR order - Anafranil SR tablets p.p.o. prolonged action 75 mg 10 pcs Novartis Pharma S.р.A
RUB 413 order
Overdose
An overdose of the drug can have serious consequences, especially in children. Symptoms are similar for all drugs in the tricyclic antidepressant .
Symptoms of an overdose appear within 4 hours after the drug enters the body, their maximum number and severity occurs within a day. The patient should be monitored for 5-6 days.
In case of overdose, the following are observed: drowsiness , anxiety, ataxia , convulsions , increased body temperature, coma , delirium , vomiting, respiratory depression, fever, severe decrease in blood pressure, arrhythmia and tachycardia , shock , stupor, heart failure up to complete cardiac arrest. Possible: anuria , cyanosis or oliguria .
As a therapy, it is necessary to urgently perform gastric lavage. If the patient is conscious, induce vomiting; if not, then intubate the trachea . Call an ambulance, give the victim enterosorbents ( activated carbon ). It is advisable to carry out the operations described above, even if more than 12 hours have passed since the overdose.
The drug does not have a specific antidote hemodialysis and peritoneal dialysis are not used. Therefore, they use modern methods of intensive therapy, eliminate convulsions, and perform artificial ventilation.
Side effects
Side effects of Anafranil are most often mild, somewhat similar to symptoms of depression . As a rule, effects of this kind disappear during treatment or after reducing and reaching the minimum active dosage.
If the adverse reactions are serious and threaten the patient’s life, the medication should be stopped.
Side effects are especially common and obvious in older people.
May be observed:
- drowsiness , dry mucous membranes, fatigue, sweating, increased appetite, tremor ;
- constipation , myoclonus , headache , visual disturbances, nausea, weight gain;
- paresthesia , hot flashes , palpitations, increased muscle tone or weakness, speech impairment, mydriasis ;
- tachycardia , severe decrease in blood pressure , minor distortions on the ECG , vomiting , diarrhea , epigastric pain, increased activity of liver enzymes;
- urticaria , galactorrhea , tinnitus, itching and skin rashes, enlarged mammary glands, distortion of taste;
- sleep disturbances, disorientation , hallucinations , anxiety and aggression, delirium , memory problems;
- convulsions, fever, ataxia , changes in the electroencephalogram ;
- glaucoma , intracardiac conduction , urinary retention, swelling, burning and swelling at the injection site;
- pneumonitis , anaphylactic and anaphylactoid reactions, purpura , leukopenia , thrombocytopenia , etc.
If the use of the drug is abruptly stopped, withdrawal syndrome occurs. Nausea, diarrhea, vomiting, irritability and anxiety, headaches and insomnia . The dosage should be reduced gradually.
During pregnancy and lactation
Experience with the drug in pregnant women is limited. There have been cases where taking the medication caused fetal developmental disorders. Therefore, the remedy can be prescribed as a last resort, when it is impossible to do without it.
Infants may experience withdrawal symptoms if the drug is stopped more than 7 weeks before birth. The active substance passes into breast milk, so during breastfeeding the drug should be discontinued (first gradually reduce the dosage).
Indications for use
Anafranil is prescribed:
- for the treatment of depression of various origins ( endogenous, neurotic, masked, involutional, reactive, organic depression );
- for depression in older people caused by constant severe pain or somatic diseases;
- for depressive states in psychopaths or schizophrenics ;
- for mood disorders of a neurotic, psychopathic or reactive nature;
- for the treatment of panic attacks and various phobias ;
- for catalepsy ( narcolepsy );
- for presenile and senile depression ;
- for migraine ;
- for the treatment of nocturnal enuresis not associated with other diseases.
