Tanyz^®-K (Tablets, Capsules) Instructions for Use

ATC Code

G04CA02 (Tamsulosin)

Active Substance

Tamsulosin (Rec.INN registered by WHO)

Clinical-Pharmacological Group

Drug used for urination disorders associated with benign prostatic hyperplasia. Alpha₁-adrenergic blocker

Pharmacotherapeutic Group

Drugs used in urology; drugs for the treatment of benign prostatic hyperplasia; alpha-adrenergic blockers

Pharmacological Action

Alpha₁-adrenergic receptor blocker; an agent for the symptomatic treatment of benign prostatic hyperplasia.

It selectively blocks postsynaptic alpha_1A-adrenergic receptors of the smooth muscles of the prostate gland, bladder neck, and prostatic part of the urethra. As a result, the tone of the smooth muscles of these structures decreases, facilitating urine outflow. Simultaneously, the symptoms of obstruction and irritation associated with benign prostatic hyperplasia are reduced. The therapeutic effect manifests approximately 2 weeks after the start of treatment.

Tamsulosin has a significantly lesser ability to block alpha_1B-adrenergic receptors of vascular smooth muscles, therefore its effect on systemic blood pressure is insignificant.

Pharmacokinetics

After oral administration, Tamsulosin is rapidly and almost completely absorbed from the gastrointestinal tract. After a single oral dose of 400 mcg, the C_max of the active substance in plasma is reached after 6 hours.

Plasma protein binding is 99%. The V_d is insignificant and amounts to 0.2 l/kg.

Tamsulosin is slowly metabolized in the liver to form pharmacologically active metabolites that retain high selectivity for alpha_1A-adrenergic receptors. Most of the active substance is present in the blood in unchanged form.

The T_1/2 of tamsulosin after a single dose is 10 hours, the terminal T_1/2 is 22 hours. It is excreted by the kidneys, 9% in unchanged form.

Indications

Treatment of dysuric disorders in benign prostatic hyperplasia.

ICD codes

Dosage Regimen

Take Tanyz^®-K orally as tablets or capsules.

Administer the recommended dose of 400 mcg once daily.

Take the dose at the same time every day, approximately 30 minutes after the same meal.

Swallow the tablet or capsule whole; do not crush or chew.

If a dose is missed, take it as soon as remembered on the same day. Do not take a double dose to make up for a forgotten one.

No dosage adjustment is required for mild to moderate renal impairment.

No dosage adjustment is required for mild to moderate hepatic impairment.

The therapeutic effect typically manifests after approximately 2 to 4 weeks of continuous treatment.

Continue treatment as long as therapeutic benefit is maintained.

Adverse Reactions

From the cardiovascular system palpitations, atrial fibrillation, arrhythmia, tachycardia, dyspnea, orthostatic hypotension.

From the central nervous system headache, dizziness, fainting.

From the digestive system: constipation, diarrhea, nausea, vomiting.

From the skin and subcutaneous tissues: skin rash, skin itching, urticaria, angioneurotic edema, Stevens-Johnson syndrome, multiforme erythema, exfoliative dermatitis.

From the reproductive system ejaculation disorders, priapism.

Other rhinitis, asthenia. Cases of intraoperative floppy iris syndrome (IFIS) during cataract and glaucoma surgery in patients taking Tamsulosin have been described.

Contraindications

Hypersensitivity to tamsulosin; orthostatic hypotension (including history), severe hepatic insufficiency; children and adolescents under 18 years of age.

With caution severe renal insufficiency (creatinine clearance less than 10 ml/min); arterial hypotension.

Use in Pregnancy and Lactation

Not applicable.

Use in Hepatic Impairment

Contraindicated in severe hepatic insufficiency.

Use in Renal Impairment

Should be used with caution in severe renal insufficiency (creatinine clearance < 10 ml/min).

Pediatric Use

Contraindicated in children and adolescents under 18 years of age.

Special Precautions

Before starting therapy with tamsulosin, the patient should be examined for the presence of other diseases that can cause the same symptoms as benign prostatic hyperplasia. Before starting treatment and regularly during therapy, a digital rectal examination and, if required, determination of prostate-specific antigen should be performed. In patients with impaired renal function, no dosage regimen adjustment is required.

There have been reports of cases of prolonged erection and priapism during therapy with alpha₁-adrenergic blockers. If an erection persists for more than 4 hours, immediate medical attention should be sought. If therapy for priapism is not administered immediately, it may lead to penile tissue damage and irreversible loss of potency.

In some patients taking or having previously taken Tamsulosin, the development of intraoperative floppy iris syndrome (IFIS) during cataract or glaucoma surgery is possible, which may lead to complications during surgery or in the postoperative period. It is not recommended to start tamsulosin therapy in patients who are scheduled for cataract or glaucoma surgery. During the preoperative examination of patients, the surgeon and ophthalmologist should take into account whether the patient is taking or has taken Tamsulosin. This is necessary to prepare for the possible development of intraoperative floppy iris syndrome during surgery.

Effect on the ability to drive vehicles and mechanisms

During the use of tamsulosin, patients should exercise caution when driving vehicles and mechanisms, as well as when engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.

Drug Interactions

With simultaneous use of tamsulosin with cimetidine, some increase in the plasma concentration of tamsulosin was noted, and with furosemide – a decrease in concentration; with other alpha₁-adrenergic blockers – a pronounced enhancement of the hypotensive effect is possible.

Diclofenac and indirect anticoagulants somewhat increase the elimination rate of tamsulosin.

Diazepam, propranolol, trichlormethiazide, chlormadinone, amitriptyline, diclofenac, glibenclamide, simvastatin and warfarin do not change the free fraction of tamsulosin in human plasma in vitro. In turn, Tamsulosin also does not change the free fractions of diazepam, propranolol, trichlormethiazide and chlormadinone.

In vitro studies, no interaction at the level of hepatic metabolism with amitriptyline, salbutamol, glibenclamide and finasteride was found.

Other alpha₁-adrenergic blockers, acetylcholinesterase inhibitors, alprostadil, anesthetics, diuretics, levodopa, antidepressants, beta-adrenergic blockers, slow calcium channel blockers, muscle relaxants, nitrates and ethanol may increase the severity of the hypotensive effect.

Concomitant administration of tamsulosin with potent inhibitors of the CYP3A4 isoenzyme may lead to an increase in the concentration of tamsulosin. Concomitant administration with ketoconazole led to an increase in the AUC and C_max of tamsulosin by 2.8 and 2.2 times, respectively.

Tamsulosin should not be used in combination with potent CYP3A4 inhibitors in patients with impaired metabolism of the CYP2D6 isoenzyme. Tamsulosin should be used with caution in combination with potent and moderate CYP3A4 inhibitors.

Storage Conditions

Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.

Dispensing Status

Rx Only

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.