Kornam, tablets 2 mg 20 pcs
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Cornam is a blocker of peripheral postsynaptic a1 adrenoreceptors.
Induces dilation of arterioles and venules, decreases OPPS and venous return to the heart, resulting in a decrease of BP.
The hypotensive effect lasts for 24 hours after a single dose of the drug.
Blocking a1 adrenoreceptors of smooth muscles of prostate and bladder neck promotes normalization of urination in patients with benign prostatic hyperplasia.
The drug helps normalize lipid metabolism: it reduces cholesterol, triglycerides and low and very low density lipoproteins in the blood while increasing the amount of high density lipoproteins.
With systematic use of Kornam there is regression of left ventricular hypertrophy.
Indications
Active ingredient
Composition
1 tablet contains terazosin (in the form of dihydrate hydrochloride) 2 or 5 mg;
20 pieces in a pack.
How to take, the dosage
In benign prostatic hyperplasia, the initial dose is 1 mg once daily before bedtime.
Gradually the dose is increased to 2-10 mg/day until optimal effect is achieved.
Therapeutic effect is usually noted in 2 weeks from the start of treatment.
The course of treatment should be 4-6 weeks to achieve a stable effect.
In case of arterial hypertension, the drug is prescribed in the initial dose of 1 mg/day before bedtime.
Gradually the dose is increased until the clinical effect is achieved.
The maintenance dose is 1-10 mg once a day.
The maximum daily dose is 20 mg.
In case of temporary discontinuation of the drug the treatment is resumed according to the same scheme.
Interaction
In concomitant use of Kornam and beta-adrenoblockers, diuretics, calcium channel blockers, ACE inhibitors may increase the antihypertensive effect. Special caution is required when concomitant administration of terazosin and antihypertensive drugs of central action.
The absorption of terazosin is reduced with concomitant administration of adsorbents and antacids.
Adrenomimetics weaken the effect of terazosin.
Concomitant use of terazosin and NSAIDs may decrease antihypertensive effect due to inhibition of prostaglandin synthesis and retention of fluid and sodium ions.
Special Instructions
To prevent the development of orthostatic arterial hypotension, treatment should begin with administration of Kornam at a dose of 1 mg/day before bedtime, after which the patient should be in bed for 6-8 hours.
The risk of orthostatic arterial hypotension (“first-dose effect”) is highest within 30-90 minutes after drug administration and increased in patients receiving beta-adrenoblockers and diuretics simultaneously, with decreased RBC, hyposolic diet, and when resuming treatment with the drug after a break (several days).
In case of temporary discontinuation of treatment, therapy is resumed with the same dose. In the course of treatment the level of specific antigen of the prostate gland does not change. Before initiating therapy of benign prostatic hyperplasia, prostate cancer must be excluded.
The patient must be informed about the increased risk of orthostatic hypotension with alcohol consumption, prolonged standing or exercise, and hot weather.
Within 12 hours after the first dose, after increasing the dose, or after discontinuing therapy, it is not recommended to engage in potentially hazardous activities that require increased attention and quick psychomotor reactions.
Contraindications
With caution, prescribe the drug in angina, CHD, hepatic or renal failure, impaired cerebral circulation, type 1 diabetes.
Side effects
Cardiovascular system: rare – orthostatic hypotension.
CNS: drowsiness, dizziness, asthenia.
Others: nasal congestion.
Cardiovascular system side: orthostatic hypotension – “first-dose effect” (observed in 1% of patients, mostly receiving concomitant diuretics or beta-adrenoblockers), manifested by dizziness, tachycardia, fainting may occur; rarely – palpitations, peripheral edema, nasal congestion.
CNS: rarely – dizziness, asthenia, somnolence, visual perception failure.
Blood system: decrease (associated with hemodilution) of hematocrit, hemoglobin, leukopenia, hypoproteinemia, hypoalbuminemia.
Other: rare – decreased potency, nausea.
Overdose
Symptoms: marked BP decrease, impaired coordination of movements, fainting.
Treatment: the patient should be laid down with the head end of the bed.
If necessary, prescribe hypertensive agents, IV fluid administration.
Hemodialysis is not effective.
Similarities
Weight | 0.014 kg |
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Shelf life | 3 years |
Conditions of storage | At a temperature not exceeding 25 °C |
Manufacturer | Lek d.d., Slovenia |
Medication form | pills |
Brand | Lek d.d. |
Other forms…
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