Ravel SR

Ravel SR is an antihypertensive drug that is used as directed by a doctor. Consider the indications for its use, medicinal properties and contraindications.

Clinico-pharmacological group of the drug - diuretic and antihypertensive drugs. The drug has vasodilator, that is vasodilating, diuretic and hypotensive properties. Its pharmacological action is similar to thiazide diuretics and sulfonamide derivatives. The active ingredient, indapamide, inhibits the absorption of sodium in the cortical segment of the nephron, while increasing the excretion of urine and the renal excretion of sodium and chloride ions.

The hypotensive effect persists for 24 hours. The medicine acts on the tone of the vessels, reduces the hypertrophy of the left ventricle and reduces the resistance of the arteriol. Efficacy is maintained in patients with impaired renal function, without affecting the concentration of lipids in the blood plasma.

Ravel SR is an effective diuretic with antihypertensive properties. The drug is taken only for medical purposes, because it requires a medical prescription.

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Indications Ravel SR

Indications for use Ravel SR is the treatment and prevention of hypertension. With this disease, there are frequent headaches, flies flies before your eyes and dizziness. But it is possible to detect the disease only with the regular measurement of blood pressure.

Without timely diagnosis, treatment and use of a medicament such as Ravel SR, side effects are possible. Patients suffer from visual impairment, kidney and heart failure. In neglected cases - heart attack, stroke and other pathologies.

[2], [3]

Release form

Form release - coated tablets prolonged action. In one package contains a blister for 20, 30 or 60 pieces. One tablet contains 1.5 mg of active ingredient indapamide.

Advantages of the tablet form are that after ingestion the tablets quickly dissolve and are absorbed, having a pharmacological effect on the lesion site.

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Pharmacodynamics

Pharmacodynamics Ravel SR indicates the antihypertensive effect of the drug. Tablets have diuretic properties, since the active ingredient refers to sulfonamide derivatives and is similar to thiazide diuretics. Indapamide destroys the reabsorption of sodium ions in the renal tubules, which leads to an increased excretion of urine from chlorine and sodium ions, enhancing diuresis.

In addition to diuretic action, the active component affects the tone of the vessels. This reduces the overall peripheral and arteriolar resistance. Antihypertensive action at high doses does not affect the level of lowering blood pressure, but increases diuresis. Therapeutic doses do not affect the carbohydrate and lipid metabolism, but, like thiazide diuretics, it reduces the hypertrophy of the left ventricle.

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Pharmacokinetics

Pharmacokinetics Ravel SR are the processes occurring with the medication after administration. Indapamide is rapidly and completely absorbed from the gastrointestinal tract. Eating significantly slows down absorption, but does not affect the quality of absorption. The maximum concentration in the blood plasma is achieved 12 hours after taking a single dose. Repeated double dosage techniques cause concentration fluctuations to decrease, but this does not lead to its cumulation. Binding to plasma proteins at the level of 75-79%.

Raval is metabolized in the liver, the elimination period is 14-24 hours. 70% is excreted as metabolites, 5% unchanged and 20% with feces as inactive metabolites. If the medication is taken by patients with renal insufficiency, this does not affect the pharmacokinetics.

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Dosing and administration

The way of application and dose is individual for each patient, therefore should be selected by the attending physician. A normal dosage is 1.5 mg once a day, that is, one tablet a day.

It is desirable to take the drug in the morning, squeezed with enough liquid. At elevated doses, medical supervision, control of heart rate and blood pressure are required.

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Use Ravel SR during pregnancy

Use of Ravel SR during pregnancy is not recommended. The drug can cause fetoplacental ischemia with the risk of delayed fetal development. Tablets are forbidden to use during the period of breastfeeding, since the active substance is excreted with the mother's milk.

The use of an antihypertensive drug is possible only if the therapeutic benefit for a woman is more important than the potential risk to the fetus. As a rule, instead of dangerous preparations, future mothers are prescribed safer means that will not harm the fetus and the female body.

Contraindications

Contraindications to the use of Ravel SR are based on the action of the active components of the pharmaceutical agent. Tablets are not used for such disorders as:

• Individual intolerance to drug components
• Hypersensitivity to sulfonamides
• Impaired liver function
• Severe renal insufficiency
• Hepatic encephalopathy
• Hypokalemia
• Children's age of patients
• Pregnancy and lactation.

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Side effects Ravel SR

Side effects of Ravel SR occur at elevated dosages or exceed the recommended treatment period. The medicine can cause arrhythmia, increased heart rate, orthostatic hypotension and hypokalemia (changes on the ECG). Most often, patients complain of headaches, nervousness, dizziness, asthenia, abdominal pain. In addition, constipation, diarrhea, dyspepsia, hepatic encephalopathy are possible.

Violations arise from all organs and systems. On the part of the urinary system, this manifests itself as polyuria, frequent infectious diseases and nocturia. Allergic reactions are possible, that is, itching, hives, spotted-papular rash and hemorrhagic vasculitis. Tablets provoke cough, sinusitis, metabolic disorders and hematopoiesis. In rare cases, the aggravation of lupus erythematosus is possible.

If Ravel is prescribed to patients with impaired liver function, but this can cause encephalopathy and the diuretic should be discontinued. Long-term treatment causes the development of hyponatremia. With insufficient nutrition and simultaneous use of several drugs by elderly patients and people with ascites, heart failure or liver cirrhosis, medical control and prevention of hypokalemia are required. 

Overdose

Overdose is possible with prolonged use of the drug and exceeding the recommended dosage. Symptoms of acute poisoning are manifested as violations of water-electrolyte balance, that is hypokalemia and hyponatremia. In addition, nausea, vomiting, dizziness, headaches, confusion, convulsions, drowsiness are possible.

Treat an overdose of gastric lavage. Patients need to take activated charcoal or any other absorbent. It also requires restoration of the water-electrolyte balance. With other adverse symptoms, symptomatic therapy is performed according to the indications.

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Interactions with other drugs

Interactions Ravel SR with other drugs is possible on medical indications. Tablets are not used with lithium preparations, as this reduces the release of lithium by the kidneys. When administered with amphotericin B for intravenous administration, stimulant laxatives or mineralocorticoids, there is a risk of an additive effect. With special care prescribe medicines digitalis and baclofen, since it increases hypotensive effect.

If the drug is used with potassium-sparing diuretics, then patients with diabetes and kidney failure may develop hyperkalemia. It requires regular monitoring of the concentration of potassium in the blood plasma and ECG parameters. Antiarrhythmics can provoke polymorphic ventricular tachycardia and bradycardia. At simultaneous application with neuroleptics and tricyclic antidepressants there is a risk of additive action.

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Storage conditions

The storage conditions for Ravel SR are similar to those for other tableted preparations. Storage temperature should not exceed 25 ° C. The drug should be kept in a dry place, protected from sunlight and inaccessible to children.

Tablets should be in their original packaging. If the above rules are not observed, the medicament loses its medicinal properties and is prohibited for use.

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Shelf life

Shelf life is 24 months from the date of issue (indicated on the packaging). At the end of the tablets are forbidden to take. If the medicine has changed color or has got an unpleasant smell it needs to be disposed of.

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