Medicinal Products

PERINDOPRIL / INDAPAMIDE KRKA 2 mg / 0.625 mg

Generic drug from Preterax
Therapeutic class: Cardiology and angiology
active ingredients: Perindopril, Indapamide
laboratory: Krka DD

Compressed
Box of 90
All forms

Indication

Treatment of essential hypertension.

DOSAGE PERINDOPRIL / INDAPAMIDE KRKA 2 mg / 0.625 mg Tablet Box of 90

Oral way.

The usual dose is one tablet of PERINDOPRIL / INDAPAMIDE KRKA per day in a single dose, preferably in the morning and before meals. If blood pressure is not controlled after one month of treatment, the dosage can be doubled.

Elderly (see section Warnings and precautions for use )

Treatment should be initiated at the normal dose of one PERINDOPRIL / INDAPAMIDE KRKA tablet per day.

Patients with renal impairment (see Warnings and Precautions section )

In severe renal impairment (creatinine clearance <30 ml / min), treatment is contraindicated. In patients with moderate renal impairment (creatinine clearance 30-60 ml / min), the maximum dose is one PERINDOPRIL / INDAPAMIDE KRKA tablet per day. In patients with a creatinine clearance greater than or equal to 60 ml / min, no dose adjustment is required.

Current medical practice includes periodic monitoring of creatinine and potassium.

Patients with hepatic impairment (see section 4.3). Contraindications, Warnings and Precautions for Use and Pharmacokinetic Properties

In case of severe hepatic impairment, treatment is contraindicated.

In patients with moderate hepatic impairment, no dose adjustment is required.

Child and teenager

PERINDOPRIL / INDAPAMIDE KRKA should not be used in children and adolescents because the efficacy and safety of perindopril in children and adolescents, alone or in combination, have not been established.

Against indications

Perindopril-related

Hypersensitivity to perindopril or other ACE inhibitors

· History of angioedema (Quincke's edema) related to taking an IEC

· Hereditary or idiopathic angioedema

· Second and third trimesters of pregnancy (see sections Warnings and precautions for use and Pregnancy and lactation ).

Linked to indapamide

· Hypersensitivity to indapamide or other sulfonamides

· Severe renal insufficiency (creatinine clearance <30 ml / min)

· Hepatic encephalopathy

· Severe hepatic insufficiency

· Hypokalemia

· This medication is generally not recommended for use with non-antiarrhythmic drugs that can cause torsades de pointes (see section 4.5 ).

· Breastfeeding (see section on Pregnancy and lactation )

Linked to PERINDOPRIL / INDAPAMIDE KRKA

Hypersensitivity to any of the excipients

Due to the lack of data, PERINDOPRIL / INDAPAMIDE KRKA should not be used in the following cases:

· Dialysis patients

· Patients with untreated decompensated heart failure.

Adverse effects Perindopril / Indapamide Krka

Administration of perindopril inhibits the renin-angiotensin-aldosterone axis and tends to reduce indapamide-induced potassium loss. Two percent of the patients treated with PERINDOPRIL / INDAPAMIDE KRKA 2 mg / 0.625 mg tablet experienced hypokalaemia (potassium level <3.4 mmol / l).

The following adverse effects could be observed during treatment and classified according to the following frequencies:

Very common (≥1 / 10) frequent (≥1 / 100, <1/10); uncommon (≥1 / 1, 000, <1/100), rare (≥1 / 10, 000, <1/1000), very rare (<1 / 10, 000), not known (can not be estimated from available data).

Blood and lymphatic system disorders

Very rare:

Thrombocytopenia, leukopenia, neutropenia, agranulocytosis, medullary aplasia, hemolytic anemia.

· Anemia (see Warnings and Precautions ) has been reported with angiotensin-converting enzyme inhibitors on specific sites (kidney transplant, hemodialysis).

Psychiatric disorders

Uncommon: mood or sleep disorders

Nervous system disorders

Frequent: paresthesia, headache, dizziness, vertigo.

Very rare: confusion.

Eye disorders

Common: blurred vision

Affections of the ear and labyrinth

Frequent: tinnitus.

Vascular disorders

Common: orthostatic hypotension or not (see Warnings and Precautions section ).

Heart conditions

Very rare: arrhythmias including bradycardia, ventricular tachycardia, atrial fibrillation, angina pectoris, and myocardial infarction, possibly secondary to excessive hypotension in high-risk patients (see Warnings and Precautions for Use section ).

Respiratory, thoracic and mediastinal disorders

Common: A dry cough has been reported with the use of angiotensin converting enzyme inhibitors. It is characterized by its persistence, as well as by its disappearance at the end of treatment. The iatrogenic etiology should be considered in the presence of this symptom. Dyspnea.

Uncommon: bronchospasm.

Very rare: eosinophilic pneumonia, rhinitis.

Gastrointestinal disorders

Common: constipation, dry mouth, nausea, epigastric pain, anorexia, vomiting, abdominal pain, taste disturbances, dyspepsia, diarrhea.

Very rare: pancreatitis.

Hepatobiliary disorders

Very rare: cytolytic or cholestatic hepatitis (see Warnings and precautions for use ).

Unknown frequency: In case of hepatic insufficiency, the occurrence of hepatic encephalopathy is possible (see sections Contraindications and Warnings and precautions for use ).

Skin and subcutaneous tissue disorders

Common: rash, pruritus, maculopapular eruptions.

Rare:

· Angioedema of the face, extremities, lips, mucous membranes, tongue, glottis and / or larynx, urticaria (see Warnings and Precautions for Use section )

· Hypersensitivity reactions, mainly dermatological, in subjects predisposed to allergic or asthmatic reactions.

· Purpura

Possible aggravation of pre-existing systemic lupus erythematosus.

Very rare: erythema multiforme, toxic epidermal necrosis, Steven Johnson syndrome.

Cases of photosensitivity have been reported (see Warnings and Precautions section ).

Muscular, Connective Tissue and Bone Disorders

Frequent: cramps.

Renal and urinary disorders

Uncommon: renal failure.

Very rare: acute renal failure.

Disorders of reproductive organs and breast

Uncommon: impotence

General disorders

Frequent: asthenia.

Uncommon: sweating.

Biological parameters

· Potassium depletion with significant decrease in serum potassium in some at-risk populations (see Warnings and Precautions for Use section ).

· Hyponatremia with hypovolemia causing dehydration and orthostatic hypotension.

· Elevation of serum uric acid and blood glucose during treatment.

· Moderate increase in plasma urea and creatinine, reversible upon discontinuation of treatment. This increase is more frequently encountered in cases of renal artery stenosis, diuretic-treated hypertension, and renal failure.

· Elevation of plasma potassium levels, usually transient.

Rare: increased serum calcium.

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