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ספירונולקטון טבע 100 מ"ג SPIRONOLACTONE TEVA 100 MG (SPIRONOLACTONE)

תרופה במרשם תרופה בסל נרקוטיקה ציטוטוקסיקה

צורת מתן:

פומי : PER OS

צורת מינון:

טבליה : TABLETS

Special Warning : אזהרת שימוש

4.4       Special warnings and precautions for use

Fluid and electrolyte balance
Fluid and electrolyte status should be regularly monitored particularly in the elderly, in those with significant renal and hepatic impairment.

Hyperkalaemia may occur in patients with impaired renal function or excessive potassium intake and can cause cardiac irregularities which may be fatal. Should hyperkalaemia develop Spironolactone Teva should be discontinued, and if necessary, active measures taken to reduce the serum potassium to normal (see section 4.3).

Reversible hyperchloraemic metabolic acidosis, usually in association with hyperkalaemia has been reported to occur in some patients with decompensated hepatic cirrhosis, even in the presence of normal renal function.

Concomitant use of Spironolactone Teva with other potassium-sparing diuretics, angiotensin- converting enzyme (ACE) inhibitors, nonsteroidal anti-inflammatory drugs, angiotensin II antagonists, aldosterone blockers, heparin, low molecular weight heparin or other drugs or conditions known to cause hyperkalaemia, potassium supplements, a diet rich in potassium or salt substitutes containing potassium, may lead to severe hyperkalaemia.

Urea
Reversible increases in blood urea have been reported in association with Spironolactone Teva therapy, particularly in the presence of impaired renal function.

Hyperkalaemia in Patients with Severe Heart Failure
Hyperkalaemia may be fatal. It is critical to monitor and manage serum potassium in patients with severe heart failure receiving spironolactone. Avoid using other potassium-sparing diuretics. Avoid using oral potassium supplements in patients with serum potassium >3.5 mEq/L. The recommended monitoring for potassium and creatinine is 1week after initiation or increase in dose of spironolactone, monthly for the first 3 months, then quarterly for a year, and then every 6 months. Discontinue or interrupt treatment for serum potassium >5 mEq/L or for serum creatinine >4 mg/dL (see section 4.2).
        Paediatric population
Potassium-sparing diuretics should be used with caution in hypertensive paediatric patients with mild renal insufficiency because of the risk of hyperkalaemia. (Spironolactone is contraindicated for use in paediatric patients with moderate or severe renal impairment; see section 4.3).

Effects on Driving

4.7      Effects on ability to drive and use machines

Somnolence and dizziness have been reported to occur in some patients. Caution is advised when driving or operating machinery until the response to initial treatment has been determined.

שימוש לפי פנקס קופ''ח כללית 1994 Hypertension, congestive heart failure, primary aldosteronism, nephrotic syndrome, premenstrual tension
תאריך הכללה מקורי בסל 01/01/1995
הגבלות תרופה שאושרה לשימוש כללי בקופ'ח

בעל רישום

TEVA ISRAEL LTD

רישום

030 32 21061 01

מחיר

0 ₪

מידע נוסף

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12.10.22 - עלון לרופא 19.06.24 - עלון לרופא

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11.08.22 - עלון לצרכן אנגלית 11.08.22 - עלון לצרכן עברית 11.08.22 - עלון לצרכן ערבית 19.06.24 - עלון לצרכן עברית 21.08.24 - עלון לצרכן אנגלית 21.08.24 - עלון לצרכן עברית 21.08.24 - עלון לצרכן ערבית 07.08.22 - החמרה לעלון 19.06.24 - החמרה לעלון 19.06.24 - החמרה לעלון

לתרופה במאגר משרד הבריאות

ספירונולקטון טבע 100 מ"ג

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