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פראצטמול פרזניוס 10 מ"ג/מ"ל PARACETAMOL FRESENIUS 10 MG/ML (PARACETAMOL)

תרופה במרשם תרופה בסל נרקוטיקה ציטוטוקסיקה

צורת מתן:

תוך-ורידי : I.V

צורת מינון:

תמיסה לאינפוזיה : SOLUTION FOR INFUSION

Special Warning : אזהרת שימוש

4.4    Special warnings and precautions for use

RISK OF MEDICATION ERRORS
Take care to avoid dosing errors due to confusion between milligram (mg) and millilitre (ml), which could result in accidental overdose and death (see section 4.2).

Prolonged or frequent use is discouraged. It is recommended that a suitable analgesic oral treatment will be used as soon as this route of administration is possible.

In order to avoid the risk of overdose, check that other medicines administered do not contain either paracetamol or propacetamol. The dose may require adjustment (see section 4.2).

Doses higher than those recommended entail the risk of very serious liver damage. Clinical signs and symptoms of liver damage (including fulminant hepatitis, hepatic failure, cholestatic hepatitis, cytolytic hepatitis) are usually first seen after two days of drug administration with a peak seen, usually after 4 – 6 days. Treatment with antidote should be given as soon as possible (See section 4.9).

Paracetamol should be used with caution in cases of:

●     hepatocellular insufficiency
●     severe renal insufficiency (creatinine clearance ≤ 30 ml/min) (see sections 4.2 and 5.2) ●     chronic alcoholism
●     chronic malnutrition (low reserves of hepatic glutathione)
●     dehydration
●     patients suffering from a genetically caused G-6-PD deficiency (favism), the occurrence of a haemolytic anaemia is possible due to the reduced allocation of glutathione following the administration of paracetamol.
Caution is advised if paracetamol is administered concomitantly with flucloxacillin due to increased risk of high anion gap metabolic acidosis (HAGMA), particularly in patients with severe renal impairment, sepsis, malnutrition and other sources of glutathione deficiency (e.g.
chronic alcoholism), as well as those using maximum daily doses of paracetamol. Close monitoring, including measurement of urinary 5-oxoproline, is recommended.

Effects on Driving

4.7    Effects on ability to drive and use machines

Not relevant.
שימוש לפי פנקס קופ''ח כללית 1994 לא צוין
תאריך הכללה מקורי בסל לא צוין
הגבלות לא צוין

בעל רישום

NEOPHARM (ISRAEL) 1996 LTD

רישום

153 99 34200 01

מחיר

0 ₪

מידע נוסף

עלון מידע לרופא

10.08.22 - עלון לרופא 28.11.23 - עלון לרופא

עלון מידע לצרכן

29.11.23 - החמרה לעלון

לתרופה במאגר משרד הבריאות

פראצטמול פרזניוס 10 מ"ג/מ"ל

קישורים נוספים

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