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סודיום כלוריד 0.9% וגלוקוז 5.0% תמיסה לעירוי בקסטר SODIUM CHLORIDE 0.9 % AND GLUCOSE 5 % SOLUTION FOR INFUSION BAXTER (GLUCOSE AS MONOHYDRATE, SODIUM CHLORIDE)

תרופה במרשם תרופה בסל נרקוטיקה ציטוטוקסיקה

צורת מתן:

תוך-ורידי : I.V

צורת מינון:

תמיסה לאינפוזיה : SOLUTION FOR INFUSION

Adverse reactions : תופעות לוואי

4.8 Undesirable effects
The following adverse reactions have been reported in post-marketing experience, listed by MedDRA System Organ Class (SOC), then where feasible, by Preferred Term in order of severity.
Frequencies cannot be estimated from the available data, as all listed adverse reactions are based on spontaneous reporting.

Adverse reactions
System Organ Class                                                 Frequency (Preferred terms) anaphylactic reaction, *
Immune system disorders                                               Not known hypersensitivity* hypernatraemia,
Metabolism and nutrition hyperglycaemia,                       Not known disorders hospital acquired hyponatraemia**

Nervous system disorders        hyponatraemic encephalopathy**        Not known 

7 of 11
Vascular disorders             phlebitis                             Not known 
Skin and subcutaneous tissue rash, pruritus                          Not known disorders
 injection site reactions including:
General disorders and pyrexia administration site chills                             Not known conditions infusion site pain infusion site vesicles
*Potential manifestation in patients with allergy to corn, see section 4.4 ** Hospital acquired hyponatraemia may cause irreversible brain injury and death due to development of acute hyponatraemic encephalopathy (see sections 4.2 and 4.4).

Other adverse reactions reported with isotonic saline and glucose infusions include: • Hyponatraemia, which may be symptomatic
• Hyperchloraemic acidosis

Adverse reactions may be associated to the medicinal product(s) added to the solution; the nature of the additive will determine the likelihood of any other adverse reactions.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important.
It allows continued monitoring of the benefit/risk balance of the medicinal product. Any suspected adverse events should be reported to the Ministry of Health according to the National Regulation by using an online form: https://sideeffects.health.gov.il/ 
שימוש לפי פנקס קופ''ח כללית 1994 לא צוין
תאריך הכללה מקורי בסל לא צוין
הגבלות לא צוין

בעל רישום

TEVA ISRAEL LTD

רישום

164 06 35835 01

מחיר

0 ₪

מידע נוסף

עלון מידע לרופא

05.04.21 - עלון לרופא 09.08.22 - עלון לרופא 12.07.24 - עלון לרופא

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לתרופה במאגר משרד הבריאות

סודיום כלוריד 0.9% וגלוקוז 5.0% תמיסה לעירוי בקסטר

קישורים נוספים

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