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עמוד הבית / אונברז בריזהלר 150 מק"ג / מידע מעלון לרופא

אונברז בריזהלר 150 מק"ג ONBREZ BREEZHALER 150 MCG (INDACATEROL AS MALEATE)

תרופה במרשם תרופה בסל נרקוטיקה ציטוטוקסיקה

צורת מתן:

שאיפה : INHALATION

צורת מינון:

אבקה לשאיפה בקפסולות קשיחות : INHALATION POWDER HARD CAPSULES

Special Warning : אזהרת שימוש

4.4   Special warnings and precautions for use

Asthma
Onbrez Breezhaler is a long-acting beta2-adrenergic agonist, which is only indicated for COPD and should not be used in asthma due to the absence of long-term outcome data in asthma.
Long-acting beta2-adrenergic agonists may increase the risk of asthma-related serious adverse events, including asthma-related deaths, when used for the treatment of asthma.

Hypersensitivity
Immediate hypersensitivity reactions have been reported after administration of Onbrez Breezhaler. If signs suggesting allergic reactions (in particular, difficulties in breathing or swallowing, swelling of tongue, lips and face, urticaria, skin rash) occur, Onbrez Breezhaler should be discontinued immediately and alternative therapy instituted.

Paradoxical bronchospasm
As with other inhalation therapy, administration of Onbrez Breezhaler may result in paradoxical bronchospasm that may be life-threatening. If paradoxical bronchospasm occurs, Onbrez Breezhaler should be discontinued immediately and alternative therapy substituted.

Deterioration of disease
Onbrez Breezhaler is not indicated for the treatment of acute episodes of bronchospasm, i.e.
as rescue therapy. In the event of deterioration of COPD during treatment with Onbrez Breezhaler, a re-evaluation of the patient and of the COPD treatment regimen should be undertaken. An increase in the daily dose of Onbrez Breezhaler beyond the maximum dose of 300 microgram is not appropriate.

Systemic effects
Although no clinically relevant effect on the cardiovascular system is usually seen after the administration of Onbrez Breezhaler at the recommended doses, as with other beta2- adrenergic agonists, indacaterol should be used with caution in patients with cardiovascular disorders (coronary artery disease, acute myocardial infarction, cardiac arrhythmias, hypertension), in patients with convulsive disorders or thyrotoxicosis, and in patients who are unusually responsive to beta2-adrenergic agonists.

Cardiovascular effects
Like other beta2-adrenergic agonists, indacaterol may produce a clinically significant cardiovascular effect in some patients as measured by increases in pulse rate, blood pressure, and/or symptoms. In case such effects occur, treatment may need to be discontinued. In addition, beta-adrenergic agonists have been reported to produce electrocardiogram (ECG) changes, such as flattening of the T wave, prolongation of QT interval, and ST segment 
ONB API JUN21 V1.1                                                     Ref EMA SmPC 15Dec2020 depression, although the clinical significance of these observations is unknown. Therefore, long-acting beta2-adrenergic agonists (LABA) or LABA containing products such as Onbrez Breezhaler should be used with caution in patients with known or suspected prolongation of the QT interval or treated with medicinal products affecting the QT interval.

Hypokalaemia
Beta2-adrenergic agonists may produce significant hypokalemia in some patients, which has the potential to produce adverse cardiovascular effects. The decrease in serum potassium is usually transient, not requiring supplementation. In patients with severe COPD, hypokalemia may be potentiated by hypoxia and concomitant treatment (see section 4.5) which may increase the susceptibility to cardiac arrhythmias.

Hyperglycaemia
Inhalation of high doses of beta2-adrenergic agonists may produce increases in plasma glucose. Upon initiation of treatment with Onbrez Breezhaler plasma glucose should be monitored more closely in diabetic patients.
During clinical studies, clinically notable changes in blood glucose were generally more frequent by 1-2% on Onbrez Breezhaler at the recommended doses than on placebo. Onbrez Breezhaler has not been investigated in patients with not well controlled diabetes mellitus.


Excipients
The capsules contain lactose. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicinal product.

Effects on Driving

4.7   Effects on ability to drive and use machines

Onbrez Breezhaler has no or negligible influence on the ability to drive and use machines.




ONB API JUN21 V1.1                                                     Ref EMA SmPC 15Dec2020

פרטי מסגרת הכללה בסל

א. התרופה האמורה תינתן לטיפול במחלת ריאות חסימתית כרונית (COPD – Chronic Obstructive Pulmonary Disease) בחולים עם FEV1 שווה או נמוך מ-70% במצב כרוני; ב. התרופה לא תינתן בשילוב עם Tiotropium או Glycopyrronium או Aclidinium. סעיף זה לא יחול על חולים עם FEV1 שווה או נמוך מ-60%. ג. תחילת הטיפול בתרופה ייעשה לפי מרשם של רופא מומחה ברפואת ריאות.

מסגרת הכללה בסל

התוויות הכלולות במסגרת הסל

התוויה תאריך הכללה תחום קליני Class Effect מצב מחלה
התרופה האמורה תינתן לטיפול במחלת ריאות חסימתית כרונית (COPD – Chronic Obstructive Pulmonary Disease) בחולים עם FEV1 שווה או נמוך מ-70% במצב כרוני 23/01/2011
שימוש לפי פנקס קופ''ח כללית 1994 לא צוין
תאריך הכללה מקורי בסל 23/01/2011
הגבלות תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת

בעל רישום

NOVARTIS ISRAEL LTD

רישום

144 76 33112 02

מחיר

0 ₪

מידע נוסף

עלון מידע לרופא

11.07.21 - עלון לרופא

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11.07.21 - עלון לצרכן אנגלית 11.07.21 - עלון לצרכן עברית 11.07.21 - עלון לצרכן ערבית 03.06.20 - החמרה לעלון 11.04.21 - החמרה לעלון

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אונברז בריזהלר 150 מק"ג

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