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עמוד הבית / פרומניקס 0.4 / מידע מעלון לרופא

פרומניקס 0.4 PROMNIX 0.4 (TAMSULOSIN HYDROCHLORIDE)

תרופה במרשם תרופה בסל נרקוטיקה ציטוטוקסיקה

צורת מתן:

פומי : PER OS

צורת מינון:

אין פרטים : MODIFIED RELEASE CAPSULES HARD

Special Warning : אזהרת שימוש

4.4. Special warnings and precautions for use

As with other alpha1 blockers, a reduction in blood pressure can occur in individual cases during treatment with Promnix 0.4, as a result of which, rarely, syncope can occur. At the first signs of orthostatic hypotension (dizziness, weakness), the patient should sit or lie down until the symptoms have disappeared.
Before therapy with Promnix 0.4 is initiated, the patient should be examined in order to exclude the presence of other conditions which can cause the same symptoms as benign prostatic hyperplasia. Digital rectal examination and, when necessary, determination of prostate specific antigen (PSA) should be performed before treatment and at regular intervals afterwards.
The treatment of severely renally impaired patients (creatinine clearance of less than 10 ml/min) should be approached with caution as these patients have not been studied.
The 'Intraoperative Floppy Iris Syndrome' (IFIS, a variant of small pupil syndrome) has been observed during cataract and glaucoma surgery in some patients on or previously treated with tamsulosin hydrochloride. IFIS may increase the risk of eye complications during and after the operation.
Discontinuing tamsulosin hydrochloride 1-2 weeks prior to cataract or glaucoma surgery is anecdotally considered helpful, but the benefit of treatment discontinuation has not been established. IFIS has also been reported in patients who had discontinued tamsulosin for a longer period prior to the surgery.
The initiation of therapy with tamsulosin hydrochloride in patients for whom cataract or glaucoma surgery is scheduled is not recommended. During pre-operative assessment, surgeons and ophthalmic teams should consider whether patients scheduled for cataract or glaucoma surgery are being or have been treated with tamsulosin in order to ensure that appropriate measures will be in place to manage the IFIS during surgery.
Tamsulosin hydrochloride should not be given in combination with strong inhibitors of CYP3A4 (e.g. ketoconazole) in patients with poor metaboliser CYP2D6 phenotype.
Tamsulosin hydrochloride should be used with caution in combination with strong (e.g.
ketoconazole) and moderate (e.g. erythromycin) inhibitors of CYP3A4 (see section 4.5).

Effects on Driving

                
שימוש לפי פנקס קופ''ח כללית 1994 לא צוין
תאריך הכללה מקורי בסל 10/01/2012
הגבלות תרופה מוגבלת לרישום ע'י רופא מומחה או הגבלה אחרת

בעל רישום

TARO INTERNATIONAL LTD, ISRAEL

רישום

137 08 31452 00

מחיר

0 ₪

מידע נוסף

עלון מידע לרופא

31.07.24 - עלון לרופא

עלון מידע לצרכן

17.01.21 - עלון לצרכן אנגלית 17.01.21 - עלון לצרכן עברית 17.01.21 - עלון לצרכן ערבית 27.02.23 - עלון לצרכן אנגלית 27.02.23 - עלון לצרכן עברית 27.02.23 - עלון לצרכן ערבית 31.07.24 - עלון לצרכן עברית 17.01.21 - החמרה לעלון 21.01.16 - החמרה לעלון 27.02.23 - החמרה לעלון 31.07.24 - החמרה לעלון

לתרופה במאגר משרד הבריאות

פרומניקס 0.4

קישורים נוספים

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