Controloc

Ülke: Ermenistan

Dil: İngilizce

Kaynak: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Aktif bileşen:

pantoprazole (pantoprazole sodium sesquihydrate)

Mevcut itibaren:

Takeda GmbH

INN (International Adı):

pantoprazole (pantoprazole sodium sesquihydrate)

Doz:

40mg

Farmasötik formu:

powder for solution for injection

Reçete türü:

Prescription

Ürün özellikleri

1
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Controloc 40 mg powder for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each vial contains 40 mg of pantoprazole.
Excipients with known effect:
Each vial contains 1 mg disodium edetate and 0.24 mg sodium hydroxide.
This medicinal product contains less than 1 mmol sodium (23 mg) per
vial, i.e. is essentially
„sodium-free‟.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder for solution for injection.
White to off-white powder (dry mass).
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
-
Reflux oesophagitis.
-
Gastric and duodenal ulcer.
-
Zollinger-Ellison-Syndrome and other pathological hypersecretory
conditions.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
This medicine should be administered by a healthcare professional and
under appropriate medical
supervision.
Intravenous administration of Controloc 40 mg powder for solution for
injection
is recommended only if oral administration is not appropriate. Data
are available on intravenous use for
up to 7 days. Therefore, as soon as oral therapy is possible,
treatment with Controloc i.v. should be
discontinued and 40 mg pantoprazole p.o. should be administered
instead. _ _
Posology
Gastric and duodenal ulcer, reflux oesophagitis
The recommended intravenous dose is one vial of Controloc 40 mg powder
for solution for injection
(40 mg pantoprazole) per day.
Zollinger-Ellison-Syndrome and other pathological hypersecretory
conditions_ _
For the long-term management of Zollinger-Ellison-Syndrome and other
pathological hypersecretory
conditions patients should start their treatment with a daily dose of
80 mg Controloc. Thereafter, the dose
can be titrated up or down as needed using measurements of gastric
acid secretion to guide. With doses
above 80 mg daily, the dose should be divided and given twice daily. A
temporary increase of the dose
above 160 mg pantoprazole is possible but should not be applied longer
than required for adequate acid
cont