CONTROLOC TABLET 40 mg

国: シンガポール

言語: 英語

ソース: HSA (Health Sciences Authority)

有効成分:

PANTOPRAZOLE

から入手可能:

TAKEDA PHARMACEUTICALS (ASIA PACIFIC) PTE. LTD.

ATCコード:

A02BC02

投薬量:

40 mg

医薬品形態:

ENTERIC COATED TABLET

構図:

PANTOPRAZOLE 40 mg

投与経路:

ORAL

処方タイプ:

Prescription Only

製:

Takeda GmbH

認証ステータス:

ACTIVE

承認日:

1996-08-14

情報リーフレット

INSTRUCTIONS FOR USE 
CONTROLOC® 40 MG 
Active ingredient: Pantoprazole sodium sesquihydrate 
Description 
Controloc: contains Pantoprazole, a proton pump inhibitors which inhibits the gastric H
+
K
+
 ATPase which 
is responsible for acid secretion in the parietal cells of the stomach. Pantoprazole is white to off‐white 
powder with a molecular weight of 432.4. Pantoprazole is freely soluble in water, very slightly soluble in 
phosphate buffer at pH 7.4, and practically insoluble in n‐hexane. Pantoprazole is a racemic mixture with 
a melting point of 138° C. 
The 
chemical 
name 
for 
Pantoprazole 
is 
sodium‐5‐(difluoromethoxy)‐2‐[[(3,4‐dimethoxy‐2‐
pyridinyl)methyl]  sulfinyl]‐1  H‐benzimidazole  sesquihydrate  and  is  represented  by  the  following 
chemical structure : 

Empirical chemical structure : C
16
H
14
F
2
N
3
NaO
4
Sx1.5H
2
O 
NAME AND STRENGTH OF ACTIVE INGREDIENT 

Active ingredient 
40mg pantoprazole (as pantoprazole sodium sesquihydrate 45.1 mg) 

Excipients 
Sodium carbonate; D‐mannitol (corresponding to 0.0036 BU);  crospovidone; povidone K 90; povidone K 
25; calcium stearate; propylene glycol;

methylhydroxypropylcellulose; 
poly(ethyl acrylate‐co‐methacrylic acid) 1:1; polysorbate 80; sodium dodecyl sulfate; triethyl citrate; 
colours (E 171, E 172);printing ink.  

PHARMACOTHERAPEUTIC / INDICATION GROUP / ACTION MECHANISM 
Selective proton pump inhibitor, substituted benzimidazole 

PHARMACODYNAMIC PROPERTIES 
Pantoprazole  is  a  substituted  benzimidazole  which  inhibits  the  secretion  of  hydrochloric  acid  in  the 
stomach  by  specific  action  on  the proton  pumps  of  the  parietal cells.  Pantoprazole  is  converted  to  its 
active form in the acidic canaliculi of the parietal cells

製品の特徴

INSTRUCTIONS FOR USE
1.
NAME OF THE MEDICINAL PRODUCT
CONTROLOC® 20 MG
CONTROLOC® 40 MG
CONTROLOC® I.V
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
_CONTROLOC® 20 MG_
1 gastro-resistant (enteric coated) tablet contains 20 mg pantoprazole
(as pantoprazole sodium) for
oral use. Active ingredient: 20mg pantoprazole (as pantoprazole sodium
sesquihydrate 22.6 mg)
_CONTROLOC® 40 MG_
1 gastro-resistant (enteric coated) tablet contains 40 mg pantoprazole
(as pantoprazole sodium) for
oral use. Active ingredient: 40mg pantoprazole (as pantoprazole sodium
sesquihydrate 45.1 mg)
_CONTROLOC® I.V_
1 vial contains 40 mg pantoprazole (as pantoprazole sodium) as powder
for solution for injection.
Sodium: This medicinal product contains less than 1 mmol sodium (23
mg) per vial. Active
ingredient: 40mg pantoprazole (as pantoprazole sodium 42.3 mg)
3.
PHARMACEUTICAL FORM
_CONTROLOC® 20 MG_
Gastro-resistant tablets, yellow, oval, biconvex, “P20” in brown
printing ink
Packs with 7 and 14 gastro-resistant tablets
_CONTROLOC® 40 MG_
Gastro-resistant tablets, yellow, oval, biconvex, “P40” in brown
printing ink
Packs with 7and 14 gastro-resistant tablets
_CONTROLOC® I.V_
Powder for solution for injection
Packs of 1 vial with 42.3mg white to off-white powder
4.
CLINICAL PARTICULARS
4.1.
THERAPEUTIC INDICATIONS
_CONTROLOC® 20 MG_
•
Mild reflux disease and associated symptoms (e.g. heartburn, acid
regurgitation, pain on
swallowing).
•
Long-term management and prevention of relapse in reflux oesophagitis.
•
Prevention of gastroduodenal ulcers induced by non-selective
non-steroidal anti-
inflammatory drugs (NSAIDs) in patients at risk with a need for
continuous NSAID treatment.
_CONTROLOC® 40 MG _
•
In combination with two appropriate antibiotics (see Dosage) for the
eradication of H.pylori in
patients with peptic ulcers with the objective of reducing the
recurrence of duodenal and gastric
ulcers caused by this microorganism.
•
Duodenal ulcer
•
Gastric ulcer
•
Moderate and severe reflux oesophagitis
_CONTROLOC®