Medicines / Non-Prescription (OTC)

ALKACITRAT

ΑΝΑΒΡΑΖΟΝΤΑ ΔΙΣΚΙΑ 2 g

Therapeutic indications: Indigestion (slow digestion, bloating).
Posology and method of administration: Oral use.
Dosage: For adults and children over 15 years: 1 to 3 tablets daily.
Method of administration : The effervescent tablets are dissolved in half a glass of water. ALKACITRAT is taken before or after meals. The duration of treatment is limited to 7 days.
Contraindications : Hypersensitivity to the active substance or to any of the excipients listed
Special warnings and precautions for use : ALKACITRAT contains 16.66 mmol sodium (or 383.2 mg) per dose. Patients on a controlled sodium diet should be considered.
Interactions with other medicines and forms of interaction : The data available to date do not indicate the existence of clinically significant interactions.
Fertility, pregnancy and lactation : Avoid during pregnancy and lactation due to lack of clinical and experimental data.
Effects on ability to drive and use machines : ALKACITRAT does not appear to affect the ability to drive and use machines.
Unwanted actions : Allergic reactions (urticaria, angioedema and rash) have been reported.
Overdose : No cases of overdose have been reported.
Pharmacodynamic properties : Pharmacotherapeutic group: Digestive and metabolic products, ATC code: A16AA06. Betaine citrate is traditionally used to treat indigestion symptoms. This information is based solely on tradition and years of experience.
List of excipients : Mannitol, Citric acid anhydrous, Sodium bicarbonate, Raspberry flavor, Sodium saccharin, Sodium benzoate, Polyethylene glycol 6000, Starch pregelatinized.
Licence number : 89058 / 10.10.2017….

Active substance: BETAINE CITRATE
Content: 2 g
Form: ΑΝΑΒΡΑΖΟΝΤΑ ΔΙΣΚΙΑ
Package: BTx10 (1 TUBE x 10), BTx10 (5 STRIPES x 2), BTx20 (10 STRIPES x 2), BTx20 (2 TUBES x 10)
Do not exceed the recommended daily dose

PEPTONORM

ΔΙΣΚΙΑ 1000 mg

For the treatment of peptic ulcer
Tablets: 1000 mg/tab

Active substance: SUCRALFATE
Content: 1000 mg
Form: ΔΙΣΚΙΑ
Package: BTx30
Do not exceed the recommended daily dose

PEPTONORM

ΠΟΣΙΜΟ ΕΝΑΙΩΡΗΜΑ 1000 mg/5ml

For the treatment of peptic ulcer.
Oral Suspension: 1000 mg/5ml

Active substance: SUCRALFATE
Content: 1000 mg/5ml
Form: ΠΟΣΙΜΟ ΕΝΑΙΩΡΗΜΑ
Package: FLx150ML
Do not exceed the recommended daily dose

PEPTONORM

ΠΟΣΙΜΟ ΕΝΑΙΩΡΗΜΑ ΣΕ ΣΥΣΚΕΥΑΣΙΑ ΜΙΑΣ ΔΟΣΗΣ 1000 mg/5ml

Για τη βραχυχρόνια (έως 8 εβδομάδες) θεραπεία του δωδεκαδακτυλικού έλκους, της χρόνιας γαστρίτιδας και της πεπτικής οισοφαγίτιδας

  • Δισκία 1000 mg/tab
  • Κοκκία για πόσιμο εναιώρημα 1000 mg/sachet
  • Πόσιμο εναιώρημα 1000 mg/5 ml
  • Εναιώρημα πόσιμο μιας δόσης 1000 mg/5 ml sachet
Active substance: SUCRALFATE
Content: 1000 mg/5ml
Form: ΠΟΣΙΜΟ ΕΝΑΙΩΡΗΜΑ ΣΕ ΣΥΣΚΕΥΑΣΙΑ ΜΙΑΣ ΔΟΣΗΣ
Package: BTx20 SACHETS x 5ML, BTx30 SACHETS x 5ML
Do not exceed the recommended daily dose

PEPTONORM

ΚΟΚΚΙΑ ΓΙΑ ΠΟΣΙΜΟ ΕΝΑΙΩΡΗΜΑ ΣΕ ΣΥΣΚΕΥΑΣΙΑ ΜΙΑΣ ΔΟΣΗΣ 1000 mg/φακελίσκο

For the treatment of peptic ulcer.
Granules Oral Suspension: 1000 mg/sachet
Suspension Single Dose: 1000 mg/5ml sachet

Active substance: SUCRALFATE
Content: 1000 mg/φακελίσκο
Form: ΚΟΚΚΙΑ ΓΙΑ ΠΟΣΙΜΟ ΕΝΑΙΩΡΗΜΑ ΣΕ ΣΥΣΚΕΥΑΣΙΑ ΜΙΑΣ ΔΟΣΗΣ
Package: BTx20 SACHETS, BTx30 SACHETS
Do not exceed the recommended daily dose

RHEOSTOP R

ΔΙΣΚΙΑ ΔΙΑΣΠΕΙΡΟΜΕΝΑ ΣΤΟ ΣΤΟΜΑ 2 mg
Active substance: LOPERAMIDE HYDROCHLORIDE
Content: 2 mg
Form: ΔΙΣΚΙΑ ΔΙΑΣΠΕΙΡΟΜΕΝΑ ΣΤΟ ΣΤΟΜΑ
Package: BTx6
Do not exceed the recommended daily dose

ZOLIDEN

ΑΝΑΒΡΑΖΟΝΤΑ ΔΙΣΚΙΑ 75 mg

Medicines for ulcer treatment/Antagonist of H2 histamine receptors.
Effervescent Granules: 300 mg/sachet
Effervescent Tablets: 150 mg/tab

Active substance: RANITIDINE HYDROCHLORIDE
Content: 75 mg
Form: ΑΝΑΒΡΑΖΟΝΤΑ ΔΙΣΚΙΑ
Package: BTx12
Do not exceed the recommended daily dose

ZOLIDEN

ΕΠΙΚΑΛΥΜΜΕΝΑ ΜΕ ΛΕΠΤΟ ΥΜΕΝΙΟ ΔΙΣΚΙΑ 75 mg
Active substance: RANITIDINE HYDROCHLORIDE
Content: 75 mg
Form: ΕΠΙΚΑΛΥΜΜΕΝΑ ΜΕ ΛΕΠΤΟ ΥΜΕΝΙΟ ΔΙΣΚΙΑ
Package: BTx10, BTx20
Do not exceed the recommended daily dose