Setlers Antacid Chewable Tablets Spearmint Flavour
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Setlers Antacid Chewable Tablets Spearmint Flavour
2 _QUALITATIVE AND
QUANTITATIVE COMPOSITION
Calcium carbonate 500mg
Excipients: Each tablet contains 0.47g sucrose
For full list of excipients see section 6.1.
3 _PHARMACEUTICAL
FORM
Chewable tablets for oral administration.
A white tablet with a bevelled edge with “Setlers” engraved on both faces of the tablet.
4. CLINICAL PARTICULARS
4.1. Therapeutic indications
For the symptomatic relief of acid indigestion, heartburn, flatulence and nausea.
4.2. Posology and method of administration
Adults, children over 12 years and elderly:
One or two tablets to be sucked or chewed whenever required, up to a maximum of 16 tablets in any 24 hours.
Children aged 6 to under 12 years: one tablet to be sucked or chewed, up to a maximum of 4 tablets in any 24 hours. Not to be given to children under 6 years of age.
The normal dose can be taken by the elderly.
Contraindications
4.3.
Patients on low phosphate diets, or receiving cardiac glycosides or with impaired hepatic or renal function.
Contraindicated in hypersensitivity to any of the ingredients
Contraindicated in hypercalcaemia, hypercalciuria (e.g. some forms of malignant disease), and calcium renal calculi.
4.4. Special warnings and precautions for use
Keep out of the reach and sight of children.
If symptoms persist consult your doctor or pharmacist.
Use with caution in diseases associated with hypercalcaemia such as sarcoidosis and some malignancies and in patients with a history of renal calculi.
Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrose-isomaltase insufficiency should not take this medicine.
4.5. Interaction with other medicinal products and other forms of interaction
Antacids of this type are known to decrease the absorption of concomitantly administered drugs due to absorption or delaying of gastric emptying or alkalinisation of gastric juice. However, the activity of cardiac glycosides such as digoxin may be increased due to the presence of calcium.
Calcium may reduce the absorption of tetracyclines, eltrombopag, bisphosphonates, fluoride, oral iron, zinc, levothyroxine and some fluoroquinolones.
Thiazide diuretics may reduce urinary calcium excretion and cause hypercalcaemia. Vitamin D increases the gastrointestinal absorption of calcium and can cause hypercalcaemia. Plasma-calcium concentrations should be monitored in patients receiving calcium together with thiazide diuretics or Vitamin D.
Antacids may damage enteric coatings designed to prevent dissolution in the stomach.
Interactions may be minimised by ensuring that Setlers Antacid Chewable Tablets Spearmint Flavour are not taken at the same time as, nor within three hours of other medications.
4.6. Pregnancy and lactation
Animal studies are insufficient with respect to effects on pregnancy, embryonal foetal development, parturition and postnatal development (see section 5.3). The potential risk for humans is unknown.
Caution should be exercised when prescribing to pregnant women.
4.7. Effects on ability to drive and use machines
None known.
4.8. Undesirable effects
Calcium carbonate can cause gastro-intestinal disturbances including flatulence and constipation.
Calcium-containing antacids can induce rebound acid secretion; however, this is unlikely to be of clinical significance in normal use.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.
4.9. Overdose
Prolonged excessive ingestion of calcium carbonate may lead to hypercalcaemia. Patients with renal impairment are most at risk. Alkalosis is a potential but rare risk. There have been rare reports of the milk-alkali syndrome.
Symptoms of hypercalcaemia may include anorexia, nausea, vomiting, constipation, abdominal pain, muscle weakness, mental disturbances, polydipsia, polyuriua, nephrocalcinosis, renal calculi and, in severe cases, cardiac arrhythmias and coma.
Treatment should be aimed at lowering serum calcium levels and may include full hydration, monitoring of other electrolytes and other standard symptomatic and supportive measures.
5. PHARMACOLOGICAL PROPERTIES 5.1. Pharmacodynamic properties
Calcium carbonate is an antacid.
5.2.
Pharmacokinetic properties
The product is formulated as a chewable tablet whose active has a local action in the gastrointestinal tract as an antacid.
5.3. Preclinical safety data
Calcium carbonate is a well established antacid active ingredient and considered to be non-toxic when administered orally at the recommended dosage. Therefore, single and repeat dose toxicity, foetal toxicity and fertility studies are not appropriate.
6.1 List of excipients
Icing Sugar (Sucrose)
Compressible Sugar (Sucrose and Maltodextrin)
Glucose
Maize starch
Spearmint flavour (Containing Sulphur Dioxide E220) Talc
Magnesium stearate Adipic acid.
6.2. Incompatibilities
None known.
6.3. Shelf life
36 months
6.4. Special precautions for storage
None
6.5 Nature and contents of container
Coated paper lined foil roll wrapper containing 12 tablets per roll. Three rolls are contained in a boxboard carton
Pack sizes: 36 tablets.
6.6. Instructions for use/handling
None.
7. MARKETING AUTHORISATION HOLDER
Thornton & Ross Limited
Linthwaite
Huddersfield
HD75QH
United Kingdom.
8. MARKETING AUTHORISATION NUMBER(S)
PL 00240/0121
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
13 th August 2003
10 DATE OF REVISION OF THE TEXT
11/09/2014