- Approval Id
- 8f36b549a85ea62b
- Drug Approval Emc Name
- Calcichew 500mg Chewable Tablets
- Drug Name
- Calcichew 500mg Chewable Tablets
- Company Name
- Neon Healthcare Ltd
- Company Address
- 8 The Chase, John Tate Road, Foxholes Business Park, Hertford, Hertfordshire, SG13 7NN, UK
- Company Website
- http://www.neonhealthcare.com
- Company Telephone
- +44 (0)1992 926 330
- Company Medical Info Direct Line
- +44 (0)1992 926 330
- Company Medical Info Email
- medinfo@neonhealthcare.com
- Company Customer Care Direct Line
- +44 (0)1992 926 330
- Company Stock Availability
- +44 (0)1992 926 330
- Atc Code
- A12AA04
- Legal Category
- Pharmacy
- Authorisation Holder
- Neon Healthcare Limited
8 The Chase
John Tate Road, Hertford
SG13 7NN
United Kingdom
- Authorisation Number
- PL 45043/0082
- Authorisation Date
- Date of first authorisation: 27 November 1987
Date of last renewal: 31 March 2005
- Instruction Authorisation Holder
- Neon Healthcare Limited
8 The Chase
John Tate Road, Hertford
SG13 7NN
United Kingdom
- Instruction Authorisation Number
- PL 45043/0082
- Instruction Authorisation Date
- Date of first authorisation: 27 November 1987
Date of last renewal: 31 March 2005
- Instruction Composition
- One chewable tablet of 500 mg contains calcium carbonate equivalent to 500mg of calcium.
Excipients with known effect:
Isomalt (E953)
For a full list of excipients, see section 6.1.
- Instruction Dosage Form
- Chewable tablet.
Round, white, uncoated and convex tablets. May have small specks.
- Instruction Clinical Particulars
- 4.1 Therapeutic indications
Calcichew 500mg Chewable Tablets are to be chewed as a supplemental source of calcium in the correction of dietary deficiencies or when normal requirements are high.
Calcichew 500mg Chewable Tablets may be used as an adjunct to conventional therapy in the prevention and treatment of osteoporosis. They may be used as a phosphate binding agent in the management of renal failure in patients on renal dialysis.4.2 Posology and method of administration
\*\*Posology\*\*
\*\*\*Adults:\*\*\*
| | |
| --- | --- |
| Adjunctive therapy in osteoporosis | 2 to 3 tablets daily. |
| Prevention and treatment of calcium deficiency | 2 to 3 tablets daily. |
| Phosphate binder: | Dose as required by the individual patient depending on serum phosphate level. |
| \*\*Special patient populations\*\* \*\*\*Elderly patients:\*\*\* Dosage as for adults. \*\*\*Paediatric patients:\*\*\* | |
| Prevention and treatment of calcium deficiency | 2 to 3 tablets daily. |
| Phosphate Binder: | Dose as required by the individual patient depending on serum phosphate level. |
\*\*\*Impaired renal function:\*\*\*
In patients with severe renal failure having a creatinine clearance of less than 30 ml/minute, dosage adjustments may be necessary dependent on serum calcium levels. See section 4.4.
\*\*\*Impaired hepatic function:\*\*\*
No dose adjustment is required.
\*\*Method of administration\*\*
Oral.
Tablets may be chewed or sucked.
For phosphate binding, the tablets should be taken just before, during or just after each meal in order to bind phosphate in the food.4.3 Contraindications
• Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
• Diseases and/or conditions resulting in hypercalcaemia and/or hypercalciuria, for example in hyperparathyroidism, vitamin D overdosage, decalcifying tumours such as plasmacytoma and skeletal metastases, in severe renal failure untreated by renal dialysis and in osteoporosis due to immobilisation.
• Renal calculi (nephrolithiasis)4.4 Special warnings and precautions for use
In renal insufficiency the tablets should be given only under controlled conditions for hyperphosphataemia. Caution should be exercised in patients with a history of renal calculi.
Monitoring is especially important in patients on concomitant treatment with cardiac glycosides or diuretics (see section 4.5).
During high dose therapy and especially during concomitant treatment with vitamin D and/or medications or nutrients (such as milk) containing calcium, there is a risk of hypercalcaemia and milk-alkali syndrome (hypercalcaemia, alkalosis and renal impairment) with subsequent kidney function impairment. In these patients, serum calcium levels should be monitored and renal function should be monitored.
Calcichew 500 mg Chewable Tablets contain isomalt (E953). Patients with rare hereditary problems of fructose intolerance should not take this medicine.4.5 Interaction with other medicinal products and other forms of interaction
Thiazide diuretics reduce the urinary excretion of calcium. Due to increased risk of hypercalcaemia, serum calcium should be regularly monitored during concomitant use of thiazide diuretics.
Calcium carbonate may interfere with the absorption of concomitantly administered tetracycline preparations. For this reason, tetracycline preparations should be administered at least two hours before, or four to six hours after, oral intake of calcium.
Hypercalcaemia may increase the toxicity of cardiac glycosides during treatment with calcium. Patients should be monitored with regard to electrocardiogram (ECG) and serum calcium levels.
If a bisphosphonate is used concomitantly, this preparation should be administered at least three hours before the intake of Calcichew 500mg Chewable Tablets since gastrointestinal absorption may be reduced.
The efficacy of levothyroxine can be reduced by the concurrent use of calcium, due to decreased levothyroxine absorption. Administration of calcium and levothyroxine should be separated by at least four hours.
The absorption of quinolone antibiotics may be impaired if administered concomitantly with calcium. Quinolone antibiotics should be taken two hours before or after intake of calcium.
Calcium salts may decrease the absorption of iron, zinc and strontium ranelate. Consequently, iron, zinc or strontium ranelate preparations should be taken two hours before or after calcium carbonate.4.6 Pregnancy and lactation
\*\*Pregnancy\*\*
Calcichew 500mg Chewable Tablets can be used during pregnancy. Daily intake should not exceed 2500 mg of calcium as permanent hypercalcaemia has been related to adverse effects on the developing foetus.
\*\*Breastfeeding\*\*
Calcium carbonate can be used during breast-feeding. Calcium passes into breast milk but at therapeutic doses no effects on the breastfed new-born are anticipated.4.7 Effects on ability to drive and use machines
Calcium carbonate has no known influence on ability to drive and use machines.4.8 Undesirable effects
Adverse reactions are listed below, by system organ class and frequency. Frequencies are defined as: uncommon (≥1/1,000 to <1/100); rare (≥1/10,000 to <1/1,000) or very rare (<1/10,000).
\*Metabolism and nutrition disorders\*
Uncommon: Hypercalcaemia and hypercalciuria.
Very rare: Milk-alkali syndrome (frequent urge to urinate; continuing headache; continuing loss of appetite; nausea or vomiting; unusual tiredness or weakness; hypercalcaemia, alkalosis and renal impairment). Seen usually only in overdose (see section 4.9).
\*Gastrointestinal disorders\*
Rare: Constipation, dyspepsia, flatulence, nausea, abdominal pain and diarrhoea.
\*Skin and subcutaneous disorders\*
Very rare: Pruritus, rash and urticaria.
\*\*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
Overdose can lead to hypercalcaemia. Symptoms of hypercalcaemia may include anorexia, thirst, nausea, vomiting, constipation, abdominal pain, muscle weakness, fatigue, mental disturbances, polydipsia, polyuria, bone pain, nephrocalcinosis, nephrolithiasis and in severe cases, cardiac arrhythmias. Extreme hypercalcaemia may result in coma and death. Persistently high calcium levels may lead to irreversible renal damage and soft tissue calcification.
Milk-alkali syndrome may still occur in patients who ingest large amounts of calcium and absorbable alkali. It is not uncommon as a cause of hypercalcaemia requiring hospitalisation. The syndrome has also been reported in a patient taking recommended doses of antacids containing calcium carbonate for chronic epigastric discomfort, and in a pregnant woman taking high, but not grossly excessive, doses of calcium (about 3 g of elemental calcium daily). Metastatic calcification can develop.
Treatment of hypercalcaemia: The treatment with calcium must be discontinued. Treatment with thiazide diuretics, lithium, vitamin A, vitamin D and cardiac glycosides must also be discontinued. Treatment: rehydration, and, according to severity of hypercalcaemia, isolated or combined treatment with loop diuretics, bisphosphonates, calcitonin and corticosteroids should be considered. Serum electrolytes, renal function and diuresis must be monitored. In severe cases, ECG and CVP should be followed.
- Instruction Pharmacology
- 5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Mineral supplements: Calcium.
ATC-code: A12AA04
An adequate intake of calcium is of importance during growth, pregnancy and breastfeeding.5.2 Pharmacokinetic properties
Absorption: The amount of calcium absorbed through the gastrointestinal tract is approximately 30% of the swallowed dose.
Distribution and biotransformation: 99% of the calcium in the body is concentrated in the hard structure of bones and teeth. The remaining 1% is present in the intra- and extracellular fluids. About 50% of the total blood-calcium content is in the physiologically active ionised form with approximately 10% being complexed to citrate, phosphate or other anions, the remaining 40% being bound to proteins, principally albumin.
Excretion and elimination: Calcium is eliminated through faeces, urine and sweat. Renal excretion depends on glomerular filtration and calcium tubular reabsorption.5.3 Preclinical safety data
There is no information of relevance to the safety assessment in addition to what is stated in other parts of the SmPC.
- Instruction Pharmaceutical Particulars
- 6.1 List of excipients
Xylitol (967)
Povidone
Magnesium stearate
Sucralose (E955)
Isomalt (E953)
Flavouring (orange)
Mono, di-fatty acid glycerides6.2 Incompatibilities
Not applicable.6.3 Shelf life
3 years.6.4 Special precautions for storage
Do not store above 30°C.
Keep the container tightly closed to protect from moisture.6.5 Nature and contents of container
Securitainer containing 100 tablets.6.6 Special precautions for disposal and other handling
No special requirements.
- Instruction Content
- ## Composition
One chewable tablet of 500 mg contains calcium carbonate equivalent to 500mg of calcium.
Excipients with known effect:
Isomalt (E953)
For a full list of excipients, see section 6.1.
## Pharmaceutical Form
Chewable tablet.
Round, white, uncoated and convex tablets. May have small specks.
## Clinical Particulars
4.1 Therapeutic indications
Calcichew 500mg Chewable Tablets are to be chewed as a supplemental source of calcium in the correction of dietary deficiencies or when normal requirements are high.
Calcichew 500mg Chewable Tablets may be used as an adjunct to conventional therapy in the prevention and treatment of osteoporosis. They may be used as a phosphate binding agent in the management of renal failure in patients on renal dialysis.4.2 Posology and method of administration
\*\*Posology\*\*
\*\*\*Adults:\*\*\*
| | |
| --- | --- |
| Adjunctive therapy in osteoporosis | 2 to 3 tablets daily. |
| Prevention and treatment of calcium deficiency | 2 to 3 tablets daily. |
| Phosphate binder: | Dose as required by the individual patient depending on serum phosphate level. |
| \*\*Special patient populations\*\* \*\*\*Elderly patients:\*\*\* Dosage as for adults. \*\*\*Paediatric patients:\*\*\* | |
| Prevention and treatment of calcium deficiency | 2 to 3 tablets daily. |
| Phosphate Binder: | Dose as required by the individual patient depending on serum phosphate level. |
\*\*\*Impaired renal function:\*\*\*
In patients with severe renal failure having a creatinine clearance of less than 30 ml/minute, dosage adjustments may be necessary dependent on serum calcium levels. See section 4.4.
\*\*\*Impaired hepatic function:\*\*\*
No dose adjustment is required.
\*\*Method of administration\*\*
Oral.
Tablets may be chewed or sucked.
For phosphate binding, the tablets should be taken just before, during or just after each meal in order to bind phosphate in the food.4.3 Contraindications
• Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
• Diseases and/or conditions resulting in hypercalcaemia and/or hypercalciuria, for example in hyperparathyroidism, vitamin D overdosage, decalcifying tumours such as plasmacytoma and skeletal metastases, in severe renal failure untreated by renal dialysis and in osteoporosis due to immobilisation.
• Renal calculi (nephrolithiasis)4.4 Special warnings and precautions for use
In renal insufficiency the tablets should be given only under controlled conditions for hyperphosphataemia. Caution should be exercised in patients with a history of renal calculi.
Monitoring is especially important in patients on concomitant treatment with cardiac glycosides or diuretics (see section 4.5).
During high dose therapy and especially during concomitant treatment with vitamin D and/or medications or nutrients (such as milk) containing calcium, there is a risk of hypercalcaemia and milk-alkali syndrome (hypercalcaemia, alkalosis and renal impairment) with subsequent kidney function impairment. In these patients, serum calcium levels should be monitored and renal function should be monitored.
Calcichew 500 mg Chewable Tablets contain isomalt (E953). Patients with rare hereditary problems of fructose intolerance should not take this medicine.4.5 Interaction with other medicinal products and other forms of interaction
Thiazide diuretics reduce the urinary excretion of calcium. Due to increased risk of hypercalcaemia, serum calcium should be regularly monitored during concomitant use of thiazide diuretics.
Calcium carbonate may interfere with the absorption of concomitantly administered tetracycline preparations. For this reason, tetracycline preparations should be administered at least two hours before, or four to six hours after, oral intake of calcium.
Hypercalcaemia may increase the toxicity of cardiac glycosides during treatment with calcium. Patients should be monitored with regard to electrocardiogram (ECG) and serum calcium levels.
If a bisphosphonate is used concomitantly, this preparation should be administered at least three hours before the intake of Calcichew 500mg Chewable Tablets since gastrointestinal absorption may be reduced.
The efficacy of levothyroxine can be reduced by the concurrent use of calcium, due to decreased levothyroxine absorption. Administration of calcium and levothyroxine should be separated by at least four hours.
The absorption of quinolone antibiotics may be impaired if administered concomitantly with calcium. Quinolone antibiotics should be taken two hours before or after intake of calcium.
Calcium salts may decrease the absorption of iron, zinc and strontium ranelate. Consequently, iron, zinc or strontium ranelate preparations should be taken two hours before or after calcium carbonate.4.6 Pregnancy and lactation
\*\*Pregnancy\*\*
Calcichew 500mg Chewable Tablets can be used during pregnancy. Daily intake should not exceed 2500 mg of calcium as permanent hypercalcaemia has been related to adverse effects on the developing foetus.
\*\*Breastfeeding\*\*
Calcium carbonate can be used during breast-feeding. Calcium passes into breast milk but at therapeutic doses no effects on the breastfed new-born are anticipated.4.7 Effects on ability to drive and use machines
Calcium carbonate has no known influence on ability to drive and use machines.4.8 Undesirable effects
Adverse reactions are listed below, by system organ class and frequency. Frequencies are defined as: uncommon (≥1/1,000 to <1/100); rare (≥1/10,000 to <1/1,000) or very rare (<1/10,000).
\*Metabolism and nutrition disorders\*
Uncommon: Hypercalcaemia and hypercalciuria.
Very rare: Milk-alkali syndrome (frequent urge to urinate; continuing headache; continuing loss of appetite; nausea or vomiting; unusual tiredness or weakness; hypercalcaemia, alkalosis and renal impairment). Seen usually only in overdose (see section 4.9).
\*Gastrointestinal disorders\*
Rare: Constipation, dyspepsia, flatulence, nausea, abdominal pain and diarrhoea.
\*Skin and subcutaneous disorders\*
Very rare: Pruritus, rash and urticaria.
\*\*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
Overdose can lead to hypercalcaemia. Symptoms of hypercalcaemia may include anorexia, thirst, nausea, vomiting, constipation, abdominal pain, muscle weakness, fatigue, mental disturbances, polydipsia, polyuria, bone pain, nephrocalcinosis, nephrolithiasis and in severe cases, cardiac arrhythmias. Extreme hypercalcaemia may result in coma and death. Persistently high calcium levels may lead to irreversible renal damage and soft tissue calcification.
Milk-alkali syndrome may still occur in patients who ingest large amounts of calcium and absorbable alkali. It is not uncommon as a cause of hypercalcaemia requiring hospitalisation. The syndrome has also been reported in a patient taking recommended doses of antacids containing calcium carbonate for chronic epigastric discomfort, and in a pregnant woman taking high, but not grossly excessive, doses of calcium (about 3 g of elemental calcium daily). Metastatic calcification can develop.
Treatment of hypercalcaemia: The treatment with calcium must be discontinued. Treatment with thiazide diuretics, lithium, vitamin A, vitamin D and cardiac glycosides must also be discontinued. Treatment: rehydration, and, according to severity of hypercalcaemia, isolated or combined treatment with loop diuretics, bisphosphonates, calcitonin and corticosteroids should be considered. Serum electrolytes, renal function and diuresis must be monitored. In severe cases, ECG and CVP should be followed.
## Pharmacological Properties
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Mineral supplements: Calcium.
ATC-code: A12AA04
An adequate intake of calcium is of importance during growth, pregnancy and breastfeeding.5.2 Pharmacokinetic properties
Absorption: The amount of calcium absorbed through the gastrointestinal tract is approximately 30% of the swallowed dose.
Distribution and biotransformation: 99% of the calcium in the body is concentrated in the hard structure of bones and teeth. The remaining 1% is present in the intra- and extracellular fluids. About 50% of the total blood-calcium content is in the physiologically active ionised form with approximately 10% being complexed to citrate, phosphate or other anions, the remaining 40% being bound to proteins, principally albumin.
Excretion and elimination: Calcium is eliminated through faeces, urine and sweat. Renal excretion depends on glomerular filtration and calcium tubular reabsorption.5.3 Preclinical safety data
There is no information of relevance to the safety assessment in addition to what is stated in other parts of the SmPC.
## Pharmaceutical Particulars
6.1 List of excipients
Xylitol (967)
Povidone
Magnesium stearate
Sucralose (E955)
Isomalt (E953)
Flavouring (orange)
Mono, di-fatty acid glycerides6.2 Incompatibilities
Not applicable.6.3 Shelf life
3 years.6.4 Special precautions for storage
Do not store above 30°C.
Keep the container tightly closed to protect from moisture.6.5 Nature and contents of container
Securitainer containing 100 tablets.6.6 Special precautions for disposal and other handling
No special requirements.
