Summary of medicine characteristics - FERROGRAD C TABLETS
1 NAME OF THE MEDICINAL PRODUCT
Ferrograd C Tablets
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
2 QUALITATIVE AND QUANTITATIVE COMPOSITIONDried Ferrous sulfate BP 325 mg (elemental iron 105 mg).
Sodium ascorbate 562.4 mg (ascorbic acid 500 mg).
3. PHARMACEUTICAL FORM
Prolonged release, film coated tablets.
Ovoid, biconvex, two layered red tablet.
4 CLINICAL PARTICULARS
4.1. Therapeutic indications
Prevention and treatment of iron deficiency anaemia and for the simultaneous treatment of vitamin C deficiency.
4.2 Posology and method of administration
Adults including the elderly
1 tablet daily. Take before food.
Children
Not recommended for children under 12 years. Above this age, as for adults.
Method of administration:
The tablets should not be sucked, chewed or kept in the mouth, but swallowed whole with water.
Tablets should be taken before meals or during meals, depending on gastrointestinal tolerance.
4.3. Contraindications
Intestinal diverticular disease or any intestinal obstruction.
Iron preparations are contra-indicated in patients with haemochromatosis and haemosiderosis.
Iron is contra-indicated in patients receiving repeated blood transfusions.
Oral iron preparations are contra-indicated when used concomitantly with parenteral iron therapy.
4.4. Special warnings and precautions for use
Ferrograd C tablets should be kept out of children's reach. Acute iron poisoning occurs rarely in adults, however it could happen if children swallow this medication.
The label will state ‘Important warning: Contains iron. Keep out of the reach and sight of children, as overdose may be fatal’. This will appear on the front of the pack within a rectangle in which there is no other information.
The prolonged release tablet and its inert plastic matrix may cause a safety hazard in some elderly or other patients suffering from delayed intestinal transit.
Iron preparations colour the faeces black, which may interfere with tests used for detection of occult blood in the stools. The guaiac test occasionally yields false positive tests for blood.
Due to the risk of mouth ulcerations and tooth discolouration, tablets should not be sucked, chewed or kept in the mouth, but swallowed whole with water.
Aspiration of iron sulfate tablets can cause necrosis of the bronchial mucosa which may result in coughing, haemoptysis, bronchostenosis and/or pulmonary infection (even if aspiration happened days to months before these symptoms occurred). Elderly patients and patients who have difficulties swallowing should only be treated with iron sulfate tablets after a careful evaluation of the individual patient’s risk of aspiration. Alternative formulations should be considered. Patients should seek medical attention in case of suspected aspiration.
4.5. Interactions with other medicinal products and other forms of interaction
Iron interacts with tetracyclines, magnesium trisilicate, trientine and zinc salts and absorption of all of these agents may be impaired.
Iron inhibits the absorption of tetracyclines from the gastrointestinal tract and tetracycline inhibits the absorption of iron. If both drugs must be given, tetracycline should be administered three hours after or two hours before oral iron supplements.
Concurrent administration of oral iron preparations with antacids, calcium supplements (calcium carbonate or phosphate), tea, coffee, eggs, food or medications containing bicarbonates, carbonate, oxalates or phosphates, milk or milk products, wholegrain breads and cereals and dietary fibre, may decrease iron absorption. Therefore, oral iron preparations should not be taken within one hour before or two hours after ingestion of such items.
Concurrent administration of oral iron preparations may interfere with the oral absorption of some quinolone anti-infective agents (e.g. ciprofloxacin, norfioxacin, ofloxacin), resulting in decreased serum and urine concentrations of the quinolones. Therefore, oral iron preparations should not be ingested with or within two hours of a dose of an oral quinolone.
Iron can decrease gastrointestinal absorption of penicillamines. Therefore, administration should be at least two hours apart if both drugs must be coadministered.
Chloramphemcol may delay response to iron therapy.
The administration of therapeutic doses of ascorbic acid may interfere with the Clinistix test for glucosuria giving a false negative result.
Ascorbic acid may enhance the absorption of iron from the gastrointestinal tract.
4.6. Pregnancy and lactation
Pregnancy
Ferrous salts are recommended for use in pregnancy, and no contraindications to such are known. No special requirements are to be anticipated.
Iron supplementation should not be routinely offered to all pregnant women in the absence of a diagnosis of iron deficiency anaemia.
Breast-feeding
Ferrous salts are recommended for use in lactation, and no contraindications to such are known. No special requirements are to be anticipated.
4.7. Effects on ability to drive and use machines
None.
4.8. Undesirable effects
Side-effects reported are similar to those associated with conventional oral iron preparations, i.e. nausea, vomiting, abdominal pain or discomfort, blackening of stools, diarrhoea and/or constipation, but the incidence of side-effects is less owing to the prolonged release nature of the formulation.
Isolated cases of allergic reaction have been reported ranging from rash to anaphylaxis.
Gastrointestinal disorders:
Not known: nausea, vomiting, abdominal pain or discomfort, blackening of stools, diarrhoea and/or constipation, mouth ulceration (in the context of incorrect administration, when the tablets are chewed, sucked or kept in mouth. Elderly patients and patients with deglutition disorders may also be at risk of oesophageal lesions or of bronchial necrosis, in case of false route).
Ascorbic acid is usually well tolerated. However, large doses are reported to cause diarrhoea and other gastrointestinal disturbances and are associated with the formation of renal calcium oxalate calculi.
Bronchial stenosis (see section 4.4)
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 Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
4.9. Overdose
Symptoms: Initial symptoms of iron overdosage include nausea, vomiting, diarrhoea, abdominal pain, haematemesis, rectal bleeding, lethargy and circulatory collapse. Hyperglycaemia and metabolic acidosis may also occur. The prolonged release characteristic may delay excessive absorption of iron, and thus allow more time for counter measures to be implemented. However, initial symptoms of overdosage may be absent due to the prolonged release formulation. Therefore, if overdosage is suspected, treatment should be implemented immediately. In severe cases, after a latent phase, relapse may occur after 24–48 hours, manifested by hypotension, coma and hepatocellular necrosis and renal failure.
Vitamin C overdosage may cause acidosis and haemolytic anaemia in predisposed individuals (glucose-6-phosphate dehydrogenase deficiency). Renal failure may occur in massive vitamin C overdose.
Treatment: The following steps are recommended to minimise or prevent further absorption of the medication:
Children:
1. Administer an emetic such as syrup of ipecacuanha.
2. Emesis should be followed by gastric lavage with desferrioxamine solution (2g/l). This should then be followed by the instillation of desferrioxamine 5 g in 50–100 ml water, to be retained in the stomach. Inducing diarrhoea in children may be dangerous and should not be undertaken in young children. Keep the patient under constant surveillance to detect possible aspiration of vomitus – maintain suction apparatus and standby emergency oxygen in case of need.
3. Unleached tablets are radio-opaque. Therefore, an abdominal x-ray should be taken to determine the number of tablets retained in the stomach following emesis and gastric lavage.
4. Severe poisoning: in the presence of shock and/or coma with high serum iron levels (serum iron >90 L.imol/l) immediate supportive measures plus i.v. infusion of desferrioxamine should be instituted. Desferrioxamine 15 mg/kg body weight should be administered every hour by slow i.v. infusion to a maximum 80 mg/kg/24 hours. Warning: hypotension may occur if the infusion rate is too rapid.
5. Less severe poisoning: i.m. desferrioxamine 1 g 4–6 hourly is recommended.
6. Serum iron levels should be monitored throughout.
Adults:
1. Administer an emetic.
2. Gastric lavage may be necessary to remove drug already released into the stomach. This should be undertaken using desferrioxamine solution (2g/l). Desferrioxamine 5 g in 50–100 ml water should be introduced into the stomach following gastric emptying. Keep the patient under constant surveillance to detect possible aspiration of vomitus; maintain suction apparatus and standby emergency oxygen in case of need.
3. Unleached tablets are radio-opaque. Therefore, an abdominal x-ray of the patient should be taken to determine the number of tablets retained in the stomach following emesis and gastric lavage. The risk/benefit ratio of x-raying pregnant women must be carefully weighed but should be avoided if possible.
4. A drink of mannitol or sorbitol should be given to induce small bowel emptying.
5. Severe poisoning: in the presence of shock and/or coma with high serum iron levels (>142 Limol/l) immediate supportive measures plus i.v. infusion of desferrioxamine should be instituted. The recommended dose of desferrioxamine is 5 mg/kg/h by slow i.v. infusion up to a maximum of 80 mg/kg/24 hours. Warning: hypotension may occur if the infusion rate is too rapid.
6. Less severe poisoning: i.m. desferrioxamine 50 mg/kg up to a maximum dose of 4 g should be given.
7.
Serum iron levels should be monitored throughout.
5 PHARMACOLOGICAL PROPERTIES
5.1. Pharmacodynamic properties
Ferrograd C combines the advantages of ferrous sulphate in the Gradumet® matrix with a large dose of vitamin C to further enhance absorption. It is indicated in iron-deficiency anaemia, especially when poor absorption is a problem, and to promote haemopoiesis in patients where an underlying vitamin C deficiency limits optimal haemoglobin formation. In patients whose haemoglobin has returned to normal, Ferrograd C may be of particular value in replenishing the depleted stores of iron.
5.2. Pharmacokinetic properties
The Gradumet device allows controlled release of ferrous sulphate over a number of hours and reduces gastro-intestinal intolerance. The device consists of an inert plastic matrix, honeycombed by thousands of narrow passages which contain ferrous sulphate together with a water soluble channelling agent. As the tablet passes down the gastro-intestinal tract the iron is leached out. The spent matrix is finally excreted in the stools.
Oral iron is absorbed better when administered between meals. However, conventional iron preparations often cause gastric irritation when taken on an empty stomach.
5.3. Preclinical safety data
There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.
6 PHARMACEUTICAL PARTICULARS
6.1. List of excipients
Tablet core:
Methylacrylate methylmethacrylate copolymer,
Magnesium stearate,
Povidone,
Macrogol 8000
Maize starch,
Purified talc,
Film coating:
Subcoat:
Povidone
Ethylcellulose,
Macrogol 400
Colour coating:
Hydroxypropylmethylcellulose
Macrogol 8000
Macrogol 400
Titanium dioxide
Dye Red Ponceau 4R Lake (E124).
Glossing:
Purified talc
Macrogol 8000
6.2. Incompatibilities
None.
6.3. Shelf life
5 years.
6.4. Special precautions for storage
Store in a cool dry place at or below 25°C.
6.5. Nature and contents of container
6.5. Nature and contents of containerCarton containing 30 (3×10) tablets in a blister (OP).
6.6. Instructions for use, handling and disposal
None.
7. MARKETING AUTHORISATION HOLDER
Via F.lli Cervi, 8
I-27010 Valle Salimbene (PV)
Italy
8. MARKETING AUTHORISATION NUMBER
PL 16250/0003
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
04/06/2004