Summary of medicine characteristics - SANDO-K
SANDO-K®
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Effervescent Tablets containing 0.6g potassium chloride Ph.Eur., 0.4g potassium bicarbonate USP
Flat, round, white effervescent tablet with a slightly rough surface, weighing 2.4g and of 22mm diameter and 4.25mm thick
4.1 Therapeutic indications
Prevention and treatment of hypokalaemic states such as those associated with:
i) Use of drugs which can induce potassium depletion eg. frusemide, thiazide diuretics, corticosteroids, carbenoxolone and cardiac glycosides, especially in combination with diuretic
ii) Potassium loss resulting from severe diarrhoea, vomiting or fistulas;
iii) Acid-base disturbances e.g. alkalosis, renal tubular acidosis, states in which there is aldosterone excess, Cushing syndrome;
iv) Decreased intake of potassium e.g. malnutrition, alcoholism, some elderly patients with deficient diets;
v) Since SANDO-K Effervescent Tablets contain Cl- they may be used in the treatment of hypokalaemia associated with hypochloraemic alkalosis.
4.2 Posology and method of administration
Oral administration, after dissolution of the tablet in water. May be taken with food if preferred.
Adults and children
Dosage is dependent upon the clinical conditions and diet of the patient, however the administration of 2 to 4 tablets daily (24 to 48 mmol K+) is likely to provide an adequate prophylactic or therapeutic dose in most patients. Large doses may be indicated in more severe hypokalaemic conditions when the dose should be regulated by the patient's response as determined by serum electrolyte levels and acid-base studies.
Dosage guidelines
A drop in serum potassium level of 1 mmol/l represents a loss of about 100–200 mmol of potassium from body stores. While serum potassium levels below 2 mmol/l may warrant intravenous replacement therapy, following are approximate guidelines in less severe potassium depletion:
For serum levels between 2–3 mmol/l, a maximum daily dose of 100–200 mmol K+ (8–16 tablets) and for serum levels between 3–4 mmol/l, a maximum daily dose of 50100 mmol K+ (4–8 tablets) should be considered.
Elderly
No evidence exists that elderly patients require different dosages or show different side-effects than younger patients. However, such patients should be carefully supervised as factors sometimes associated with ageing, such as poor diet or impaired renal function, may indirectly affect the dosage or tolerability.
4.3 Contraindications
Severe renal impairment with oliguria, inadequately treated Addison's disease, hyperkalaemia from any cause, crush injuries and acute dehydration.
4.4 Special warnings and precautions for use
Periodic evaluation of the patient's clinical status, serum electrolytes and the ECG should be carried out when replacement therapy is undertaken. This is particularly important in patients with cardiac disease and in those receiving digitalis. Care should be taken to avoid dosage in excess of requirements for patients with impaired renal function. Caution is also necessary in patients receiving potassium-sparing diuretics and ACE-inhibitors, and in patients with myotonia congenita or severe haemolysis. In patients with acidosis, the acid-base balance should be monitored. In patients with hypertension, it should be remembered that correction of hypokalaemia may lower blood pressure.
4.5 Interaction with other medicinal products and other forms of interaction
If co-administered with potassium-sparing diuretics and ACE-inhibitors, the risk of hyperkalaemia must be considered.
4.6 Fertility, Pregnancy and lactation
No clinical problems have been encountered during pregnancy and lactation.
Nevertheless, the benefit of treatment should be considered in relation to the risks before SANDO-K is given to pregnant or nursing women.
4.7 Effects on ability to drive and use machines
No effects known.
4.8 Undesirable effects
Abdominal discomfort, diarrhoea, nausea and vomiting may occur. If there are any signs of gastric irritancy, SANDO-K, in common with all other potassium salts, should be given with or after food. Gastric irritancy has occurred but this is rare since the tablets dissolve in water and are taken in solution, thus preventing high local concentrations. A moderate hyperkalaemia may be asymptomatic; if suspected reference to the section on overdosage is recommended.
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 national reporting system in the United Kingdom: Yellow Card Scheme
Website: www.mhra.gov.uk/yellowcard
4.9 Overdose
Hyperkalaemia. Poisoning is usually minimal below 6.5 mmol per litre but may be severe above 8 mmol per litre. However, comparatively low doses may cause adverse effects when excretion is delayed as in renal insufficiency. The absolute toxicity is dependent on other electrolytes and acid-base levels.
Hyperkalaemic symptoms include paraesthesia of the extremities, listlessness, mental confusion, weakness, paralysis, hypotension, cardiac arrhythmias, heart block and cardiac arrest.
Hyperkalaemia is often asymptomatic. However, increasing serum potassium levels can be detected by changes in the ECG; initially the appearance of tall, peaked T waves, followed by a widening of the QRS complex bending into the abnormal T waves. P-wave voltage decreases and the PR interval is prolonged.
Severe cardiac toxicity may be treated with calcium gluconate (10–20ml of a 10% injection given over 1–5 minutes with ECG monitoring). The effect may be transient and the injection may need to be repeated.
Raised serum potassium levels respond to administration of dextrose (300–500ml/hr of 10 or 25% solution), dextrose and insulin (as for dextrose with 10 units of insulin per 20g dextrose), or sodium bicarbonate solution.
Cation exchange resins may be used, or in severe cases peritoneal dialysis or haemodialysis may be necessary.
Caution should be exercised in patients who are digitalised and who may experience acute digitalis intoxication in the course of potassium removal.
| 5.1 | Pharmacodynamic properties |
| The potassium ion is essential to the maintenance of body function, being involved in the synthesis of protein, metabolism of carbohydrate and storage of energy reserves. It interacts with sodium in the operation of the trans-membrane pump and at the site of exchange in the kidney, exchanges with sodium ion to maintain body homeostasis. A close relationship between potassium ion and magnesium ion has also been noted; a deficit in one ion has been associated with low levels of the other. The diet of a healthy adult will provide an adequate intake of potassium (considered to be 20.5 to 33.3 mmol potassium daily) from a total intake of 60–100 mmol potassium. Total body potassium in an adult is about 3,500 mmol depending on the non-fat body tissues. A deficient intake or failure to conserve potassium leads to symptoms of hypokalaemia. |
5.2 Pharmacokinetic properties
Unless a deficiency is present, requiring a supplement, sufficient potassium is taken into the body through the daily diet. The chloride salt of potassium is readily absorbed from the gastro-intestinal tract. Potassium enters the intracellular fluid to maintain a concentration of about 150 mEq/l and the normal range of concentration of potassium in the plasma is considered to be 3.5 – 5 mEq/l.
Excretion of potassium is mainly by the distal tubules of the kidney, by the faeces (5 to 10 mmol/day) and a smaller amount in perspiration.
Metabolic, drug induced, or dietary deficiencies in potassium intake may require administration of a supplement.
5.3 Preclinical safety data
SANDO-K Effervescent Tablets contain potassium chloride and postassium bicarbonate (both of which are the subject of pharmacopoeial monographs). The physiological, pharmacological and clinical toxicity of potassium salts are well documented and limited animal data are therefore available.
6.1 List of excipients
Dioctyle sodium sulfosuccinate BPC , Colloidal anhydrous silica EP, Talc (acid washed) EP, Sodium saccharin BP, Icing sugar, CP HSE, Pulverised sugar, EP, Citric acid anhydrous 30/60 EP, Polyethylene glycol 4000 EP, Purified water EP.
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
36 Months.
6.4 Special precautions for storage
Do not store above 25°C. Store in the original container. Keep the container tightly closed.
6.5 Nature and contents of container
High density polypropylene tube with polyethylene bellowed stopper containing integral silica gel dessicant capsule. Pack size 20.
6.6 Special precautions for disposal
6.6 Special precautions for disposalNot applicable