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Calcium chloride

Updated 2 Feb 2023 | Calcium supplements

Presentation

Sterile aqueous solution of calcium chloride for slow intravenous injection or infusion.

This product is available in two strengths:

Calcium chloride dihydrate 7.35%
Each 5ml ampoule contains 2.5mmol of Ca
Each 10ml ampoule contains 5mmol of Ca

Calcium chloride dihydrate 14.7%
Each 5ml ampoule contains 5mmol of Ca
Each 10ml ampoule contains 10mmol of Ca

Drugs List

  • calcium chloride 10mmol/10ml (14.7%) injection
  • calcium chloride 2.5mmol/5ml (7.35%) injection
  • calcium chloride 5mmol/10ml (7.35%) injection
  • calcium chloride 5mmol/5ml (14.7%) injection
  • Therapeutic Indications

    Uses

    Hypocalcaemia
    Electrolyte imbalance

    Dosage

    Adults

    Precise dosage should be determined by the condition of the patient.
    An initial intravenous dose of 10mmol (by slow injection or after dilution, by infusion) may be given. The rate should not exceed 1mmol per minute.
    A further infusion of up to 10mmol per day be given.
    Plasma calcium must be monitored.

    Elderly

    See dosage Adults

    Children

    Children over 12 years
    See dosage Adults

    Children 2 to 12 years:
    Precise dosage should be determined by the condition of the patient.
    An initial intravenous dose of 0.5 - 3.5mmol (by infusion after dilution with at least 4 times its volume of sodium chloride 0.9%) may be given. The dose may be repeated every 1 to 3 days. Plasma calcium must be monitored.

    Children under 2 years:
    Precise dosage should be determined by the condition of the patient.
    An initial intravenous dose of less than 0.5mmol (by infusion after dilution with at least 4 times its volume of sodium chloride 0.9%) may be given. The dose may be repeated every 1 to 3 days. Plasma calcium must be monitored.

    Patients with Renal Impairment

    Use with caution in renal impairment, due to the increased risk of hypercalcaemia and renal calculi.

    Administration

    For slow intravenous use only.

    When possible solutions should be warmed to body temperature.

    Inject slowly through a small needle into a large vein to minimise venous irritation and avoid undesirable effects. Calcium chloride is considered to be the most irritant of the injectable calcium salts. Care should be taken to avoid extravasation.

    Infusions should be diluted with at least 4 times its volume of sodium chloride.

    Infant injections should not be given thorough the scalp.

    Incompatibilities

    Calcium salts are incompatible with a wide range of drugs. Complexes may form resulting in the formation of a precipitate. Generally the mixing of calcium with carbonates, citrates, oxidising agents, phosphates, sulfates, tartrates, tetracyclines or parenteral mixtures including total parenteral nutrition should be avoided.

    Contraindications

    Patients receiving cardiac glycosides
    Respiratory acidosis
    Respiratory failure
    Hypercalcaemia
    Hypercalciuria
    Nephrolithiasis
    History of nephrolithiasis
    Chronic renal impairment
    Digitalis toxicity

    For slow intravenous use only - other routes are contraindicated due to the risk of necrosis.

    Precautions and Warnings

    Sarcoidosis
    Renal impairment (see 'Dosage; Renal impairment' section)
    Cardiac disease

    A moderate fall in blood pressure due to vasodilatation may accompany the injection.

    Not suitable for the treatment of hypocalcaemia caused by renal impairment (due to calcium chloride's acidifying nature).

    The severe tissue necrosis caused upon extravasation of calcium chloride may limit the choice of this calcium salt to life threatening indications.

    Excessive amounts of calcium may lead to hypercalcaemia. Symptoms may include: anorexia, nausea, vomiting, constipation, abdominal pain, muscle weakness, mental disturbances, polydipsia, polyuria, bone pain, nephrocalcinosis, renal calculi, cardiac arrhythmias and coma.

    Calcium chloride is considered to be the most irritant of the injectable calcium salts. Severe tissue necrosis and sloughing may occur. Care should be taken to avoid extravasation or accidental injection into perivascular tissues.

    If calcium chloride is administered too rapidly, may lead to many of the symptoms of hypercalcaemia and in addition; chalky (calcium) taste, hot flushes, a sense of oppression, tingling sensations and peripheral vasodilatation.

    Monitoring of calcium serum levels is necessary following intravenous administration of calcium.

    Monitor serum electrolytes

    Pregnancy (see Pregnancy section).
    Breastfeeding (see Lactation section).

    Pregnancy and Lactation

    Pregnancy

    Evaluate risk / benefit of treatment in pregnancy.

    There are no studies on the effects of calcium chloride on pregnant women. No problems have been documented. However calcium crosses the placenta and absorption of calcium is increased during pregnancy.

    The use of all medication in pregnancy should be avoided whenever possible; particularly in the first trimester. Non-drug treatments should also be considered. When essential, a medication with the best safety record over time should be chosen, employing the lowest effective dose for the shortest possible time. Polypharmacy should be avoided. Teratogens taken in the pre-embryonic period, often quoted as lasting until 14-17 days post-conception, are believed to have an all-or-nothing effect. Where drugs have a short half-life, and when the date of conception is certain, this may allow women to be reassured where drug exposure has occurred within this time frame. Further advice may be available from the UK National Teratology Information Service (NTIS) and through ToxBase, available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).

    Lactation

    Use with caution in lactation

    Calcium is excreted in breast milk, but there are no data on the effects, if any, on the infant.

    Neonates, infants born prematurely, those with low birth weight, those with an unstable gastrointestinal function or who have serious illnesses may require special consideration. For any infant, if a drug is prescribed to the nursing mother, it should be at the lowest practical dose and for the shortest time. When drug administration is unavoidable and breastfeeding is to continue, minimisation of exposure of the infant to the drug may sometimes be achieved by timing the maternal doses to just after a feeding episode. Infants exposed to drugs via breast milk should be monitored for unusual signs or symptoms. Interactions between the drug received by the infant from the mother's milk and medication prescribed for the infant should also be considered, for example, when the drug given to the infant may prevent metabolism of the drug received via breast milk.
    Specialist advice is available from the UK Drugs in Lactation Advisory Service at https://www.midlandsmedicines.nhs.uk/content.asp?section=6&subsection=17&pageIdx=1

    Effects on Ability to Drive and Operate Machinery

    Some side effects may effect the patients ability to drive or operate machinery.

    Counselling

    Advise patients that side effects may effect their ability to drive or operate machinery

    Side Effects

    Gastro-intestinal symptoms
    Bradycardia
    Arrhythmias
    Irritation (after intravenous injection)
    Decrease in blood pressure
    Hot flushes
    Tingling sensation
    Peripheral vasodilatation
    Sense of oppression
    Symptoms of hypercalcaemia
    Hypertension
    Drowsiness
    Nausea
    Sweating
    Flushing

    Overdosage

    It is strongly recommended that the UK National Poisons Information Service be consulted on cases of suspected or actual overdose where there is doubt over the degree of risk or about appropriate management.

    The following number will direct the caller to the relevant local centre (0844) 892 0111

    Information may be obtained if you have access to ToxBase the primary clinical toxicology database of the National Poisons Information Service. This is available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).

    Shelf Life and Storage

    None stated.

    Further Information

    Last Full Review Date: May 2011

    Reference Sources

    British National Formulary, 61st Edition (2011) Pharmaceutical Press, London.

    BNF for Children (2010-2011) Pharmaceutical Press, London.

    Martindale: The Complete Drug Reference, 37th edition (2011) ed. Sweetman, S. Pharmaceutical Press, London.

    Summary of Product Characteristics: Calcium chloride injection 5mmol in 10ml. Martindale Pharmaceuticals (Macarthys Laboratories Ltd). Revised December 2000.

    Summary of Product Characteristics: Calcium chloride injection 10mmol in 10ml. Martindale Pharmaceuticals (Macarthys Laboratories Ltd). Revised January 2001.

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