NALOXONE

Naloxone injection is for intravenous (iv), intramuscular (im) or subcutaneous (sc) injection.

Opioid overdosage (known or suspected) Adults:

An initial dose of 400 micrograms to 2mg of naloxone may be administered intravenously. If the desired degree of counteraction and improvement in respiratory function is not obtained it may be repeated at two to three minute intervals.

If no response is observed after 10mg of naloxone being administered the diagnosis of opioid-induced or partial opioid induced toxicity should be questioned. Intramuscular or subcutaneous administration may be necessary if dosing by the intravenous route is not feasible.

Post-operative Use:

When naloxone is used post-operatively, the dose should be titrated for each patient in order to obtain respiratory response while maintaining analgesia. 0 micrograms/kg body weight is usually sufficient, but a full two minutes should be allowed between each 100 microgram increment of naloxone administered.

e. long or short acting) of drug used. Alternatively, naloxone may be administered as an intravenous infusion (see below).

Children:

The usual initial dose in children is 5-10 micrograms per kg body-weight given intravenously. If this does not result in the desired degree of clinical improvement, a subsequent dose of 100 micrograms per body weight may be administered.

Naloxone may be administered intramuscularly or subcutaneously in divided doses. Intravenous Infusion (iv) In situations where one of the longer acting opioids is known or suspected to be the cause of the symptoms, IV infusion of naloxone is recommended to produce sustained antagonism to the opioid (without antagonism of pain relief) rather than repeated injection.

9%) or 5% dextrose in water or saline. Mixtures should be used within 24 hours. Any remaining unused solution must then be discarded. The rate of administration should be titrated in accordance with the patient’s response.

8 Undesirable effects). Naloxone may antagonise the analgesic effects of the opioids in the control of postoperative pain. 5 Interaction with other medicinal products and other forms of interaction Naloxone should be used with caution in patients who are opioid dependent (including patients being treated with methadone), as it may precipitate an acute withdrawal syndrome.

g. g. alfentanil, fentanyl, remifentanil). 6 Pregnancy and lactation Naloxone crosses the placenta; adequate and well-controlled studies in humans have not been done, therefore naloxone, like all drugs, should be used with caution during pregnancy.

Risk-benefit must be considered before naloxone is administered to a pregnant woman who is known or suspected to be opioid dependent because naloxone may precipitate withdrawal in the foetus as well as the mother. It is not generally advisable to give naloxone just prior to delivery as blocking endogenous endorphins may affect the ability of the foetus to withstand the stress of delivery.

It is not known if naloxone is distributed into breast milk Problems in humans have not been documented. 7 Effects on ability to drive and use machines None known. 8 Undesirable effects Cardiac disorders: atrial and ventricular dysrhythmias, including atrial premature contractures, ventricular tachycardia and fibrillation, asystole, hypotension, hypertension, left ventricular failure and cardiac arrest.

Gastrointestinal disorders:

Nausea and vomiting.

General disorders and administration site conditions:

Opioid withdrawal symptoms- sweating, yawning, rhinorrhoea, sneezing, muscle tremor, weakness, anxiety, irritability, restlessness, nausea, vomiting, diarrhoea, abdominal and muscle cramps, piloerection, increases in heart rate (tachycardia), blood pressure and temperature (fever).

Acute withdrawal syndrome may include, but is not limited to the above listed signs and symptoms. Acute withdrawal effects after naloxone have only been reported in individuals physically dependent on opioids or after large doses of opioids.

Nervous system disorders: tingling/numbness of the extremities, trembling and generalised convulsions. Psychiatric disorders: behavioural changes, including violent behaviour, nervousness, restlessness, excitement, irritability.

Respiratory, thoracic and mediastinal disorders:

Pulmonary oedema and dyspnoea. 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.

uk/yellowcard.

Patients who have responded satisfactorily to naloxone should be kept under observation. Repeated doses may be necessary since the duration of action of some opioids may exceed that of naloxone. Naloxone is not effective against respiratory depression caused by non-opioid drugs.

8 Undesirable effects). Naloxone may antagonise the analgesic effects of the opioids in the control of postoperative pain.

Naloxone should not be given to patients who are known to be hypersensitive to it.