Suspected acute opioid overdose or intoxication

Active Ingredient: Naloxone

Indication for Naloxone

Population group: only children (1 year - 12 years old) , adolescents (12 years - 18 years old) , adults (18 years old or older)
Therapeutic intent: Curative procedure

For this indication, competent medicine agencies globally authorize below treatments:

0.01 mg/kg and thereafter, if satisfactory clinical response is not achieved, an additional injection of 0.1 mg/kg

For:

Dosage regimens

Intravenous, 0.01 milligrams naloxone per kilogram of body weight, one dose. Afterwards, intravenous, 0.1 milligrams naloxone per kilogram of body weight, one dose.

Detailed description

The usual starting dose is 0.01 mg naloxone hydrochloride per kg i.v. If the satisfactory clinical response is not achieved, the dose can be increased in the next injection to 0.1 mg/kg. Depending on the individual patient, an i.v. infusion may also be necessary.

0.01 mg/kg and thereafter, if satisfactory clinical response is not achieved, an additional injection of 0.1 mg/kg

For:

Dosage regimens

Intramuscular, 0.01 milligrams naloxone per kilogram of body weight, one dose. Afterwards, intramuscular, 0.01 milligrams naloxone per kilogram of body weight, one dose.

Detailed description

The usual starting dose is 0.01 mg naloxone hydrochloride per kg i.v. If the satisfactory clinical response is not achieved, the dose can be increased in the next injection to 0.1 mg/kg. Depending on the individual patient, an i.v. infusion may also be necessary. If i.v. administration is not possible, naloxone can also be injected i.m. (initial dose 0.01 mg/kg), divided into several doses.

0.4-2 mg and thereafter, if the desired clinical response is not achieved, repeat every 2-3 min up to a total dose of 10 mg

For:

Dosage regimens

Intravenous, between 0.4 milligrams naloxone and 2 milligrams naloxone, once every 2 to 3 minutes.

Detailed description

The initial dose is usually 0.4-2 mg naloxone hydrochloride i.v. If the desired improvement in the respiratory depression is not obtained immediately after i.v. administration, the injections can be repeated at intervals of 2-3 minutes.

If 10 mg naloxone hydrochloride does not produce a significant improvement, this suggests that the depression is wholly or partially caused by other pathological conditions or active substances other than opioids.

0.4-2 mg and thereafter, if the desired clinical response is not achieved, repeat every 2-3 min up to a total dose of 10 mg

For:

Route of admnistration

Defined daily dose

Dosage regimen

$d time(s) per day every $document.frequencyDenominator day(s)

Detailed description

The initial dose is usually 0.4-2 mg naloxone hydrochloride i.v. If the desired improvement in the respiratory depression is not obtained immediately after i.v. administration, the injections can be repeated at intervals of 2-3 minutes.

Naloxone can also be injected intramuscularly (initial dose usually 0.4-2 mg) if intravenous administration is not possible.

If 10 mg naloxone hydrochloride does not produce a significant improvement, this suggests that the depression is wholly or partially caused by other pathological conditions or active substances other than opioids.

1 spray of 2 or 4 mg into one nostril and if the desired response is not obtained, repeat every 2-3 min

For:

Dosage regimens

Regimen A: Intrasinal, 2 milligrams naloxone, once every 2 to 3 minutes.

Regimen B: Intrasinal, 4 milligrams naloxone, once every 2 to 3 minutes.

Detailed description

Naloxone nasal spray is indicated for the emergency treatment of known or suspected opioid overdose, as manifested by respiratory and/or central nervous system depression.

It is intended for immediate administration as emergency therapy in settings where opioids may be present.

It is not a substitute for emergency medical care.

Initial Dosing

The recommended initial dose in adults and pediatric patients is one spray delivered by intranasal administration into one nostril.

Repeat Dosing

Seek emergency medical assistance as soon as possible after administering the first dose of naloxone nasal spray.

The requirement for repeat doses of naloxone nasal spray depends upon the amount, type, and route of administration of the opioid being antagonized.

Administer naloxone nasal spray in alternate nostrils with each dose.

If the patient responds to naloxone nasal spray and relapses back into respiratory depression before emergency assistance arrives, administer an additional dose of naloxone nasal spray and continue surveillance of the patient.

If the desired response is not obtained after 2 or 3 minutes, administer an additional dose of naloxone nasal spray. If there is still no response and additional doses are available, administer additional doses of naloxone nasal spray every 2 to 3 minutes until emergency medical assistance arrives.

Additional supportive and/or resuscitative measures may be helpful while awaiting emergency medical assistance.

Active ingredient

Naloxone

Naloxone hydrochloride, a semisynthetic morphine derivative (N-allyl-nor-oxymorphone), is a specific opioid antagonist that acts competitively at opioid receptors. It reveals very high affinity for the opioid receptor sites and therefore displaces both opioid agonists and partial antagonists, such as pentazocine, for example, but also nalorphine.

Read more about Naloxone

Related medicines

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