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Naloxone

Generic Name
Naloxone
Brand Names
Kloxxado, Narcan, Suboxone, Targin, Targiniq, Zimhi, Zubsolv, Nyxoid
Drug Type
Small Molecule
Chemical Formula
C19H21NO4
CAS Number
465-65-6
Unique Ingredient Identifier
36B82AMQ7N
Background

Naloxone is an opioid antagonist medication used to block or reverse the effects of opioid drugs, particularly within the setting of drug overdoses which are rapidly becoming a leading cause of death worldwide. More specifically, naloxone has a high affinity for μ-opioid receptors, where it acts as an inverse agonist, causing the rapid removal of any other drugs bound to these receptors. When taken in large quantities, opioid medications such as morphine, hydromorphone, methadone, heroin, or fentanyl are capable of causing life-threatening symptoms such as respiratory depression, reduced heart rate, slurred speech, drowsiness, and constricted pupils. If untreated, this can progress to vomiting, absent pulse and breathing, loss of consciousness, and even death. Naloxone is indicated for the rapid reversal of these symptoms of central nervous system depression in opioid overdose. It's important to note that naloxone only works on opioid receptors within the body, and is therefore not capable of reversing the effects of non-opioid medications such as stimulants like methamphetamine or cocaine, or benzodiazepines like lorazepam or diazepam.

Also known as the brand name product Narcan, naloxone is currently available by intramuscular (IM) or subcutaneous (SubQ) injection, nasal spray, or intravenous (IV) infusion. Naloxone IM injections are commonly available in the form of "kits", which is ideal for making overdose treatment accessible and readily available for administration by minimally trained individuals within the community. Kits commonly include the supplies necessary to treat an overdose in a non-medical setting such as alcohol swabs, syringes, a rescue breathing mask, and instructions for use. Frequently also carried by medical and emergency personnel and at events known to be associated with heavy drug use like music festivals, naloxone kits are considered a key component of harm reduction strategies. There are over-the-counter nasal sprays available.

When injected intramuscularly (IM), naloxone acts within three to five minutes. Administration of naloxone is associated with very few side effects. Notably, if injected into a person not currently using opioid medications, there would be no noticeable effects at all. However, for individuals using opioid medications or experiencing an overdose, IM injection of naloxone rapidly reverses opioid effects and can cause the injected individual to immediately experience withdrawal symptoms. Common symptoms of opioid withdrawal include nausea, vomiting, sweating, runny nose, aches, and diarrhea. Although certainly physically uncomfortable, opioid withdrawal symptoms are not life-threatening; administration of naloxone is, therefore, appropriate for any person appearing to have any symptoms of an opioid overdose. Due to its short duration of action, persons injected with naloxone should be monitored for responsiveness and potentially injected a second time or taken to the hospital.

Naloxone is also available within the combination product Suboxone with the opioid medication buprenorphine. Suboxone is used for the maintenance treatment of opioid dependence and addiction. When taken orally, naloxone has no pharmacological effect and does not reduce the effectiveness of the opioid effect of buprenorphine. The primary purpose of including naloxone within Suboxone is to act as a deterrent to injection, as injected naloxone would rapidly reverse the effects of buprenorphine.

Naloxone was granted FDA approval on 13 April 1971.

Indication

Naloxone nasal sprays are indicated for the reversal of an opioid overdose or suspected opioid overdose: it is intended for immediate administration as emergency therapy in settings where opioids may be present. Intramuscular, intravenous, and subcutaneous injections are indicated for complete or partial reversal of opioid depression, diagnosis of known or suspected opioid overdose, and as an adjunct therapy in the treatment of septic shock.

Sublingual tablets and films are formulated with buprenorphine for the treatment of opioid dependence. Naloxone is also formulated with pentazocine as an oral tablet for severe pain.

Intramuscular or subcutaneous naloxone autoinjectors are used for the emergency treatment of people 12 years of age and older where the use of high-potency opioids such as fentanyl analogues as a chemical weapon, is suspected.

Naloxone has been used off-label for the treatment of neuraxial opioid-induced pruritus.

Associated Conditions
Opioid Dependence, Opioid Overdose, Pruritus, Respiratory Depression, Septic Shock, Severe Pain, Moderate Pain, Suspected Opioid Overdose
Associated Therapies
Emergency Care

Role of Endorphins in the Perception of Dyspnea in Patients With Chronic Obstructive Pulmonary Disease

Not Applicable
Completed
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Drug: intravenous injection of normal saline or naloxone
First Posted Date
2007-04-10
Last Posted Date
2007-11-02
Lead Sponsor
Dartmouth-Hitchcock Medical Center
Target Recruit Count
17
Registration Number
NCT00458419
Locations
🇺🇸

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, United States

Optimal Dose of Prophylactic Naloxone in Reducing Opioid-Induced Side Effects in Children/Adolescents

Phase 2
Completed
Conditions
Nausea
Pain
Pruritus
Interventions
First Posted Date
2006-05-26
Last Posted Date
2017-07-19
Lead Sponsor
Johns Hopkins University
Target Recruit Count
75
Registration Number
NCT00330343
Locations
🇺🇸

John Hopkins Hospital, Baltimore, Maryland, United States

Opioid Receptors Influence Ischemia-Reperfusion Injury

Not Applicable
Suspended
Conditions
Ischemia-Reperfusion Injury
First Posted Date
2005-09-16
Last Posted Date
2008-03-28
Lead Sponsor
Radboud University Medical Center
Target Recruit Count
40
Registration Number
NCT00184938
Locations
🇳🇱

Radboud University Nijmegen Medical Centre / Department of Pharmacology and Toxicology, Nijmegen, Gelderland, Netherlands

Tramadol to Reduce Opioid Withdrawal Symptoms

Phase 2
Completed
Conditions
Opioid-Related Disorders
First Posted Date
2005-09-02
Last Posted Date
2017-01-12
Lead Sponsor
National Institute on Drug Abuse (NIDA)
Target Recruit Count
16
Registration Number
NCT00142896
Locations
🇺🇸

Johns Hopkins University (BPRU) Bayview Campus, Baltimore, Maryland, United States

Characterization of Pain Processing Mechanisms in Irritable Bowel Syndrome

Phase 2
Completed
Conditions
Irritable Bowel Syndrome
First Posted Date
2005-04-18
Last Posted Date
2009-01-21
Lead Sponsor
US Department of Veterans Affairs
Registration Number
NCT00108446
Locations
🇺🇸

Malcom Randall VAMC, Gainesville, Florida, United States

Naloxone in Treating Constipation in Patients Who Are Receiving Opioids for Chronic Pain

Phase 3
Conditions
Constipation, Impaction, and Bowel Obstruction
Unspecified Adult Solid Tumor, Protocol Specific
First Posted Date
2004-04-05
Last Posted Date
2018-12-13
Lead Sponsor
Dana-Farber Cancer Institute
Registration Number
NCT00020605
Locations
🇺🇸

Brigham and Women's Hospital, Boston, Massachusetts, United States

Determine the Safety of a Sublingual Tablet Formulation of Buprenorphine and Naloxone by Extending the Combination Tablet Availability to Physicians in Office-Based Practice

Phase 4
Completed
Conditions
Opiate Dependence
First Posted Date
2001-01-01
Last Posted Date
2009-01-21
Lead Sponsor
US Department of Veterans Affairs
Target Recruit Count
600
Registration Number
NCT00007527
Locations
🇺🇸

Paul Casadonte, M.D. VAMC New York, New York, New York, United States

🇺🇸

Andrew Saxon, M.D.-Addictions Treatment (116ATC), Seattle, Washington, United States

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