MedPath

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

Health Canada Approves Hikma's KLOXXADO® 8 mg Nasal Spray for Opioid Overdose Treatment

• Health Canada has approved KLOXXADO® (naloxone HCl) Nasal Spray 8 mg for treating known or suspected opioid overdoses in adults, providing a higher-dose alternative to existing treatments. • Emergent BioSolutions will lead commercial efforts in Canada under a six-year agreement with Hikma, with the product expected to be available by prescription as early as 2026. • The approval comes as Canada faces an ongoing opioid crisis with 22 lives lost daily to overdoses in 2023, though expanded naloxone distribution has contributed to decreasing death rates in recent years.

Scienture Launches REZENOPY, Most Potent Naloxone Nasal Spray for Opioid Overdose Treatment

• Scienture Holdings has secured exclusive U.S. rights to launch REZENOPY, a 10mg naloxone HCl nasal spray, marking the highest-strength opioid overdose treatment available in the market. • Through collaboration with Kindeva Drug Delivery, REZENOPY will be manufactured and distributed, addressing the growing opioid crisis with annual naloxone market sales reaching $189 million. • The FDA-approved treatment offers enhanced effectiveness against potent opioids, featuring a quick-acting nasal delivery system designed for emergency overdose situations.

FDA Approves Test to Identify Patients at Risk of Opioid Use Disorder

The FDA has approved the AvertD test, a DNA analysis tool designed to identify patients at risk of developing opioid use disorder before they are prescribed opioid analgesics. This approval comes as part of efforts to combat the ongoing opioid epidemic in the US.

FDA Approves Journavx, a Novel Non-Opioid Painkiller, Offering New Hope for Acute Pain Management

• The FDA has approved Journavx (suzetrigine), a first-in-class non-opioid analgesic, for treating moderate to severe acute pain in adults, offering a safer alternative to opioids. • Journavx works by selectively blocking pain signals in the peripheral nervous system, reducing pain without the addictive potential and severe side effects associated with opioids. • Clinical trials demonstrated Journavx's effectiveness in reducing pain after surgeries, with a safety profile comparable to placebo, though it didn't outperform opioid-acetaminophen combinations. • Priced at $15.50 per pill, Journavx faces challenges in accessibility due to its higher cost compared to generic opioids, but it represents a significant step in combating the opioid crisis.
© Copyright 2025. All Rights Reserved by MedPath