Opioid overdose

Short description: Toxicity due to excessive consumption of opiates

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"Heroin overdose" redirects here. For other uses, see heroin.

Opioid overdose

Other names| Narcotic overdose, opioid poisoning
A naloxone kit distributed in British Columbia, Canada
Specialty| Toxicology, emergency medicine
Symptoms| Respiratory depression, small pupils, unconsciousness
Complications| Permanent brain damage
Causes| Opioids (morphine, codeine, heroin, fentanyl, tramadol, methadone, etc.)
Risk factors| Opioid dependence, metabolic disorders, use of high doses of opioids, injection of opioids, use with antidepressants, alcohol, benzodiazepines, and cocaine.[1][2]
Diagnostic method| Based on symptoms[3]
Differential diagnosis| Low blood sugar, alcohol intoxication, head trauma, stroke[4]
Prevention| Improved access to naloxone, treatment of opioid dependence
Treatment| Supporting a person's breathing and naloxone
Deaths| over 110,000 (2017)

An opioid overdose is toxicity due to excessive consumption of opioids, such as morphine, codeine, heroin, fentanyl, tramadol, Oxycodone, and methadone.[3][5] This preventable pathology can be fatal if it leads to respiratory depression, a lethal condition that can cause hypoxia from slow and shallow breathing.[3] Other symptoms include small pupils[note 1] and unconsciousness; however, its onset can depend on the method of ingestion, the dosage and individual risk factors.[6] Although there were over 110,000 deaths in 2017 due to opioids, individuals who survived also faced adverse complications, including permanent brain damage.[7][8]

Opioid overdoses are diagnosed based on symptoms and examination.[3] Risk factors for opioid overdose include high levels of opioid dependence, use of opioids via injection, high-dose opioid usage, having a mental disorder or having a predisposition for one, and use of opioids in combination with other substances, such as alcohol, benzodiazepines, or cocaine.[1][9][2] Dependence on prescription opioids can occur from their use to treat chronic pain in individuals.[1] Additionally, if following a period of detoxification, which allows the tolerance level to fall, the risk of overdose upon return to use is high.[1]

Initial treatment of an overdose involves supporting the person's breathing and providing oxygen to reduce the risk of hypoxia.[10] Naloxone is then recommended to those who cannot reverse the opioid's effects through breathing.[10][3] Giving naloxone via nasal administration or as an injection into a muscle has shown to be equally effective.[11] Other efforts to prevent deaths from overdose include increasing access to naloxone and treatment for opioid dependence.[1][12]

Drug use contributes to 500,000 deaths worldwide, with opioid overdose resulting in approximately 115,000 of these deaths in 2018.[1] This is up from 18,000 deaths in 1990.[13][14] In 2018, approximately 269 million people had engaged in drug usage at least once, 58 million of which used opioids.[1] Drug use disorders have affected around 35.6 million people worldwide in 2018.[1] The WHO estimates that 70% of deaths due to drug use are in relation to opioids, with 30% being due to overdose.[1] It is believed that the opioid epidemic has partly been caused due to assurances that prescription opioids were safe, by the pharmaceutical industry in the 1990s.[15] This led to unwarranted trust and a subsequent heavy reliance on opioids.[15] Though there are treatment interventions which can effectively reduce the risk of overdose in people with opioid dependence, less than 10% of affected individuals receive it.[1]

## Contents

* 1 Signs and symptoms
* 2 Causes
* 2.1 Co-ingestion
* 3 Risk factors
* 3.1 Metabolic disorders
* 3.2 Mental health
* 4 Mechanism
* 5 Prevention
* 6 Treatments
* 6.1 Naloxone
* 6.1.1 Access to Naloxone
* 6.2 Basic Life Support
* 6.3 Other Treatments
* 7 Epidemiology
* 7.1 United States
* 8 Awareness
* 9 See also
* 10 Notes
* 11 References
* 12 External links

## Signs and symptoms

Opiate overdose symptoms and signs can be referred to as the "opioid toxidrome triad": decreased level of consciousness, pinpoint pupils, and respiratory depression. Other signs and symptoms include seizures and muscle spasms. Sometimes, an opiate overdose can lead to such a decreased level of consciousness that the person will not wake up.

Pinpoint pupils, or miosis, caused by opioids

Because of their effect on the part of the brain that regulates breathing, opioids can cause very slow or stopped breathing during overdoses, leading to hypoxia[16] or death if left untreated.[1] Hypoxia is typically caused by respiratory depression.[17][18] The brain uses oxygen to regulate the homeostasis of the body. In animal studies, it was found that opioids act on specific regions of the central nervous system associated with respiratory regulation, including the medulla and pons.[18] During cerebral hypoxia, the brain lacks sufficient oxygen supply.[17] Prolonged lack of oxygenation from respiratory depression can lead to detrimental damage to the brain and spinal cord and can leave the person unable to walk or function normally, even if treatment with naloxone is given.[17]

Alcohol also causes respiratory depression and, therefore, when taken with opioids, can increase the risk of respiratory depression and death.[1]

In young children, opioid overdose may not be apparent right away. This is due to absorption, distribution, and metabolism differences between young children and adults and the higher amount of opioid ingestion per kilogram of body weight.[3]

## Causes

Fentanyl. 2 mg (white powder to the right) is a lethal dose in most people.[19] US penny is 19 mm (0.75 in) wide.

Risk factors for opioid overdose include opioid dependence, injecting opioids, using high doses of opioids, and use together with alcohol, benzodiazepines, or cocaine.[1][2] The risk is particularly high following detoxification.[1] Dependence on prescription opioids can occur from their use to treat chronic pain.[1] In young children, an overdose is usually due to opioids that are intended for their parents, older siblings, or grandparents.[20] In mothers who take codeine during breastfeeding, opioid overdoses have occurred in their baby.[21] Codeine is, therefore, not recommended for those who are breastfeeding.[21]

### Co-ingestion

Opioid overdoses are often associated with benzodiazepines, tranquilisers (e.g. xylazine) or alcohol use.[22][23] Other central nervous system depressants, muscle relaxers, pain relievers, anti-convulsants, anxiolytics, treatment drugs of a psychoactive or epileptic variety or any other such drug with its active function meant to calm or mitigate neuronal signaling (barbiturates, etc.) can additionally cause a worsened condition with less likelihood of recovery cumulative to each added drug. This includes drugs less immediately classed to a slowing of the metabolism such as with GABAergic like GHB or glutamatergic antagonists like PCP or ketamine.

## Risk factors

End organ dysfunction (liver disease), which may lead to decreased drug clearance, is a risk factor for opioid overdose.[24] Other risk factors for opioid overdose include sleep disordered breathing disorders such as sleep apnea, pulmonary diseases (such as asthma or chronic obstructive pulmonary disease) which may reduce ventilation and concomitant use of sedating medications such as benzodiazepines, gabapentinoids, muscle relaxants and other central nervous system depressants.[24] Benzodiazepine use with opioids increases the risk of overdose death by four-fold, whereas concomitant use with gabapentintoids such as gabapentin or pregabalin increases the risk of overdose death by nearly two-fold.[24]

Higher doses of prescription opioids, as well as long-acting formulations, are associated with an increased risk of overdose.[24] In those on long-term opioid treatment for chronic pain, daily morphine equivalents greater than 200 mg were associated with death from opioid related causes (including overdose) in 3.8% of men and 2.2% of women.[24] Opioids are the most common cause for serious accidental poisonings of children in the UK.[25]

### Metabolic disorders

Opioids are primarily metabolized in the liver, before being excreted through urine. Opioids are metabolized by phase 1 and/or phase 2 metabolism, which can lead to the activation or inhibition of these drugs.[26][3] Phase 1 metabolism is the CYP pathway which consists of different cytochrome P450s – a set of enzymes that catalyze hydrolysis, reduction, and oxidation reactions – to create an active metabolite.[27] In contrast, Phase 2 metabolism causes the opioids to undergo conjugation, with little to no interaction with the CYP pathway.[27] The opioids undergo phase 1 and phase 2 metabolism until they are hydrophilic enough to be renally excreted.[26]

Various factors play a role in how an opioid is metabolized. In phase 1 metabolism, the CYP family has several polymorphisms, which can account for the difference in therapeutic responses within each individual.[28] This diversification leads to opioids being modified at varying rates, which can cause the drug to remain in the bloodstream for either a longer or shorter period.[28] Therefore, these polymorphisms control opioid tolerance and facilitate overdose.

### Mental health

Evidence suggests that mental health can be a significant facilitator for opioid use disorder.[29] Given that opioids are prescribed for pain management, mental health disorders, such as depression, have been shown to increase use of opioids when treating conditions associated with chronic pain.[29] Evidence has shown that individuals with mood and anxiety disorders have an increased likelihood of being prescribed opioids and continuing usage for lengthy periods of time, consequently increasing likelihood for dependence.[30] As such, affected individuals have almost double the risk of using opioids for pain relief in the long-term.[30] Additionally, mental health challenges associated with trauma, economic depression, social environments conducive to substance use and risk-taking behaviours have been shown to increase opioid misuse.[31] Furthermore, mental health challenges associated with cardiovascular disease, sleep disorders, and HIV can cause opioid dependence and subsequent overdose.[32] Notably, cyclic behaviours can be observed between mental illness and opioid use disorder where individuals with mental health diagnoses engage in opioid use which further perpetuates mental health challenges and increased drug usage.[32]

## Mechanism

Mu opioid receptor (a GPCR)

Opioids bind with neural opioid receptors to provoke analgesic, sedative, and euphoric effects.[16] Opioids function by stimulating specific G-protein coupled receptors distributed throughout the body—including the brain, skin and spinal cord.[16] Three of the major opioid receptors include mu, kappa, delta, and nociception, each playing a role in eliciting the effects associated with opioids.[33] An opioid overdose results from over-activation of these receptors, which can cause permanent brain damage from cerebral hypoxia or neurotoxicity.[34][7]

Mu receptors have an analgesic effect on the brain, and are found in various parts of the nervous system including the cerebral cortex and thalamus.[16] They can be found in the nucleus accumbens, the pleasure centre of the brain, as well as the amygdala.[16] Kappa receptors, in the hypothalamus, produce a similar analgesic effect. They bind with dynorphins to stimulate anti-reward effects (dysphoria) and other negative effects of withdrawal. While mu receptors are the source of addiction, kappa receptors contribute to continued use. They generate dysphoria in response to increasing stress levels via corticotropin-releasing factor (CRF).[16] This increases erratic shifts in mood during the withdrawal period and can prompt relapse.[16] Delta receptors, found in the basal ganglia of the limbic system, have been shown to reduce anxiety by binding with enkephalins, although this requires further research.[16] The most recent addition to these receptors are nociception opioid receptors. Although they have been determined to be receptors to certain ligands from opioids, their role is not yet fully understood.[35]

When opioids are ingested, the ligand binds to these constitutively active receptors to reduce neural activity.[33] This is accomplished by inhibiting adenylyl cyclase and cyclic AMP, which are necessary for communication within the central nervous system.[33] There is research indicating that opioids reduce pain by disrupting ion channels and vesicle fusion.[33]

Prolonged exposure to opioids can cause these receptors to become internalized, leading to increased tolerance and increased opioid use.[17]

## Prevention

Opioid overdoses can often be prevented.[36][37] Clear protocols for staff at emergency departments and urgent care centers can reduce opioid prescriptions for individuals presenting in these settings who engage in drug seeking behaviors or who have a history of a substance use disorder.[38] Drug seeking behaviors include but are not limited to obsessiveness or impatience when it comes to attaining medications, seeking multiple pain adjunct medications, and inconsistent physiological presentation.[39] A prescription monitoring program may help determine if an individual is receiving a high doses of opioids or combinations of medications such as benzodiazepines and opioids that put them at high risk.[40] Limited amount of evidence suggests opioid therapy with extended-release or long-acting formulations may increase the risk of an unintentional overdose compared to shorter-acting agents.[41] Routinely screening using tools such as the CAGE-AID and the Drug Abuse Screening Test (DAST-10) in adults and the CRAFFT in those aged 14–18 years is recommended.[36] The revised risk index for overdose or severe opioid induced respiratory depression (RIOSORD) is a validated screening tool that may be used to estimate the risk of overdose in people using opioids, or the rapid opioid dependence screen may be used as a more rapid and succinct method to screen for opioid use disorder.[24] Other "drug seeking" behaviors and physical indications of drug use should be used as clues to perform formal screenings.[36]

There are several medication-assisted treatments available for people with opioid use disorder or opioid dependence who are at higher risk for opioid overdose.[1][42] The selection of treatment depends on various factors, such as a person's preference, accessibility, and history of treatment.[42] Examples of medication-assisted treatments are buprenorphine (with or without naloxone), naltrexone, and methadone.[43][44] Methadone and buprenorphine are associated with reduced mortality in those with opioid use disorder as well as higher drug treatment program retention, lower illicit drug use, and decreased overdose deaths.[24] The mortality benefit of long-term naltrexone use in those with opioid use disorder is less well-established.[24] After a non-fatal opioid overdose, subsequent methadone or buprenorphine initiation and use reduce the risk of overdose death by 59% and 38%, respectively. Initiating buprenorphine in the emergency department is associated with lower mortality and increased adherence to opioid use disorder treatment programs.[24] Peer support groups have tentative evidence of benefit.[45] There is also some evidence indicating benefits in community-based overdose education and naloxone distribution programs.[46] Buprenorphine and methadone can help decrease drug cravings.[42] Combining pharmacologic treatments with behavioral therapy, such as support or recovery groups, can increase the likelihood of overcoming addiction and reduce the risk of an opioid overdose.

File:P20250716MR-0146 President Donald Trump attends a signing ceremony for the HALT Fentanyl Act.jpgPresident Trump with families of overdose victims after signing the HALT Fentanyl Act, 16 July 2025

Individuals diagnosed with opioid dependence should be prescribed naloxone to prevent overdose. They should be directed to one of the treatment options available, such as needle exchange programs and treatment centers.[36][37] A naloxone prescription is also recommended when risk factors for opioid overdose are present, such as a history of overdose, substance use disorder, or higher doses of opioids.[40] With the CDC recommending naloxone be provided to all people on long term opioids who have risk factors for overdose, including a history of a substance use disorder, daily morphine equivalents greater than 50 mg or concurrent benzodiazepine use.[24] Brief motivational interviewing can also be performed and has been shown to improve people's motivation to change their behavior.[36][47] Despite these opportunities, the dissemination of prevention interventions in the US has been hampered by the lack of coordination and sluggish federal government response.[37]

Unused or old opioids should not be stored in the home as there is a risk of people using the drugs for non-medical purposes. Among adolescents and young-adults, non-medical use of prescription opioids is associated with a subsequent 13-fold increased risk of heroin use later in life.[24] Opioids that are no longer being used may be taken to drug take back programs at local pharmacies, healthcare facilities or law enforcement agencies for safe disposal. The United States Food and Drug Administration also has a "flush list"; a list of medications that may be safely disposed of by flushing down the toilet.[48]

In the United States, 49 states and the District of Columbia have expanded naloxone access at a pharmacy level via standing order, protocol order, naloxone-specific collaborative practice agreement, or pharmacist prescriptive authority.[49]

## Treatments

If someone is suspected to have overdosed on opioids, call for medical attention, administer naloxone, and provide basic life support as soon as possible.[50]

Free Narcan and test strips at a community event in Hopland, California

### Naloxone

Main article: Chemistry:Naloxone

Naloxone works by temporarily blocking the effects of opioids, including respiratory depression and sedation.[50][3] Naloxone is safe and side effects are rare, generally limited to allergic reactions.[51] It should be given if there is any suspicion of an opioid overdose. Naloxone is available to the public in the United States in two routes of administration: intranasal and intramuscular/subcutaneous. Intranasal forms include Narcan, approved in 2015, and Kloxxado, approved in 2021.[52] Formulations that are injectable into the intramuscular or subcutaneous spaces include Evzio, approved in 2014, and Zimhi, approved in 2021.[53][54] The doses are approved for both children and adults and may be repeated every 2–3 minutes.[52][53][54] Synthetic opioids like fentanyl and carfentanil are much more potent than prescription opioids and heroin.[55] There is some debate about whether increased doses of naloxone are required to reverse overdose from synthetic opioids; however, this concern has prompted FDA approval of higher dose naloxone formulations such as Kloxxado and Zimhi.[52][56] The effects of naloxone last for approximately 30-90 minutes, at which point opioids present in the body may begin to take effect again depending on the specific opioids duration of action. Therefore, transport to a hospital is indicated after naloxone administration, and the medication may need to be re-administered.[24]

Naloxone Formulations for Public Use in the US  Brand name  | Route of Administration  | Dose  | Additional Considerations

|
|
|

Narcan[57] | Intranasal  | 4 mg  |
Kloxxado[58] | Intranasal  | 8 mg  |
Evzio[53] | Intramuscular/subcutaneous auto-injector  | 2 mg  |
Zimhi[54] | Intramuscular/subcutaneous prefilled syringe  | 5 mg  | For individuals 12 years of age or older

#### Access to Naloxone

The examples and perspective in this section deal primarily with the United States and do not represent a worldwide view of the subject. You may improve this section, discuss the issue on the talk page, or create a new article, as appropriate. (February 2024) (Learn how and when to remove this template message)

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Opioid overdose should be reversed as soon as possible. To shorten the time between overdose and naloxone administration, multiple programs have been enacted to improve naloxone access for drug users, caregivers, and first responders.[59] In the US, these efforts include FDA approval of intranasal and injectable naloxone over the counter, professional organizations recommending physicians to co-prescribe naloxone when opioids are used for pain management, free community overdose education and naloxone distribution (OEND) programs, and efforts to train non-medical first responders such as firefighters and police to use naloxone. These actions have reduced opioid-related deaths at the state and national levels and are cost-effective.[59][60]

In the UK, naloxone is a prescription-only medicine, but drug treatment services can supply it without a prescription. In an emergency, anyone can use it as a life-saving measure.[61]

In August 2024, a new device was developed by researchers at MIT and Brigham and Women's Hospital that can be implanted under the skin, which rapidly releases naloxone when an overdose is detected.[62]

### Basic Life Support

Opioid overdose leads to death when people stop breathing.[63] Bystanders trained in first aid can evaluate people who have overdosed and provide basic life support including rescue breathing via bag valve mask or mouth to mouth. If the person who has overdosed does not have a pulse, rescuers should begin CPR.[50]

### Other Treatments

Another medication that can be used to treat opioid overdoses is Nalmefene, which is an opioid derivative structurally similar to Naltrexone. It works similarly to Naloxone but has a longer half-life.[64] It is approved for intravenous, intramuscular, and subcutaneous administration by prescription only, unlike the over the counter formulations of naloxone.[65]

## Epidemiology

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See also: Chemistry:Opioid epidemic

A two milligram dose of fentanyl powder (on pencil tip) is a lethal amount for most people.[66]

In 2016, the World Health Organization estimated that 34 million people used opioids and 19 million used opiates.[1] Of these, about 27 million people had opioid dependence, with the majority—but a decreasing number—using illicit heroin.[1] In 2015, 118,000 people died from opioid use disorders, causing almost one-third of all drug-related deaths.[1]

### United States

Of the 70,200 overdose deaths in the US in 2017, opioids were involved in 47,600, with three male deaths for each female death.[2] This is an increase from 2016 where over 64,000 died from drug overdose, and opioids were involved in over 42,000.[67] In 2017, the five states with the highest rates of death due to drug overdose were West Virginia (57.8 per 100,000), Ohio (46.3 per 100,000), Pennsylvania (44.3 per 100,000), Kentucky (37.2 per 100,000), and New Hampshire (37.0 per 100,000).[68]

Concerning the 2017 data in the charts below, deaths from the various drugs add up to more than 70,200 because multiple substances are involved in many of the deaths.[2] According to the National Safety Council, the lifetime odds of dying from an overdose in the United States is 1 in 96.[69]

In 2023, the most opioid overdose deaths were among Whites (47,754), followed by Blacks (16,481), Latinos (11,310), Native Americans (1,170), and Asians (695).[70]

File:Drug overdose death rates per 100,000 by state. US map.svgDrug overdose deaths in the US per 100,000 people by state.[71][68]

* Charts of deaths involving specific opioids and classes of opioids
* US yearly deaths involving other synthetic opioids, predominately Fentanyl.[2]

* US yearly deaths involving prescription opioids. Non-methadone synthetics is a category dominated by illegally acquired fentanyl, and has been excluded.[2]

* US yearly overdose deaths involving heroin.[2]

## Awareness

The Substance Abuse and Mental Health Services Administration hosts an annual health observance known as National Prevention Week. Every third week of May, they encourage communities across the country to unite to share stories about positive mental and behavioral health and the importance of implementing prevention methods.[72] They also sponsor Recovery Month every September. Recovery Month aims to raise awareness about mental and substance use disorders and to honor individuals who recover, promoting the positive message that prevention works and that treatment is effective.[73]

International Overdose Awareness Day is on 31 August to remember those who have died from an overdose, to decrease the stigma of drug-related deaths, and to promote the prevention of overdose.[74]

## See also

* Harm reduction
* List of deaths from drug overdose and intoxication
* Responsible drug use

## Notes

1. ↑ In the case of pethidine (brand name Demerol) in particular, extreme overdose may produce dilated pupils instead, due to this drug's tendency to produce non-opioid central nervous system toxicity and excitation at elevated doses.[citation needed]

## References

1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 1.17 1.18 "Information sheet on opioid overdose". World Health Organization. November 2014. https://www.who.int/substance_abuse/information-sheet/en/.
2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 "Overdose Death Rates". National Institute on Drug Abuse. 20 January 2022. https://nida.nih.gov/research-topics/trends-statistics/overdose-death-rates.
3. ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 "Management of opioid analgesic overdose". The New England Journal of Medicine 367 (2): 146–155. July 2012. doi:10.1056/NEJMra1202561. PMID 22784117.
4. ↑ Emergency Medicine: Expert Consult -- Online. Elsevier Health Sciences. 2008. p. PT4876. ISBN 978-1-4377-2129-4. https://books.google.com/books?id=Q2Ag9OKC7awC&pg=PT4876.
5. ↑ "Opioids and the treatment of chronic pain: controversies, current status, and future directions". Experimental and Clinical Psychopharmacology 16 (5): 405–416. October 2008. doi:10.1037/a0013628. PMID 18837637.
6. ↑ Medical emergencies in the dental office (6th ed.). St. Louis, Mo.: Mosby. 2007. ISBN 978-0-323-07594-7. OCLC 769189432.
7. ↑ 7.0 7.1 "Cellular and molecular mechanisms involved in the neurotoxicity of opioid and psychostimulant drugs". Brain Research Reviews 58 (1): 192–208. June 2008. doi:10.1016/j.brainresrev.2008.03.002. PMID 18440072.
8. ↑ "Opioids, cocaine, cannabis and illicit drugs". Our World in Data. 16 March 2018. https://ourworldindata.org/illicit-drug-use.
9. ↑ "Understanding Risk Factors for Opioid Overdose in Clinical Populations to Inform Treatment and Policy". Journal of Addiction Medicine 10 (6): 369–381. 2016. doi:10.1097/ADM.0000000000000245. PMID 27525471.
10. ↑ 10.0 10.1 "Part 12: Pediatric Advanced Life Support: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care". Circulation 132 (18 Suppl 2): S526–S542. November 2015. doi:10.1161/cir.0000000000000266. PMID 26473000.
11. ↑ "Management of Suspected Opioid Overdose With Naloxone in Out-of-Hospital Settings: A Systematic Review". Annals of Internal Medicine 167 (12): 867–875. December 2017. doi:10.7326/M17-2224. PMID 29181532.
12. ↑ "Opioid epidemic: 6 key steps that states should take now". American Medical Association. 9 September 2019. https://www.ama-assn.org/delivering-care/opioids/opioid-epidemic-6-key-steps-states-should-take-now.
13. ↑ "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet 388 (10053): 1459–1544. October 2016. doi:10.1016/s0140-6736(16)31012-1. PMID 27733281.
14. ↑ GBD 2013 Mortality and Causes of Death Collaborators (January 2015). "Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013". Lancet 385 (9963): 117–171. doi:10.1016/S0140-6736(14)61682-2. PMID 25530442.
15. ↑ 15.0 15.1 "Opioid Overdose Crisis". 1 June 2017. https://www.drugabuse.gov/drugs-abuse/opioids/opioid-overdose-crisis.
16. ↑ 16.0 16.1 16.2 16.3 16.4 16.5 16.6 16.7 "Historical Review: Opiate Addiction and Opioid Receptors". Cell Transplantation 28 (3): 233–238. March 2019. doi:10.1177/0963689718811060. PMID 30419763.
17. ↑ 17.0 17.1 17.2 17.3 "Respiratory depression and brain hypoxia induced by opioid drugs: Morphine, oxycodone, heroin, and fentanyl". Neuropharmacology 151: 219–226. June 2019. doi:10.1016/j.neuropharm.2019.02.008. PMID 30735692.
18. ↑ 18.0 18.1 "Progress in understanding mechanisms of opioid-induced gastrointestinal adverse effects and respiratory depression". Neuropharmacology 131: 238–255. March 2018. doi:10.1016/j.neuropharm.2017.12.032. PMID 29273520.
19. ↑ Fentanyl. Image 4 of 17. US DEA (Drug Enforcement Administration). See archive with caption: "photo illustration of 2 milligrams of fentanyl, a lethal dose in most people".
20. ↑ "Methadone and buprenorphine toxicity in children". The American Journal on Addictions 19 (1): 89–95. January 2010. doi:10.1111/j.1521-0391.2009.00002.x. PMID 20132125.
21. ↑ 21.0 21.1 "Codeine should not be prescribed for breastfeeding mothers or children under the age of 12". Acta Paediatrica 104 (6): 550–556. June 2015. doi:10.1111/apa.13012. PMID 25809057.
22. ↑ "Concomitant use of benzodiazepines in opiate overdose and the association with a poorer outcome". BestBets. July 2005. http://www.bestbets.org/bets/bet.php?id=1007.
23. ↑ "Concomitant use of alcohol in opiate overdose and the association with a poorer outcome". BestBets. July 2005. http://www.bestbets.org/bets/bet.php?id=1006.
24. ↑ 24.00 24.01 24.02 24.03 24.04 24.05 24.06 24.07 24.08 24.09 24.10 24.11 Babu, Kavita M.; Brent, Jeffrey; Juurlink, David N. (6 June 2019). "Prevention of Opioid Overdose". New England Journal of Medicine 380 (23): 2246–2255. doi:10.1056/NEJMra1807054. PMID 31167053.
25. ↑ King, Charlotte; Anderson, Mark; Agarwal, Abhishek; Fakis, Apostolos; Parry, Christopher M; Lynn, Richard Michael; Hawcutt, Daniel B; Starkey, Elizabeth Sarah (12 February 2025). "Severe accidental poisonings in children: a British Paediatric Surveillance Unit nationwide prospective study" (in en). Archives of Disease in Childhood 110 (8): archdischild–2024–328196. doi:10.1136/archdischild-2024-328196. ISSN 0003-9888. PMID 39939143. https://adc.bmj.com/lookup/doi/10.1136/archdischild-2024-328196.
26. ↑ 26.0 26.1 "Opioid metabolism". Mayo Clinic Proceedings 84 (7): 613–624. July 2009. doi:10.1016/S0025-6196(11)60750-7. PMID 19567715.
27. ↑ 27.0 27.1 "Drug Metabolism - Clinical Pharmacology" (in en-US). https://www.merckmanuals.com/professional/clinical-pharmacology/pharmacokinetics/drug-metabolism.
28. ↑ 28.0 28.1 "Polymorphic cytochrome P450 enzymes (CYPs) and their role in personalized therapy". PLOS ONE 8 (12). 10 December 2013. doi:10.1371/journal.pone.0082562. PMID 24340040. Bibcode: 2013PLoSO...882562P.
29. ↑ 29.0 29.1 "Depression and prescription opioid misuse among chronic opioid therapy recipients with no history of substance abuse". Annals of Family Medicine 10 (4): 304–311. 2012. doi:10.1370/afm.1371. PMID 22778118.
30. ↑ 30.0 30.1 "Prescription Opioid Use among Adults with Mental Health Disorders in the United States". Journal of the American Board of Family Medicine 30 (4): 407–417. 1 July 2017. doi:10.3122/jabfm.2017.04.170112. PMID 28720623.
31. ↑ "Risk Factors for Opioid-Use Disorder and Overdose" (in en-US). Anesthesia and Analgesia 125 (5): 1741–1748. November 2017. doi:10.1213/ANE.0000000000002496. PMID 29049118.
32. ↑ 32.0 32.1 "COVID-19: The Hidden Impact on Mental Health and Drug Addiction". Frontiers in Psychiatry 11. 29 July 2020. doi:10.3389/fpsyt.2020.00767. PMID 32848937.
33. ↑ 33.0 33.1 33.2 33.3 "Endogenous and Exogenous Opioids in Pain". Annual Review of Neuroscience 41: 453–473. July 2018. doi:10.1146/annurev-neuro-080317-061522. PMID 29852083.
34. ↑ "Heroin". July 2017. https://www.drugabuse.gov/publications/drugfacts/heroin.
35. ↑ "Molecular mechanisms of opioid receptor-dependent signaling and behavior". Anesthesiology 115 (6): 1363–1381. December 2011. doi:10.1097/ALN.0b013e318238bba6. PMID 22020140.
36. ↑ 36.0 36.1 36.2 36.3 36.4 "Reducing the health consequences of opioid addiction in primary care". The American Journal of Medicine 126 (7): 565–571. July 2013. doi:10.1016/j.amjmed.2012.11.031. PMID 23664112. In press
37. ↑ 37.0 37.1 37.2 "Prevention of fatal opioid overdose". JAMA 308 (18): 1863–1864. November 2012. doi:10.1001/jama.2012.14205. PMID 23150005.
38. ↑ "Emergency Department and Urgent Care Clinicians Use Protocol To Reduce Opioid Prescriptions for Patients Suspected of Abusing Controlled Substances". Agency for Healthcare Research and Quality. 12 March 2014. https://innovations.ahrq.gov/profiles/emergency-department-and-urgent-care-clinicians-use-protocol-reduce-opioid-prescriptions.
39. ↑ "A systematic approach to identifying drug-seeking patients". Family Practice Management 15 (4): A3–A5. April 2008. PMID 18444310.
40. ↑ 40.0 40.1 "CDC Guideline for Prescribing Opioids for Chronic Pain--United States, 2016". JAMA 315 (15): 1624–1645. April 2016. doi:10.1001/jama.2016.1464. PMID 26977696.
41. ↑ "Prescription opioid duration of action and the risk of unintentional overdose among patients receiving opioid therapy". JAMA Internal Medicine 175 (4): 608–615. April 2015. doi:10.1001/jamainternmed.2014.8071. PMID 25686208.
42. ↑ 42.0 42.1 42.2 "ASAM National Practice Guideline for the Use of Medications in the Treatment of Addiction Involving Opioid Use". https://www.asam.org/docs/default-source/practice-support/guidelines-and-consensus-docs/asam-national-practice-guideline-supplement.pdf.
43. ↑ "Current and Emerging Options to Combat the Opioid Epidemic". AJMC. https://www.ajmc.com/journals/supplement/2018/combating-opioid-epidemic/current-and-emerging-options-to-combat-the-opioid-epidemic?p=3.
44. ↑ "Buprenorphine maintenance versus placebo or methadone maintenance for opioid dependence". The Cochrane Database of Systematic Reviews 2014 (2). February 2014. doi:10.1002/14651858.CD002207.pub4. PMID 24500948.
45. ↑ "Benefits of peer support groups in the treatment of addiction". Substance Abuse and Rehabilitation 7: 143–154. September 2016. doi:10.2147/SAR.S81535. PMID 27729825.
46. ↑ "A Review of Opioid Overdose Prevention and Naloxone Prescribing: Implications for Translating Community Programming Into Clinical Practice". Substance Abuse 36 (2): 240–253. 16 March 2015. doi:10.1080/08897077.2015.1010032. PMID 25774771. Bibcode: 2015JPkR...36..240M.
47. ↑ "Randomized controlled trial of a brief intervention for problematic prescription drug use in non-treatment-seeking patients". Addiction 104 (1): 109–117. January 2009. doi:10.1111/j.1360-0443.2008.02421.x. PMID 19133895.
48. ↑ "Drug Disposal: FDA's Flush List for Certain Medicines" (in en). 1 October 2020. https://www.fda.gov/drugs/disposal-unused-medicines-what-you-should-know/drug-disposal-fdas-flush-list-certain-medicines.
49. ↑ "PDAPS - Naloxone Overdose Prevention Laws". http://pdaps.org/datasets/laws-regulating-administration-of-naloxone-1501695139.
50. ↑ 50.0 50.1 50.2 "Responding to a suspected opioid overdose | NIOSH | CDC" (in en-us). 19 July 2021. https://www.cdc.gov/niosh/topics/opioids/response.html.
51. ↑ "Naloxone DrugFacts" (in en). 11 January 2022. https://nida.nih.gov/publications/drugfacts/naloxone.
52. ↑ 52.0 52.1 52.2 "Higher-Dose Naloxone Nasal Spray (Kloxxado) for Opioid Overdose". JAMA 326 (18): 1853–1854. November 2021. doi:10.1001/jama.2021.15948. PMID 34751711.
53. ↑ 53.0 53.1 53.2 "EVZIO® (naloxone hydrochloride injection) Auto-Injector for intramuscular or subcutaneous use". October 2016. https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/209862lbl.pdf.
54. ↑ 54.0 54.1 54.2 "ZIMHI (naloxone hydrochloride injection) for intramuscular or subcutaneous use". October 2021. https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212854s000lbl.pdf.
55. ↑ "Fentanyl, fentanyl analogs and novel synthetic opioids: A comprehensive review". Neuropharmacology 134 (Pt A): 121–132. May 2018. doi:10.1016/j.neuropharm.2017.10.016. PMID 29042317. https://escholarship.org/uc/item/8xh0s7nf.
56. ↑ "Higher doses of naloxone are needed in the synthetic opioid era". Substance Abuse Treatment, Prevention, and Policy 14 (1). February 2019. doi:10.1186/s13011-019-0195-4. PMID 30777088.
57. ↑ "NARCAN® (naloxone hydrochloride) nasal spray". November 2015. https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/208411lbl.pdf.
58. ↑ "KLOXXADO (naloxone hydrochloride) nasal spray". April 2021. https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/212045s000lbl.pdf.
59. ↑ 59.0 59.1 "Expanding Access to Naloxone: A Review of Distribution Strategies" (in en-US). 29 May 2019. https://ldi.upenn.edu/our-work/research-updates/expanding-access-to-naloxone-a-review-of-distribution-strategies/.
60. ↑ "Naloxone for Opioid Overdose: Life-Saving Science" (in en). 30 March 2017. https://nida.nih.gov/publications/naloxone-opioid-overdose-life-saving-science.
61. ↑ "Widening the availability of naloxone". 18 February 2019. https://www.gov.uk/government/publications/widening-the-availability-of-naloxone/widening-the-availability-of-naloxone.
62. ↑ "An implantable sensor could reverse opioid overdoses" (in en). 14 August 2024. https://news.mit.edu/2024/implantable-sensor-could-reverse-opioid-overdoses-0814.
63. ↑ "Non-analgesic effects of opioids: opioid-induced respiratory depression". Current Pharmaceutical Design 18 (37): 5994–6004. 2012. doi:10.2174/138161212803582469. PMID 22747535.
64. ↑ "Nalmefene: a long-acting opioid antagonist. Clinical applications in emergency medicine". The Journal of Emergency Medicine 16 (3): 471–475. May 1998. doi:10.1016/s0736-4679(98)00019-5. PMID 9610980.
65. ↑ "Revex (nalmefene hydrochloride injection)". https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020459s006lbl.pdf.
66. ↑ "One Pill Can Kill". https://www.dea.gov/onepill.
67. ↑ National Center for Health Statistics. "Provisional Counts of Drug Overdose Deaths, as of 8/6/2017". United States: Centers for Disease Control and Prevention. https://www.cdc.gov/nchs/data/health_policy/monthly-drug-overdose-death-estimates.pdf. Source lists US totals for 2015 and 2016 and statistics by state.
68. ↑ 68.0 68.1 Drug Overdose Deaths. Centers for Disease Control and Prevention, National Center for Injury Prevention and Control. Click on a map year. The data table is below the map. Number of deaths for each state, and the age-adjusted death rates for each state. Also, place the cursor on the map states to get data.
69. ↑ "Odds of Dying". https://injuryfacts.nsc.org/all-injuries/preventable-death-overview/odds-of-dying/.
70. ↑ "Opioid Overdose Deaths by Race/Ethnicity". Kaiser Family Foundation. 2023. https://www.kff.org/mental-health/state-indicator/opioid-overdose-deaths-by-raceethnicity/?currentTimeframe=0&sortModel={"colId":"Location","sort":"asc"}.
71. ↑ Drug Overdose Mortality by State. Pick the year from the menu below the map. From National Center for Health Statistics for the Centers for Disease Control and Prevention. The numbers are in the data table below the map and by running your cursor over the map at the source. The CSV data link is below the table.
72. ↑ "About National Prevention Week". 8 November 2013. https://www.samhsa.gov/prevention-week/about.
73. ↑ "Home | RecoveryMonth.gov" (in en). https://www.recoverymonth.gov/.
74. ↑ "International Overdose Awareness Day - August 31, 2019" (in en-us). MMWR. Morbidity and Mortality Weekly Report 68 (34): 737. August 2019. doi:10.15585/mmwr.mm6834a1. PMID 31466079.

## External links

* WHO fact sheet on opioid overdose
* Community management of opioid overdose. World Health Organization. 2014. ISBN 978-92-4-154881-6. http://apps.who.int/iris/bitstream/10665/137462/1/9789241548816_eng.pdf?ua=1.

Classification|

* ICD-10: F11.0, T40.0-T40.2
* ICD-9-CM: 305.5, 965.0

|

External resources|

* eMedicine: emerg/330

* v
* t
* e

Psychoactive substance-related disorder (F10–F19, 291–292; 303–305)

General|

* SID
* Substance intoxication / Drug overdose
* Substance-induced psychosis
* Withdrawal:
* Craving
* Neonatal withdrawal
* Post-acute-withdrawal syndrome (PAWS)
* SUD
* Substance abuse / Substance-related disorders
* Physical dependence / Psychological dependence / Substance dependence

Combined
substance use|

* SUD
* Polysubstance dependence
* SID
* Combined drug intoxication (CDI)

Alcohol|

| SID|

| Cardiovascular diseases|

* Alcoholic cardiomyopathy
* Alcohol flush reaction

|

Gastrointestinal diseases|

* Alcoholic liver disease (ALD):
* Alcoholic hepatitis
* Auto-brewery syndrome

Endocrine diseases|

* Alcoholic ketoacidosis (AKA)

Nervous
system diseases|

* Alcohol-related dementia (ARD)
* Alcohol intoxication
* Hangover

Neurological
disorders|

* Alcoholic hallucinosis
* Alcoholic polyneuropathy
* Alcohol-related brain damage
* Alcohol withdrawal syndrome:
* Alcoholic hallucinosis
* Delirium tremens (DTs)
* Fetal alcohol spectrum disorder (FASD)
* Fetal alcohol syndrome (FAS)
* Korsakoff syndrome
* Korsakoff psychosis
* Positional alcohol nystagmus (PAN)
* Wernicke–Korsakoff syndrome (WKS)
* Wernicke encephalopathy (WE)

Respiratory tract diseases|

* Alcohol-induced respiratory reactions
* Alcoholic lung disease

SUD|

* Alcoholism (alcohol use disorder (AUD))
* Binge drinking

Caffeine|

* SID
* Caffeine-induced anxiety disorder
* Caffeine-induced sleep disorder
* Caffeinism
* SUD
* Caffeine dependence

Cannabis|

* SID
* Cannabinoid hyperemesis syndrome (CHS)
* SUD
* Amotivational syndrome
* Cannabis use disorder (CUD)
* Synthetic cannabinoid use disorder

Cocaine|

* SID
* Cocaine intoxication
* Prenatal cocaine exposure (PCE)
* SUD
* Cocaine dependence

Hallucinogen|

* SID
* Acute intoxication from hallucinogens (bad trip)
* Hallucinogen persisting perception disorder (HPPD)

Nicotine|

* SID
* Nicotine poisoning
* Nicotine withdrawal
* SUD
* Nicotine dependence

Opioids|

* SID
* Opioid overdose
* SUD
* Opioid use disorder (OUD)

Sedative /
hypnotic|

* SID
* Kindling (sedative–hypnotic withdrawal)
* benzodiazepine: SID
* Benzodiazepine overdose
* Benzodiazepine withdrawal
* SUD
* Benzodiazepine use disorder (BUD)
* Benzodiazepine dependence
* barbiturate: SID
* Barbiturate overdose
* SUD
* Barbiturate dependence

Stimulants|

* SID
* Stimulant psychosis
* amphetamine: SUD
* Amphetamine dependence

Volatile
solvent|

* SID
* Sudden sniffing death syndrome (SSDS)
* Toluene toxicity
* SUD
* Inhalant abuse

* v
* t
* e

* Poisoning
* Toxicity
* Overdose (T36–T65, 960–989)

History of poison

Inorganic|

| Metals|

| Toxic metals|

* Beryllium
* Cadmium
* Lead
* Mercury
* Nickel
* Silver
* Thallium
* Tin

|

Dietary minerals|

* Chromium
* Cobalt
* Copper
* Iron
* Manganese
* Zinc

Metalloids|

* Arsenic

Nonmetals|

* Sulfuric acid
* Selenium
* Chlorine
* Fluoride

Organic|

| Phosphorus|

* Pesticides
* Aluminium phosphide
* Organophosphates

|

Nitrogen|

* Cyanide
* Nicotine
* Nitrogen dioxide poisoning

CHO|

* alcohol
* Ethanol
* Ethylene glycol
* Methanol
* Carbon monoxide
* Oxygen
* Toluene

Pharmaceutical|

| Drug overdoses|

| Nervous|

* Anticholinesterase
* Aspirin
* Barbiturates
* Benzodiazepines
* Cocaine
* Lithium
* Opioids
* Paracetamol
* Tricyclic antidepressants

|

Cardiovascular|

* Digoxin
* Dipyridamole

Vitamin poisoning|

* Vitamin A
* Vitamin D
* Vitamin E
* Megavitamin-B6 syndrome

Biological1|

| Fish / seafood|

* Ciguatera
* Haff disease
* Ichthyoallyeinotoxism
* Scombroid
* Shellfish poisoning
* Amnesic
* Diarrhetic
* Neurotoxic
* Paralytic

|

Other vertebrates|

* amphibian venom
* Batrachotoxin
* Bombesin
* Bufotenin
* Physalaemin
* birds / quail
* Coturnism
* snake venom
* Alpha-Bungarotoxin
* Ancrod
* Batroxobin

Arthropods|

* Arthropod bites and stings
* bee sting / bee venom
* Apamin
* Melittin
* scorpion venom
* Charybdotoxin
* spider venom
* Latrotoxin / Latrodectism
* Loxoscelism
* tick paralysis

Plants / fungi|

* Cinchonism
* Ergotism
* Lathyrism
* Locoism
* Mushrooms
* Strychnine

1 including venoms, toxins, foodborne illnesses.

* v
* t
* e

Opioid receptor modulators

MOR|

* Agonists (abridged; see here for a full list): 3-HO-PCP
* 7-Acetoxymitragynine
* 7-Hydroxymitragynine
* ψ-Akuammigine
* α-Chlornaltrexamine
* α-Narcotine
* Acetyldihydrocodeine
* Acetylfentanyl
* Acrylfentanyl
* Adrenorphin (metorphamide)
* AH-7921
* Akuammicine
* Akuammidine
* Alfentanil
* Anileridine
* Apparicine
* β-Endorphin
* BAM-12P
* BAM-18P
* BAM-22P
* Benzhydrocodone
* Benzylmorphine
* Bezitramide
* Biphalin
* BU08070
* Buprenorphine
* Butorphan
* Butorphanol
* Butyrfentanyl
* BW373U86
* Carfentanil
* Casokefamide
* Cebranopadol
* Chloroxymorphamine
* Codeine
* DADLE
* DAMGO (DAGO)
* Dermorphin
* Desmetramadol (desmethyltramadol)
* Desomorphine
* Dextromoramide
* Dextropropoxyphene (propoxyphene)
* Dezocine
* Dimenoxadol
* Dimethylaminopivalophenone
* Eluxadoline
* Diamorphine (heroin)
* Dihydrocodeine
* Dihydroetorphine
* Dihydromorphine
* Dinalbuphine sebacate
* Diphenoxylate
* Dipipanone
* Dynorphin A
* Embutramide
* Endomorphin-1
* Endomorphin-2
* Eseroline
* Ethylmorphine
* Etorphine
* Fentanyl
* Fluorophen
* Frakefamide
* Furanylfentanyl
* Hemorphin-4
* Herkinorin
* Hodgkinsine
* Hydrocodone
* Hydromorphinol
* Hydromorphone
* IBNtxA
* Ketamine
* Ketobemidone
* Kratom
* Laudanosine
* Lefetamine
* Leu-enkephalin
* Levacetylmethadol
* Levomethorphan
* Levorphanol
* Lexanopadol
* Loperamide
* Loxicodegol
* Matrine
* Meptazinol
* Met-enkephalin (metenkefalin)
* Methadone
* Metkefamide
* Metopon
* Mitragynine
* Mitragynine pseudoindoxyl
* Morphiceptin
* Morphine
* Nalbuphine
* NalBzOH
* Nalmexone
* Naltalimide
* Neopine
* NFEPP
* Nicocodeine
* Nicodicodine
* Nicomorphine
* NKTR-181
* Norketamine
* Octreotide
* Oliceridine
* OM-3-MNZ
* Oripavine
* Oxycodone
* Oxymorphazone
* Oxymorphonazine
* Oxymorphone
* Oxymorphone phenylhydrazone
* OxyPNPH
* Papaver somniferum (opium)
* Pentazocine
* Pericine
* Pethidine (meperidine)
* Phenazocine
* Phencyclidine
* Piminodine
* Piritramide
* PL-017
* Prodine
* Propiram
* PZM21
* Racemethorphan
* Racemorphan
* Remifentanil
* Salsolinol
* SC-17599
* Sinomenine
* Sufentanil
* Tapentadol
* Tetrahydropapaveroline
* TH-030418
* Thebaine
* Thienorphine
* Tianeptine
* Tilidine
* Tramadol
* Trimebutine
* TRIMU 5
* TRV734
* Tubotaiwine
* U-47700
* Valorphin
* Viminol
* Xorphanol

* PAMs: BMS-986121
* BMS-986122

* Antagonists: (3S,4S)-Picenadol
* 2-(S)-N,N-(R)-Viminol
* 3CS-nalmefene
* 4-Caffeoyl-1,5-quinide
* 4′-Hydroxyflavanone
* 4',7-Dihydroxyflavone
* 6β-Naltrexol
* 6β-Naltrexol-d4
* 18-MC
* α-Gliadin
* β-Chlornaltrexamine
* β-Funaltrexamine
* Akuammine
* Alvimopan
* AM-251
* Apigenin
* AT-076
* Axelopran
* Bevenopran
* Catechin
* Catechin gallate
* Clocinnamox
* CTAP
* CTOP
* Cyclofoxy
* Cyprodime
* Diacetylnalorphine
* Diprenorphine
* ECG
* EGC
* Epicatechin
* Eptazocine
* Gemazocine
* Ginsenoside R
* Hyperoside
* Ibogaine
* Levallorphan
* Lobeline
* LY-255582
* LY-2196044
* Methocinnamox
* Methylnaltrexone
* Methylsamidorphan chloride
* Naldemedine
* Nalmefene
* Nalodeine (N-allylnorcodeine)
* Nalorphine
* Nalorphine dinicotinate
* Naloxazone
* Naloxegol
* Naloxol
* Naloxonazine
* Naloxone
* Naltrexazone
* Naltrexonazine
* Naltrexone
* Naltrindole
* Naringenin
* Noribogaine
* Oxilorphan
* Pawhuskin A
* Rimonabant
* Quadazocine
* Samidorphan
* Taxifolin

* Unknown/unsorted: Cannabidiol
* Coronaridine
* Cyproterone acetate
* Dihydroakuuamine
* Tabernanthine
* Tetrahydrocannabinol

DOR|

* Agonists: 3CS-nalmefene
* 6'-GNTI
* 7-SIOM
* ADL-5747 (PF-04856881)
* ADL-5859
* Alazocine (SKF-10047)
* Amoxapine
* AR-M100390 (ARM390)
* AZD2327
* β-Endorphin
* BAM-18P
* Biphalin
* BU-48
* Butorphan
* Butorphanol
* BW373U86
* Casokefamide
* Cebranopadol
* Codeine
* Cyclazocine
* DADLE
* Deltorphin A
* Deltorphin I
* Deltorphin II
* Desmethylclozapine
* Desmetramadol (desmethyltramadol)
* Dezocine
* Diamorphine (heroin)
* Dihydroetorphine
* Dihydromorphine
* DPDPE
* DPI-221
* DPI-3290
* DSLET
* Ethylketazocine
* Etorphine
* Fentanyl
* FIT
* Fluorophen
* Hemorphin-4
* Hydrocodone
* Hydromorphone
* Ibogaine
* Isomethadone
* JNJ-20788560
* KNT-127
* Kratom
* Laudanosine
* Leu-enkephalin
* Levomethorphan
* Levorphanol
* Lexanopadol
* Lofentanil
* Met-enkephalin (metenkefalin)
* Metazocine
* Metkefamide
* Mitragynine
* Mitragynine pseudoindoxyl
* Morphine
* N-Phenethyl-14-ethoxymetopon
* Norbuprenorphine
* NalBzOH
* Oripavine
* Oxycodone
* Oxymorphone
* Pethidine (meperidine)
* Proglumide
* Racemethorphan
* Racemorphan
* RWJ-394674
* Samidorphan
* SB-235863
* SNC-80
* SNC-162
* TAN-67 (SB-205,607)
* TH-030418
* Thebaine
* Thiobromadol (C-8813)
* Tonazocine
* Tramadol
* TRV250
* Xorphanol
* Zenazocine

* Antagonists: 4',7-Dihydroxyflavone
* 5'-NTII
* 6β-Naltrexol
* 6β-Naltrexol-d4
* α-Santolol
* β-Chlornaltrexamine
* Apigenin
* AT-076
* Axelopran
* Bevenopran
* BNTX
* Catechin
* Catechin gallate
* Clocinnamox
* Diacetylnalorphine
* Diprenorphine
* ECG
* EGC
* Eluxadoline
* Epicatechin
* ICI-154129
* ICI-174864
* LY-255582
* LY-2196044
* Methylnaltrexone
* Methylnaltrindole
* N-Benzylnaltrindole
* Nalmefene
* Nalorphine
* Naltrexone
* Naltriben
* Naltrindole
* Naloxone
* Naringenin
* Noribogaine
* Pawhuskin A
* Quadazocine
* SDM25N
* SoRI-9409
* Taxifolin
* Thienorphine

* Unknown/unsorted: 18-MC
* Cannabidiol
* Coronaridine
* Cyproterone acetate
* Tabernanthine
* Tetrahydrocannabinol

KOR|

* Agonists: 3CS-nalmefene
* 6'-GNTI
* 8-CAC
* 18-MC
* 14-Methoxymetopon
* β-Chlornaltrexamine
* β-Funaltrexamine
* Adrenorphin (metorphamide)
* Akuuamicine
* Alazocine (SKF-10047)
* Allomatrine
* Apadoline
* Asimadoline
* BAM-12P
* BAM-18P
* BAM-22P
* Big dynorphin
* Bremazocine
* BRL-52537
* Butorphan
* Butorphanol
* BW373U86
* Cebranopadol
* Ciprefadol
* CR665
* Cyclazocine
* Cyclorphan
* Cyprenorphine
* Desmetramadol (desmethyltramadol)
* Diamorphine (heroin)
* Diacetylnalorphine
* Difelikefalin
* Dihydroetorphine
* Dihydromorphine
* Dinalbuphine sebacate
* Diprenorphine
* Dynorphin A
* Dynorphin B (rimorphin)
* Eluxadoline
* Enadoline
* Eptazocine
* Erinacine E
* Ethylketazocine
* Etorphine
* Fedotozine
* Fentanyl
* Gemazocine
* GR-89696
* GR-103545
* Hemorphin-4
* Herkinorin
* HS665
* Hydromorphone
* HZ-2
* Ibogaine
* ICI-199,441
* ICI-204,448
* Ketamine
* Ketazocine
* Laudanosine
* Leumorphin (dynorphin B-29)
* Levallorphan
* Levomethorphan
* Levorphanol
* Lexanopadol
* Lofentanil
* LPK-26
* Lufuradom
* Matrine
* MB-1C-OH
* Menthol
* Metazocine
* Metkefamide
* Mianserin
* Mirtazapine
* Morphine
* Moxazocine
* MR-2034
* N-MPPP
* Nalbuphine
* NalBzOH
* Nalfurafine
* Nalmefene
* Nalodeine (N-allylnorcodeine)
* Nalorphine
* Naltriben
* Niravoline
* Norbuprenorphine
* Norbuprenorphine-3-glucuronide
* Noribogaine
* Norketamine
* Oripavine
* Oxilorphan
* Oxycodone
* Pentazocine
* Pethidine (meperidine)
* Phenazocine
* Proxorphan
* Racemethorphan
* Racemorphan
* RB-64
* Salvinorin A (salvia)
* Salvinorin B ethoxymethyl ether
* Salvinorin B methoxymethyl ether
* Samidorphan
* Spiradoline (U-62,066)
* TH-030418
* Thienorphine
* Tifluadom
* Tricyclic antidepressants (e.g., amitriptyline, desipramine, imipramine, nortriptyline)
* U-50488
* U-54,494A
* U-69,593
* Xorphanol

* Antagonists: 4′-Hydroxyflavanone
* 4',7-Dihydroxyflavone
* 5'-GNTI
* 6'-GNTI
* 6β-Naltrexol
* 6β-Naltrexol-d4
* β-Chlornaltrexamine
* Buprenorphine/samidorphan
* Amentoflavone
* ANTI
* Apigenin
* Arodyne
* AT-076
* Aticaprant
* Axelopran
* AZ-MTAB
* Binaltorphimine
* BU09059
* Buprenorphine
* Catechin
* Catechin gallate
* CERC-501 (LY-2456302)
* Clocinnamox
* Cyclofoxy
* Dezocine
* DIPPA
* EGC
* ECG
* Epicatechin
* Hyperoside
* JDTic
* LY-255582
* LY-2196044
* LY-2444296
* LY-2459989
* LY-2795050
* MeJDTic
* Methylnaltrexone
* ML190
* ML350
* MR-2266
* N-Fluoropropyl-JDTic
* Naloxone
* Naltrexone
* Naltrindole
* Naringenin
* Norbinaltorphimine
* Noribogaine
* Pawhuskin A
* PF-4455242
* RB-64
* Quadazocine
* Taxifolin
* UPHIT
* Zyklophin

* Unknown/unsorted: Akuammicine
* Akuammine
* Coronaridine
* Cyproterone acetate
* Dihydroakuuamine
* Ibogamine
* Tabernanthine

NOP|

* Agonists: (Arg14,Lys15)Nociceptin
* ((pF)Phe4)Nociceptin(1-13)NH2
* (Phe1Ψ(CH2-NH)Gly2)Nociceptin(1-13)NH2
* Ac-RYYRWK-NH2
* Ac-RYYRIK-NH2
* BU08070
* Buprenorphine
* Cebranopadol
* Dihydroetorphine
* Etorphine
* JNJ-19385899
* Levomethorphan
* Levorphanol
* Levorphanol
* Lexanopadol
* MCOPPB
* MT-7716
* NNC 63-0532
* Nociceptin (orphanin FQ)
* Nociceptin (1-11)
* Nociceptin (1-13)NH2
* Norbuprenorphine
* Racemethorphan
* Racemorphan
* Ro64-6198
* Ro65-6570
* SCH-221510
* SCH-486757
* SR-8993
* SR-16435
* TH-030418

* Antagonists: (Nphe1)Nociceptin(1-13)NH2
* AT-076
* BAN-ORL-24
* BTRX-246040 (LY-2940094)
* J-113,397
* JTC-801
* NalBzOH
* Nociceptin (1-7)
* Nocistatin
* SB-612,111
* SR-16430
* Thienorphine
* Trap-101
* UFP-101

Unsorted|

* β-Casomorphins
* Amidorphin
* BAM-20P
* Cytochrophin-4
* Deprolorphin
* Gliadorphin (gluteomorphin)
* Gluten exorphins
* Hemorphins
* Kava constituents
* MEAGL
* MEAP
* NEM
* Neoendorphins
* Nepetalactone (catnip)
* Peptide B
* Peptide E
* Peptide F
* Peptide I
* Rubiscolins
* Soymorphins

Others|

* Enkephalinase inhibitors: Amastatin
* BL-2401
* Candoxatril
* D -Phenylalanine
* Dexecadotril (retorphan)
* Ecadotril (sinorphan)
* Kelatorphan
* Racecadotril (acetorphan)
* RB-101
* RB-120
* RB-3007
* Opiorphan
* Selank
* Semax
* Spinorphin
* Thiorphan
* Tynorphin
* Ubenimex (bestatin)

* Propeptides: β-Lipotropin (proendorphin)
* Prodynorphin
* Proenkephalin
* Pronociceptin
* Proopiomelanocortin (POMC)

* Others: Kyotorphin (met-enkephalin releaser/degradation stabilizer)

See also: Receptor/signaling modulators • Signaling peptide/protein receptor modulators

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Original source: https://en.wikipedia.org/wiki/Opioid overdose. Read more

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*[MOR]: μ-opioid receptor
*[DOR]: δ-opioid receptor
*[KOR]: κ-opioid receptor
*[NOP]: Nociceptin receptor