|By mouth, rectal, subcutaneous injection, intramuscular injection|
|Metabolism||Liver: CYP2D6 (to morphine), CYP3A4 (to norcodeine), UGT2B7 (to 3- and 6-glucuronides of codeine, norcodeine, and morphine)|
• Others (e.g., conjugates)
|Onset of action||15–30 minutes|
|Elimination half-life||2.5–3 hours|
|Duration of action||4–6 hours|
|Chemical and physical data|
|Molar mass||299.364 g/mol g·mol−1|
|3D model (JSmol)|
|(what is this?)|
Codeine is an opiate used to treat pain, as a cough medicine, and for diarrhea. It is typically used to treat mild to moderate degrees of pain. Greater benefit may occur when combined with paracetamol (acetaminophen) or a nonsteroidal anti-inflammatory drug (NSAID) such as aspirin or ibuprofen. Evidence does not support its use for acute cough suppression in children or adults. In Europe it is not recommended as a cough medicine in those under twelve years of age. It is generally taken by mouth. It typically starts working after half an hour with maximum effect at two hours. Its effects last for about four to six hours.
Common side effects include vomiting, constipation, itchiness, lightheadedness, and drowsiness. Serious side effects may include breathing difficulties and addiction. It is unclear if its use in pregnancy is safe. Care should be used during breastfeeding as it may result in opiate toxicity in the baby. Its use as of 2016 is not recommended in children. Codeine works following being broken down by the liver into morphine. How quickly this occurs depends on a person’s genetics.
Codeine was discovered in 1832 by Pierre Jean Robiquet. In 2013 about 361,000 kilograms of codeine were produced while 249,000 kilograms were used. This makes it the most commonly taken opiate. It is on the World Health Organization’s List of Essential Medicines, the most effective and safe medicines needed in a health system. The wholesale cost in the developing world is between 0.04 and 0.29 USD per dose as of 2014. In the United States it costs about one dollar a dose. Codeine occurs naturally and makes up about 2% of opium.
- 1 Medical uses
- 2 Side effects
- 3 Pharmacology
- 4 Chemistry
- 5 History
- 6 Society and culture
- 6.1 Names
- 6.2 Recreational use
- 6.3 Detection
- 6.4 Legal status
- 6.4.1 Australia
- 6.4.2 Canada
- 6.4.3 Denmark
- 6.4.4 France
- 6.4.5 Germany, Switzerland, and Austria
- 6.4.6 Greece
- 6.4.7 Hong Kong
- 6.4.8 India
- 6.4.9 Iran
- 6.4.10 Ireland
- 6.4.11 Italy
- 6.4.12 Japan
- 6.4.13 Maldives
- 6.4.14 Nigeria
- 6.4.15 Romania
- 6.4.16 The Russian Federation
- 6.4.17 South Africa
- 6.4.18 Sri Lanka
- 6.4.19 United Arab Emirates
- 6.4.20 United Kingdom
- 6.4.21 United States
- 7 References
- 8 External links
Codeine is used to treat mild to moderate pain and to relieve cough. Codeine is also used to treat diarrhea and diarrhea-predominant irritable bowel syndrome, although loperamide (which is available without a prescription for milder diarrhea), diphenoxylate, paregoric or even laudanum are more frequently used to treat severe diarrhea.
There is weak evidence that it is useful in cancer pain but it is associated with increased side effects. The American Academy of Pediatrics does not recommend its use in children due to side effects. The FDA lists age under 12 years old as a contraindication to use.
Furthermore, codeine has been found as an endogenous compound, along with morphine, in the brains of non-human primates with depolarized neurons, indicating that codeine may function as a neurotransmitter or neuromodulator in the central nervous system.
Evidence does not support its use for acute cough suppression in children or adults. In Europe it is not recommended as a cough medicine in those under twelve years of age. There is some tentative evidence it can reduce a chronic cough in adults.
Codeine is marketed as both a single-ingredient drug and in combination preparations with paracetamol (as co-codamol: e.g., brands Paracod, Panadeine, and the Tylenol-with-codeine series, including Tylenol 3 and 1,2,4); with aspirin (as co-codaprin); or with ibuprofen (as Nurofen Plus). These combinations provide greater pain relief than either agent alone (drug synergy).
Codeine is also commonly marketed in products containing codeine with other pain killers or muscle relaxers, as well as codeine mixed with phenacetin (Emprazil with codeine No. 1, 2, 3, 4 and 5), naproxen, indomethacin, diclofenac, and others, as well as more complex mixtures, including such mixtures as aspirin + paracetamol + codeine ± caffeine ± antihistamines and other agents, such as those mentioned above.
Codeine-only products can be obtained with a prescription as a time release tablet. Codeine is also marketed in cough syrups with zero to a half-dozen other active ingredients, and a linctus (e.g., Paveral) for all of the uses for which codeine is indicated.
Injectable codeine is available for subcutaneous or intramuscular injection only; intravenous injection is contraindicated as this can result in non-immune mast-cell degranulation and resulting anaphylactoid reaction. Codeine suppositories are also marketed in some countries.
Common adverse effects associated with the use of codeine include drowsiness and constipation. Less common are itching, nausea, vomiting, dry mouth, miosis, orthostatic hypotension, urinary retention, euphoria, dysphoria, and coughing. Rare adverse effects include anaphylaxis, seizure, acute pancreatitis, and respiratory depression. As with all opiates, longer-term effects can vary, but can include diminished libido, apathy, and memory loss. Some people may have allergic reactions to codeine, such as the swelling of skin and rashes.
Tolerance to many of the effects of codeine, including its therapeutic effects, develops with prolonged use. This occurs at different rates for different effects, with tolerance to the constipation-inducing effects developing particularly slowly for instance.
A potentially serious adverse drug reaction, as with other opioids, is respiratory depression. This depression is dose-related and is a mechanism for the potentially fatal consequences of overdose. As codeine is metabolized to morphine, morphine can be passed through breast milk in potentially lethal amounts, fatally depressing the respiration of a breastfed baby.
In August 2012, the United States Federal Drug Administration issued a warning about deaths in pediatric patients < 6 years old after ingesting “normal” doses of paracetamol with codeine after tonsillectomy; this warning was upgraded to a black box warning in February 2013.
Some patients are very effective converters of codeine to its active form, morphine, resulting in lethal blood levels. The FDA is presently recommending very cautious use of codeine in young tonsillectomy patients: use the drug in the lowest amount that can control the pain, use “as needed” and not “around the clock”, and seek immediate medical attention if a child on codeine exhibits excessive sedation or abnormally noisy breathing.
Withdrawal and dependence
As with other opiate-based pain killers, chronic use of codeine can cause physical dependence. When physical dependence has developed, withdrawal symptoms may occur if a person suddenly stops the medication. Withdrawal symptoms include: drug craving, runny nose, yawning, sweating, insomnia, weakness, stomach cramps, nausea, vomiting, diarrhea, muscle spasms, chills, irritability, and pain. To minimize withdrawal symptoms, long-term users should gradually reduce their codeine medication under the supervision of a healthcare professional.
There is also no evidence that CYP2D6 inhibition is useful in treating codeine dependence, though the metabolism of codeine to morphine (and hence further metabolism to glucuronide morphine conjugates) does have an effect on the abuse potential of codeine. However, CYP2D6 has been implicated in the toxicity and death of neonates when codeine is administered to lactating mothers, particularly those with increased 2D6 activity (“ultra-rapid” metabolizers).
|Codeine||79 nM||>1,000 nM||>1,000 nM||ND|||
|Morphine||1.8 nM||90 nM||317 nM||1:50:176|||
Codeine is an opioid. It is a selective agonist of the μ-opioid receptor (MOR). Codeine itself has relatively weak affinity for the MOR. Instead of acting directly on the MOR, codeine functions as a prodrug of its major active metabolite morphine, which is a far more potent MOR agonist in comparison.
Mechanism of action
Codeine is an opioid and an agonist of the mu opioid receptor. It acts on the central nervous system to have an analgesic effect. It is metabolised in the liver to produce morphine which is ten times more potent agonist of the mu receptor. Opioid receptors are G-Protein coupled receptors that positively and negatively regulate synaptic transmission through downstream signalling. Binding of codeine or morphine to the mu opioid receptor results hyperpolarization of the neuron leading to the inhibition of release of nociceptive neurotransmitters causing an analgesic effect and increased pain tolerance due to reduced neuronal excitability.
The conversion of codeine to morphine occurs in the liver and is catalyzed by the cytochrome P450 enzyme CYP2D6. CYP3A4 produces norcodeine and UGT2B7 conjugates codeine, norcodeine, and morphine to the corresponding 3- and 6- glucuronides. Srinivasan, Wielbo and Tebbett speculate that codeine-6-glucuronide is responsible for a large percentage of the analgesia of codeine, and, thus, these patients should experience some analgesia. Many of the adverse effects will still be experienced in poor metabolizers. Conversely, 0.5-2% of the population are “extensive metabolizers”; multiple copies of the gene for 2D6 produce high levels of CYP2D6 and will metabolize drugs through that pathway more quickly than others.
Some medications are CYP2D6 inhibitors and reduce or even completely block the conversion of codeine to morphine. The most well-known of these are two of the selective serotonin reuptake inhibitors, paroxetine (Paxil) and fluoxetine (Prozac) as well as the antihistamine diphenhydramine (Benadryl), and the antidepressant bupropion (Wellbutrin, also known as Zyban). Other drugs, such as rifampicin and dexamethasone, induce CYP450 isozymes and thus increase the conversion rate.
CYP2D6 converts codeine into morphine, which then undergoes glucuronidation. Life-threatening intoxication, including respiratory depression requiring intubation, can develop over a matter of days in patients who have multiple functional alleles of CYP2D6, resulting in ultra-rapid metabolism of opioids such as codeine into morphine.
Studies on codeine’s analgesic effect are consistent with the idea that metabolism by CYP2D6 to morphine is important, but some studies show no major differences between those who are poor metabolizers and extensive metabolizers. Evidence supporting the hypothesis that ultrarapid metabolizers may get greater analgesia from codeine due to increased morphine formation is limited to case reports.
Due to increased metabolism of codeine to morphine, ultrarapid metabolizers (those possessing more than 2 functional copies of the CYP2D6 allele) are at increased risk of adverse drug effects related to morphine toxicity. Guidelines released by the Clinical Pharmacogenomics Implementation Consortium (CPIC) advise against administering codeine to ultrarapid metabolizers, where this genetic information is available. The CPIC also suggests that codeine use be avoided in poor metabolizers, due to its lack of efficacy in this group.
Codeine and its salts are readily absorbed from the gastrointestinal tract and ingestion of codeine phosphate produces peak plasma concentrations in about one hour. Plasma half life is between 3 and 4 hours and oral/intramuscular analgesic potency ratio is approximately equal to 1:1.5. The most common conversion ratio, given on equianalgesia charts used in the United States, Canada, the UK, Republic of Ireland, the European Union, Russia and elsewhere as 130 mg IM equals 200 mg PO—both of which are equivalent to 10 mg of morphine sulphate IV and 60 mg of morphine sulphate PO. The salt:freebase ratio of the salts of both drugs in use are roughly equivalent, and do not generally make a clinical difference.
Codeine is metabolised by O- and N-demethylation in the liver to morphine and norcodeine. Codeine and its metabolites are excreted almost entirely by the kidney, mainly as conjugates with glucuronic acid.
The active metabolites of codeine, notably morphine, exert their effects by binding to and activating the μ-opioid receptor.
Relation to other opioids
Codeine has been used in the past as the starting material and prototype of a large class of mainly mild to moderately strong opioids; such as hydrocodone (1920 in Germany), oxycodone (1916 in Germany), dihydrocodeine (1908 in Germany), and its derivatives such as nicocodeine (1956 in Austria). However, these opioids are no longer synthesized from codeine and are usually synthesized from other opium alkaloids; specifically thebaine. Other series of codeine derivatives include isocodeine and its derivatives, which were developed in Germany starting around 1920. In general, the various classes of morphine derivatives such as ketones, semisynthetics like dihydromorphine, halogeno-morphides, esters, ethers, and others have codeine, dihydrocodeine, and isocodeine analogues. The codeine ester acetylcodeine is a common active impurity in street heroin as some codeine tends to dissolve with the morphine when it is extracted from opium in underground heroin and morphine base labs.
As an analgesic, codeine compares weakly to other opiates. Related to codeine in other ways are codoxime, thebacon, codeine-N-oxide (genocodeine), related to the nitrogen morphine derivatives as is codeine methobromide, and heterocodeine, which is a drug six times stronger than morphine and 72 times stronger than codeine due to a small re-arrangement of the molecule, viz. moving the methyl group from the 3 to the 6 position on the morphine carbon skeleton.
Drugs bearing resemblance to codeine in effects due to close structural relationship are variations on the methyl groups at the 3 position including ethylmorphine a.k.a. codethyline (Dionine) and benzylmorphine (Peronine). While having no narcotic effects of its own, the important opioid precursor thebaine differs from codeine only slightly in structure. Pseudocodeine and some other similar alkaloids not currently used in medicine are found in trace amounts in opium as well.
Codeine, or 3-methylmorphine, is an alkaloid found in the opium poppy, Papaver somniferum var. album, a plant in the papaveraceae family. Opium poppy has been cultivated and utilized throughout human history for a variety of medicinal (analgesic, anti-tussive and anti-diarrheal) and hypnotic properties linked to the diversity of its active components, which include morphine, codeine and papaverine.
Codeine is found in concentrations of 1% to 3% in opium prepared by the latex method from unripe pods of Papaver somniferum. The name codeine is derived from the Ancient Greek κώδεια (kṓdeia, “poppy head”). The relative proportion of codeine to morphine, the most common opium alkaloid at 4% to 23%, tends to be somewhat higher in the poppy straw method of preparing opium alkaloids.
Until the beginning of the 19th century, raw opium was used in diverse preparations known as laudanum (see Thomas de Quincey‘s Confessions of an English Opium-Eater, 1821) and paregoric elixirs, a number of which were popular in England since the beginning of the 18th century; the original preparation seems to have been elaborated in Leiden, the Netherlands around 1715 by a chemist named Lemort; in 1721 the London Pharmacopoeia mentions an Elixir Asthmaticum, replaced by the term Elixir Paregoricum (“pain soother”) in 1746.
The progressive isolation of opium’s several active components opened the path to improved selectivity and safety of the opiates-based pharmacopeia.
Morphine had already been isolated in Germany by Friedrich Sertürner in 1804. Codeine was first isolated in 1832 in France by Pierre Robiquet, already famous for the discovery of alizarin, the most widespread red dye, while working on refined morphine extraction processes. Robiquet is also credited with discovering caffeine independently of Pelletier, Caventou, and Runge. This paved the way for the elaboration of a new generation of safer, codeine-based specific antitussive and antidiarrheal formulations.
Codeine is the most widely used opiate in the world, and is one of the most commonly used drugs overall according to numerous reports by organizations including the World Health Organization and its League of Nations predecessor agency. It is one of the most effective orally administered opioid analgesics and has a wide safety margin. Its strength ranges from 8% to 12% of morphine in most people; differences in metabolism can change this figure as can other medications, depending on its route of administration.
While codeine can be directly extracted from opium, its original source, most codeine is synthesized from the much more abundant morphine through the process of O-methylation, through a process first completed in the late 20th century by Robert C. Corcoran and Junning Ma.
By 1972, the effects of the War On Drugs had caused widespread shortages of illicit and licit opiates because of a scarcity of natural opium, poppy straw, and other sources of opium alkaloids, and the geopolitical situation was growing difficult for the United States. After much of the opium and morphine in the US National Stockpile of Strategic & Critical Materials was tapped in order to ease severe shortages of medicinal opiates — the codeine-based antitussives in particular — in late 1973, researchers were tasked with finding a way to synthesize codeine and its derivatives. They quickly succeeded using petroleum or coal tar and a process developed at the United States’ National Institutes of Health.
Numerous codeine salts have been prepared since the drug was discovered. The most commonly used are the hydrochloride (freebase conversion ratio 0.805), phosphate (0.736), sulphate (0.859), and citrate (0.842). Others include a salicylate NSAID, codeine salicylate (0.686), a bromide (codeine methylbromide, 0.759), and at least four codeine-based barbiturates, the cyclohexenylethylbarbiturate (0.559), cyclopentenylallylbarbiturate (0.561), diallylbarbiturate (0.561), and diethylbarbiturate (0.619). The latter was introduced as Codeonal in 1912, indicated for pain with nervousness. Codeine methylbromide is also considered a separate drug for various purposes.
Codeine and morphine, as well as opium, were used in an attempt to treat diabetes in the 1880s and thereafter, as recently as the 1950s.
Society and culture
It is often sold as a salt in the form of either codeine sulfate or codeine phosphate in the United States, United Kingdom and Australia. Codeine hydrochloride is more common worldwide and the citrate, hydroiodide, hydrobromide, tartrate, and other salts are also seen. The chemical name for codeine is morphinan-6-ol, 7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-, (5α,6α)-
Codeine is also available in conjunction with the anti-nausea medication promethazine in the form of a syrup. Brand named as Phenergan with Codeine or in generic form as promethazine with codeine. In the 1990s it started to be mixed with soft drinks to be used as a recreational drug and was called ‘syrup’, ‘lean’, or ‘purple drank‘. Rapper Pimp C, from the group UGK, died from an overdose of this combination.
Codeine and its major metabolites may be quantitated in blood, plasma or urine to monitor therapy, confirm a diagnosis of poisoning or assist in a medico-legal death investigation. Drug abuse screening programs generally test urine, hair, sweat or saliva. Many commercial opiate screening tests directed at morphine cross-react appreciably with codeine and its metabolites, but chromatographic techniques can easily distinguish codeine from other opiates and opioids. It is important to note that codeine usage results in significant amounts of morphine as an excretion product. Furthermore, heroin contains codeine (or acetyl codeine) as an impurity and its use will result in excretion of small amounts of codeine. Poppy seed foods represent yet another source of low levels of codeine in one’s biofluids. Blood or plasma codeine concentrations are typically in the 50–300 µg/L range in persons taking the drug therapeutically, 700–7000 µg/L in chronic users and 1000–10,000 µg/L in cases of acute fatal over dosage.
Codeine is produced in the human body along the same biosynthetic pathway as morphine. Urinary concentrations of endogenous codeine and morphine have been found to significantly increase in individuals taking L-DOPA for the treatment of Parkinson’s disease.
Around the world, codeine is, contingent on its concentration, a Schedule II and III drug under the Single Convention on Narcotic Drugs. In Australia, Canada, New Zealand, Sweden, the United Kingdom, the United States and many other countries, codeine is regulated under various narcotic control laws. In some countries it is available without a medical prescription in combination preparations from licensed pharmacists in doses up to 20 mg, or 30 mg when sold combined with 500 mg paracetamol.
In Australia, Since February 1, 2018, preparations containing codeine are not available without a prescription.
Preparations containing pure codeine (e.g., codeine phosphate tablets or codeine phosphate linctus) are available on prescription and are considered S8 (Schedule 8, or “Controlled Drug Possession without authority illegal”). Schedule 8 preparations are subject to the strictest regulation of all medications available to consumers.
In Canada tablets containing 8 mg of codeine combined with 15 mg of caffeine and 300 mg of acetaminophen are sold as T1s (Tylenol Number 1) without a prescription. A similar tablet called “A.C. & C.” (which stands for Acetylsalicylic acid with Caffeine and Codeine) containing 325–375 mg of acetylsalicylic acid (Aspirin) instead of acetaminophen is also available without a prescription. Both tablets are kept behind the counter and must be dispensed by a pharmacist who may limit quantities. Names of many codeine and dihydrocodeine products in Canada tend to follow the narcotic content number system (Tylenol With Codeine No. 1, 2, 3, 4 &c) mentioned below in the section on the United States; it came to be in its current form with the Pure Food & Drug Act of 1906.
Codeine became a prescription-only medication in the province of Manitoba on February 1, 2016. A pharmacist may issue a prescription, and all purchases are logged to a central database to prevent overprescribing.
In Denmark codeine is sold over the counter in dosages up to 9.6 mg (with aspirin, brand name Kodimagnyl); anything stronger requires a prescription.
In France, before 2017 most preparations containing codeine did not require a doctor’s prescription. Example products containing codeine include Néocodion (codeine and camphor), Tussipax (ethylmorphine and codeine), Paderyl (codeine alone), Codoliprane (codeine with paracetamol), Prontalgine and Migralgine (codeine, paracetamol and caffeine). In 2017 the law was changed making mandatory a prescription for all codeine products along with ethylmorphine and dextromethorphan 
Germany, Switzerland, and Austria
Codeine is listed under the Betäubungsmittelgesetz in Germany and the similarly named narcotics and controlled substances law in Switzerland. In Austria, the drug is listed under the Suchtmittelgesetz in categories corresponding to their classification under the Single Convention on Narcotic Drugs. Dispensing of products containing codeine and similar drugs (dihydrocodeine, nicocodeine, benzylmorphine, ethylmorphine etc.), in general, requires a prescription order from a doctor or the discretion of the pharmacist.
Municipal and provincial regulations may impact availability, in particular in Austria and Switzerland, which allows cities and provinces to regulate the selling of the least-regulated schedule of the SMG/BtMG. Individual chemists’ shops can opt out of providing them or imposing volume, frequency, or single-purchase limitations and other things of the same store. Plain codeine hydrochloride tablets as well as other non-injectable forms of codeine and its midrange derivatives can be dispensed in this way; the same goes for most chemical classes of benzodiazepines, the majority of non-barbiturate sedative/hypnotics, and at least a handful of barbiturates.
Title 76 of the Schengen treaty has made it possible for countries within the signatory states to import and export drugs with various provisos, recording and ordering requirements, and various other rules.
Codeine is classed as an illegal drug in Greece, and individuals possessing it could conceivably be arrested, even if they were legitimately prescribed it in another country. It is sold only with a doctor’s prescription (Lonarid-N, Lonalgal).
In Hong Kong, codeine is regulated under Laws of Hong Kong, Dangerous Drugs Ordinance, Chapter 134, Schedule 1. It can be used legally only by health professionals and for university research purposes. The substance can be given by pharmacists under a prescription. Anyone who supplies the substance without prescription can be fined $10,000 (HKD). The maximum penalty for trafficking or manufacturing the substance is a $5,000,000 (HKD) fine and life imprisonment. Possession of the substance for consumption without license from the Department of Health is illegal with a $1,000,000 (HKD) fine and/or 7 years of jail time.
Codeine preparations require a prescription in India. A preparation of paracetamol and codeine is available in India. Codeine is also present in various cough syrups as codeine phosphate including chlorpheniramine maleate. Pure codeine is also available as codeine sulphate tablets. Codeine containing cough medicine has been banned in India with effect from 14 March 2016. The Ministry of Health and Family Welfare has found no proof of its efficacy against cough control.
Preparations of codeine in Iran normally comes with paracetamol or guaifenesin, and can be purchased over-the-counter. Pure codeine is also available as codeine phosphate 30 mg tablets and special permit required to purchasing. Iran’s deputy health minister reported that codeine combinations is Iran’s best selling OTC medication.
In Ireland, new regulations came into effect on 1 August 2010 concerning codeine, due to worries about the overuse of the drug. Codeine remains a semi non-prescriptive, over-the-counter drug up to a limit of 12.8 mg per pill, but codeine products must be out of the view of the public to facilitate the legislative requirement that these products “are not accessible to the public for self-selection”. In practice, this means customers must ask pharmacists for the product containing codeine in name, and the pharmacist makes a judgement whether it is suitable for the patient to be using codeine, and that patients are fully advised of the correct use of these products. Products containing more than 12.8 mg codeine are available on prescription only.
Low dose codeine is available over the counter at pharmacies but not higher doses.
The Maldives takes an infamously strict line on medicines, with many common drugs, notably anything with containing codeine being banned unless you have a notarized and authenticated doctor’s prescription. Visitors breaking the rules, even inadvertently, have been deported or imprisoned.
Codeine is not allowed without a medical prescription. Codeine is sold under the name Farmacod and its concentration does not exceed 15 mg. There is a known combination of acetylsalicylic acid, paracetamol and codeine phosphate hemihydrate named Aspaco that is allowed without a medical prescription but its case is signed with an exclamation red symbol which means that driving won’t be allowed during treatment. There are no sanctions whether the drug is given without a prescription.
The Russian Federation
According to ITAR-Tass and Austria Presse-Agentur, OTC availability of codeine products was rescinded nationwide in 2012 because of the discovery of the Krokodil method of underground desomorphine synthesis. Opponents of the move point out that codeine has not been available OTC in 22 of Russia’s oblasts for years and the demand will call forth its own supply, meaning that only legitimate end users are negatively impacted (activist quoted in Pravda story on issue).
Codeine is available over the counter in South Africa. Certain pharmacies require people to write down their name and address to ensure they are not buying too much over a short period although many do not require this at all. According to Dr Lochan Naidoo, the former president of the National Narcotics Control Board, making the drugs more difficult to obtain could lead to even worse problems where people in withdrawal would turn to illicit drugs to get their fix. Although codeine is freely available, South Africa has a fairly low annual prevalence rate of opiate use at 0.3% compared to the United States at 0.57% where all opiates are strictly regulated.
Codeine preparations are available as over the counter pharmacy medicines in Sri Lanka. The most common preparation is Panadeine, which contains 500 mg of Paracetamol and 8 mg of Codeine. But cough syrup containing Codeine is banned, even with a prescription.
United Arab Emirates
The UAE takes an exceptionally strict line on medicines, with many common drugs, notably anything containing codeine being banned unless one has a notarized and authenticated doctor’s prescription. Visitors breaking the rules, even inadvertently, have been deported or imprisoned. The US Embassy to the UAE maintains an unofficial list of what may not be imported.
In the United Kingdom, the sale and possession of codeine are restricted separately under law.
Neat codeine and higher-strength codeine formulations are generally prescription-only medicines (POM) meaning that the sale of such products is restricted under the Medicines Act 1968. Lower-strength products containing combinations of up to 12.8 mg of codeine per dosage unit, combined with paracetamol, ibuprofen or aspirin are available over the counter at pharmacies. Codeine linctus of 15 mg per 5 ml is also available at some pharmacies, although a purchaser would have to request it specifically from the pharmacist.
Under the Misuse of Drugs Act 1971 codeine is a Class B controlled substance or a Class A drug when prepared for injection. The possession of controlled substances without a prescription is a criminal offence. However, certain preparations of codeine are exempt from this restriction under Schedule 5 of the Misuse of Drugs Regulations 2001. It is thus legal to possess codeine without a prescription, provided that it is compounded with at least one other active or inactive ingredient and that the dosage of each tablet, capsule, etc. does not exceed 100 mg or 2.5% concentration in the case of liquid preparations. The exemptions do not to apply to any preparation of codeine designed for injection.
In the United States, codeine is regulated by the Controlled Substances Act. Federal law dictates that codeine be a Schedule II controlled substance when used in products for pain-relief that contain codeine alone or more than 80 mg per dosage unit. Codeine without aspirin or acetaminophen (Tylenol) is very rarely available or prescribed in order to discourage abuse. Tablets of codeine in combination with aspirin or acetaminophen (paracetamol) and intended for pain relief are listed as Schedule III, allowing electronic fills and refills without a physical paper-copy of the physician ordered prescription.
Cough syrups are classed as Schedule III, IV or V, depending on formulation. For example, the acetaminophen/codeine antitussive liquid is a Schedule IV controlled substance.
Some states have chosen to reclassify codeine preparations at a more restrictive schedule in order to lower the instances of its abuse. Minnesota, for instance, has chosen to reclassify Schedule V some codeine preparations (e.g. Cheratussin) as a Schedule II controlled substance.
In some jurisdictions where codeine is a Schedule V substance, it is available as an antitussive liquid, combined with paracetamol, aspirin or terpin hydrate, in limited strengths and quantities without a prescription (at the discretion of the dispensing pharmacist). In most jurisdictions such sales are entered into a dispensed-narcotics database, requiring customer signature, to limit excessive use.
- Shen H, He MM, Liu H, et al. (August 2007). “Comparative metabolic capabilities and inhibitory profiles of CYP2D6.1, CYP2D6.10, and CYP2D6.17”. Drug Metab. Dispos. 35 (8): 1292–300. doi:10.1124/dmd.107.015354. PMID 17470523.
- “Codeine”. The American Society of Health-System Pharmacists. Archived from the original on 18 January 2016. Retrieved 5 January 2016.
- Prommer, E (2010). “Role of codeine in palliative care”. Journal of Opioid Management. 7 (5): 401–6. PMID 22165039.
- Paul, IM (February 2012). “Therapeutic options for acute cough due to upper respiratory infections in children”. Lung. 190 (1): 41–4. doi:10.1007/s00408-011-9319-y. PMID 21892785.
- Schroeder, K.; Fahey, T. (2004-10-18). “Over-the-counter medications for acute cough in children and adults in ambulatory settings”. The Cochrane Database of Systematic Reviews (4): CD001831. doi:10.1002/14651858.CD001831.pub2. ISSN 1469-493X. PMID 15495019.
- Tobias, J. D.; Green, T. P.; Cote, C. J. (19 September 2016). “Codeine: Time To Say “No““. Pediatrics. 138 (4): e20162396. doi:10.1542/peds.2016-2396. PMID 27647717.
- Newton, David (2015). Prescription Drug Abuse: A Reference Handbook. ABC-CLIO. p. 20. ISBN 978-1-4408-3979-5. Archived from the original on 4 February 2017.
- Narcotic Drugs 2014 (pdf). INTERNATIONAL NARCOTICS CONTROL BOARD. 2015. p. 21. ISBN 9789210481571. Archived (PDF) from the original on 2 June 2015.
- “WHO Model List of Essential Medicines (19th List)” (PDF). World Health Organization. April 2015. Archived (PDF) from the original on 13 December 2016. Retrieved 8 December 2016.
- “Codeine”. International Drug Price Indicator Guide. Retrieved 10 January 2016.
- Stefano Guandalini; Haleh Vaziri (8 November 2010). Diarrhea: Diagnostic and Therapeutic Advances. New York, USA: Humana Press. p. 452. ISBN 978-1-60761-182-0.
- Straube, C; Derry, S; Jackson, KC; Wiffen, PJ; Bell, RF; Strassels, S; Straube, S (19 Sep 2014). “Codeine, alone and with paracetamol (acetaminophen), for cancer pain”. The Cochrane Database of Systematic Reviews. 9 (9): CD006601. doi:10.1002/14651858.CD006601.pub4. PMID 25234029.
- Commissioner, Office of the. “Press Announcements – FDA statement from Douglas Throckmorton, M.D., deputy center director for regulatory programs, Center for Drug Evaluation and Research, on new warnings about the use of codeine and tramadol in children & nursing mothers”. www.fda.gov. Archived from the original on 20 April 2017. Retrieved 21 April 2017.
- Neri C; Guama M; et.al Endogenous morphine and codeine in the brain of non human primate. Medical Science Montier 2004, 10, MS1-MS5.
- Paul IM (February 2012). “Therapeutic options for acute cough due to upper respiratory infections in children”. Lung. 190 (1): 41–4. doi:10.1007/s00408-011-9319-y. PMID 21892785.
- McCrory DC, et al. (January 2013). “Assessment and Management of Chronic Cough”. AHRQ Comparative Effectiveness Reviews. PMID 23367526.
- “Codeine – adverse effects”. Medscape reference – Drugs, Diseases & Procedures. WebMD LLC. Archived from the original on 18 August 2012. Retrieved 27 September 2012.
- CTV News, Codeine use while breastfeeding may be dangerous Archived 1 September 2008 at the Wayback Machine, Wed. 20 August 2008
- Koren G, Cairns J, Chitayat D, Gaedigk A, Leeder SJ (August 2006). “Pharmacogenetics of morphine poisoning in a breastfed neonate of a codeine-prescribed mother”. Lancet. 368 (9536): 704. doi:10.1016/S0140-6736(06)69255-6. PMID 16920476.
- “Safety review update of codeine use in children; new Boxed Warning and Contraindication on use after tonsillectomy and/or adenoidectomy”. FDA. 20 February 2013. Archived from the original on 4 September 2014.
- “Opioids: Information for Health Professionals” (PDF). Alberta Health Services. Archived (PDF) from the original on 12 March 2017. Retrieved 9 March 2017.
- Fernandes LC, Kilicarslan T, Kaplan HL, Tyndale RF, Sellers EM, Romach MK (June 2002). “Treatment of codeine dependence with inhibitors of cytochrome P450 2D6”. J Clin Psychopharmacol. 22 (3): 326–9. doi:10.1097/00004714-200206000-00014. PMID 12006904.
- Kathiramalainathan K, Kaplan HL, Romach MK, et al. (2000). “Inhibition of cytochrome P450 2D6 modifies codeine abuse liability”. J Clin Psychopharmacol. 20 (4): 435–44. doi:10.1097/00004714-200008000-00008. PMID 10917405.
- Willmann S, Edginton AN, Coboeken K, Ahr G, Lippert J (2009). “Risk to the Breast-Fed Neonate From Codeine Treatment to the Mother: A Quantitative Mechanistic Modeling Study”. Clinical Pharmacology & Therapeutics. 86 (6): 634–43. doi:10.1038/clpt.2009.151. PMID 19710640.
- Raynor K, Kong H, Chen Y, Yasuda K, Yu L, Bell GI, Reisine T (1994). “Pharmacological characterization of the cloned kappa-, delta-, and mu-opioid receptors”. Mol. Pharmacol. 45 (2): 330–4. PMID 8114680.
- Corbett AD, Paterson SJ, Kosterlitz HW (1993). “Selectivity of Ligands for Opioid Receptors”. In Herz A, Akil H, Simon EJ. Opioids. Handbook of Experimental Pharmacology. 104 / 1. Springer Verlag. pp. 645–679. doi:10.1007/978-3-642-77460-7_26. ISBN 978-3-642-77462-1. ISSN 0171-2004.
- King (25 October 2010). Pharmacology for Women’s Health. Jones & Bartlett Publishers. pp. 332–. ISBN 978-1-4496-1073-9.
- David H. Chestnut; Cynthia A Wong; Lawrence C Tsen; Warwick D Ngan Kee; Yaakov Beilin; Jill Mhyre (28 February 2014). Chestnut’s Obstetric Anesthesia: Principles and Practice. Elsevier Health Sciences. pp. 611–. ISBN 978-0-323-11374-8.
- Adriana P. Tiziani (1 June 2013). Havard’s Nursing Guide to Drugs. Elsevier Health Sciences. pp. 933–. ISBN 978-0-7295-8162-2.
- Rhonda J. Moore (5 January 2012). Handbook of Pain and Palliative Care: Biobehavioral Approaches for the Life Course. Springer Science & Business Media. pp. 499–. ISBN 978-1-4419-1651-8.
- Papich, Mark G. (1 January 2016). “Codeine”. Saunders Handbook of Veterinary Drugs (Fourth Edition). W.B. Saunders: 183–184. doi:10.1016/b978-0-323-24485-5.00175-3.
- Papich, Mark G. (1 January 2016). “Codeine”. Saunders Handbook of Veterinary Drugs (Fourth Edition). W.B. Saunders: 183–184. doi:10.1016/b978-0-323-24485-5.00175-3.
- Hitchings, Anderw; Lonsdale, Dagan; Burrage, Daniel; Baker, Emma (2015). Top 100 drugs : clinical pharmacology and practical prescribing. p. 168. ISBN 978-0-7020-5516-4.
- Stefano GB, Ptáček R, Kuželová H, Kream RM (2012). “Endogenous morphine: up-to-date review 2011” (PDF). Folia Biol. (Praha). 58 (2): 49–56. PMID 22578954. Archived (PDF) from the original on 24 August 2016.
Positive evolutionary pressure has apparently preserved the ability to synthesize chemically authentic morphine, albeit in homeopathic concentrations, throughout animal phyla.
- Srinivasan V, Wielbo D, Tebbett IR (1997). “Analgesic effects of codeine-6-glucuronide after intravenous administration”. European Journal of Pain. 1 (3): 185–90. doi:10.1016/S1090-3801(97)90103-8. PMID 15102399.
- Lurcott G (1998). “The effects of the genetic absence and inhibition of CYP2D6 on the metabolism of codeine and its derivatives, hydrocodone and oxycodone”. Anesth Prog. 45 (4): 154–6. PMC 2148980. PMID 10483388.
- Gasche Y, Daali Y, Fathi M, et al. (December 2004). “Codeine intoxication associated with ultrarapid CYP2D6 metabolism”. N. Engl. J. Med. 351 (27): 2827–31. doi:10.1056/NEJMoa041888. PMID 15625333.
- Caraco Y (December 2004). “Genes and the response to drugs”. N. Engl. J. Med. 351 (27): 2867–9. doi:10.1056/NEJMe048278. PMID 15625340.
- Gardiner, S. J.; Begg, E. J. (2006). “Pharmacogenetics, Drug-Metabolizing Enzymes, and Clinical Practice”. Pharmacological Reviews. 58 (3): 521–590. doi:10.1124/pr.58.3.6. PMID 16968950.
- Crews, KR; Gaedigk, A; Dunnenberger, HM; Leeder, JS; Klein, TE; Caudle, KE; Haidar, CE; Shen, DD; Callaghan, JT; Sadhasivam, S; Prows, CA; Kharasch, ED; Skaar, TC (April 2014). “Clinical Pharmacogenetics Implementation Consortium Guidelines for Cytochrome P450 2D6 Genotype and Codeine Therapy: 2014 Update”. Clin Pharmacol Ther. 95 (4): 376–382. doi:10.1038/clpt.2013.254. PMC 3975212. PMID 24458010.
- The Merck Index, 13th Edition: Morphine Hydrochloride
- http://www.medicines.org.uk/emc/medicine/23910#PHARMACOKINETIC_PROPS Archived 30 July 2014 at the Wayback Machine
- Report of Committee on drug addiction, 1929-1941″. National Research Council (US).
- Andreas Luch (2009). Molecular, clinical and environmental toxicology. Springer. p. 20. ISBN 978-3-7643-8335-0.
- Wisniak, Jaime (2013-03-01). “Pierre-Jean Robiquet”. Educación Química. 24: 139–149. doi:10.1016/S0187-893X(13)72507-2. ISSN 0187-893X.
- Opiates.com – Codeine Archived 13 October 2011 at the Wayback Machine
- Science Daily (March 2010) – “Unlocking the Opium Poppy’s Biggest Secret: Genes That Make Codeine, Morphine” Archived 27 November 2011 at the Wayback Machine
- Elmhurt College – Narcotic Analgesic Drugs Archived 29 July 2003 at the Wayback Machine
- Corcoran, R. C.; Ma, J. Solid-phase synthesis of codeine from morphine. NV, United States Patent 6,204,337, 2001.
- The American Practitioner. 1912.
- DEA, ibid
- Fraser, Thomas R (1889). “The Relative Value of Opium, Morphine, and Codeine in Diabetes Mellitus”. British Medical Journal. 1 (1464): 118–19. doi:10.1136/bmj.1.1464.118. PMC 2154578. PMID 20752554.
- Merck Index
- Anonymous Codeine. In The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals; O’Neil, M. J., Ed.; Merck: Whitehouse Station, NJ, 2006; pp 2417.
- Boekhout van Solinge, Tim (1996). “7. La politique de soins des années quatre-vingt-dix”. L’héroïne, la cocaïne et le crack en France. Trafic, usage et politique (in French). Amsterdam: CEDRO Centrum voor Drugsonderzoek, Universiteit van Amsterdam. pp. 247–262.
- Leinwand, Donna (18 October 2006). “DEA warns of soft drink-cough syrup mix”. USA Today. Archived from the original on 28 November 2006. Retrieved 23 October 2006.
- “Pimp C’s death caused by overdose and sleep condition – Houston Chronicle”. Chron.com. 4 February 2008. Archived from the original on 31 December 2013. Retrieved 12 January 2014.
- Hogshire, Jim (June 1999). Pills-A-Go-Go: A Fiendish Investigation into Pill Marketing, Art, History & Consumption. Los Angeles: Feral House. pp. 216–223. ISBN 978-0-922915-53-8.
- Savchuk, S. A.; Barsegyan, S. S.; Barsegyan, I. B.; Kolesov, G. M. (2011). “Chromatographic study of expert and biological samples containing desomorphine”. Journal of Analytical Chemistry. 63 (4): 361–70. doi:10.1134/S1061934808040096.
- Thevis M, Opfermann G, Schänzer W (2003). “Urinary concentrations of morphine and codeine after consumption of poppy seeds”. J. Anal. Toxicol. 27 (1): 53–6. doi:10.1093/jat/27.1.53. PMID 12587685.
- Cone EJ, Welch P, Paul BD, Mitchell JM (1991). “Forensic drug testing for opiates, III. Urinary excretion rates of morphine and codeine following codeine administration”. J. Anal. Toxicol. 15 (4): 161–6. doi:10.1093/jat/15.4.161. PMID 1943064.
- Baselt R (2008). Disposition of Toxic Drugs and Chemicals in Man (8th ed.). Foster City CA: Biomedical Publications. pp. 355–360.
- International Narcotics Control Board. “List of Narcotic Drugs under International Control” (PDF). Archived from the original (PDF) on 10 May 2012. Retrieved 24 May 2006.
- “Painkillers with codeine won’t be available over the counter from 2018”. ABC.net.au. Archived from the original on 21 December 2016. Retrieved 20 December 2016.
- “Tylenol 1 to require prescription in Manitoba in February 2016”. www.cbc.ca. Archived from the original on 31 May 2016. Retrieved 4 June 2016.
- Foley, M; Breindahl, T; Hindersson, P; Deluca, P; Kimergård, A (January 2016). “Misuse of ‘over-the-counter’ codeine analgesics: does formulation play a role?”. Public Health. 130: 95–6. doi:10.1016/j.puhe.2015.10.006. PMID 26612458.
- “vital list of codein”. vidal.com. Archived from the original on 21 July 2011. Retrieved 12 January 2011.
- Wilkes, Deborah. “OTCToolbox – France restricts dextromethorphan and codeine”. www.otctoolbox.com.
- “Pharmacies in Greece”. About.com. Archived from the original on 6 October 2010. Retrieved 10 October 2009.
- Laws of Hong Kong, Dangerous Drugs Ordinance, Chapter 134 “Archived copy”. Archived from the original on 16 October 2012. Retrieved 16 October 2016.CS1 maint: Archived copy as title (link)
- “Pfizer, Abbott shares tank after ban on Corex, Phensedyl and 327 other drugs – The Economic Times”. The Economic Times. Archived from the original on 17 November 2016. Retrieved 14 March 2016.
- “Codeine regulations cause a few headaches”. The Irish Times. 8 August 2010. Archived from the original on 3 September 2010.
- Office of The Attorney General, Regulation 5(1)(e) of the Regulation of Retail Pharmacy Businesses Regulations 2008 (S.I. 488 of 2008) Archived 27 July 2011 at the Wayback Machine
- “Non-Prescription Medicinal Products Containing Codeine: Draft Guidance for Pharmacists”. Pharmaceutical Society of Ireland. Archived from the original on 21 May 2013.
- “Nigeria bans all codeine cough syrup”. BBC News. 1 May 2018. Retrieved 3 May 2018.
- “Archived copy”. Archived from the original on 17 October 2016. Retrieved 16 October 2016.CS1 maint: Archived copy as title (link)
- “Misuse of Drugs Act 1971”. Legislation.gov.uk. Archived from the original on 8 November 2013. Retrieved 12 January 2014.
- “Misuse of Drugs Act 1971”. Legislation.gov.uk. Archived from the original on 28 January 2014. Retrieved 12 January 2014.
- “The Misuse of Drugs Regulations 2001”. Legislation.gov.uk. 9 December 2013. Archived from the original on 29 January 2014. Retrieved 12 January 2014.
- Valeant Pharmaceuticals. “Prescribing Information for Capital with Codeine (paracetamol with codeine) showing Schedule V designation” (PDF). Archived (PDF) from the original on 17 July 2011. Retrieved 25 February 2011.
- “152.02 SCHEDULES OF CONTROLLED SUBSTANCES”. State of Minnesota. Archived from the original on 30 July 2013. Retrieved 30 May 2013.
- U.S. National Center for Biotechnology Information: Medical Genetics Summaries – Codeine Therapy and CYP2D6 Genotype