Everything about Codeine totally explained
This article is about the drug.
| PubChem = 5284371
| DrugBank = APRD00120
| C=18 | H=21 | N=1 | O=3
| molecular_weight = 299.364 g/mol
| bioavailability = ~90% Oral
| elimination_half-life = 2.5–3 hours
| metabolism =
Hepatic, via
CYP2D6 (Cytochrome P450 2D6)
| legal_AU = S8
| legal_CA = Schedule I
| legal_NZ = Class C
| legal_SG = Class B
| legal_UK = Class B
| legal_US = Schedule II
| legal_status =
| routes_of_administration = oral, intra-rectally,
SC,
IM
}}
Codeine (
INN) or
methylmorphine is an
opiate used for its
analgesic,
antitussive and
antidiarrheal properties. It is by far the most widely used opiate in the world and very likely most commonly used drug overall according to numerous reports over the years by organizations such as the
World Health Organization and its League of Nations predecessor agency and others. It is one of the most effective orally-administered
opioid analgesics and has a wide safety margin. It is from 8 to 12 percent of the strength of morphine in most people; differences in metabolism can change this figure as can other medications.
Codeine is an
alkaloid found in
opium and other poppy saps like
Papaver bracteatum the Iranian poppy. It was first isolated in 1830 in
France by
Jean-Pierre Robiquet, in concentrations ranging from 0.3 to 3.0
percent. While codeine can be extracted from opium, most codeine is synthesized from
morphine through the process of O-
methylation.
Although it's a naturally-occurring opiate, codeine can also be made by complete synthesis as well. The effects of the Nixon
War On Drugs by 1972 or so had caused across-the-board 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 getting less helpful for the United States. After a large percentage of the opium and morphine in the
US National Stockpile of Strategic & Critical Materials had to be tapped in order to ease severe shortages of medicinal opiates -- the codeine-based antitussives in particular -- in late 1973, researchers were tasked with and quickly succeeded in finding a way that codeine and its derivatives and precursors can be synthesised from scratch from petroleum or coal tar using a process developed at the United States' National Institutes of Health.
Codeine is marketed as the salts codeine sulphate and codeine phosphate in the United States and Canada. Codeine hydrochloride is more commonly marketed in continental Europe and other regions, and codeine hydroiodide and codeine bitartrate round out the top five most-used codeine salts worldwide. Codeine is usually present in raw opium as free alkaloid in addition to codeine meconate, codeine pectinate, and possibly other naturally-occurring codeine salts. Dozens of other salts of codeine have been developed over the last 175 years including some with special properties of other drug groups such as codeine
salicylate and codeine-based salts of barbituric acid (
barbiturates). Codeine citrate, nitrate, picrate, acetate, hydrobromide and others are occasionally encountered on the pharmaceutical market and in research.
Codeine is the starting material and prototype of a large class of mainly mild to moderately strong opioids such as
hydrocodone,
dihydrocodeine and its derivatives such as
nicocodeine,
oxycodone etc. Related to codeine in other ways are
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.
Indications
Approved indications for codeine include:
Codeine is sometimes marketed in combination preparations with the analgesic,
acetaminophen (
paracetamol), as
co-codamol,
paracod,
panadeine, or
Tylenol 3, with the analgesic,
acetylsalicylic acid (
aspirin), as
co-codaprin or with the
NSAID (non-steroidal
anti-inflammatory drug),
ibuprofen, as
Herron Blue or
Nurofen Plus. These combinations provide greater pain relief than either agent alone (drug
synergy). Codeine is also commonly compounded with other pain killers or muscle relaxers such as
Fioricet with Codeine,
Soma Compound/Codeine, etc. Codeine-only products can be obtained with a prescription as a time release tablet (eg. Codeine Contin(r) 100mg) and Perduretas (50 mg).
The narcotic content number in the US names of codeine tablets and combination products like Tylenol With Codeine No. 3, Emprin With Codeine No. 4 are as follows: No. 1 - 7½ or 8 mg (1/8 grain), No. 2 - 15 or 16 mg (1/4 grain), No. 3 - 30 or 32 mg (1/2 grain), No. 4 - 60 or 64 mg (1 grain). The Canadian 222 series is identical to the above list 222=1/8 grain, 292=1/4 grain, 293=1/2 grain, and 294=1 grain of codeine.
Injectable codeine is available for subcutaneous or intramuscular injecton; intravenous injection can cause a serious reaction which can progress to anaphylaxis. Codeine suppositories are also marketed in some countries.
Controlled substance
In
Australia,
New Zealand,
Romania,
Canada and many other countries, codeine is regulated. In some countries it's available without prescription in combination preparations from licensed pharmacists in doses up to 15 mg/tablet in Australia, 8 mg/tablet in Canada, 20 mg/tablet in New Zealand, and 10mg/tablet in Israel.
In Canada, codeine can be sold over the counter only in combination with two or more ingredients, which has resulted in the prevalence of AC&C (
aspirin, codeine, and
caffeine), and similar combinations using acetaminophen (
paracetamol) rather than aspirin. Caffeine, being a stimulant, tends to offset the sedative effects of codeine. It also can
increase the effectiveness and absorption rate of analgesics in some circumstances.
Codeine is listed under the
Betäubungsmittelgesetz in
Germany and the similarly-named narcotics & 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 &c.) generally require a prescription order from a doctor or the discretion of the pharmacist. Municipal and provincial regulations may impact the range of products which can be dispensed in the latter case.
In
Hong Kong, codeine is regulated under Schedule 1 of
Hong Kong's Chapter 134
Dangerous Drugs Ordinance. 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 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.
However, codeine is available without prescription from licensed pharmacists in doses up to 0.1% (5mg/5ml) according to Hong Kong "Dangerous Drugs Ordinance".
In the
United Kingdom, codeine tablets are prescription only medicines, with the exception of co-codamol 8/500 where 8mg of codeine phosphate is combined with 500mg paracetamol which is available as a pharmacy supervised medicine. This applies as well to Nurofen Plus, which contains 200mg
Ibuprofen with 12.8mg Codeine per tablet.
Intramuscular injection of codeine is a controlled drug under the
Misuse of Drugs Act 1971.
In the
United States, codeine is regulated by the
Controlled Substances Act. It is a Schedule II controlled substance for pain-relief products containing codeine alone or more than 90 mg per dosage unit. In combination with aspirin or acetaminophen (
paracetamol/Tylenol) it's listed as Schedule III or V, depending on formula. Preparations for cough or diarrhoea containing small amounts of codeine in combination with two or more other active ingredients are Schedule V in the US, and in some states may be dispensed in amounts up to 4 fl. oz. per 48 hours without a prescription. Schedule V specifically consigns the product to state and local regulation beyond certain required record-keeping requirements (a dispensary log must be maintained for two years in a ledger from which pages can't easily be removed and/or are pre-numbered and the pharmacist must ask for a picture ID such as a driving licence) and also which maintain controlled substances in the closed system at the root of the régime intended by the Controlled Substances Act of 1970 -- for example the codeine in these products was a Schedule II substance when the company making the Schedule V product acquired it for mixing up the end product. In locales where dilute codeine preparations are non-prescription, anywhere from very few to perhaps a moderate percentage of pharmacists will sell these preparations without a prescription. However, many states have their own laws that do require a prescription for Schedule V drugs. Other drugs which are present in Schedule V narcotic preparations like the codeine syrups are
ethylmorphine and
dihydrocodeine.
Paregoric and
hydrocodone were transferred to Schedule III from Schedule V even if the preparation contains two or more other active ingredients, and
diphenoxylate is usually covered by state prescription laws even though this relative of
pethidine is a Schedule V substance when adulterated with atropine to prevent abuse.
Codeine is also available outside the United States as an
over-the-counter drug in liquid cough-relief formulations. Internationally, codeine is a Schedule II drug under the
Single Convention on Narcotic Drugs.
Pharmacokinetics
Codeine is considered a
prodrug, since it's metabolised
in vivo to the primary active compounds
morphine and
codeine-6-glucuronide. Roughly 5-10% of codeine will be converted to morphine, with the remainder either free, conjugated to form codeine-6-glucuronide (~70%), or converted to
norcodeine (~10%) and
hydromorphone (~1%). It is less potent than morphine and has a correspondingly lower
dependence-liability than morphine. Like all opiates, codeine is addictive unless used infrequently. However, the withdrawal symptoms are relatively mild and as a consequence codeine is considerably less addictive than the other opiates.
Theoretically, a dose of approximately 200 mg (oral) of codeine must be administered to give analgesia equivalent to 30 mg (oral) of morphine (Rossi, 2004). However, codeine is generally not used in single doses of greater than 60 mg (and no more than 240 mg in 24 hours). When analgesia beyond this is required, stronger opioids such as
hydrocodone or
oxycodone are favored. Because codeine needs to be metabolized to an active form, there's a
ceiling effect around 400-450 mg. This low ceiling further contributes to codeine being less addictive than the other opiates.
The conversion of codeine to morphine occurs in the liver and is catalysed by the
cytochrome P450 enzyme
CYP2D6.
CYP3A4 produces norcodeine and
UGT2B7 conjugates codeine, norcodeine and morphine to the corresponding 3- and 6- glucuronides. Approximately 6–10% of the Caucasian population, 2% of Asians, and 1% of Arabs have poorly functional CYP2D6 and codeine should be less effective for analgesia in these patients (Rossi, 2004), although it's speculated 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 those deficient in 2D6. Conversely, 0.5-2% of the population has multiple copies of the 2D6 gene and will metabolise 2D6 dependent drugs more efficiently than others.
Some medications are CYP2D6 inhibitors and reduce or even completely eliminate the efficacy of codeine. The most well-known of these are the
selective serotonin reuptake inhibitors, such as
fluoxetine (Prozac) and
citalopram (Celexa). Other drugs, such as
rifampicin and
dexamethasone, induce expression of CYP450 isozymes and thus increase the rate of metabolism.
It is important to note that whereas usually a CYP2D6 extensive metaboliser (EM) will need a higher dose of 2D6-metabolized drug for a sufficient therapeutic effect and a poor metaboliser (PM) may suffer from drug toxicity due to excessive plasma concentration, with the pro-drug Codeine, the opposite is true. Thus, an EM may have an adverse toxicity effect and a PM may have little or no pain relief.
Pharmacology
Codeine is a
prodrug, itself inactive, but demethylated to the active
morphine by the liver enzyme
CYP2D6. Because of the wide variability in CYP2D6 activity among humans, the effect of codeine can vary between individuals. In persons with little or no CYP2D6 function, codeine has little or no effect.
Adverse effects
Common adverse drug reactions associated with the use of codeine include
euphoria,
itching,
nausea,
vomiting,
drowsiness,
dry mouth,
miosis,
orthostatic hypotension,
urinary retention and
constipation.
Tolerance to many of the effects of codeine develops with prolonged use, including therapeutic effects. The rate at which this occurs develops 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 the mechanism for the potentially fatal consequences of overdose.
Another side effect commonly noticed is the lack of sexual drive and increased complications in erectile dysfunction.
Codeine has also been known to interact negatively with some
psychiatric medications such as
reboxetine and
venlafaxine.
Codeine is also available in conjunction with the anti-nausea medication
promethazine in the form of a syrup. Brand named as Phenergan VC with Codeine or generically as promethazine with codeine this medication is quickly becoming one of the most highly abused codeine preparations. Although there are various forms of this syrup varying in strengths, the highly publicized "purple" version (grape flavored) is the most sought after. In this form, there are 60mg of codeine per liquid ounce which makes it the strongest of the codeine syrups. This "
Purple Drank" is frequently referenced and praised in the
southern rap and
Houston-based hip-hop community where it's mixed with the soft drink
Sprite. There are many songs that mention this narcotic mixed drink, such as
Three Six Mafia's "
Sippin' On Some Syrup" and
Paul Wall's "
Sippin' The Barre". The common nicknames associated with codeine infused cough syrup are purple, yellow, red, barre, drank, Texas tea, purple drank, hulk, syrup, sizzerp and there continues to be more added everyday.
In the
United Kingdom,
Ireland,
Australia,
New Zealand, and
Canada tablets which combine codeine and
paracetamol (acetaminophen) are widely available, and these can be consumed at higher-than-recommended doses for recreational effect. In doing so, users run the serious risk of
hepatotoxicity associated with large doses of paracetamol. While the combination of codeine with
paracetamol at higher-than-recommended doses can possibly cause hepatotoxicity (
liver damage), combination with
ibuprofen can result in
kidney problems/failure and additional
stomach pain and
nausea, and combination with
aspirin can lead to internal
hemorrhaging, particularly
gastrointestinal hemorrhage.
Codeine is also demethylated by reaction with
pyridine to illicitly synthesize morphine. Pyridine is toxic and
carcinogenic, so morphine illicitly produced in this manner (and potentially contaminated with pyridine) may be particularly harmful.
Further Information
Get more info on 'Codeine'.
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