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Wikipedia

Dihydrocodeine

Dihydrocodeine is a semi-synthetic opioid analgesic prescribed for pain or severe dyspnea, or as an antitussive, either alone or compounded with paracetamol (acetaminophen) (as in co-dydramol) or aspirin. It was developed in Germany in 1908 and first marketed in 1911.[4]

Dihydrocodeine
Clinical data
Other names6α-Hydrocodol[1]
AHFS/Drugs.comInternational Drug Names
Dependence
liability
Moderate-high
Addiction
liability
Moderate-high
Routes of
administration
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability20%[3]
Metabolism
Mainly hepatic, through CYP3A4 and CYP2D6
Elimination half-life4 hours[3]
Identifiers
  • 4,5α-epoxy-3-methoxy-17-methylmorphinan-6α-ol
CAS Number
  • 125-28-0 N
PubChem CID
  • 5284543
IUPHAR/BPS
  • 7594
DrugBank
  • DB01551 Y
ChemSpider
  • 4447600 Y
UNII
  • N9I9HDB855
KEGG
  • D07831 Y
ChEMBL
  • ChEMBL1595 N
CompTox Dashboard (EPA)
  • DTXSID5022936
ECHA InfoCard100.004.303
Chemical and physical data
FormulaC18H23NO3
Molar mass301.386 g·mol−1
3D model (JSmol)
  • Interactive image
  • O[C@@H]1[C@@H]2OC3=C(OC)C=CC4=C3[C@@]2([C@H]5CC1)CCN(C)[C@@H]5C4
  • InChI=1S/C18H23NO3/c1-19-8-7-18-11-4-5-13(20)17(18)22-16-14(21-2)6-3-10(15(16)18)9-12(11)19/h3,6,11-13,17,20H,4-5,7-9H2,1-2H3/t11-,12+,13-,17-,18-/m0/s1 Y
  • Key:RBOXVHNMENFORY-DNJOTXNNSA-N Y
 NY (what is this?)  (verify)

Commonly available as tablets, solutions, elixirs, and other oral forms, dihydrocodeine is also available in some countries as an injectable solution for deep subcutaneous and intra-muscular administration. As with codeine, intravenous administration should be avoided, as it could result in anaphylaxis and life-threatening pulmonary edema. In the past, dihydrocodeine suppositories were used. Dihydrocodeine is available in suppository form on prescription. Dihydrocodeine is used as an alternative to codeine.

It was first described in 1911 and approved for medical use in 1948.[5] Dihydrocodeine was developed during the search for more effective cough medication, especially to help reduce the spread of tuberculosis, pertussis, and pneumonia in the years from c.a. 1895 to 1915. It is similar in chemical structure to codeine. Dihydrocodeine is twice as strong as codeine.[6] Although dihydrocodeine does have extremely active metabolites, in the form of dihydromorphine and dihydromorphine-6-glucuronide (one hundred times more potent), these metabolites are produced in such small amounts that they do not have clinically significant effects.[7]

Dihydrocodeine is also the original member and chemical base of a number of similar semi-synthetic opioids such as acetyldihydrocodeine, dihydrocodeinone enol acetate, dihydroisocodeine, nicocodeine, and nicodicodeine.

Medical uses Edit

Approved indication for dihydrocodeine is the management of moderate to moderately severe pain as well as coughing and shortness of breath. As is the case with other drugs in this group, the antitussive dose tends to be less than the analgesic dose, and dihydrocodeine is a powerful cough suppressant like all other members of the immediate codeine family (see below) and their cousins hydrocodone, oxycodone and ethylmorphine, whole opium preparations, and the strong opioid hydromorphone.[8][9]

For use against pain, dihydrocodeine is usually formulated as tablets or capsules containing 15–16 mg or 30–32 mg with or without other active ingredients such as aspirin, paracetamol (acetaminophen), ibuprofen, or others.[10][11]

Controlled-release dihydrocodeine is available for both pain and coughing, as indicated below, as waxy tablets containing 60 to 120 mg of the drug. Some formulations, intended for use against coughing and the like, have other active ingredients such as antihistamines, decongestants and others.[12] Other oral formulations, such as packets of effervescent powder, sublingual drops, elixirs and the like are also available in many locations.[13]

Injectable dihydrocodeine is most often given as a deep subcutaneous injection.[14]

Side effects Edit

As with other opioids, tolerance and physical and psychological dependence develop with repeated dihydrocodeine use. All opioids can impair the mental or physical abilities required for the performance of potentially hazardous tasks such as driving or operating machinery if taken in large doses.[15][16]

Itching and flushing and other effects of blood vessel dilation are also common side-effects, due to histamine release in response to the drug using one or more types of receptors in the CNS or other responses elsewhere in the body.[17] First-generation antihistamines such as tripelennamine (Pyrabenzamine), clemastine (Tavist), hydroxyzine (Atarax), diphenhydramine (Benadryl), cyproheptadine (Periactin), brompheniramine (Dimetapp), chlorphenamine (Chlor-Trimeton), doxylamine (NyQuil) and phenyltoloxamine (Percogesic Original Formula) not only combat the histamine-driven side-effects, but are analgesic-sparing (potentiating) in various degrees.[18][19] The antihistamine promethazine (Phenergan) may also have a positive effect on hepatic metabolism of dihydrocodeine as it does with codeine. Higher doses of promethazine may interfere with most other opioids with the exception of the pethidine family (Demerol and the like) by this or other unknown mechanisms.[20]

As with all drugs, side-effects depend on the person taking the medication. They can range in severity from mild to extreme, from headaches to difficulty breathing.[21][22]

Constipation is the one side-effect of dihydrocodeine and almost all opioids which is near-universal.[23][24] It results from the slowing of peristalsis in the gut and is a reason dihydrocodeine, ethylmorphine, codeine, opium preparations, and morphine are used to stop diarrhoea and combat irritable bowel syndrome (IBS) in its diarrhoeal and cyclical forms as well as other conditions causing hypermotility or intestinal cramping.[25] Opium/opioid preparations are used often as a last resort where pain is severe and the bowels are organically loose. It is generally better to treat IBS with a non psycho-tropic opioid such as loperamide hydrochloride which stays contained in the bowel,[26] thereby not causing drowsy effects and allowing many people to work using machines etc. For IBS, hyoscine butylbromide (Buscopan in the UK) and mebeverine hydrochloride (Colofac) can be effective with or without an opium related compound.[26]

Regulation Edit

Australia
In Australia, dihydrocodeine is a 'pharmacist only' Schedule 3 drug, only when indicated for cough suppression, and compounded with one or more other therapeutically active substances not exceeding 15 mg dihydrocodeine per dose.[27] Schedule 3 drugs, while still OTC, can only be dispensed after consultation with a pharmacist. It is a Schedule 4 (prescription only) drug when compounded with one or more other therapeutically active substances and not exceeding 100 mg dihydrocodeine per dose.[27] Any Dihydrocodeine preparation not falling within Schedules 3 or 4, including single ingredient dihydrocodeine preparations, are categorised as Schedule 8 (controlled drugs), which can only be dispensed in accordance with the stricter requirements of the state or territory in which they are prescribed (and which vary between states and territories).[27][28][29]
Hong Kong
In Hong Kong, dihydrocodeine is regulated under Schedule 1 of Hong Kong's Chapter 134 Dangerous Drugs Ordinance. It can only be used legally by health professionals and for university research purposes. A pharmacist can dispense Dihydrocodeine when furnished with a doctors prescription. Anyone who supplies the substance without a prescription can be fined $10000 (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 a licence from the Department of Health, is illegal and carries a $1,000,000 (HKD) fine or 7 years imprisonment.
Japan
In Japan, dihydrocodeine is available without a prescription; used in cough medicines such as New Bron Solution-ACE. Dihydrocodeine is used as an antitussive in many products as a Dextromethorphan alternative. Medicines in Japan which contain dihydrocodeine are coupled with caffeine to offset the sedative effects and discourage recreational use. Cough medicines containing dihydrocodeine are controlled similarly to dextromethorphan in the United States, in that its sale is strictly limited by purchase quantity and is restricted to persons 20 and older for purchase.
United Kingdom
In the United Kingdom, dihydrocodeine is a Class B drug; but, it is available over-the-counter in small amounts (less than 8 mg), when combined with paracetamol (see co-dydramol). Dihydrocodeine is listed in Schedule 5 of the Misuse of Drugs Regulations 2001 whereby it is exempt from prohibition on possession provided that it is in the form of a single preparation not being designed for injection and less than 100 mg (calculated as free base) or with a total concentration less than 2.5% (calculated as free base). Illegal possession of dihydrocodeine can result in up to 5 years in prison or an unlimited fine.
United States
In the US, pure dihydrocodeine is a DEA Schedule II substance, although preparations containing small amounts of dihydrocodeine can also be classified as Schedule III or Schedule V, depending on the concentration of dihydrocodeine relative to other active constituents, such as paracetamol (acetaminophen). This scheduling is similar to the UK's. The DEA's ACSCN for dihydrocodeine free base and all salts is 9120. The 2013 annual aggregate manufacturing quota is 250 kilos.

International treaties and the controlled-substances laws of most countries, such as the German Betäubungsmittelgesetz, regulate dihydrocodeine at the same level as codeine. Dihydrocodeine-based pharmaceuticals are especially used where chronic pain patients are able to have essentially OTC access to them provided they are registered with the provincial or national government as such a patient.

Controlled-release dihydrocodeine is a non-prescription item in some places, especially the 60 mg strength. A report by the Ivo Šandor Organisation in 2004 listed Andorra, Spain, Gibraltar and Austria as having varying degrees of access to these and other dihydrocodeine, nicocodeine and codeine products.

Chemistry Edit

It is available as the following salts, in approximate descending order of frequency of use: bitartrate, phosphate, hydrochloride, tartrate, hydroiodide, methyliodide, hydrobromide, sulfate, and thiocyanate. The salt to free base conversion factors are 0.67 for the bitartrate, 0.73 for the phosphate, and 0.89 for the hydrochloride.

Dihydrocodeine is the parent drug of a series of moderately strong narcotics including, among others, hydrocodone, nicocodeine, nicodicodeine, thebaine and acetyldihydrocodeine.

Whereas converting codeine to morphine is a difficult and unrewarding task, dihydrocodeine can be converted to dihydromorphine with very high yields (over 95%). Dihydromorphine is widely used in Japan. The dihydromorphine can be quantitatively converted to hydromorphone using potassium tert butoxide.

Dihydrocodeine can be presumptively detected by the Froehde reagent.

Recreational use Edit

As dihydrocodeine can provide a euphoric high when taken in higher-than-therapeutic doses, it is quite commonly used recreationally. The typical recreational dose can be anything from 70 mg to 500 mg, or, in users with tolerance, even more. Potentiators and adjuvants are often included when dihydrocodeine is used in an unsupervised fashion, especially carisoprodol, glutethimide, hydroxyzine and first-generation antihistamines, both to intensify the effect and lessen side-effects such as itching.[30]

History Edit

Two famous users of dihydrocodeine were William S. Burroughs, who described it as "twice as strong as codeine and almost as good as heroin" and Hermann Göring, who was a known morphine addict (Hitler referred to him as the "morphinist"), consumed up to 100 tablets (3 grams) of dihydrocodeine per day and was captured by the Allies with a large quantity of the drug in a suitcase, reportedly more than 20,000 tablets[citation needed]. Another account suggest Hermann Göring was taking 20 tablets in the morning and 20 at night to ward off morphine withdrawals. Germany was experiencing a massive shortage of morphine, and as a result Göring used massive amounts of dihydrocodeine.[31] He also used morphine and oxycodone, beginning with therapeutic use of morphine after being wounded in the groin during the November 1923 Beer Hall Putsch in Munich and then used dihydrocodeine in the early 1930s for toothache.[32][33]

Society and culture Edit

Brand names Edit

Brand names for dihydrocodeine products include Drocode, Paracodeine, Parzone, Rikodeine, Trezix, Synalgos DC, Panlor DC, Panlor SS, Contugesic, New Bron Solution-ACE, Huscode, Drocode, Paracodin, Paramol (UK), Codidol, Dehace, DHC Continus, Didor Continus, Dicogesic, Codhydrine, Dekacodin, DH-Codeine, Didrate, Dihydrin, Hydrocodin, Nadeine, Novicodin, Rapacodin, Fortuss, Remedeine, Dico, Synalgos-DC (US), and DF-118.[34]

Preparations and availability Edit

 
Package of 100 Dihydrocodeine Tablets

Dihydrocodeine products which can be purchased over the counter in many European and Pacific Rim countries generally contain from 2 to 20 mg of dihydrocodeine per dosing unit combined with one or more other active ingredients such as paracetamol (acetaminophen), aspirin, ibuprofen, antihistamines, decongestants, vitamins, medicinal herb preparations, and other such ingredients. In a subset of these countries and foreign possessions, 30 mg tablets and 60 mg controlled-release tablets are available over the counter and chemists may very well be able to dispense the 90 and 120 mg strengths at their discretion.

In the United States, the most common analgesic brands with dihydrocodeine are: DHC Plus (16 and 32 mg), Panlor SS (32 mg), ZerLor (32 mg), Panlor DC (16 mg) and Synalgos DC (16 mg). These combination products also include paracetamol (acetaminophen) and caffeine. Aspirin is used in the case of Synalgos DC.

Dihydrocodeine is sometimes marketed in combination preparations with paracetamol as co-dydramol (BAN) to provide greater pain relief than either agent used singly (see Synergy § Drug synergy).

In the UK and other countries, 30 mg tablets containing only dihydrocodeine as the active ingredient are available, also a 40 mg Dihydrocodeine tablet is available in the UK as DF-118 Forte.

The original dihydrocodeine product, Paracodin, is an elixir of dihydrocodeine hydroiodide also available as a Tussionex-style suspension in many European countries.

In many European countries and elsewhere in the world, the most commonly found dihydrocodeine preparations are extended-release tablets made by encasing granules of the ingredient mixture, almost always using the bitartrate salt of dihydrocodeine, of four different sizes in a wax-based binder. The usual strengths are 60, 90, and 120 mg. Common trade names for the extended-release tablets are Didor Continus, Codidol, Codi-Contin, Dicodin (made in France and the major product containing the tartrate salt), Contugesic, DHC, and DHC Continus.

Dihydrocodeine is available in Japan as tablets which contain 2.5 mg of dihydrocodeine phosphate and caffeine, the decongestant d,l-methylephedrine HCl, and the antihistamine chlorpheniramine, and packets of granules which effervesce like Alka-Seltzer with 10 mg of dihydrocodeine with lysozyme and chlorpheniramine, marketed for OTC sale as New Bron Solution-ACE. These two formulations may have once contained phenyltoloxamine citrate as the antihistamine component.

Elsewhere in the Pacific Rim, Dicogesic in analogous to Glaxo/Smith-Kline's DF-118.

The manufacturer of New Bron Solution-ACE; SS Pharmaceutical Co., Ltd, also markets an ibuprofen with dihydrocodeine product called S.Tac EVE, which also includes d,l-methylephedrine HCl, chlorpheniramine, anhydrous caffeine, and vitamins B1 and C.

The Panlor series is manufactured by Pan-American Laboratories of Covington, Louisiana, and they also market several dihydrocodeine-based prescription cough syrups in the United States.

References Edit

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External links Edit

  • "Dihydrocodeine". Drug Information Portal. U.S. National Library of Medicine.

  Media related to Dihydrocodeine at Wikimedia Commons

dihydrocodeine, confused, with, hydrocodone, codeine, this, article, require, cleanup, meet, wikipedia, quality, standards, specific, problem, significant, portions, unreferenced, vague, incorrect, information, additionally, areas, that, cited, highly, inappro. Not to be confused with hydrocodone or codeine This article may require cleanup to meet Wikipedia s quality standards The specific problem is significant portions of unreferenced vague or incorrect information Additionally the areas that are cited are highly inappropriate citations Please help improve this article if you can August 2014 Learn how and when to remove this template message Dihydrocodeine is a semi synthetic opioid analgesic prescribed for pain or severe dyspnea or as an antitussive either alone or compounded with paracetamol acetaminophen as in co dydramol or aspirin It was developed in Germany in 1908 and first marketed in 1911 4 DihydrocodeineClinical dataOther names6a Hydrocodol 1 AHFS Drugs comInternational Drug NamesDependenceliabilityModerate highAddictionliabilityModerate highRoutes ofadministrationoralsubcutaneousintramuscularrectalpossibly sublingual buccalATC codeN02AA08 WHO Legal statusLegal statusAU S3 Pharmacist only S3 S4 S8 depending on dose and other constituents BR Class A2 Narcotic drugs 2 CA Schedule I DE Prescription only Anlage III for higher doses UK Class B US Schedule II Schedule III in drug combination Pharmacokinetic dataBioavailability20 3 MetabolismMainly hepatic through CYP3A4 and CYP2D6Elimination half life4 hours 3 IdentifiersIUPAC name 4 5a epoxy 3 methoxy 17 methylmorphinan 6a olCAS Number125 28 0 NPubChem CID5284543IUPHAR BPS7594DrugBankDB01551 YChemSpider4447600 YUNIIN9I9HDB855KEGGD07831 YChEMBLChEMBL1595 NCompTox Dashboard EPA DTXSID5022936ECHA InfoCard100 004 303Chemical and physical dataFormulaC 18H 23N O 3Molar mass301 386 g mol 13D model JSmol Interactive imageSMILES O C H 1 C H 2OC3 C OC C CC4 C3 C 2 C H 5CC1 CCN C C H 5C4InChI InChI 1S C18H23NO3 c1 19 8 7 18 11 4 5 13 20 17 18 22 16 14 21 2 6 3 10 15 16 18 9 12 11 19 h3 6 11 13 17 20H 4 5 7 9H2 1 2H3 t11 12 13 17 18 m0 s1 YKey RBOXVHNMENFORY DNJOTXNNSA N Y N Y what is this verify Commonly available as tablets solutions elixirs and other oral forms dihydrocodeine is also available in some countries as an injectable solution for deep subcutaneous and intra muscular administration As with codeine intravenous administration should be avoided as it could result in anaphylaxis and life threatening pulmonary edema In the past dihydrocodeine suppositories were used Dihydrocodeine is available in suppository form on prescription Dihydrocodeine is used as an alternative to codeine It was first described in 1911 and approved for medical use in 1948 5 Dihydrocodeine was developed during the search for more effective cough medication especially to help reduce the spread of tuberculosis pertussis and pneumonia in the years from c a 1895 to 1915 It is similar in chemical structure to codeine Dihydrocodeine is twice as strong as codeine 6 Although dihydrocodeine does have extremely active metabolites in the form of dihydromorphine and dihydromorphine 6 glucuronide one hundred times more potent these metabolites are produced in such small amounts that they do not have clinically significant effects 7 Dihydrocodeine is also the original member and chemical base of a number of similar semi synthetic opioids such as acetyldihydrocodeine dihydrocodeinone enol acetate dihydroisocodeine nicocodeine and nicodicodeine Contents 1 Medical uses 2 Side effects 3 Regulation 4 Chemistry 5 Recreational use 6 History 7 Society and culture 7 1 Brand names 7 2 Preparations and availability 8 References 9 External linksMedical uses EditApproved indication for dihydrocodeine is the management of moderate to moderately severe pain as well as coughing and shortness of breath As is the case with other drugs in this group the antitussive dose tends to be less than the analgesic dose and dihydrocodeine is a powerful cough suppressant like all other members of the immediate codeine family see below and their cousins hydrocodone oxycodone and ethylmorphine whole opium preparations and the strong opioid hydromorphone 8 9 For use against pain dihydrocodeine is usually formulated as tablets or capsules containing 15 16 mg or 30 32 mg with or without other active ingredients such as aspirin paracetamol acetaminophen ibuprofen or others 10 11 Controlled release dihydrocodeine is available for both pain and coughing as indicated below as waxy tablets containing 60 to 120 mg of the drug Some formulations intended for use against coughing and the like have other active ingredients such as antihistamines decongestants and others 12 Other oral formulations such as packets of effervescent powder sublingual drops elixirs and the like are also available in many locations 13 Injectable dihydrocodeine is most often given as a deep subcutaneous injection 14 Side effects EditAs with other opioids tolerance and physical and psychological dependence develop with repeated dihydrocodeine use All opioids can impair the mental or physical abilities required for the performance of potentially hazardous tasks such as driving or operating machinery if taken in large doses 15 16 Itching and flushing and other effects of blood vessel dilation are also common side effects due to histamine release in response to the drug using one or more types of receptors in the CNS or other responses elsewhere in the body 17 First generation antihistamines such as tripelennamine Pyrabenzamine clemastine Tavist hydroxyzine Atarax diphenhydramine Benadryl cyproheptadine Periactin brompheniramine Dimetapp chlorphenamine Chlor Trimeton doxylamine NyQuil and phenyltoloxamine Percogesic Original Formula not only combat the histamine driven side effects but are analgesic sparing potentiating in various degrees 18 19 The antihistamine promethazine Phenergan may also have a positive effect on hepatic metabolism of dihydrocodeine as it does with codeine Higher doses of promethazine may interfere with most other opioids with the exception of the pethidine family Demerol and the like by this or other unknown mechanisms 20 As with all drugs side effects depend on the person taking the medication They can range in severity from mild to extreme from headaches to difficulty breathing 21 22 Constipation is the one side effect of dihydrocodeine and almost all opioids which is near universal 23 24 It results from the slowing of peristalsis in the gut and is a reason dihydrocodeine ethylmorphine codeine opium preparations and morphine are used to stop diarrhoea and combat irritable bowel syndrome IBS in its diarrhoeal and cyclical forms as well as other conditions causing hypermotility or intestinal cramping 25 Opium opioid preparations are used often as a last resort where pain is severe and the bowels are organically loose It is generally better to treat IBS with a non psycho tropic opioid such as loperamide hydrochloride which stays contained in the bowel 26 thereby not causing drowsy effects and allowing many people to work using machines etc For IBS hyoscine butylbromide Buscopan in the UK and mebeverine hydrochloride Colofac can be effective with or without an opium related compound 26 Regulation EditAustralia In Australia dihydrocodeine is a pharmacist only Schedule 3 drug only when indicated for cough suppression and compounded with one or more other therapeutically active substances not exceeding 15 mg dihydrocodeine per dose 27 Schedule 3 drugs while still OTC can only be dispensed after consultation with a pharmacist It is a Schedule 4 prescription only drug when compounded with one or more other therapeutically active substances and not exceeding 100 mg dihydrocodeine per dose 27 Any Dihydrocodeine preparation not falling within Schedules 3 or 4 including single ingredient dihydrocodeine preparations are categorised as Schedule 8 controlled drugs which can only be dispensed in accordance with the stricter requirements of the state or territory in which they are prescribed and which vary between states and territories 27 28 29 Hong Kong In Hong Kong dihydrocodeine is regulated under Schedule 1 of Hong Kong s Chapter 134 Dangerous Drugs Ordinance It can only be used legally by health professionals and for university research purposes A pharmacist can dispense Dihydrocodeine when furnished with a doctors prescription Anyone who supplies the substance without a prescription can be fined 10000 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 a licence from the Department of Health is illegal and carries a 1 000 000 HKD fine or 7 years imprisonment Japan In Japan dihydrocodeine is available without a prescription used in cough medicines such as New Bron Solution ACE Dihydrocodeine is used as an antitussive in many products as a Dextromethorphan alternative Medicines in Japan which contain dihydrocodeine are coupled with caffeine to offset the sedative effects and discourage recreational use Cough medicines containing dihydrocodeine are controlled similarly to dextromethorphan in the United States in that its sale is strictly limited by purchase quantity and is restricted to persons 20 and older for purchase United Kingdom In the United Kingdom dihydrocodeine is a Class B drug but it is available over the counter in small amounts less than 8 mg when combined with paracetamol see co dydramol Dihydrocodeine is listed in Schedule 5 of the Misuse of Drugs Regulations 2001 whereby it is exempt from prohibition on possession provided that it is in the form of a single preparation not being designed for injection and less than 100 mg calculated as free base or with a total concentration less than 2 5 calculated as free base Illegal possession of dihydrocodeine can result in up to 5 years in prison or an unlimited fine United States In the US pure dihydrocodeine is a DEA Schedule II substance although preparations containing small amounts of dihydrocodeine can also be classified as Schedule III or Schedule V depending on the concentration of dihydrocodeine relative to other active constituents such as paracetamol acetaminophen This scheduling is similar to the UK s The DEA s ACSCN for dihydrocodeine free base and all salts is 9120 The 2013 annual aggregate manufacturing quota is 250 kilos International treaties and the controlled substances laws of most countries such as the German Betaubungsmittelgesetz regulate dihydrocodeine at the same level as codeine Dihydrocodeine based pharmaceuticals are especially used where chronic pain patients are able to have essentially OTC access to them provided they are registered with the provincial or national government as such a patient Controlled release dihydrocodeine is a non prescription item in some places especially the 60 mg strength A report by the Ivo Sandor Organisation in 2004 listed Andorra Spain Gibraltar and Austria as having varying degrees of access to these and other dihydrocodeine nicocodeine and codeine products Chemistry EditThis section does not cite any sources Please help improve this section by adding citations to reliable sources Unsourced material may be challenged and removed August 2015 Learn how and when to remove this template message It is available as the following salts in approximate descending order of frequency of use bitartrate phosphate hydrochloride tartrate hydroiodide methyliodide hydrobromide sulfate and thiocyanate The salt to free base conversion factors are 0 67 for the bitartrate 0 73 for the phosphate and 0 89 for the hydrochloride Dihydrocodeine is the parent drug of a series of moderately strong narcotics including among others hydrocodone nicocodeine nicodicodeine thebaine and acetyldihydrocodeine Whereas converting codeine to morphine is a difficult and unrewarding task dihydrocodeine can be converted to dihydromorphine with very high yields over 95 Dihydromorphine is widely used in Japan The dihydromorphine can be quantitatively converted to hydromorphone using potassium tert butoxide Dihydrocodeine can be presumptively detected by the Froehde reagent Recreational use EditAs dihydrocodeine can provide a euphoric high when taken in higher than therapeutic doses it is quite commonly used recreationally The typical recreational dose can be anything from 70 mg to 500 mg or in users with tolerance even more Potentiators and adjuvants are often included when dihydrocodeine is used in an unsupervised fashion especially carisoprodol glutethimide hydroxyzine and first generation antihistamines both to intensify the effect and lessen side effects such as itching 30 History EditTwo famous users of dihydrocodeine were William S Burroughs who described it as twice as strong as codeine and almost as good as heroin and Hermann Goring who was a known morphine addict Hitler referred to him as the morphinist consumed up to 100 tablets 3 grams of dihydrocodeine per day and was captured by the Allies with a large quantity of the drug in a suitcase reportedly more than 20 000 tablets citation needed Another account suggest Hermann Goring was taking 20 tablets in the morning and 20 at night to ward off morphine withdrawals Germany was experiencing a massive shortage of morphine and as a result Goring used massive amounts of dihydrocodeine 31 He also used morphine and oxycodone beginning with therapeutic use of morphine after being wounded in the groin during the November 1923 Beer Hall Putsch in Munich and then used dihydrocodeine in the early 1930s for toothache 32 33 Society and culture EditBrand names Edit Brand names for dihydrocodeine products include Drocode Paracodeine Parzone Rikodeine Trezix Synalgos DC Panlor DC Panlor SS Contugesic New Bron Solution ACE Huscode Drocode Paracodin Paramol UK Codidol Dehace DHC Continus Didor Continus Dicogesic Codhydrine Dekacodin DH Codeine Didrate Dihydrin Hydrocodin Nadeine Novicodin Rapacodin Fortuss Remedeine Dico Synalgos DC US and DF 118 34 Preparations and availability Edit This section does not cite any sources Please help improve this section by adding citations to reliable sources Unsourced material may be challenged and removed August 2015 Learn how and when to remove this template message nbsp Package of 100 Dihydrocodeine TabletsDihydrocodeine products which can be purchased over the counter in many European and Pacific Rim countries generally contain from 2 to 20 mg of dihydrocodeine per dosing unit combined with one or more other active ingredients such as paracetamol acetaminophen aspirin ibuprofen antihistamines decongestants vitamins medicinal herb preparations and other such ingredients In a subset of these countries and foreign possessions 30 mg tablets and 60 mg controlled release tablets are available over the counter and chemists may very well be able to dispense the 90 and 120 mg strengths at their discretion In the United States the most common analgesic brands with dihydrocodeine are DHC Plus 16 and 32 mg Panlor SS 32 mg ZerLor 32 mg Panlor DC 16 mg and Synalgos DC 16 mg These combination products also include paracetamol acetaminophen and caffeine Aspirin is used in the case of Synalgos DC Dihydrocodeine is sometimes marketed in combination preparations with paracetamol as co dydramol BAN to provide greater pain relief than either agent used singly see Synergy Drug synergy In the UK and other countries 30 mg tablets containing only dihydrocodeine as the active ingredient are available also a 40 mg Dihydrocodeine tablet is available in the UK as DF 118 Forte The original dihydrocodeine product Paracodin is an elixir of dihydrocodeine hydroiodide also available as a Tussionex style suspension in many European countries In many European countries and elsewhere in the world the most commonly found dihydrocodeine preparations are extended release tablets made by encasing granules of the ingredient mixture almost always using the bitartrate salt of dihydrocodeine of four different sizes in a wax based binder The usual strengths are 60 90 and 120 mg Common trade names for the extended release tablets are Didor Continus Codidol Codi Contin Dicodin made in France and the major product containing the tartrate salt Contugesic DHC and DHC Continus Dihydrocodeine is available in Japan as tablets which contain 2 5 mg of dihydrocodeine phosphate and caffeine the decongestant d l methylephedrine HCl and the antihistamine chlorpheniramine and packets of granules which effervesce like Alka Seltzer with 10 mg of dihydrocodeine with lysozyme and chlorpheniramine marketed for OTC sale as New Bron Solution ACE These two formulations may have once contained phenyltoloxamine citrate as the antihistamine component Elsewhere in the Pacific Rim Dicogesic in analogous to Glaxo Smith Kline s DF 118 The manufacturer of New Bron Solution ACE SS Pharmaceutical Co Ltd also markets an ibuprofen with dihydrocodeine product called S Tac EVE which also includes d l methylephedrine HCl chlorpheniramine anhydrous caffeine and vitamins B1 and C The Panlor series is manufactured by Pan American Laboratories of Covington Louisiana and they also market several dihydrocodeine based prescription cough syrups in the United States References Edit Karch SB 9 October 2007 Pharmacokinetics and Pharmacodynamics of Abused Drugs CRC Press pp 56 ISBN 978 1 4200 5460 6 Anvisa 2023 03 31 RDC Nº 784 Listas de Substancias Entorpecentes Psicotropicas Precursoras e Outras sob Controle Especial Collegiate Board Resolution No 784 Lists of Narcotic Psychotropic Precursor and Other Substances under Special Control in Brazilian Portuguese Diario Oficial da Uniao published 2023 04 04 Archived from the original on 2023 08 03 Retrieved 2023 08 03 a b Rowell FJ Seymour RA Rawlins MD 1983 Pharmacokinetics of intravenous and oral dihydrocodeine and its acid metabolites European Journal of Clinical Pharmacology 25 3 419 424 doi 10 1007 BF01037958 PMID 6628531 S2CID 29370394 Stolerman I 31 July 2010 Encyclopedia of Psychopharmacology Springer Science amp Business Media ISBN 9783540686989 Fischer J Ganellin CR 2006 Analogue based Drug Discovery John Wiley amp Sons p 52X ISBN 9783527607495 Equivalence table in French PDF Archived from the original PDF on 1 February 2013 Retrieved 12 April 2018 Schmidt H Vormfelde SV Walchner Bonjean M Klinder K Freudenthaler S Gleiter CH et al March 2003 The role of active metabolites in dihydrocodeine effects International Journal of Clinical Pharmacology and Therapeutics 41 3 95 106 doi 10 5414 cpp41095 PMID 12665158 Leppert W July 2010 Dihydrocodeine as an opioid analgesic for the treatment of moderate to severe chronic pain Current Drug Metabolism 11 6 494 506 doi 10 2174 138920010791636211 PMID 20540693 Myovant Sciences and Pfizer Receive U S FDA Approval of Myfembree a Once Daily Treatment for the Management of Moderate to Severe Pain Associated With Endometriosis Drugs com Archived from the original on 5 September 2022 Retrieved 5 September 2022 Dihydrocodeine painkiller nhs uk 25 October 2019 Retrieved 5 September 2022 Multum Cerner 12 January 2022 Acetaminophen caffeine and dihydrocodeine Uses Side Effects amp Warnings Drugs com Retrieved 5 September 2022 Cowan DA Woffendin G Noormohammadi A July 1988 Two assays for dihydrocodeine in plasma and in urine and their use to determine the bioavailability of a controlled release product Journal of Pharmaceutical Sciences 77 7 606 609 doi 10 1002 jps 2600770711 PMID 3171947 Di Girolamo G Opezzo JA Lopez MI Schere D Keller G Gonzalez CD et al October 2007 Relative bioavailability of new formulation of paracetamol effervescent powder containing sodium bicarbonate versus paracetamol tablets a comparative pharmacokinetic study in fed subjects Expert Opinion on Pharmacotherapy 8 15 2449 2457 doi 10 1517 14656566 8 15 2449 PMID 17931082 S2CID 45519503 Kim H Park H Lee SJ August 2017 Effective method for drug injection into subcutaneous tissue Scientific Reports 7 1 9613 Bibcode 2017NatSR 7 9613K doi 10 1038 s41598 017 10110 w PMC 5575294 PMID 28852051 Bailey CP Connor M February 2005 Opioids cellular mechanisms of tolerance and physical dependence Current Opinion in Pharmacology 5 1 60 68 doi 10 1016 j coph 2004 08 012 PMID 15661627 Adriaensen H Vissers K Noorduin H Meert T 2003 Opioid tolerance and dependence an inevitable consequence of chronic treatment Acta Anaesthesiologica Belgica 54 1 37 47 PMID 12703345 Ashina K Tsubosaka Y Nakamura T Omori K Kobayashi K Hori M et al 2015 Histamine Induces Vascular Hyperpermeability by Increasing Blood Flow and Endothelial Barrier Disruption In Vivo PLOS ONE 10 7 e0132367 Bibcode 2015PLoSO 1032367A doi 10 1371 journal pone 0132367 PMC 4497677 PMID 26158531 Antihistamines LiverTox Clinical and Research Information on Drug Induced Liver Injury Bethesda MD National Institute of Diabetes and Digestive and Kidney Diseases 2012 PMID 31643232 retrieved 2022 09 05 Fookes C 2019 02 05 List of Common Antihistamines Uses amp Side Effects Drugs com Retrieved 5 September 2022 Southard BT Al Khalili Y 2022 Promethazine StatPearls Treasure Island FL StatPearls Publishing PMID 31335081 Retrieved 5 September 2022 Dihydroergotamine Side Effects Common Severe Long Term Drugs com Retrieved 5 September 2022 Dihydrocodeine Drugs and Lactation Database LactMed Bethesda MD National Library of Medicine US 2006 PMID 29999751 retrieved 2022 09 05 Canty SL May 1994 Constipation as a side effect of opioids Oncology Nursing Forum 21 4 739 745 PMID 8047473 Aspirin caffeine dihydrocodeine Side Effects Common Severe Long Term Drugs com Retrieved 5 September 2022 Irritable bowel syndrome Symptoms and causes Mayo Clinic Retrieved 5 September 2022 a b Opioid Induced Hyperalgesia How Opioids Can Increase Pain Hospital for Special Surgery Retrieved 5 September 2022 a b c Scheduling delegate s final decisions June 2017 Hua AC Shen F Ge X July 2015 State based legal requirement for Schedule 8 prescriptions why so complicated The Medical Journal of Australia 203 2 64 66 doi 10 5694 mja14 01587 PMID 26175237 S2CID 37916675 Poisons Standard November 2016 Australian Government Retrieved 29 December 2016 El Hai J 2013 The Nazi and the psychiatrist Hermann Goring Dr Douglas M Kelley and a fatal meeting of minds at the end of WWII First ed PublicAffairs Hachette UK ISBN 978 1 61039 156 6 Dolibois J 16 November 2000 Pattern of Circles An Ambassador s Story Kent State University Press p 88 ISBN 978 0 87338 702 6 Ramen F January 2000 Hermann Goring Hitler s Second in command The Rosen Publishing Group ISBN 978 0 8239 3307 5 World leaders that had serious drug addictions Gaijinass 12 July 2010 Retrieved 26 July 2016 Dihydrocodeine drugs com international Retrieved 14 August 2015 External links Edit Dihydrocodeine Drug Information Portal U S National Library of Medicine nbsp Media related to Dihydrocodeine at Wikimedia Commons Portal nbsp Medicine Retrieved from https en wikipedia org w index php title Dihydrocodeine amp oldid 1168565820, wikipedia, wiki, book, books, library,

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