Chemistry:Diphenoxylate
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| Other names | R-1132, NIH-756 |
| AHFS/Drugs.com | Monograph |
| Routes of administration | Oral |
| Drug class | Opioid Antidiarrheal |
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| Pharmacokinetic data | |
| Protein binding | 74–95% |
| Elimination half-life | 12–14 hours |
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| Chemical and physical data | |
| Formula | C30H32N2O2 |
| Molar mass | 452.598 g·mol−1 |
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Diphenoxylate is a centrally active opioid drug of the phenylpiperidine series that is used as a combination drug with atropine for the treatment of diarrhea. Diphenoxylate is an opioid and acts by slowing intestinal contractions; the atropine is present to prevent drug abuse and overdose. It should not be given to children due to the risk that they will stop breathing and should not be used in people with Clostridium difficile infection.
Medical use
Diphenoxylate is used to treat diarrhea in adults; it is only available as a combination drug with a subtherapeutic dose of atropine to prevent abuse.[1]
It should not be used in children due to the risk of respiratory depression.[1] It does not appear harmful to a fetus but the risks have not been fully explored.[1]
It should not be taken with other central depressants like alcohol, as they can increase its risks.[1]
It should not be used for people with diarrhea caused by an infection, for example with Clostridium difficile infection, since the slowing of peristalsis can prevent clearing of the infectious organism.[1]
Adverse effects
The drug label (in some jurisdictions) has warnings with regard to the risk of respiratory depression, anticholinergic toxicity and opioid overdose, the risk of dehydration and electrolyte imbalance that people with severe diarrhea always run, and toxic megacolon in people with ulcerative colitis.[1]
Other adverse effects include numbness in the hands and feet, euphoria, depression, lethargy, confusion, drowsiness, dizziness, restlessness, headache, hallucinations, edema, hives, swollen gums, itchiness, vomiting, nausea, loss of appetite, and stomach pain.[1]
Pharmacology
Diphenoxylate is rapidly metabolized to difenoxin; it is eliminated mostly in feces but also in urine.[1]
Like other opioids, diphenoxylate acts by slowing intestinal contractions, allowing the body to consolidate intestinal contents and prolong transit time, thus allowing the intestines to draw moisture out of them at a normal or higher rate and therefore stop the formation of loose and liquid stools; the atropine is an anticholinergic and is present to prevent drug abuse and overdose.[2]
History and chemistry
Diphenoxylate was first synthesized by Paul Janssen at Janssen Pharmaceutica in 1956 as part of a medicinal chemistry investigation of opioids.[3]
Diphenoxylate is made by combining a precursor of normethadone with norpethidine. Loperamide (Imodium) and bezitramide are analogs. [4] Like loperamide, it has a methadone-like structure and a piperidine moiety.[5]
Society and culture
Pricing
In 2017 Hikma Pharmaceuticals raised the price of its liquid formulation of generic diphenoxylate-atropine in the US by 430%, from $16 to $84.00.[6]
Regulation
In the United States, drugs containing diphenoxylate combined with atropine salts are classified as Schedule V controlled substances.[7][1] (Diphenoxlate by itself is a Schedule II controlled substance.)
It is on Schedule III of the Single Convention on Narcotic Drugs, only in forms that contain, according to the Yellow List: "not more than 2.5 milligrams of diphenoxylate calculated as base and a quantity of atropine sulfate equivalent to at least 1 per cent of the dose of diphenoxylate".[8]
Research
Diphenoxylate and atropine have been studied in small trials as a treatment for fecal incontinence; it appears to be less efficacious and have more adverse effects when compared with loperamide or codeine.[9]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 "US label: Diphenoxylate hydrochloride and atropine sulfate tablets". FDA. 12 February 2018. https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/012462s048lbl.pdf. For label updates see FDA index page for NDA 012462
- ↑ "Management of acute cancer treatment-induced diarrhea". Seminars in Oncology Nursing 19 (4 Suppl 3): 11–6. November 2003. doi:10.1053/j.soncn.2003.09.009. PMID 14702928.
- ↑ Florey, Klaus (1991). Profiles of Drug Substances, Excipients and Related Methodology, Volume 19. Academic Press. p. 342. ISBN 9780080861142. https://books.google.com/books?id=5ndDXC2L5Q8C&pg=PA342.
- ↑ (in en) Opioid Analgesics: Chemistry and Receptors. Springer Science & Business Media. 2013. p. 312. ISBN 9781489905857. https://books.google.com/books?id=vwAHCAAAQBAJ&pg=PA312.
- ↑ Patrick, Graham L. (2013) (in en). An Introduction to Medicinal Chemistry. OUP Oxford. p. 644. ISBN 9780199697397. https://books.google.com/books?id=Pj7xJRuhZxUC&pg=PA644.
- ↑ Crow, David (20 August 2017). "Hikma hikes price of US medicines by up to 430%". Financial Times. https://www.ft.com/content/05ae5a46-8457-11e7-94e2-c5b903247afd.
- ↑ "Diphenoxylate" (in en). MedlinePlus. 15 April 2018. https://medlineplus.gov/druginfo/meds/a601045.html.
- ↑ "Yellow List: List of Narcotic Drugs Under International Control, 50th Edition". International Narcotics Control Board. 2011. p. 8. http://www.incb.org/documents/Narcotic-Drugs/Yellow_List/NAR_2011_YellowList_50edition_EN.pdf.
- ↑ "Drug treatment for faecal incontinence in adults". The Cochrane Database of Systematic Reviews 2013 (6): CD002116. June 2013. doi:10.1002/14651858.CD002116.pub2. PMID 23757096.
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