Diphenoxylate

Diphenoxylate is a centrally active opioid drug of the phenylpiperidine series that is used in 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.

Diphenoxylate
Clinical data
Other namesR-1132, NIH-756
AHFS/Drugs.comMonograph
Routes of
administration
Oral
ATC code
Legal status
Legal status
  • AU: S8 (Controlled)
  • CA: Schedule I
  • DE: Prescription only (Anlage II for higher doses) if combined with atropine sulphate
  • UK: Class A
  • US: Schedule II (alone) and V (with atropine)
Pharmacokinetic data
Protein binding74-95%
Elimination half-life12–14 hours
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.011.837
Chemical and physical data
FormulaC30H32N2O2
Molar mass452.587 g/mol g·mol−1
3D model (JSmol)
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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 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 piperdine 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 are classified as a Schedule V controlled substance.[7][1]

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. "US label: Diphenoxylate hydrochloride and atropine sulfate tablets" (PDF). FDA. 12 February 2018. For label updates see FDA index page for NDA 012462
  2. Stern, J; Ippoliti, C (November 2003). "Management of acute cancer treatment-induced diarrhea". Seminars in Oncology Nursing. 19 (4 Suppl 3): 11–6. doi:10.1053/j.soncn.2003.09.009. PMID 14702928.
  3. Florey, Klaus (1991). Profiles of Drug Substances, Excipients and Related Methodology, Volume 19. Academic Press. p. 342. ISBN 9780080861142.
  4. Casy, A. F.; Parfitt, R. T. (2013). Opioid Analgesics: Chemistry and Receptors. Springer Science & Business Media. p. 312. ISBN 9781489905857.
  5. Patrick, Graham L. (2013). An Introduction to Medicinal Chemistry. OUP Oxford. p. 644. ISBN 9780199697397.
  6. Crow, David (20 August 2017). "Hikma hikes price of US medicines by up to 430%". Financial Times.
  7. "Diphenoxylate". MedlinePlus. 15 April 2018. Retrieved 10 May 2018.
  8. "Yellow List: List of Narcotic Drugs Under International Control, 50th Edition" (PDF). International Narcotics Control Board. 2011. p. 8. Retrieved 10 May 2018.
  9. Omar, MI; Alexander, CE (11 June 2013). "Drug treatment for faecal incontinence in adults". The Cochrane Database of Systematic Reviews (6): CD002116. doi:10.1002/14651858.CD002116.pub2. PMID 23757096.

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