Chemistry:Domperidone

From HandWiki
Short description: Peripheral D2 receptor antagonist
Domperidone
Domperidone 2D structure.svg
Domperidone-from-xtal-3D-bs-17.png
Clinical data
Trade namesMotilium, many others
Other namesR-33812; R33812; KW-5338; KW5338; NSC-299589; NSC299589
AHFS/Drugs.comMicromedex Detailed Consumer Information
Pregnancy
category
  • AU: B2
  • US: N (Not classified yet)
Routes of
administration		By mouth (tablet), rectal (suppository)[1]
Drug classD2 receptor antagonist; Prolactin releaser
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only)
  • CA: ℞-only
  • UK: POM (Prescription only)
  • US: Not Approved
Pharmacokinetic data
Protein binding~92%[1]
MetabolismHepatic (CYP3A4/5) and intestinal (first-pass)[1][2]
MetabolitesAll inactive[1][2]
Onset of action30–60 minutes[3]
Elimination half-life7–9 hours[4][1][5]
ExcretionFeces: 66%[1]
Urine: 32%[1]
Breast milk: small quantities[1]
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC22H24ClN5O2
Molar mass425.92 g·mol−1
3D model (JSmol)
Melting point242.5 °C (468.5 °F)
  (verify)

Domperidone, sold under the brand name Motilium among others, is a dopamine antagonist medication which is used to treat nausea and vomiting and certain gastrointestinal problems like gastroparesis (delayed gastric emptying). It raises the level of prolactin in the human body and is used to induce and promote breast milk production.[1][6] It may be taken by mouth or rectally.[1][7][8]

Side effects of domperidone include headache, dry mouth, abdominal cramps, diarrhea, and elevated prolactin levels.[1][6][9] Secondary to increased prolactin levels, breast changes, milk outflow, menstrual irregularities, and hypogonadism can occur.[1][6][9] Domperidone may also cause QT prolongation and has rarely been associated with serious cardiac complications such as sudden cardiac death.[10][11][12][13] However, the risks are small and occur more with high doses.[13][14] Domperidone acts as a peripherally selective antagonist of the dopamine D2 and D3 receptors.[1][6] Due to its low entry into the brain, the side effects of domperidone are different from those of other dopamine receptor antagonists like metoclopramide and it produces little in the way of central nervous system adverse effects.[1][6] However, domperidone can nonetheless increase prolactin levels as the pituitary gland is outside of the blood–brain barrier.[15]

Domperidone was discovered in 1974 and was introduced for medical use in 1979.[16][17][18] It was developed by Janssen Pharmaceutica.[16][17] Domperidone is available over-the-counter in many countries, for instance in Europe and elsewhere throughout the world.[19][1] It is not approved for use in the United States .[20][21][1] However, it is available in the United States for people with severe and treatment-refractory gastrointestinal motility problems under an expanded access individual-patient investigational new drug application.[22] An analogue of domperidone called deudomperidone is also currently under development for potential use in the United States and other countries.[23][24][25]


Medical uses

Nausea and vomiting

There is some evidence that domperidone has antiemetic activity.[1] It is recommended by the Canadian Headache Society for treatment of nausea associated with acute migraine.[26]

Gastroparesis

Gastroparesis is a medical condition characterised by delayed emptying of the stomach when there is no mechanical gastric outlet obstruction. Its cause is most commonly idiopathic, a diabetic complication or a result of abdominal surgery. The condition causes nausea, vomiting, fullness after eating, early satiety (feeling full before the meal is finished), abdominal pain and bloating. Domperidone can be used to increase the transit of food through the stomach by increasing gastrointestinal peristalsis and hence to treat gastroparesis.[1][6] It may be useful in idiopathic and diabetic gastroparesis.[27][28] However, increased rate of gastric emptying induced by drugs like domperidone does not always correlate well with relief of symptoms.[29]

Lactation

The hormone prolactin stimulates lactation. Dopamine, released by the hypothalamus, stops the release of prolactin from the pituitary gland. Domperidone, by acting as an anti-dopaminergic agent, results in increased prolactin secretion, and thus promotes lactation as a galactogogue. Domperidone moderately increases the volume of expressed breast milk in mothers of preterm babies where breast milk expression is inadequate, and appears to be safe for short-term use for this purpose.[30][31][32] In the United States, domperidone is not approved for this use.[21][33]

A study called the EMPOWER trial was designed to assess the effectiveness and safety of domperidone in assisting mothers of preterm babies to supply breast milk for their infants.[34] The study randomized 90 mothers of preterm babies to receive either domperidone 10 mg orally three times daily for 28 days (Group A) or placebo 10 mg orally three times daily for 14 days followed by domperidone 10 mg orally three times daily for 14 days (Group B). Mean milk volumes at the beginning of the intervention were similar between the 2 groups. After the first 14 days, 78% of mothers receiving domperidone (Group A) achieved a 50% increase in milk volume, while 58% of mothers receiving placebo (Group B) achieved a 50% increase in milk volume.[35]

To induce lactation, domperidone is used at a dosage of 10 to 20 mg 3 or 4 times per day by mouth.[9] Effects may be seen within 24 hours or may not be seen for 3 or 4 days.[9] The maximum effect occurs after 2 or 3 weeks of treatment, and the treatment period generally lasts for 3 to 8 weeks.[9] A 2012 review shows that no studies support prophylactic use of galactagogue medications, including domperidone, at any stage of pregnancy,.[36]

Other uses

Parkinson's disease

Parkinson's disease is a degenerative neurological condition where a decrease in dopamine in the brain leads to rigidity (stiffness of movement), tremor and other symptoms and signs. Poor gastrointestinal function, nausea and vomiting is a major problem for people with Parkinson's disease because most medications used to treat Parkinson's disease are given by mouth. These medications, such as levodopa, can cause nausea as a side effect. Furthermore, anti-nausea drugs, such as metoclopramide, which do cross the blood–brain barrier, may worsen the extrapyramidal symptoms of Parkinson's disease. Domperidone can be used to relieve nausea and gastrointestinal symptoms in Parkinson's disease; it blocks peripheral D2 receptors but minimally crosses the blood–brain barrier in normal doses, so has no effect on the extrapyramidal symptoms of the disease.[37][38][39]

Other gastrointestinal uses

Domperidone may be used in functional dyspepsia in both adults and children.[40][41] It has also been found effective in the treatment of reflux in children.[42] However some specialists consider its risks prohibitory of the treatment of infantile reflux.[43]

Available forms

Domperidone is available for use by oral administration in the form of tablets, orally disintegrating tablets, and suspension, and by rectal administration in the form of suppositories.[7][8] The oral tablets are available in the strength of 10 mg.[1] Domperidone has been studied for use by intramuscular injection and an intravenous formulation was previously available, but the medication is now only available in forms for oral and rectal administration.[1]

Contraindications

Domperidone is contraindicated with QT-prolonging drugs like amiodarone.[44]

Side effects

Side effects associated with domperidone include dry mouth, abdominal cramps, diarrhea, nausea, rash, itching, hives, and hyperprolactinemia (the symptoms of which may include breast enlargement, galactorrhea, breast pain/tenderness, gynecomastia, hypogonadism, and menstrual irregularities).[9]

Due to blockade of D2 receptors in the central nervous system, D2 receptor antagonists like metoclopramide and antipsychotics can also produce a variety of additional side effects including drowsiness, akathisia, restlessness, insomnia, lassitude, fatigue, extrapyramidal symptoms, dystonia, Parkinsonian symptoms, tardive dyskinesia, and depression.[1][6] However, this is not the case with domperidone, because, unlike other D2 receptor antagonists, it minimally crosses the blood–brain barrier, and for this reason, is rarely associated with such side effects.[1][6] However, domperidone theoretically might be able to produce some blockade of central D2 receptors at higher doses, in turn producing side effects similar to those of centrally permeable D2 receptor antagonists like antipsychotics.[45]

Elevated prolactin levels

Due to D2 receptor blockade, domperidone causes hyperprolactinemia.[46] Hyperprolactinemia can suppress the secretion of gonadotropin-releasing hormone (GnRH) from the hypothalamus, in turn suppressing the secretion of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) and resulting in hypogonadism and low levels of the sex hormones estradiol and testosterone.[47] Accordingly, 10 to 15% of females have been reported to experience mammoplasia (breast enlargement), mastodynia (breast pain/tenderness), galactorrhea (inappropriate or excessive milk production/secretion), and amenorrhea (cessation of menstrual cycles) with domperidone therapy.[46] Males may experience low libido, erectile dysfunction, and impaired spermatogenesis, as well as galactorrhea and gynecomastia.[47][48] D2 receptor antagonists like antipsychotics and domperidone may also increase the risk of prolactinomas, but more research is needed to confirm this.[49][50][51]

Rare reactions

Cardiac complications

Domperidone use is associated with an increased risk of sudden cardiac death (by 70%)[10] most likely through its prolonging effect of the cardiac QT interval and ventricular arrhythmias.[52][53] The cause is thought to be blockade of hERG voltage-gated potassium channels.[11][12] The risks are dose-dependent, and appear to be greatest with high/very high doses via intravenous administration and in the elderly, as well as with drugs that interact with domperidone and increase its circulating concentrations (namely CYP3A4 inhibitors).[14][13] Conflicting reports exist, however.[54] In neonates and infants, QT prolongation is controversial and uncertain.[55][56]

UK drug regulatory authorities (MHRA) have issued the following restriction on domperidone in 2014 due to increased risk of adverse cardiac effects:[57]

Domperidone (Motilium) is associated with a small increased risk of serious cardiac side effects. Its use is now restricted to the relief of nausea and vomiting and the dosage and duration of use have been reduced. It should no longer be used for the treatment of bloating and heartburn. Domperidone is now contraindicated in those with underlying cardiac conditions and other risk factors. Patients with these conditions and patients receiving long-term treatment with domperidone should be reassessed at a routine appointment, in light of the new advice.

However, a 2015 Australian review concluded the following:[13]

Based on the results of the two TQT (the regulatory agency gold standard for assessment of QT prolongation) domperidone does not appear to be strongly associated with QT prolongation at oral doses of 20 mg QID in healthy volunteers. Further, there are limited case reports supporting an association with cardiac dysfunction, and the frequently cited case-control studies have significant flaws. While there remains an ill-defined risk at higher systemic concentrations, especially in patients with a higher baseline risk of QT prolongation, our review does not support the view that domperidone presents intolerable risk.

Possible central toxicity in infants

In United Kingdom a legal case involved the death of two children of a mother whose three children had all had hypernatraemia. She was charged with poisoning the children with salt. One of the children, who was born at 28 weeks gestation with respiratory complications and had a fundoplication for gastroesophageal reflux and failure to thrive was prescribed domperidone. An advocate for the mother suggested the child may have had neuroleptic malignant syndrome as a side effect of domperidone due to the drug crossing the child's immature blood–brain barrier.[58]

Interactions

In healthy volunteers, the CYP3A4 inhibitor ketoconazole increased the Cmax and AUC concentrations of domperidone by 3- to 10-fold.[59] This was accompanied by a QT interval prolongation of about 10–20 milliseconds when domperidone 10 mg four times daily and ketoconazole 200 mg twice daily were administered, whereas domperidone by itself at the dosage assessed produced no such effect.[59] As such, domperidone with ketoconazole or other CYP3A4 inhibitors is a potentially dangerous combination.[59]

Pharmacology

Pharmacodynamics

Domperidone is a peripherally selective dopamine D2 and D3 receptor antagonist.[6] It has no clinically significant interaction with the D1 receptor, unlike metoclopramide.[6] The medication provides relief from nausea by blocking D2 receptors in the chemoreceptor trigger zone and from gastrointestinal symptoms by blocking D2 receptors in the gut.[15][1] It blocks D2 receptors in the lactotrophs of the anterior pituitary gland increasing release of prolactin which in turn increases lactation.[15][60][61] Domperidone may be more useful in some patients and cause harm in others by way of the genetics of the person, such as polymorphisms in the drug transporter gene ABCB1 (which encodes P-glycoprotein), the voltage-gated potassium channel KCNH2 gene (hERG/Kv11.1), and the α1D-adrenergic receptor ADRA1D gene.[62]

Effects on prolactin levels

A single 20 mg oral dose of domperidone has been found to increase mean serum prolactin levels (measured 90 minutes post-administration) in non-lactating women from 8.1 ng/mL to 110.9 ng/mL (a 13.7-fold increase).[6][63][64][65] This was similar to the increase in prolactin levels produced by a single 20 mg oral dose of metoclopramide (7.4 ng/mL to 124.1 ng/mL; 16.7-fold increase).[64][65] After two weeks of repeated administration (30 mg/day in both cases), the increase in prolactin levels produced by domperidone was reduced (53.2 ng/mL; 6.6-fold above baseline), but the increase in prolactin levels produced by metoclopramide, conversely, was heightened (179.6 ng/mL; 24.3-fold above baseline).[6][65] This indicates that acute and continuous administration of both domperidone and metoclopramide is effective in increasing prolactin levels, but that there are different effects on the secretion of prolactin with repeated use.[64][65] The mechanism of the difference is unknown.[65] The increase in prolactin levels observed with the two drugs was much greater in women than in men.[64][65] This appears to be due to the higher estrogen levels in women, as estrogen stimulates prolactin secretion from the pituitary gland.[66]

For comparison, normal prolactin levels in women are less than 20 ng/mL, prolactin levels peak at 100 to 300 ng/mL at parturition in pregnant women, and in lactating women, prolactin levels have been found to be 90 ng/mL at 10 days postpartum and 44 ng/mL at 180 days postpartum.[67][68]

Pharmacokinetics

Absorption

The absolute bioavailability of domperidone is low (13–17% or approximately 15%).[4][1] This is due to extensive first-pass metabolism in the intestines and liver.[4] Conversely, its bioavailability is high via intramuscular injection (90%).[1] The onset of action of domperidone taken orally is about 30 to 60 minutes.[3][1] Peak levels of domperidone following an oral dose occur after about 60 minutes.[4] Domperidone exposure increases proportionally with doses in the 10 to 20 mg dose range.[4] There is a 2- to 3-fold accumulation in levels of domperidone with frequent repeated oral administration of domperidone (four times per day (every 5 hours) for 4 days).[4] The oral bioavailability of domperidone is somewhat increased, and time to peak slightly increased when it is taken with food and bioavailability is decreased by prior concomitant administration of cimetidine and sodium bicarbonate.[4]

Distribution

The plasma protein binding of domperidone is 91 to 93%.[4] The tissue distribution of domperidone based on animal studies is wide, but concentrations are low in the brain.[4] The drug is a substrate for the P-glycoprotein (ABCB1) transporter, and animal studies suggest that this is the reason for the low central nervous system penetration of domperidone.[69] Small amounts of domperidone cross the placenta in animals.[4]

Metabolism

Domperidone is extensively metabolized in the liver and intestines with oral administration.[4][2][70] This occurs via hydroxylation and N-dealkylation.[4] Domperidone is almost exclusively metabolized by CYP3A4/5, though minor contributions by CYP1A2, CYP2D6, and CYP2C8 have been reported.[70][2] CYP3A4 is the major enzyme involved in the N-dealkylation of domperidone, while CYP3A4, CYP1A2, and CYP2E1 are involved in its aromatic hydroxylation.[4] All of the metabolites of domperidone are inactive as D2 receptor ligands.[1][2] Overall and peak levels of domperidone are increased by about 2.9- and 1.5-fold in moderate hepatic impairment, respectively.[4]

Elimination

Domperidone is eliminated 31% in urine and 66% in feces.[4] The proportion of domperidone excreted unchanged is small (10% in feces and 1% in urine).[4] The elimination half-life of domperidone is about 7 to 9 hours in healthy individuals.[4][1] However, the elimination half-life of domperidone can be prolonged to 20 hours in people with several renal dysfunction.[4][1]

Chemistry

Domperidone is a derivative of benzimidazolinone. It is structurally related to butyrophenone neuroleptics like haloperidol.[71][72]

History

Domperidone was synthesized at Janssen Pharmaceutica in 1974 following their research on antipsychotic drugs.[17][16] Janssen pharmacologists discovered that some of antipsychotic drugs had a significant effect on dopamine receptors in the central chemoreceptor trigger zone that regulated vomiting, and started searching for a dopamine antagonist that would not pass the blood–brain barrier, thereby being free of the extrapyramidal side effects that were associated with drugs of this type.[17] This led to the discovery of domperidone as a strong antiemetic with minimal central effects.[17][73] Domperidone was patented in the United States in 1978, with the patent filed in 1976.[citation needed] In 1979, domperidone was first marketed, under the brand name Motilium, in Switzerland and West Germany.[18] Domperidone was subsequently introduced in the forms of orally disintegrating tablets (based on Zydis technology) in 1999.[74] Janssen Pharmaceutical has brought domperidone before the United States Federal Drug Administration (FDA) several times, including in the 1990s, but it has not been approved.

In April 2014, the Co-ordination Group for Mutual Recognition and Decentralised Procedures – Human (CMDh) published official press-release suggesting to restrict the use of domperidone-containing medicines. It also approved earlier published suggestions by Pharmacovigilance Risk Assessment Committee (PRAC) to use domperidone only for treating nausea and vomiting and reduce maximum daily dosage to 10 mg.[7]

Society and culture

Generic names

Domperidone is the generic name of the drug and its INN, USAN, BAN, and JAN.[75][76][77]

Regulatory approval

It was reported in 2007 that domperidone is available in 58 countries, including Canada ,[1] but the uses or indications of domperidone vary between nations. In Italy it is used in the treatment of gastroesophageal reflux disease and in Canada, the drug is indicated in upper gastrointestinal motility disorders and to prevent gastrointestinal symptoms associated with the use of dopamine agonist antiparkinsonian agents.[78] In the United Kingdom , domperidone is only indicated for the treatment of nausea and vomiting and the treatment duration is usually limited to 1 week.

In the United States, domperidone is not currently a legally marketed human drug and it is not approved for sale in the United States. On 7 June 2004, FDA issued a public warning that distributing any domperidone-containing products is illegal.[20]

It is available over-the-counter to treat gastroesophageal reflux and functional dyspepsia in many countries, such as Ireland, the Netherlands, Italy, South Africa , Mexico, India , Chile , and China .[19]

Domperidone is not generally approved for use in the United States. There is an exception for use in people with treatment-refractory gastrointestinal symptoms under an FDA Investigational New Drug application.[1]

Formulations

Research

Domperidone has been studied as a potential hormonal contraceptive to prevent pregnancy in women.[82]

References

  1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 1.17 1.18 1.19 1.20 1.21 1.22 1.23 1.24 1.25 1.26 1.27 1.28 1.29 1.30 "Domperidone: review of pharmacology and clinical applications in gastroenterology". The American Journal of Gastroenterology 102 (9): 2036–2045. September 2007. doi:10.1111/j.1572-0241.2007.01255.x. PMID 17488253. 
  2. ↑ 2.0 2.1 2.2 2.3 2.4 "Identification of the cytochrome P450 enzymes involved in the metabolism of domperidone". Xenobiotica; the Fate of Foreign Compounds in Biological Systems 34 (11–12): 1013–1023. 2008. doi:10.1080/00498250400015301. PMID 15801545. 
  3. ↑ 3.0 3.1 "Domperidone: Anti-sickness medicine used to treat nausea and vomiting". 7 January 2020. https://www.nhs.uk/medicines/domperidone/. 
  4. ↑ 4.00 4.01 4.02 4.03 4.04 4.05 4.06 4.07 4.08 4.09 4.10 4.11 4.12 4.13 4.14 4.15 4.16 4.17 "Domperidone 10mg Tablets - Summary of Product Characteristics (SMPC) - (Emc)". https://www.medicines.org.uk/emc/product/556/smpc. 
  5. ↑ Cite error: Invalid <ref> tag; no text was provided for refs named Rose2004
  6. ↑ 6.00 6.01 6.02 6.03 6.04 6.05 6.06 6.07 6.08 6.09 6.10 6.11 "Domperidone: a peripherally acting dopamine2-receptor antagonist". The Annals of Pharmacotherapy 33 (4): 429–440. April 1999. doi:10.1345/aph.18003. PMID 10332535. 
  7. ↑ 7.0 7.1 7.2 "CMDh confirms recommendations on restricting use of domperidone-containing medicines: European Commission to take final legal decision". European Medicines Agency. 2014-04-25. http://www.ema.europa.eu/ema/index.jsp?curl=pages/news_and_events/news/2014/04/news_detail_002083.jsp. 
  8. ↑ 8.0 8.1 "MOTILIUM INSTANTS PL 13249/0028". Medicines and Healthcare products Regulatory Agency. 2010-02-23. http://www.mhra.gov.uk/home/groups/par/documents/websiteresources/con076114.pdf. 
  9. ↑ 9.0 9.1 9.2 9.3 9.4 9.5 "Domperidone. Discovering new choices for lactating mothers". AWHONN Lifelines 7 (1): 54–60. 2003. doi:10.1177/1091592303251726. PMID 12674062. 
  10. ↑ 10.0 10.1 "Domperidone and Risk of Ventricular Arrhythmia and Cardiac Death: A Systematic Review and Meta-analysis". Clinical Drug Investigation 36 (2): 97–107. February 2016. doi:10.1007/s40261-015-0360-0. PMID 26649742. 
  11. ↑ 11.0 11.1 "Domperidone and long QT syndrome". Current Drug Safety 5 (3): 257–262. July 2010. doi:10.2174/157488610791698334. PMID 20394569. 
  12. ↑ 12.0 12.1 "Cardiac safety concerns for domperidone, an antiemetic and prokinetic, and galactogogue medicine". Expert Opinion on Drug Safety 13 (1): 131–138. January 2014. doi:10.1517/14740338.2014.851193. PMID 24147629. https://eprints.qut.edu.au/65613/2/65613.pdf. 
  13. ↑ 13.0 13.1 13.2 13.3 "Domperidone safety: a mini-review of the science of QT prolongation and clinical implications of recent global regulatory recommendations". The New Zealand Medical Journal 128 (1416): 66–74. June 2015. PMID 26117678. 
  14. ↑ 14.0 14.1 "[Cardiac adverse effects of domperidone in adult patients: a systematic review]". Revista Médica de Chile 143 (1): 14–21. January 2015. doi:10.4067/S0034-98872015000100002. PMID 25860264. 
  15. ↑ 15.0 15.1 15.2 "Use of domperidone as a galactagogue drug: a systematic review of the benefit-risk ratio". Journal of Human Lactation 31 (1): 57–63. February 2015. doi:10.1177/0890334414561265. PMID 25475074. 
  16. ↑ 16.0 16.1 16.2 "Dose-effect study of domperidone as a galactagogue in preterm mothers with insufficient milk supply, and its transfer into milk". British Journal of Clinical Pharmacology 66 (2): 283–289. August 2008. doi:10.1111/j.1365-2125.2008.03207.x. PMID 18507654. 
  17. ↑ 17.0 17.1 17.2 17.3 17.4 "Plant Product Analogues and Compounds Derived from Them". Drug discovery : a history. Chichester: John Wiley & Sons Ltd. 2005. p. 125. ISBN 978-0-471-89979-2. 
  18. ↑ 18.0 18.1 "Domperidone". Pharmaceutical Manufacturing Encyclopedia, 3rd Edition (Vol. 1-4). William Andrew Publishing. 2013. p. 138. ISBN 9780815518563. https://books.google.com/books?id=_J2ti4EkYpkC&pg=PA1381. Retrieved 2014-12-12. 
  19. ↑ 19.0 19.1 "A case of sudden cardiac death following Domperidone self-medication". Forensic Science International 254: e1–e3. September 2015. doi:10.1016/j.forsciint.2015.06.004. PMID 26119456. 
  20. ↑ 20.0 20.1 "How to Obtain". Food and Drug Administration. 10 February 2015. https://www.fda.gov/drugs/developmentapprovalprocess/howdrugsaredevelopedandapproved/approvalapplications/investigationalnewdrugindapplication/ucm368736.htm. 
  21. ↑ 21.0 21.1 "Domperidone for lactating women". CMAJ 171 (7): 725–726. September 2004. doi:10.1503/cmaj.1041054. PMID 15451832. 
  22. ↑ "How to Request Domperidone for Expanded Access Use". FDA. 2 February 2021. https://www.fda.gov/drugs/investigational-new-drug-ind-application/how-request-domperidone-expanded-access-use. 
  23. ↑ "Deudomperidone - CinRx Pharma - AdisInsight". https://adisinsight.springer.com/drugs/800050807. 
  24. ↑ "Nausea and Vomiting in 2021: A Comprehensive Update". Journal of Clinical Gastroenterology 55 (4): 279–299. April 2021. doi:10.1097/MCG.0000000000001485. PMID 33471485. 
  25. ↑ "Antiemetic therapy for gastroparesis". Gastroparesis. Elsevier. 2021. pp. 341–359. doi:10.1016/B978-0-12-818586-5.00025-9. ISBN 9780128185865. 
  26. ↑ "Canadian Headache Society Guideline: acute drug therapy for migraine headache". The Canadian Journal of Neurological Sciences. Le Journal Canadien des Sciences Neurologiques 40 (5 Suppl 3): S1–S80. September 2013. doi:10.1017/S0317167100118943. PMID 23968886. 
  27. ↑ "Pathophysiology and pharmacotherapy of gastroparesis: current and future perspectives". Expert Opinion on Pharmacotherapy 14 (9): 1171–1186. June 2013. doi:10.1517/14656566.2013.795948. PMID 23663133. 
  28. ↑ "Domperidone in the management of symptoms of diabetic gastroparesis: efficacy, tolerability, and quality-of-life outcomes in a multicenter controlled trial. DOM-USA-5 Study Group". Clinical Therapeutics 20 (3): 438–453. 1998. doi:10.1016/S0149-2918(98)80054-4. PMID 9663360. 
  29. ↑ "The relation between symptom improvement and gastric emptying in the treatment of diabetic and idiopathic gastroparesis". The American Journal of Gastroenterology 108 (9): 1382–1391. September 2013. doi:10.1038/ajg.2013.118. PMID 24005344. 
  30. ↑ "Domperidone for increasing breast milk volume in mothers expressing breast milk for their preterm infants: a systematic review and meta-analysis". BJOG 125 (11): 1371–1378. October 2018. doi:10.1111/1471-0528.15177. PMID 29469929. 
  31. ↑ "Audit of domperidone use as a galactogogue at an Australian tertiary teaching hospital". Journal of Human Lactation 29 (1): 32–37. February 2013. doi:10.1177/0890334412459804. PMID 23015150. 
  32. ↑ "Medications for increasing milk supply in mothers expressing breastmilk for their preterm hospitalised infants". The Cochrane Database of Systematic Reviews 3 (3): CD005544. March 2012. doi:10.1002/14651858.CD005544.pub2. PMID 22419310. 
  33. ↑ "FDA warns against women using unapproved drug, domperidone to increase milk production." U.S. Food and Drug Administration 7 June 2004.
  34. ↑ "Enhancing breast milk production with Domperidone in mothers of preterm neonates (EMPOWER trial)". BMC Pregnancy and Childbirth 12: 87. August 2012. doi:10.1186/1471-2393-12-87. PMID 22935052. 
  35. ↑ "Enhancing Human Milk Production With Domperidone in Mothers of Preterm Infants". Journal of Human Lactation 33 (1): 181–187. February 2017. doi:10.1177/0890334416680176. PMID 28107101. 
  36. ↑ "Medications for increasing milk supply in mothers expressing breastmilk for their preterm hospitalised infants". The Cochrane Database of Systematic Reviews (3): CD005544. March 2012. doi:10.1002/14651858.cd005544.pub2. PMID 22419310. 
  37. ↑ "Parkinson's Disease and Current Treatments for Its Gastrointestinal Neurogastromotility Effects". Current Treatment Options in Gastroenterology 16 (4): 489–510. December 2018. doi:10.1007/s11938-018-0201-3. PMID 30361854. 
  38. ↑ "Antidopaminergic therapy for managing comorbidities in patients with Parkinson's disease". American Journal of Health-System Pharmacy 65 (5): 414–419. March 2008. doi:10.2146/ajhp060624. PMID 18281732. 
  39. ↑ "Gastrointestinal motility problems in patients with Parkinson's disease. Effects of antiparkinsonian treatment and guidelines for management". Drugs & Aging 10 (4): 249–258. April 1997. doi:10.2165/00002512-199710040-00002. PMID 9108986. 
  40. ↑ "Influence of hippophae rhamnoides on two appetite factors, gastric emptying and metabolic parameters, in children with functional dyspepsia". Hellenic Journal of Nuclear Medicine 16 (1): 38–43. 2013. PMID 23529392. https://www.nuclmed.gr/wp/wp-content/uploads/2017/03/42-4.pdf. 
  41. ↑ "Itopride therapy for functional dyspepsia: a meta-analysis". World Journal of Gastroenterology 18 (48): 7371–7377. December 2012. doi:10.3748/wjg.v18.i48.7371. PMID 23326147. 
  42. ↑ "7.2 Gastrointestinal Drugs". Illustrated Medical Pharmacology. JP Medical Ltd. 2013. p. 677. ISBN 978-9350906552. https://books.google.com/books?id=Le28AQAAQBAJ&pg=PA677. Retrieved 2014-10-31.  (Google Books)
  43. ↑ "Fear that reflux treatment for babies will be denied under new Nice guidance". The Daily Telegraph. 2014-08-01. https://www.telegraph.co.uk/health/healthnews/11005559/Fear-that-reflux-treatment-for-babies-will-be-denied-under-new-Nice-guidance.html. 
  44. ↑ 44.0 44.1 Swannick G. (ed.) "MIMS Australia." December 2013
  45. ↑ "Domperidone as an unintended antipsychotic". Canadian Pharmacists Journal 147 (2): 76–77. March 2014. doi:10.1177/1715163514521969. PMID 24660005. 
  46. ↑ 46.0 46.1 Joslin's Diabetes Mellitus: Edited by C. Ronald Kahn ... [et Al.]. Lippincott Williams & Wilkins. 2005. pp. 1084–. ISBN 978-0-7817-2796-9. https://books.google.com/books?id=ohgjG0qAvfgC&pg=PA1084. 
  47. ↑ 47.0 47.1 Male Infertility: Problems and Solutions. Springer Science & Business Media. 20 October 2010. pp. 83–. ISBN 978-1-60761-193-6. https://books.google.com/books?id=YthJpK5clTMC&pg=PA83. 
  48. ↑ Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk. Lippincott Williams & Wilkins. 28 March 2012. pp. 442–. ISBN 978-1-4511-5359-0. https://books.google.com/books?id=ScPvM03B3lUC&pg=PA442. 
  49. ↑ "Antipsychotics and hyperprolactinaemia: mechanisms, consequences and management". Clinical Endocrinology 74 (2): 141–147. February 2011. doi:10.1111/j.1365-2265.2010.03814.x. PMID 20455888. 
  50. ↑ "A review of hyperprolactinaemia and severe mental illness: are there implications for clinical biochemistry?". Annals of Clinical Biochemistry 47 (Pt 4): 292–300. July 2010. doi:10.1258/acb.2010.010025. PMID 20592331. 
  51. ↑ "Antipsychotics and pituitary tumors: an analysis of the European pharmacovigilance database (EudraVigilance)". International Clinical Psychopharmacology 34 (2): 89–92. March 2019. doi:10.1097/YIC.0000000000000247. PMID 30531551. 
  52. ↑ "Domperidone and ventricular arrhythmia or sudden cardiac death: a population-based case-control study in the Netherlands". Drug Safety 33 (11): 1003–1014. November 2010. doi:10.2165/11536840-000000000-00000. PMID 20925438. 
  53. ↑ "Risk of serious ventricular arrhythmia and sudden cardiac death in a cohort of users of domperidone: a nested case-control study". Pharmacoepidemiology and Drug Safety 19 (9): 881–888. September 2010. doi:10.1002/pds.2016. PMID 20652862. 
  54. ↑ "Cardiovascular safety profile and clinical experience with high-dose domperidone therapy for nausea and vomiting". The American Journal of the Medical Sciences 349 (5): 421–424. May 2015. doi:10.1097/MAJ.0000000000000439. PMID 25828198. 
  55. ↑ "Effect of domperidone on QT interval in neonates". The Journal of Pediatrics 153 (5): 663–666. November 2008. doi:10.1016/j.jpeds.2008.05.013. PMID 18589449. 
  56. ↑ "Effect of domperidone on the QTc interval in premature infants". Journal of Perinatology 30 (1): 50–53. January 2010. doi:10.1038/jp.2009.96. PMID 19626027. 
  57. ↑ "Domperidone: Risks of cardiac side effects". http://www.mhra.gov.uk/Safetyinformation/DrugSafetyUpdate/CON418518. 
  58. ↑ "Distinguishing between salt poisoning and hypernatraemic dehydration in children". BMJ 326 (7381): 157–160. January 2003. doi:10.1136/bmj.326.7381.157. PMID 12531853. 
  59. ↑ 59.0 59.1 59.2 Meyler's Side Effects of Antimicrobial Drugs. Elsevier. 27 November 2009. pp. 2244–. ISBN 978-0-08-093293-4. https://books.google.com/books?id=Zu2s5QBqiEkC&pg=PT2244. 
  60. ↑ Saeb-Parsy K. "Instant pharmacology." John Wiley & Sons, 1999 ISBN:0471976393, 9780471976394 p216.
  61. ↑ "Effects of domperidone on gastric emptying: a crossover study using a continuous real-time 13C breath test (BreathID system)". Hepato-Gastroenterology 58 (106): 637–641. 2011. PMID 21661445. 
  62. ↑ "Domperidone treatment for gastroparesis: demographic and pharmacogenetic characterization of clinical efficacy and side-effects". Digestive Diseases and Sciences 56 (1): 115–124. January 2011. doi:10.1007/s10620-010-1472-2. PMID 21063774. 
  63. ↑ "Galactogogues: medications that induce lactation". Journal of Human Lactation 18 (3): 274–279. August 2002. doi:10.1177/089033440201800311. PMID 12192964. 
  64. ↑ 64.0 64.1 64.2 64.3 "Domperidone: secretion in breast milk and effect on puerperal prolactin levels". British Journal of Obstetrics and Gynaecology 92 (2): 141–144. February 1985. doi:10.1111/j.1471-0528.1985.tb01065.x. PMID 3882143. 
  65. ↑ 65.0 65.1 65.2 65.3 65.4 65.5 "Plasma prolactin levels after acute and subchronic oral administration of domperidone and of metoclopramide: a cross-over study in healthy volunteers". Clinical Endocrinology 12 (5): 435–440. May 1980. doi:10.1111/j.1365-2265.1980.tb02733.x. PMID 7428183. 
  66. ↑ "Effects of domperidone on serum prolactin levels in human beings". Endocrinologia Japonica 27 (4): 521–525. August 1980. doi:10.1507/endocrj1954.27.521. PMID 7460861. 
  67. ↑ Breastfeeding and Human Lactation. Jones & Bartlett Learning. January 2005. pp. 76–. ISBN 978-0-7637-4585-1. https://books.google.com/books?id=aiVesab_2bwC&pg=PA76. 
  68. ↑ Principles and Practice of Endocrinology and Metabolism. Lippincott Williams & Wilkins. 2001. pp. 147–. ISBN 978-0-7817-1750-2. https://books.google.com/books?id=FVfzRvaucq8C&pg=PA147. 
  69. ↑ Applied Pharmacology. Elsevier Health Sciences. 2011. pp. 184–. ISBN 978-1-4377-0310-8. https://books.google.com/books?id=nYPy70d1E50C&pg=PA184. 
  70. ↑ 70.0 70.1 "Drug-drug interactions in pharmacologic management of gastroparesis". Neurogastroenterology and Motility 27 (11): 1528–1541. November 2015. doi:10.1111/nmo.12614. PMID 26059917. 
  71. ↑ Hospital Formulary. HFM Publishing Corporation. 1991. p. 171. https://books.google.com/books?id=3oVMAQAAIAAJ. "Domperidone, a benzimidazole derivative, is structurally related to the butyrophenone tranquilizers (eg, haloperidol (Haldol, Halperon])." 
  72. ↑ Receptors as Supramolecular Entities: Proceedings of the Biannual Capo Boi Conference, Cagliari, Italy, 7-10 June 1981. Elsevier Science. 22 October 2013. pp. 3–. ISBN 978-1-4831-5550-0. https://books.google.com/books?id=8VAJAwAAQBAJ&pg=PA3. 
  73. ↑ "Apomorphine: from experimental tool to therapeutic aid". The Triumph of Psychopharacology and the Story of CINP. CINP. 2010. p. 54. ISBN 978-9634081814. http://cinp.org/fileadmin/documents/history/books/VOL2_opt.pdf. 
  74. ↑ "The Zydis Oral Fast-Dissolving Dosage Form". Modified-Release Drug Delivery Technology. CRC Press. 2002. p. 200. ISBN 9780824708696. https://books.google.com/books?id=mw9W82MLYZ8C&pg=PA200. Retrieved 2014-10-31. 
  75. ↑ The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. 14 November 2014. pp. 466–. ISBN 978-1-4757-2085-3. https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA466. 
  76. ↑ Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 366–. ISBN 978-3-88763-075-1. https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA366. 
  77. ↑ "Domperidone". https://www.drugs.com/international/domperidone.html. 
  78. ↑ "Domperidone - heart rate and rhythm disorders." Canadian adverse reactions newsletter. Government of Canada. January 2007 17(1)
  79. ↑ "Motilium nog enkel op voorschrift". standaard.be. 2013-05-07. https://www.standaard.be/cnt/dmf20130507_00571810. 
  80. ↑ "ipcalabs.com". ipcalabs.com. http://www.ipcalabs.com/. 
  81. ↑ "torrentpharma.com". torrentpharma.com. http://www.torrentpharma.com/. 
  82. ↑ "Effect of domperidone-induced hyperprolactinaemia on the menstrual cycle; a placebo-controlled study". Journal of Obstetrics and Gynaecology 5 (4): 263–264. 1985. doi:10.3109/01443618509067772. ISSN 0144-3615. 

External links



Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Domperidone&oldid=3329302"