Antiemetic
(Redirected from Anti-nausea)
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An antiemetic is a drug that is effective against vomiting and nausea. Antiemetics are typically used to treat motion sickness and the side effects of opioid analgesics, general anaesthetics, and chemotherapy directed against cancer. They may be used for severe cases of gastroenteritis, especially if the patient is dehydrated.[1][2]
Some antiemetics previously thought to cause birth defects appear safe for use by pregnant women in the treatment of morning sickness and the more serious hyperemesis gravidarum.[3][4]
Types
[edit]- 5-HT3 receptor antagonists block serotonin receptors in the central nervous system and gastrointestinal tract. As such, they can be used to treat post-operative and cytotoxic drug nausea & vomiting. However, they can also cause constipation or diarrhea, dry mouth, and fatigue.
- Dolasetron (Anzemet) can be administered in tablet form or in an injection.
- Granisetron (Kytril, Sancuso) can be administered in tablet (Kytril), oral solution (Kytril), injection (Kytril), or in a single transdermal patch to the upper arm (SANCUSO).
- Ondansetron (Zofran) is administered in an oral tablet form, orally dissolving tablet form, orally dissolving film, sublingual, or in an IV/IM injection.
- Tropisetron (Setrovel, Navoban) can be administered in oral capsules or in injection form.
- Palonosetron (Aloxi) can be administered in an injection or in oral capsules.
- Dopamine antagonists act on the brainstem and are used to treat nausea and vomiting associated with cancer, radiation sickness, opioids, cytotoxic drugs and general anaesthetics. Side effects include muscle spasms and restlessness.
- Amisulpride (Barhemsys), administered by intravenous injection.
- Domperidone (Motilium)
- Droperidol
- Olanzapine (Zyprexa)
- Haloperidol (limited in usefulness by extra-pyramidal and sedative side-effects)
- Alizapride
- Prochlorperazine (Compazine, Stemzine, Buccastem, Stemetil, Phenotil)
- Chlorpromazine (Use limited by sedating properties)
- Metoclopramide
- NK1 receptor antagonist
- Aprepitant (Emend) is a commercially available NK1 receptor antagonist
- Casopitant is an investigational NK1 receptor antagonist
- Rolapitant (Varubi) another recently approved drug from this class
- Antihistamines (H1 histamine receptor antagonists) are effective in many conditions, including motion sickness, morning sickness in pregnancy, and to combat opioid nausea. H1 receptors in central areas include area postrema and vomiting center in the vestibular nucleus. Also, many of the antihistamines listed here also block muscarinic acetylcholine receptors.
- Cinnarizine (UK only)
- Cyclizine
- Diphenhydramine (Benadryl)
- Dimenhydrinate (Gravol, Dramamine)
- Doxylamine (Bonjesta, Unisom)
- Mirtazapine (Remeron) is an antidepressant that also has antiemetic effects.[5][6] It is a potent histamine H1 receptor antagonist, Ki=1.6 nM,[7] and also exhibits notable 5-HT3 antagonism.[6]
- Meclizine (Bonine, Antivert)
- Promethazine (Pentazine, Phenergan, Promacot) can be administered via a rectal suppository, intravenous injection, oral tablet or oral suspension for adults and children over 2 years of age.
- Hydroxyzine (Vistaril)
- Cannabinoids are used in patients with cachexia, cytotoxic nausea, and vomiting, or who are unresponsive to other agents. These may cause changes in perception, dizziness, and loss of coordination.
- Cannabis, also known as medical marijuana in the United States, is a Schedule I drug.[8][9]
- Nabilone
- Dronabinol (Marinol/Syndros) is a Schedule II drug in the U.S. when in an oral solution (Syndros),[10] and Schedule III when in sesame oil and encapsulated in a soft gelatin capsule (Marinol).[11]
- Some synthetic cannabinoids such as Nabilone (Cesamet) or the JWH series.
- Sativex is an oral spray containing THC and CBD.[12] It is currently legal in Canada and a few countries in Europe and the US as of June 25, 2018[update] [13][14]
- Benzodiazepines (GABA receptor positive allosteric modulators)
- Midazolam (Versed) is given at the onset of anesthesia and has been shown in recent trials to be as effective as ondansetron, but most effective when used in combination with ondansetron.[15]
- Lorazepam (Ativan) is said to be very good as an adjunct treatment for nausea along with first line medications such as Compazine. [citation needed]
- Anticholinergics
- Hyoscine (also known as scopolamine)
- Atropine
- Steroids
- Dexamethasone (Decadron) is given in low dose at the onset of a general anesthetic as an effective antiemetic. It is also used in chemotherapy as a single drug as well as with other antiemetics such as 5-HT3 receptor antagonists and NK1 receptor antagonist, but the specific mechanism of action is not fully understood.[16]
- Other
- Trimethobenzamide is thought to work on the CTZ
- Ginger contains 5-HT3 antagonists gingerols, shogaols,[17] and galanolactone.[18] Preliminary clinical data suggests ginger may be effective for treatment of nausea and/or vomiting in a number of settings.[19][20][21]
- Emetrol is also claimed to be an effective antiemetic.
- Propofol is given intravenously. It has been used in an acute care setting in hospital as a rescue therapy for emesis.[22]
- Muscimol is purported to have antiemetic activity.[23]
- Ajwain is purported to be antiemetic. It is a popular spice in India, Ethiopia and Eritrea.[citation needed]
See also
[edit]- Cancer and nausea
- Emetic – substances that induce nausea and vomiting
References
[edit]- ^ Manteuffel, Jacob (2009). "Use of antiemetics in children with acute gastroenteritis: Are they safe and effective?". Journal of Emergencies, Trauma, and Shock. 2 (1): 3–5. doi:10.4103/0974-2700.44674. ISSN 0974-2700. PMC 2700583. PMID 19561947.
- ^ Fedorowicz, Zbys; Jagannath, Vanitha A; Carter, Ben (2011-09-07). "Antiemetics for reducing vomiting related to acute gastroenteritis in children and adolescents". The Cochrane Database of Systematic Reviews. 2011 (9): CD005506. doi:10.1002/14651858.CD005506.pub5. ISSN 1469-493X. PMC 6768985. PMID 21901699.
- ^ Quinlan, Jeffrey D.; Hill, D. Ashley (1 June 2003). "Nausea and Vomiting in Pregnancy - American Family Physician". American Family Physician. 68 (1): 121–128. Retrieved 2015-10-09.
- ^ Schaefer, Christof; Scialli, Anthony; Rost van Tonningen, Margreet (2001). "Antiemetics and hyperemesis gravidarum". Drugs During Pregnancy and Lactation: Handbook of Prescription Drugs and Comparative Risk Assessment. Gulf Professional Publishing. ISBN 978-0-444-50763-1.
- ^ Pae C-U (2006). "Low-dose mirtazapine may be successful treatment option for severe nausea and vomiting". Progress in Neuro-Psychopharmacology and Biological Psychiatry. 30 (6): 1143–5. doi:10.1016/j.pnpbp.2006.03.015. PMID 16632163. S2CID 31784303.
- ^ a b Kast RE, Foley KF (July 2007). "Cancer chemotherapy and cachexia: mirtazapine and olanzapine are 5-HT3 antagonists with good antinausea effects". European Journal of Cancer Care. 16 (4): 351–4. doi:10.1111/j.1365-2354.2006.00760.x. PMID 17587360.
- ^ National Institute of Mental Health. PDSD Ki Database (Internet) [cited 2013 Sep 27]. Chapel Hill (NC): University of North Carolina. 1998-2013. Available from: "PDSP Database - UNC". Archived from the original on 2013-11-08. Retrieved 2013-12-01.
- ^ Vincent, Beverly J.; McQuiston, Debra J.; Einhorn, Lawrence H.; Nagy, Catherine M.; Brames, Mary J. (1983-05-01). "Review of Cannabinoids and their Antiemetic Effectiveness". Drugs. 25 (1): 52–62. doi:10.2165/00003495-198300251-00006. ISSN 1179-1950. PMID 6301800. S2CID 22426920.
- ^ "Drug Scheduling". www.dea.gov. Retrieved 2019-02-21.
- ^ "2017 - Final Rule: Placement of FDA-Approved Products of Oral Solutions Containing Dronabinol [(-)-delta-9-trans-tetrahydrocannabinol (delta-9-THC)] in Schedule II". www.deadiversion.usdoj.gov. Archived from the original on 2018-03-28. Retrieved 2019-02-21.
- ^ "Schedules of Controlled Substances: Rescheduling of the Food and Drug Administration Approved Product Containing Synthetic Dronabinol [(-)-greek-DSUP9/SUP -(trans)-Tetrahydrocannabinol] in Sesame Oil and Encapsulated in Soft Gelatin Capsules From Schedule II to Schedule III". Federal Register. 1999-08-04. Retrieved 2024-06-28.
- ^ Sastre-Garriga, Jaume; Vila, Carlos; Clissold, Stephen; Montalban, Xavier (2011-05-11). "THC and CBD oromucosal spray (Sativex ® ) in the management of spasticity associated with multiple sclerosis". Expert Review of Neurotherapeutics. 11 (5): 627–637. doi:10.1586/ern.11.47. ISSN 1473-7175. PMID 21456949.
- ^ Wadsworth, E; Hammond, D (2019-03-04). "International differences in patterns of cannabis use among youth: Prevalence, perceptions of harm, and driving under the influence in Canada, England & United States". Addictive Behaviors. 90: 171–175. doi:10.1016/j.addbeh.2018.10.050. ISSN 0306-4603. PMC 6324962. PMID 30412908.
- ^ Rahman, Lu (2021-02-03). "Medical cannabis and regulatory framework in Europe". Drug Discovery World (DDW). Retrieved 2024-08-18.
- ^ Honarmand, Azim; Safavi, Mohammadreza; Chegeni, Mansoureh; Hirmanpour, Anahita; Nazem, Masoud; Sarizdi, Seyyad Hamid (January 2016). "Prophylactic antiemetic effects of Midazolam, Ondansetron, and their combination after middle ear surgery". Journal of Research in Pharmacy Practice. 5 (1): 16–21. doi:10.4103/2279-042X.176556. ISSN 2319-9644. PMC 4776542. PMID 26985431.
- ^ Grunberg, S. M. (1 February 2007). "Antiemetic activity of corticosteroids in patients receiving cancer chemotherapy: dosing, efficacy, and tolerability analysis". Annals of Oncology. 18 (2): 233–240. doi:10.1093/annonc/mdl347. ISSN 0923-7534. PMID 17108149.
- ^ Abdel-Aziz H, Windeck T, Ploch M, Verspohl EJ (2006-01-13), "Mode of action of gingerols and shogaols on 5-HT3 receptors: binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum", Eur J Pharmacol, 530 (1–2): 136–43, doi:10.1016/j.ejphar.2005.10.049, PMID 16364290
- ^ Huang, Q.; Iwamoto, Y.; Aoki, S.; Tanaka, N.; Tajima, K.; Yamahara, J.; Takaishi, Y.; Yoshida, M.; Tomimatsu, T.; Tamai, Y. (1991). "Anti-5-hydroxytryptamine3 effect of galanolactone, diterpenoid isolated from ginger". Chemical & Pharmaceutical Bulletin. 39 (2): 397–399. doi:10.1248/cpb.39.397. PMID 2054863.
- ^ Marx, WM; Teleni L; McCarthy AL; Vitetta L; McKavanagh D; Thomson D; Isenring E. (2013). "Ginger (Zingiber officinale) and chemotherapy-induced nausea and vomiting: a systematic literature review" (PDF). Nutr Rev. 71 (4): 245–54. doi:10.1111/nure.12016. PMID 23550785. S2CID 19187673. Archived from the original (PDF) on 2020-05-07. Retrieved 2019-12-16.
- ^ Ernst, E.; Pittler, M. H. (March 2000). "Efficacy of ginger for nausea and vomiting: a systematic review of randomized clinical trials". British Journal of Anaesthesia. 84 (3): 367–371. doi:10.1093/oxfordjournals.bja.a013442. ISSN 0007-0912. PMID 10793599.
- ^ O'Connor, Anahad (August 21, 2007). "The Claim: Eating Ginger Can Cure Motion Sickness". The New York Times.
- ^ Kampo, Sylvanus; Afful, Alfred Parker; Mohammed, Shiraj; Ntim, Michael; Buunaaim, Alexis D. B.; Anabah, Thomas Winsum (2019-09-14). "Sub-hypnotic dose of propofol as antiemetic prophylaxis attenuates intrathecal morphine-induced postoperative nausea and vomiting, and pruritus in parturient undergoing cesarean section — a randomized control trial". BMC Anesthesiology. 19 (1): 177. doi:10.1186/s12871-019-0847-y. ISSN 1471-2253. PMC 6745062. PMID 31521119.
- ^ Gov, Us. "MUSCIMOL - CAMEO Chemicals". NOAA. Retrieved 2021-03-09.
Major chemical drug groups – based upon the Anatomical Therapeutic Chemical Classification System | |
|---|---|
| gastrointestinal tract / metabolism (A) | |
| blood and blood forming organs (B) | |
| cardiovascular system (C) | |
| skin (D) | |
| genitourinary system (G) | |
| endocrine system (H) | |
| infections and infestations (J, P, QI) | |
| malignant disease (L01–L02) | |
| immune disease (L03–L04) | |
| muscles, bones, and joints (M) | |
| brain and nervous system (N) |
|
| respiratory system (R) | |
| sensory organs (S) | |
| other ATC (V) | |
