"Thiethylperazine"

Thiethylperazine An official website of the United States government Here's how you know Log inAccess keysNCBI HomepageMyNCBI HomepageMain ContentMain NavigationBookshelfSearch databaseBooksAll DatabasesAssemblyBiocollectionsBioProjectBioSampleBooksClinVarConserved DomainsdbGaPdbVarGeneGenomeGEO DataSetsGEO ProfilesGTRHomoloGeneIdentical Protein GroupsMedGenMeSHNLM Levels and EffectsSummary of Use during LactationBased on minimal excretion of other phenothiazine derivatives, it appears that occasional short-term use of thiethylperazine for the treatment of nausea and vomiting poses little risk to the breastfed infant.Drug LevelsMaternal Levels. Relevant published information was not found as of the revision date.Infant Levels. Relevant published information

and thiethylperazine in patients undergoing cancer chemotherapy. N Z Med J 91(662):449–451CAS Google Scholar Ahmedzai S, Carlyle DL, Calder IT, Moran F (1983) Anti-emetic efficacy and toxicity of nabilone, a synthetic cannabinoid, in lung cancer chemotherapy. Br J Cancer 48(5):657–663. https://doi.org/10.1038/bjc.1983.247Article CAS Google Scholar Niiranen A, Mattson K (1985) A cross-over comparison of nabilone

or Metoclopramide or metopimazine or nabilone or netupitant or norchlorpromazine or Olanzapine or Ondansetron or Palonosetron or pancopride or Prochlorperazine or Promazine or promethazine or ramosetron or renzapride or ricasetron or rolapitant or Scopolamine or sulpiride or telmapitant or tetrahydrocannabinol or Thiethylperazine or transmer or Trifluoperazine or Triflupromazine or trimethobenzamide

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(LactMed) - GlossaryLactMed Selected ReferencesDrugs and Lactation Database (LactMed) - About Dietary SupplementsBreastfeeding LinksRelated informationPubChem SubstancePubMedSimilar articles in PubMedReview Thiethylperazine.[Drugs and Lactation Database (...]Review Trifluoperazine.[Drugs and Lactation Database (...]Review Perphenazine.[Drugs and Lactation Database (...]Review Chlorpromazine.[Drugs

, 12, 22] * * Terbinafine [2, 3, 7, 12, 22, 37] AntihistaminesAntihistamines include the following: * * Brompheniramine [3, 7, 19] * * Cinnarizine + thiethylperazine [3, 7, 19] AntihypertensivesAntihypertensives include the following: * * Clonidine [2, 10, 12] * * Methyldopa [2, 10, 12] * * Olmesartan [38] * * Reserpine [2] ACE inhibitors include the following [39

, 12, 22] * * Terbinafine [2, 3, 7, 12, 22, 37] AntihistaminesAntihistamines include the following: * * Brompheniramine [3, 7, 19] * * Cinnarizine + thiethylperazine [3, 7, 19] AntihypertensivesAntihypertensives include the following: * * Clonidine [2, 10, 12] * * Methyldopa [2, 10, 12] * * Olmesartan [38] * * Reserpine [2] ACE inhibitors include the following [39

Anaphylactic reaction and unrelated, subsequent, known side effects during therapy with thiethylperazine. We report the first case presenting with successive anaphylactic reaction and extra-pyramidal syndrome after treatment with thiethylperazine maleate (thiethylperazine). Both reactions were caused due to this anti-emetic drug, but an additive effect of clemastine fumarate, prescribed to treat

Randomized crossover comparison of high-dose intravenous metoclopramide versus a five-drug antiemetic regimen. In a randomized open crossover study, the antiemetic efficacy of a five-drug antiemetic regimen consisting of metoclopramide, dexamethasone, diazepam, diphenhydramine, and thiethylperazine was compared to that of high-dose metoclopramide. Thirteen patients treated with cisplatin

in which the antiemetic activity of thiethylperazine (6.5 mg p.o. every 8 h X 5 days) was compared with that of the combination of thiethylperazine (same dosage) plus amitriptyline (25 mg p.o. every 8 h X 5 days). This combination was designed to obtain a simultaneous blockade of the dopamine D-2, histamine H-1, and muscarinic cholinergic receptors of the central structures responsible for emesis (chemoreceptor trigger zone and vomiting center). The combination significantly decreased both the number of emetic episodes (P less than 0.05) and the duration of emesis (P less than 0.01) compared with thiethylperazine alone. The combination was also preferred by a significantly higher number of the patients (P less than 0.001) who were exposed to both the types of antiemetic treatment under trial