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Oxatomide, sold under the brand name Tinset among others, is a first-generation antihistamine of the diphenylmethylpiperazine family which is marketed in Europe, Japan, and a number of other countries. It was discovered at Janssen Pharmaceutica in 1975. Oxatomide lacks any anticholinergic effects. In addition to its H1 receptor antagonism, it also possesses antiserotonergic activity similarly to hydroxyzine. It was patented in 1976 and came into medical use in 1981.

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  • أوكساتومايد (ar)
  • Oxatomide (it)
  • Oxatomide (en)
  • Oxatomida (pt)
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  • أوكساتومايد Oxatomide هو مضاد هيستامين من الجيل الأول من صف الفينيل ببيرازين. لا يملك أي تأثيرات مضادة للكولنرجي. بالإضافة إلى أنه يعمل كمناهض لمستقبلات H1, فهو يملك فعل مضاد للسيروتونين. وهو يعد من مثبتات الخلايا البدينة. (ar)
  • Oxatomide, sold under the brand name Tinset among others, is a first-generation antihistamine of the diphenylmethylpiperazine family which is marketed in Europe, Japan, and a number of other countries. It was discovered at Janssen Pharmaceutica in 1975. Oxatomide lacks any anticholinergic effects. In addition to its H1 receptor antagonism, it also possesses antiserotonergic activity similarly to hydroxyzine. It was patented in 1976 and came into medical use in 1981. (en)
  • L'oxatomide (noto anche con la sigla R35443, durante la fase degli studi sperimentali) è un farmaco antistaminico di prima generazione appartenente alla classe della . Il farmaco possiede un'attività di tipo antiserotoninergico. L'oxatomide è un derivato piperazinico antagonista dei recettori H1 dell'istamina. Il farmaco sembra anche possedere attività stabilizzante i mastociti attraverso inibizione del rilascio intracellulare del calcio e del release di sostanze bioattive dai mastociti. Non presenta attività . (it)
  • Oxatomida, vendido sob o nome de marca Tinset entre outros, é um da família das difenilmetilpiperazinas, o qual é comercializado na Europa, Japão e uma variedade de outros países. Foi descoberta na Janssen Farmacêutica em 1975. Oxatomida carece de quaisquer efeitos anticolinérgicos. Em adição a seu antagonismo ao receptor H1, também possui atividade antiserotonérgica similarmente a hidroxizina. (pt)
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  • AE06 (en)
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