DEXDOR

This brand name is authorized in Austria, Cyprus, Estonia, Spain, Finland, France, Croatia, Ireland, Lithuania, Netherlands, Poland, United Kingdom

Active ingredients

The drug DEXDOR contains one active pharmaceutical ingredient (API):

1 Dexmedetomidine
UNII 1018WH7F9I - DEXMEDETOMIDINE HYDROCHLORIDE

Dexmedetomidine is a selective alpha-2 receptor agonist with a broad range of pharmacological properties. It has a sympatholytic effect through decrease of the release of noradrenaline in sympathetic nerve endings. The sedative effects are mediated through decreased firing of locus coeruleus, the predominant noradrenergic nucleus, situated in the brainstem.

Read about Dexmedetomidine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
DEXDOR Concentrate for solution for infusion European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
N05CM18 Dexmedetomidine N Nervous system → N05 Psycholeptics → N05C Hypnotics and sedatives → N05CM Other hypnotics and sedatives
Discover more medicines within N05CM18

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1540336, 1540347, 1540358, 1540369
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 11718002, 11718006
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 390699, 470397
Country: FR Base de données publique des médicaments Identifier(s): 64634939
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 195381, 195385, 195388
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1062981, 1062982, 1062984, 1062986, 1072972
Country: NL Z-Index G-Standaard Identifier(s): 15742199, 15742210, 15742229
Country: NL Z-Index G-Standaard, PRK Identifier(s): 99791, 99805, 99813
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100254789

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