ESMYA

This brand name is authorized in Croatia, Ecuador, Estonia, Finland, Hong Kong SAR China, Ireland, Israel, Lithuania, Netherlands, Poland, Romania, Singapore, Spain, UK.

Active ingredients

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

1
UNII YF7V70N02B - ULIPRISTAL ACETATE
 

Ulipristal is an orally-active synthetic selective progesterone receptor modulator which acts via high-affinity binding to the human progesterone receptor. When used for emergency contraception the mechanism of action is inhibition or delay of ovulation via suppression of the luteinising hormone (LH) surge. Pharmacodynamic data show that even when taken immediately before ovulation is scheduled to occur (when LH has already started to rise), ulipristal acetate is able to postpone follicular rupture for at least 5 days.

 
Read more about Ulipristal

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ESMYA Tablet MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
G03XB02 G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03X Other sex hormones and modulators of the genital system → G03XB Antiprogestogens
Discover more medicines within G03XB02

Authorization and marketing

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

Country Identification scheme Identifier(s)
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 563-MEE-1214
EE Ravimiamet 1557435, 1636567, 1681062
ES Centro de información online de medicamentos de la AEMPS 12750001
FI Lääkealan turvallisuus- ja kehittämiskeskus 536013
GB Medicines & Healthcare Products Regulatory Agency 202926
HK Department of Health Drug Office 62553
IE Health Products Regulatory Authority 88109
IL מִשְׂרַד הַבְּרִיאוּת 7819
LT Valstybinė vaistų kontrolės tarnyba 1065205, 1068705, 1075188, 1075189, 1075190
NL Z-Index G-Standaard, PRK 101877
PL Rejestru Produktów Leczniczych 100274622
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W61258001
SG Health Sciences Authority 14685P

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.