OPTRUMA

This brand name is authorized in Austria, Estonia, Spain, France, Croatia, Ireland, Italy, Lithuania, Poland, Romania, Tunisia

Active ingredients

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

1 Raloxifene
UNII 4F86W47BR6 - RALOXIFENE HYDROCHLORIDE

As a selective oestrogen receptor modulator (SERM), raloxifene has selective agonist or antagonist activities on tissues responsive to oestrogen. It acts as an agonist on bone and partially on cholesterol metabolism (decrease in total and LDL-cholesterol), but not in the hypothalamus or in the uterine or breast tissues.

Read about Raloxifene

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
OPTRUMA Film-coated tablet 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
G03XC01 Raloxifene 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 → G03XC Selective estrogen receptor modulators
Discover more medicines within G03XC01

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): 1197761, 1197772, 1197783, 1197794
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 98074002
Country: FR Base de données publique des médicaments Identifier(s): 69445593
Country: IT Agenzia del Farmaco Identifier(s): 034154017, 034154029
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1030349, 1030350, 1030351, 1030352
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100125603
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W51630001, W51630002, W51630003, W51630004
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 4323012

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