THYMOGLOBULINE

This brand name is authorized in Brazil, Croatia, Ecuador, France, Ireland, Israel, Japan, Lithuania, Malta, Poland, Singapore, South Africa, Tunisia, Turkey.

Active ingredients

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

1
UNII D7RD81HE4W - LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN
 

Antithymocyte immunoglobulin is a selective immunosuppressive agent mostly acting on T lymphocytes. Antithymocyte immunoglobulin is used for the prevention and treatment of graft rejection after solid organ transplantation, usually in combination with other immunosuppressive drugs.

 
Read more about Antithymocyte immunoglobulin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 THYMOGLOBULINE Powder for solution for infusion 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
L04AA04 Antithymocyte immunoglobulin (rabbit) L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AA Selective immunosuppressants
Discover more medicines within L04AA04

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 576720070080617
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 72-MBE-1016
FR Base de données publique des médicaments 62850870
HR Agencija za lijekove i medicinske proizvode HR-H-671425021
IL מִשְׂרַד הַבְּרִיאוּת 6996
JP 医薬品医療機器総合機構 6399423F1026
LT Valstybinė vaistų kontrolės tarnyba 1015566
MT Medicines Authority MA596/00201
PL Rejestru Produktów Leczniczych 100066697
SG Health Sciences Authority 03951P
TN Direction de la Pharmacie et du Médicament 1383021H
TR İlaç ve Tıbbi Cihaz Kurumu 8699809799189
ZA Health Products Regulatory Authority W/30.2/75

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