FIBROVEIN

This brand name is authorized in Estonia, France, Hong Kong SAR China, Malta, New Zealand, Poland, Romania, UK.

Active ingredients

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

1
UNII Q1SUG5KBD6 - SODIUM TETRADECYL SULFATE
 

Sodium tetradecyl sulfate is a sclerosing agent. Intravenous injection causes intima inflammation and thrombus formation. This usually occludes the injected vein. Subsequent formation of fibrous tissue results in partial or complete vein obliteration that may or may not be permanent.

 
Read more about Sodium tetradecyl sulfate

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 FIBROVEIN Solution for injection 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
C05BB04 Sodium tetradecyl sulfate C Cardiovascular system → C05 Vasoprotectives → C05B Antivaricose therapy → C05BB Sclerosing agents for local injection
Discover more medicines within C05BB04

Authorization and marketing

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

Country Identification scheme Identifier(s)
EE Ravimiamet 1820236
FR Base de données publique des médicaments 60021771, 62685543, 68264234, 69320675
GB Medicines & Healthcare Products Regulatory Agency 227981, 227983, 227985, 227987, 227989
HK Department of Health Drug Office 62315, 62316, 62317, 62318
MT Medicines Authority AA565/09403, AA770/16401, AA770/16402
NZ Medicines and Medical Devices Safety Authority 1253, 1254, 1255, 1256
PL Rejestru Produktów Leczniczych 100375464, 100375470, 100375487, 100375493
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W67003001, W67003002, W67003003, W67004001, W67005001, W67006001, W67006002, W67006003, W67006004

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