ATC Group: B01AE07 Dabigatran etexilate

The World Health Organization's ATC classification organizes medical drugs based on therapeutic properties, chemical composition, and anatomy. It helps make essential medicines readily available globally and is widely used in the pharmaceutical industry.

Position of B01AE07 in the ATC hierarchy

Level Code Title
1 B Blood and blood forming organs
2 B01 Antithrombotic agents
3 B01A Antithrombotic agents
4 B01AE Direct thrombin inhibitors
5 B01AE07 Dabigatran etexilate

Defined daily dose

The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. The DDD is a unit of measurement and does not necessarily reflect the recommended or Prescribed Daily Dose. Therapeutic doses for individual patients and patient groups will often differ from the DDD as they will be based on individual characteristics (such as age, weight, ethnic differences, type and severity of disease) and pharmacokinetic considerations.

Route Amount
ORAL - Oral 0.3 g

Active ingredients in B01AE07

Active Ingredient Description
Dabigatran

Dabigatran etexilate is a small molecule prodrug which does not exhibit any pharmacological activity. After oral administration, dabigatran etexilate is rapidly absorbed and converted to dabigatran by esterase-catalysed hydrolysis in plasma and in the liver. Dabigatran is a potent, competitive, reversible direct thrombin inhibitor and is the main active principle in plasma.

Related product monographs

Title Information Source Document Type  
PRADAXA 110mg Hard capsule European Medicines Agency (EU) MPI, EU: SmPC
PRADAXA 150mg Hard capsule European Medicines Agency (EU) MPI, EU: SmPC
PRADAXA 75mg Hard capsule European Medicines Agency (EU) MPI, EU: SmPC
PRADAXA Coated granules European Medicines Agency (EU) MPI, EU: SmPC

Medicines in this ATC group

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Note the following: The list of brand names is continuously updated, and thus does not include the total of products circulating worldwide.