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.

Code Route Amount Notes
ORAL Oral 0.3 g

Active ingredients in B01AE07

Active Ingredient

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

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

United States medicines

Medicines classified under this ATC code globally

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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.