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Dabigatran

Dabigatran etexilate
Dabigatran etexilate structure.svg
Clinical data
Trade names Pradaxa, Pradax, Prazaxa
License data
Pregnancy
category
  • US: C (Risk not ruled out)
Routes of
administration
oral
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability 3–7%
Protein binding 35%
Biological half-life 12–17 hours
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
ChEMBL
Chemical and physical data
Formula C34H41N7O5
Molar mass 627.734 g/mol
3D model (Jmol)
 NYesY (what is this?)  

Dabigatran (Pradaxa, Prazaxa) is an anticoagulant medication that can be taken by mouth. It is being studied for various uses and in some cases is an alternative to warfarin, since it does not have to be monitored by blood tests, but offers similar results in terms of efficacy.

In case of major bleeding, there is an antidote, idarucizumab (sold under the brand name Praxbind). A large study sponsored by the manufacturer found that idarucizumab effectively reversed anticoagulation by dabigatran within minutes.

It is in the class of a direct thrombin inhibitor. It was developed by the pharmaceutical company Boehringer Ingelheim.

Dabigatran is used to prevent strokes in those with atrial fibrillation not caused by heart valve issues, as well as deep vein thrombosis and pulmonary embolism in persons who have been treated for 5–10 days with parenteral anticoagulant (usually low molecular weight heparin), and to prevent deep vein thrombosis and pulmonary embolism in some circumstances.

It appears to be as effective as warfarin in preventing nonhemorrhagic strokes and embolic events in those with atrial fibrillation not due to valve problems.

Dabigatran is contraindicated in patients who have active pathological bleeding, since dabigatran can increase bleeding risk and can also cause serious and potentially life-threatening bleeds. Dabigatran is also contraindicated in patients who have a history of serious hypersensitivity reaction to dabigatran (e.g. anaphylaxis or anaphylactic shock). The use of dabigatran should also be avoided in patients with mechanical prosthetic heart valve due to the increased risk of thromboembolic events (e.g. valve thrombosis, stroke, and myocardial infarction) and major bleeding associated with dabigatran in this population.


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