USA - engelsk - NLM (National Library of Medicine)

camber pharmaceuticals, inc. - dabigatran etexilate mesylate (unii: sc7nuw5iit) (dabigatran - unii:i0vm4m70gc) - dabigatran etexilate capsules are indicated to reduce the risk of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation. dabigatran etexilate capsules are indicated for the treatment of deep venous thrombosis and pulmonary embolism in adult patients who have been treated with a parenteral anticoagulant for 5 to 10 days. dabigatran etexilate capsules are indicated to reduce the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients who have been previously treated. pediatric use information is approved for boehringer ingelheim pharmaceuticals, inc.’s pradaxa (dabigatran etexilate) capsules. however, due to boehringer ingelheim pharmaceuticals, inc.’s marketing exclusivity rights, this drug product is not labeled with that information. dabigatran etexilate capsules are contraindicated in patients with: • active pathological bleeding [see warnings and precautions ( 5.2) and adverse reactions ( 6.1)] • history of a seri

Frankrike - fransk - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

eg labo - laboratoires eurogenerics - dabigatran étexilate 150 mg sous forme de : mésilate de dabigatran étexilate - gélule - pour une gélule > dabigatran étexilate 150 mg sous forme de : mésilate de dabigatran étexilate - classe pharmacothérapeutique: agents antithrombotiques - classe pharmacothérapeutique antithrombotiques, inhibiteurs directs de la thrombine - code atc : b01ae07dabigatran etexilate eg labo contient le dabigatran étexilate comme substance active et appartient à un groupe de médicaments appelé anticoagulants. il agit en bloquant une substance présente dans l’organisme qui intervient dans la formation des caillots sanguins.dabigatran etexilate eg labo est utilisé chez l’adulte pour : prévenir la formation de caillots sanguins dans le cerveau (avc) et dans d’autres vaisseaux sanguins du corps chez les patients souffrant d’une forme de rythme cardiaque irrégulier appelée fibrillation atriale non valvulaire, associée à au moins un facteur de risque supplémentaire. traiter les caillots sanguins dans les veines des jambes et des poumons, et pour prévenir la réapparition de caillots sanguins dans les veines des jambes et des poumons.dabigatran etexilate eg labo est utilisé chez l’enfant pour : traiter les caillots sanguins et prévenir la réapparition de caillots sanguins.

Frankrike - fransk - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

eg labo - laboratoires eurogenerics - dabigatran étexilate 110 mg sous forme de : mésilate de dabigatran étexilate - gélule - pour une gélule > dabigatran étexilate 110 mg sous forme de : mésilate de dabigatran étexilate - classe pharmacothérapeutique : agents antithrombotiques, inhibiteurs directs de la thrombine, code atc : b01ae07 .dabigatran etexilate eg labo contient le dabigatran étexilate comme substance active et appartient à un groupe de médicaments appelé anticoagulants. il agit en bloquant une substance présente dans l’organisme qui intervient dans la formation des caillots sanguins.dabigatran etexilate eg labo est utilisé chez l’adulte pour : prévenir la formation de caillots sanguins dans les veines suite à une intervention chirurgicale pour prothèse totale de genou ou de hanche. prévenir la formation de caillots sanguins dans le cerveau (avc) et dans d’autres vaisseaux sanguins du corps chez les patients souffrant d’une forme de rythme cardiaque irrégulier appelée fibrillation atriale non valvulaire, associée à au moins un facteur de risque supplémentaire. traiter les caillots sanguins dans les veines des jambes et des poumons, et pour prévenir la réapparition de caillots sanguins dans les veines des jambes et des poumons.dabigatran etexilate eg labo est utilisé chez l’enfant pour : traiter les caillots sanguins et prévenir la réapparition de caillots sanguins.

Hellas - gresk - Εθνικός Οργανισμός Φαρμάκων

win medica ΦΑΡΜΑΚΕΥΤΙΚΗ ΑΝΩΝΥΜΗ ΕΤΑΙΡΕΙΑ Δ.Τ. win medica a.e. Οιδίποδος 1-3 & Παράδρομος Αττικής Οδού 33-35, 152 38 Χαλάνδρι 210.7488821 - dabigatran etexilate - caps (ΚΑΨΑΚΙΟ, ΣΚΛΗΡΟ) - 110mg/cap - dabigatran etexilate 110mg - dabigatran etexilate

Hellas - gresk - Εθνικός Οργανισμός Φαρμάκων

win medica ΦΑΡΜΑΚΕΥΤΙΚΗ ΑΝΩΝΥΜΗ ΕΤΑΙΡΕΙΑ Δ.Τ. win medica a.e. Οιδίποδος 1-3 & Παράδρομος Αττικής Οδού 33-35, 152 38 Χαλάνδρι 210.7488821 - dabigatran etexilate - caps (ΚΑΨΑΚΙΟ, ΣΚΛΗΡΟ) - 75mg/cap - dabigatran etexilate 75mg - dabigatran etexilate

Hellas - gresk - Εθνικός Οργανισμός Φαρμάκων

win medica ΦΑΡΜΑΚΕΥΤΙΚΗ ΑΝΩΝΥΜΗ ΕΤΑΙΡΕΙΑ Δ.Τ. win medica a.e. Οιδίποδος 1-3 & Παράδρομος Αττικής Οδού 33-35, 152 38 Χαλάνδρι 210.7488821 - dabigatran etexilate - caps (ΚΑΨΑΚΙΟ, ΣΚΛΗΡΟ) - 150mg/cap - dabigatran etexilate 150mg - dabigatran etexilate

USA - engelsk - NLM (National Library of Medicine)

american health packaging - dabigatran etexilate mesylate (unii: sc7nuw5iit) (dabigatran - unii:i0vm4m70gc) - dabigatran etexilate capsules are indicated to reduce the risk of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation. dabigatran etexilate capsules are indicated for the treatment of deep venous thrombosis and pulmonary embolism in adult patients who have been treated with a parenteral anticoagulant for 5 to 10 days. dabigatran etexilate capsules are indicated to reduce the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients who have been previously treated. pediatric use information is approved for boehringer ingelheim pharmaceuticals, inc.’s pradaxa (dabigatran etexilate) capsules. however, due to boehringer ingelheim pharmaceuticals, inc.’s marketing exclusivity rights, this drug product is not labeled with that information. dabigatran etexilate capsules are contraindicated in patients with: - active pathological bleeding [see warnings and precautions (5.2) and adverse reactions (6.1)] - history of a serious hypersensitivity

USA - engelsk - NLM (National Library of Medicine)

ascend laboratories, llc - dabigatran etexilate mesylate (unii: sc7nuw5iit) (dabigatran - unii:i0vm4m70gc) - dabigatran etexilate capsules is indicated to reduce the risk of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation. dabigatran etexilate capsules is indicated for the treatment of deep venous thrombosis and pulmonary embolism in adult patients who have been treated with a parenteral anticoagulant for 5 to 10 days.  dabigatran etexilate capsules is indicated to reduce the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients who have been previously treated. dabigatran etexilate capsules is indicated for the prophylaxis of deep vein thrombosis and pulmonary embolism, in adult patients who have undergone hip replacement surgery.  pediatric use information is approved for boehringer ingelheim pharmaceuticals, inc.’s pradaxa (dabigatran etexilate) capsules. however, due to boehringer ingelheim pharmaceuticals, inc.’s marketing exclusivity rights, this drug product is not labeled with that information. dabigatran etexilate capsules is contraindic

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

boehringer ingelheim pty ltd - dabigatran etexilate mesilate, quantity: 172.95 mg (equivalent: dabigatran etexilate, qty 150 mg) - capsule, hard - excipient ingredients: dimeticone 350; purified talc; hyprolose; purified water; indigo carmine; hypromellose; carrageenan; acacia; potassium chloride; titanium dioxide; tartaric acid; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - prevention of venous thromboembolic events in adult patients who have undergone major orthopaedic surgery of the lower limb (elective total hip or knee replacement). (see section 4.2 dose and method of administration for details of treatment duration). prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation and at least one additional risk factor for stroke. treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and for the prevention of recurrent dvt and pe in adults.

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

boehringer ingelheim pty ltd - dabigatran etexilate mesilate, quantity: 126.83 mg (equivalent: dabigatran etexilate, qty 110 mg) - capsule, hard - excipient ingredients: hyprolose; hypromellose; tartaric acid; dimeticone 350; potassium chloride; acacia; purified talc; titanium dioxide; carrageenan; indigo carmine; purified water; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - prevention of venous thromboembolic events in adult patients who have undergone major orthopaedic surgery of the lower limb (elective total hip or knee replacement). (see section 4.2 dose and method of administration for details of treatment duration). prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation and at least one additional risk factor for stroke. treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and for the prevention of recurrent dvt and pe in adults.