Vitamin K
Related entities
Findings (27)
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130
None
adverseVitamin K antagonist use during pregnancy in women with Fontan physiology was significantly associated with bleeding events compared to no antithrombotic therapy (OR 11.7, 95% CI 1.06-130, p=0.032).
Effect: adverse; OR 11.7; CI: 95% CI 1.06 to 130