PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 11062276-3 2000 METHODS: A LMWH, enoxaparin 1 mg/kg BID, was used as bridging anticoagulation therapy in 24 consecutive patients admitted to a university stroke center in whom the treatment plan included transition from acute to chronic anticoagulation. Enoxaparin 17-27 BH3 interacting domain death agonist Homo sapiens 36-39 15249498-3 2004 The recommended dose of enoxaparin of 1 mg/kg BID was used throughout the population except when physicians decided on dose reduction because of a history of a recent bleeding event or because of a high bleeding risk. Enoxaparin 24-34 BH3 interacting domain death agonist Homo sapiens 46-49 22345487-2 2012 Two enoxaparin regimens are approved for thromboprophylaxis, one in the United States (30 mg twice daily [bid]) and another in the rest of the world (40 mg once daily [qd]). Enoxaparin 4-14 BH3 interacting domain death agonist Homo sapiens 106-109 29958743-2 2018 Considering his clinical stability and sPESI 0, enoxaparin 1 mg/kg BID was started for 24 h, and the patient was then considered for early discharge with apixaban 10 mg BID. Enoxaparin 48-58 BH3 interacting domain death agonist Homo sapiens 67-70 28781584-6 2017 Lovenox 90 mg subcutaneous twice daily (1 mg/kg BID) was started together with warfarin to keep INR 2-3. Enoxaparin 0-7 BH3 interacting domain death agonist Homo sapiens 48-51 28228055-14 2017 Weight-based enoxaparin dosing (0.5 mg/kg/dose BID) is an option in trauma patients considered to be at a lower risk of bleeding complications. Enoxaparin 13-23 BH3 interacting domain death agonist Homo sapiens 47-50 26031274-2 2015 Presently, standard dose enoxaparin (30 mg BID) is used as chemical prophylaxis, regardless of weight or physiologic status. Enoxaparin 25-35 BH3 interacting domain death agonist Homo sapiens 43-46 23519234-7 2013 Adjusted indirect comparison showed that bid enoxaparin was significantly more effective in preventing VTE than enoxaparin once daily (relative risk [RR], 0.71; 95% CI, 0.61-0.83; P < .00001). Enoxaparin 45-55 BH3 interacting domain death agonist Homo sapiens 41-44 23519234-8 2013 For major and clinically relevant hemorrhage, adjusted indirect comparison showed that enoxaparin bid was nonsignificantly associated with increased risk of bleeding (RR 1.27; 95% CI, 0.97-1.65; P = .08) above that of enoxaparin once daily. Enoxaparin 87-97 BH3 interacting domain death agonist Homo sapiens 98-101 23519234-8 2013 For major and clinically relevant hemorrhage, adjusted indirect comparison showed that enoxaparin bid was nonsignificantly associated with increased risk of bleeding (RR 1.27; 95% CI, 0.97-1.65; P = .08) above that of enoxaparin once daily. Enoxaparin 218-228 BH3 interacting domain death agonist Homo sapiens 98-101 22824193-5 2012 Patients who underwent therapeutic anticoagulation with a heparin infusion or enoxaparin (1 mg/kg BID) were evaluated for neurologic deterioration or hemorrhage extension by CT scan. Enoxaparin 78-88 BH3 interacting domain death agonist Homo sapiens 98-101 20825842-9 2011 From the 28 patients enrolled, 75% (group 1, n = 21) received at least 0.9 mg/kg per dose BID and 25% (group 2, n = 7) received less than 0.9 mg/kg per dose BID of enoxaparin. Enoxaparin 164-174 BH3 interacting domain death agonist Homo sapiens 157-160