xilate capsules to 75 mg twice daily when administered concomitantly with the p-gp inhibitors dronedarone or systemic ketoconazole. the use of the p-gp inhibitors verapamil, amiodarone, quinidine, clarithromycin, and ticagrelor does not require a dose adjustment of dabigatran etexilate capsules. these results should not be extrapolated to other p-gp inhibitors [see warnings and precautions (5.5), use in specific populations (8.6), and clinical pharmacology (12.3)] . the concomitant use of dabigatran etexilate capsules and p-gp inhibitors in patients with severe renal impairment (crcl 15 to 30 ml/min) should be avoided [see warnings and precautions (5.5), use in specific populations (8.6), and clinical pharmacology (12.3)] . 7.2 treatment and reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients avoid use of dabigatran etexilate capsules and p-gp inhibitors in patients with crcl <50 ml/min [see warnings and precautions (5.5), use in specific populations (8.6), and clinical pharmacology (12.3)] . 7.3 prophylaxis of deep vein thrombosis and pulmonary embolism in adult patients following hip replacement surgery in patients with crcl ≥50 ml/min who have concomitant administration of p-gp inhibitors such as dronedarone or systemic ketoconazole, it may be helpful to separate the timing of administration of dabigatran etexilate capsules and the p-gp inhibitor by several hours. the concomitant use of dabigatran etexilate capsules and p-gp inhibitors in patients with crcl <50 ml/min should be avoided [see warnings and precautions (5.5), use in specific populations (8.6) and clinical pharmacology (12.2, 12.3)] . 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.

ep venous thrombosis and pulmonary embolism in adult patients who have been treated with a parenteral anticoagulant for 5 to 10 days. 1.3 reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients 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. 1.4 prophylaxis of deep vein thrombosis and pulmonary embolism in adult patients following hip replacement surgery 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.

of bleeding and can cause significant and, sometimes, fatal bleeding. promptly evaluate any signs or symptoms of blood loss (e.g., a drop in hemoglobin and/or hematocrit or hypotension). discontinue dabigatran etexilate capsules in patients with active pathological bleeding [see dosage and administration (2.4)]. risk factors for bleeding include the concomitant use of other drugs that increase the risk of bleeding (e.g., anti-platelet agents, heparin, fibrinolytic therapy, and chronic use of nsaids). dabigatran etexilate capsules’s anticoagulant activity and half-life are increased in patients with renal impairment [see clinical pharmacology (12.2)]. reversal of anticoagulant effect: in adults, a specific reversal agent (idarucizumab) for dabigatran etexilate capsules is available when reversal of the anticoagulant effect of dabigatran is needed: for emergency surgery/urgent procedures in life-threatening or uncontrolled bleeding in pediatric patients, the efficacy and safety of idarucizumab have not been established. hemodialysis can remove dabigatran; however the clinical experience supporting the use of hemodialysis as a treatment for bleeding is limited [see overdosage (10)] . prothrombin complex concentrates, or recombinant factor viia may be considered but their use has not been evaluated in clinical trials. protamine sulfate and vitamin k are not expected to affect the anticoagulant activity of dabigatran. consider administration of platelet concentrates in cases where thrombocytopenia is present or long-acting antiplatelet drugs have been used. 5.3 spinal/epidural anesthesia or puncture when neuraxial anesthesia (spinal/epidural anesthesia) or spinal puncture is employed, patients treated with anticoagulant agents are at risk of developing an epidural or spinal hematoma which can result in long-term or permanent paralysis [see boxed warning] . to reduce the potential risk of bleeding associated with the concurrent use of dabigatran etexilate capsules and epidural or spinal anesthesia/analgesia or spinal puncture, consider the pharmacokinetic profile of dabigatran [see clinical pharmacology (12.3)]. placement or removal of an epidural catheter or lumbar puncture is best performed when the anticoagulant effect of dabigatran is low; however, the exact timing to reach a sufficiently low anticoagulant effect in each patient is not known. should the physician decide to administer anticoagulation in the context of epidural or spinal anesthesia/analgesia or lumbar puncture, monitor frequently to detect any signs or symptoms of neurological impairment, such as midline back pain, sensory and motor deficits (numbness, tingling, or weakness in lower limbs), bowel and/or bladder dysfunction. instruct patients to immediately report if they experience any of the above signs or symptoms. if signs or symptoms of spinal hematoma are suspected, initiate urgent diagnosis and treatment including consideration for spinal cord decompression even though such treatment may not prevent or reverse neurological sequelae. 5.4 thromboembolic and bleeding events in patients with prosthetic heart valves the safety and efficacy of dabigatran etexilate capsules in adult patients with bileaflet mechanical prosthetic heart valves was evaluated in the re-align trial, in which patients with bileaflet mechanical prosthetic heart valves (recently implanted or implanted more than three months prior to enrollment) were randomized to dose-adjusted warfarin or 150 mg, 220 mg, or 300 mg of dabigatran etexilate capsules twice a day. re-align was terminated early due to the occurrence of significantly more thromboembolic events (valve thrombosis, stroke, transient ischemic attack, and myocardial infarction) and an excess of major bleeding (predominantly post-operative pericardial effusions requiring intervention for hemodynamic compromise) in the dabigatran etexilate capsules treatment arm as compared to the warfarin treatment arm. these bleeding and thromboembolic events were seen both in patients who were initiated on dabigatran etexilate capsules postoperatively within three days of mechanical bileaflet valve implantation, as well as in patients whose valves had been implanted more than three months prior to enrollment. therefore, the use of dabigatran etexilate capsules is contraindicated in all patients with mechanical prosthetic valves [see contraindications (4)]. the use of dabigatran etexilate capsules for the prophylaxis of thromboembolic events in patients with atrial fibrillation in the setting of other forms of valvular heart disease, including the presence of a bioprosthetic heart valve,has not been studied and is not recommended. 5.5 effect of p-gp inducers and inhibitors on dabigatran exposure the concomitant use of dabigatran etexilate capsules with p-gp inducers (e.g., rifampin) reduces exposure to dabigatran and should generally be avoided [see clinical pharmacology (12.3)] . p-gp inhibition and impaired renal function are the major independent factors that result in increased exposure to dabigatran [see clinical pharmacology (12.3)]. concomitant use of p-gp inhibitors in patients with renal impairment is expected to produce increased exposure of dabigatran compared to that seen with either factor alone. reduction of risk of stroke and systemic embolism in non-valvular atrial fibrillation in adult patients reduce the dose of dabigatran etexilate capsules to 75 mg twice daily when dronedarone or systemic ketoconazole is co-administered with dabigatran etexilate capsules in patients with moderate renal impairment (crcl 30 to 50 ml/min). avoid use of dabigatran etexilate capsules and p-gp inhibitors in patients with severe renal impairment (crcl 15 to 30 ml/min) [see drug interactions (7.1) and use in specific populations (8.6)] . treatment and reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients avoid use of dabigatran etexilate capsules and concomitant p-gp inhibitors in patients with crcl <50 ml/min [see drug interactions (7.2) and use in specific populations (8.6)] . prophylaxis of deep vein thrombosis and pulmonary embolism in adult patients following hip replacement surgery avoid use of dabigatran etexilate capsules and concomitant p-gp inhibitors in patients with crcl <50 ml/min [see drug interactions (7.3) and use in specific populations (8.6)] . 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. 5.6 increased risk of thrombosis in patients with triple-positive antiphospholipid syndrome direct-acting oral anticoagulants (doacs), including dabigatran etexilate capsules, are not recommended for use in patients with triple-positive antiphospholipid syndrome (aps). for patients with aps (especially those who are triple-positive [positive for lupus anticoagulant, anticardiolipin, and anti-beta 2-glycoprotein i antibodies]), treatment with doacs has been associated with increased rates of recurrent thrombotic events compared with vitamin k antagonist therapy.

2.7 ) • temporarily discontinue dabigatran etexilate capsules before invasive or surgical procedures when possible, then restart promptly ( 2.8 ) 2.1 important dosage information dabigatran etexilate is available in different dosage forms and not all dosage forms are approved for the same indications and age groups. in addition, there are differences between the dosage forms with respect to dosing due to differences in bioavailability. do not substitute different dosage forms on a milligram-to-milligram basis and do not combine more than one dosage form to achieve the total dose [see clinical pharmacology (12.3)]. 2.2 recommended dabigatran etexilate capsules dose for adults indication dosage reduction in risk of stroke and systemic embolism in non-valvular af crcl >30 ml/min: crcl 15 to 30 ml/min: crcl <15 ml/min or on dialysis: 150 mg twice daily 75 mg twice daily dosing recommendations cannot be provided crcl 30 to 50 ml/min with concomitant use of p-gp inhibitors: crcl <30 ml/min with concomitant use of p-gp inhibitors: reduce dose to 75 mg twice daily if given with p-gp inhibitors dronedarone or systemic ketoconazole. avoid coadministration treatment of dvt and pe reduction in the risk of recurrence of dvt and pe crcl >30 ml/min: crcl ≤30 ml/min or on dialysis: 150 mg twice daily dosing recommendations cannot be provided crcl <50 ml/min with concomitant use of p-gp inhibitors: avoid coadministration prophylaxis of dvt and pe following hip replacement surgery crcl >30 ml/min: 110 mg for first day, then 220 mg once daily crcl ≤30 ml/min or on dialysis: dosing recommendations cannot be provided crcl <50 ml/min with concomitant use of p-gp inhibitors: avoid coadministration reduction of risk of stroke and systemic embolism in non-valvular atrial fibrillation in adult patients for patients with creatinine clearance (crcl) >30 ml/min, the recommended dose of dabigatran etexilate capsules is 150 mg taken orally, twice daily. for patients with severe renal impairment (crcl 15 to 30 ml/min), the recommended dose of dabigatran etexilate capsules is 75 mg twice daily [see use in specific populations (8.6) and clinical pharmacology (12.3)]. dosing recommendations for patients with a crcl <15 ml/min or on dialysis cannot be provided. treatment of deep venous thrombosis and pulmonary embolism in adult patients for patients with crcl >30 ml/min, the recommended dose of dabigatran etexilate capsules is 150 mg taken orally, twice daily, after 5 to 10 days of parenteral anticoagulation. dosing recommendations for patients with a crcl ≤30 ml/min or on dialysis cannot be provided [see use in specific populations (8.6) and clinical pharmacology (12.3)]. reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients for patients with crcl >30 ml/min, the recommended dose of dabigatran etexilate capsules is 150 mg taken orally, twice daily after previous treatment. dosing recommendations for patients with a crcl ≤30 ml/min or on dialysis cannot be provided [see use in specific populations (8.6) and clinical pharmacology (12.3)] . prophylaxis of deep vein thrombosis and pulmonary embolism in adult patients following hip replacement surgery for patients with crcl >30 ml/min, the recommended dose of dabigatran etexilate capsules is 110 mg taken orally 1-4 hours after surgery and after hemostasis has been achieved, then 220 mg taken once daily for 28 to 35 days. if dabigatran etexilate capsules is not started on the day of surgery, after hemostasis has been achieved initiate treatment with 220 mg once daily. dosing recommendations for patients with a crcl ≤30 ml/min or on dialysis cannot be provided [see dosage and administration (2.4), use in specific populations (8.6) and clinical pharmacology (12.2, 12.3)] . 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. 2.4 dosage adjustments adult patients with renal impairment assess renal function prior to initiation of treatment with dabigatran etexilate capsules. periodically assess renal function as clinically indicated (i.e., more frequently in clinical situations that may be associated with a decline in renal function) and adjust therapy accordingly. discontinue dabigatran etexilate capsules in patients who develop acute renal failure while on dabigatran etexilate capsules and consider alternative anticoagulant therapy. generally, in adult patients, the extent of anticoagulation does not need to be assessed. when necessary, use aptt or ect, and not inr, to assess for anticoagulant activity in adult patients on dabigatran etexilate capsules [see warnings and precautions (5.2) and clinical pharmacology (12.2)] . reduction of risk of stroke and systemic embolism in non-valvular atrial fibrillation in patients with moderate renal impairment (crcl 30 to 50 ml/min), concomitant use of the p-gp inhibitor dronedarone or systemic ketoconazole can be expected to produce dabigatran exposure similar to that observed in severe renal impairment. reduce the dose of dabigatran etexilate capsules to 75 mg twice daily [see warnings and precautions (5.5), drug interactions (7.1) and clinical pharmacology (12.3)] . treatment and reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism dosing recommendations for patients with crcl≤30 ml/min cannot be provided. avoid use of concomitant p-gp inhibitors in patients with crcl <50 ml/min [see warnings and precautions (5.5), drug interactions (7.2) and clinical pharmacology (12.3)] . prophylaxis of deep vein thrombosis and pulmonary embolism following hip replacement surgery dosing recommendations for patients with crcl ≤30 ml/min or on dialysis cannot be provided. avoid use of concomitant p-gp inhibitors in patients with crcl <50 ml/min [see dosage and administration (2.5), warnings and precautions (5.5), drug interactions (7.3) and clinical pharmacology (12.2, 12.3)] . pediatric patients with renal impairment 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. 2.5 administration dabigatran etexilate capsules should be swallowed whole. dabigatran etexilate capsules should be taken with a full glass of water. breaking, chewing, or emptying the contents of the capsule can result in increased exposure [ s ee clinical pharmacology (12.3)] . if a dose of dabigatran etexilate capsules is not taken at the scheduled time, the dose should be taken as soon as possible on the same day; the missed dose should be skipped if it cannot be taken at least 6 hours before the next scheduled dose. the dose of dabigatran etexilate capsules should not be doubled to make up for a missed dose. consider administration with food if gastrointestinal distress occurs with dabigatran etexilate capsules. 2.6 converting from or to warfarin when converting patients from warfarin therapy to dabigatran etexilate capsules, discontinue warfarin and start dabigatran etexilate capsules when the inr is below 2.0. when converting from dabigatran etexilate capsules to warfarin, adjust the starting time of warfarin as follows: adults for crcl ≥50 ml/min, start warfarin 3 days before discontinuing dabigatran etexilate capsules. for crcl 30 to 50 ml/min, start warfarin 2 days before discontinuing dabigatran etexilate capsules. for crcl 15 to 30 ml/min, start warfarin 1 day before discontinuing dabigatran etexilate capsules. for crcl <15 ml/min, no recommendations can be made. because dabigatran etexilate capsules can increase inr, the inr will better reflect warfarin’s effect only after dabigatran etexilate capsules has been stopped for at least 2 days [see clinical pharmacology (12.2)]. 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. 2.7 converting from or to parenteral anticoagulants for adult patients currently receiving a parenteral anticoagulant, start dabigatran etexilate capsules 0 to 2 hours before the time that the next dose of the parenteral drug was to have been administered or at the time of discontinuation of a continuously administered parenteral drug (e.g., intravenous unfractionated heparin). for adult patients currently taking dabigatran etexilate capsules wait 12 hours (crcl ≥30 ml/min) or 24 hours (crcl <30 ml/min) after the last dose of dabigatran etexilate capsules before initiating treatment with a parenteral anticoagulant [see clinical pharmacology (12.3)] . 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. 2.8 discontinuation for surgery and other interventions if possible, discontinue dabigatran etexilate capsules in adults 1 to 2 days (crcl ≥50 ml/min) or 3 to 5 days (crcl <50 ml/min) before invasive or surgical procedures because of the increased risk of bleeding. consider longer times for patients undergoing major surgery, spinal puncture, or placement of a spinal or epidural catheter or port, in whom complete hemostasis may be required [see use in specific populations (8.6) and clinical pharmacology (12.3)] . if surgery cannot be delayed, there is an increased risk of bleeding [see warnings and precautions (5.2)] . this risk of bleeding should be weighed against the urgency of intervention [see warnings and precautions (5.1, 5.3)] . use a specific reversal agent (idarucizumab) in case of emergency surgery or urgent procedures when reversal of the anticoagulant effect of dabigatran is needed in adults. efficacy and safety of idarucizumab have not been established in pediatric patients [see warnings and precautions (5.2)]. refer to the idarucizumab prescribing information for additional information. restart dabigatran etexilate capsules as soon as medically appropriate. 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.

ials experience because clinical trials are conducted under widely varying conditions, adverse reactions rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. adult trials reduction of risk of stroke and systemic embolism in non-valvular atrial fibrillation the re-ly (randomized evaluation of long-term anticoagulant therapy) study provided safety information on the use of two doses of dabigatran etexilate capsules and warfarin [see clinical studies (14.1)] . the numbers of patients and their exposures are described in table 2. limited information is presented on the 110 mg dosing arm because this dose is not approved. table 2 summary of treatment exposure in re-ly dabigatran etexilate capsules 110 mg twice daily dabigatran etexilate capsules 150 mg twice daily warfarin total number treated 5,983 6,059 5,998 exposure > 12 months 4,936 4,939 5,193 > 24 months 2,387 2,405 2,470 mean exposure (months) 20.5 20.3 21.3 total patient-years 10,242 10,261 10,659 drug discontinuation in re-ly the rates of adverse reactions leading to treatment discontinuation were 21% for dabigatran etexilate capsules 150 mg and 16% for warfarin. the most frequent adverse reactions leading to discontinuation of dabigatran etexilate capsules were bleeding and gastrointestinal events (i.e., dyspepsia, nausea, upper abdominal pain, gastrointestinal hemorrhage, and diarrhea). bleeding [see warnings and precautions (5.2)] table 3 shows the number of adjudicated major bleeding events during the treatment period in the re-ly study, with the bleeding rate per 100 subject-years (%). major bleeding is defined as bleeding accompanied by one or more of the following: a decrease in hemoglobin of ≥2 g/dl, a transfusion of ≥2 units of packed red blood cells, bleeding at a critical site or with a fatal outcome. intracranial hemorrhage included intracerebral (hemorrhagic stroke), subarachnoid, and subdural bleeds. table 3 adjudicated major bleeding events in treated patients a event dabigatran etexilate capsules 150 mg n = 6,059 n (%/year b ) warfarin n = 5,998 n (%/year b ) dabigatran etexilate capsules 150 mg vs warfarin hr (95% ci) major bleeding c 350 (3.47) 374 (3.58) 0.97 (0.84, 1.12) intracranial hemorrhage (ich) d 23 (0.22) 82 (0.77) 0.29 (0.18, 0.46) hemorrhagic stroke e 6 (0.06) 40 (0.37) 0.16 (0.07, 0.37) other ich 17 (0.17) 46 (0.43) 0.38 (0.22, 0.67) gastrointestinal 162 (1.59) 111 (1.05) 1.51 (1.19, 1.92) fatal bleeding f 7 (0.07) 16 (0.15) 0.45 (0.19, 1.10) ich 3 (0.03) 9 (0.08) 0.35 (0.09, 1.28) non-intracranial g 4 (0.04) 7 (0.07) 0.59 (0.17, 2.02) a patients during treatment or within 2 days of stopping study treatment. major bleeding events within each subcategory were counted once per patient, but patients may have contributed events to multiple subcategories. b annual event rate per 100 pt-years = 100 * number of subjects with event/subject-years. subject-years is defined as cumulative number of days from first drug intake to event date, date of last drug intake + 2, death date (whatever occurred first) across all treated subjects divided by 365.25. in case of recurrent events of the same category, the first event was considered. c defined as bleeding accompanied by one or more of the following: a decrease in hemoglobin of ≥2 g/dl, a transfusion of 2 or more units of packed red blood cells, bleeding at a critical site or with fatal outcome. d intracranial bleed included intracerebral (hemorrhagic stroke), subarachnoid, and subdural bleeds. e on-treatment analysis based on the safety population, compared to itt analysis presented in section 14 clinical studies. f fatal bleed: adjudicated major bleed as defined above with investigator reported fatal outcome and adjudicated death with primary cause from bleeding. g non-intracranial fatal bleed: adjudicated major bleed as defined above and adjudicated death with primary cause from bleeding but without symptomatic intracranial bleed based on investigator’s clinical assessment. there was a higher rate of any gastrointestinal bleeds in patients receiving dabigatran etexilate capsules 150 mg than in patients receiving warfarin (6.6% vs 4.2%, respectively). the risk of major bleeds was similar with dabigatran etexilate capsules 150 mg and warfarin across major subgroups defined by baseline characteristics (see figure 1), with the exception of age, where there was a trend toward a higher incidence of major bleeding on dabigatran etexilate capsules (hazard ratio 1.2, 95% ci: 1.0 to 1.5) for patients ≥75 years of age. figure 1 adjudicated major bleeding by baseline characteristics including hemorrhagic stroke treated patients note: the figure above presents effects in various subgroups all of which are baseline characteristics and all of which were pre-specified. the 95% confidence limits that are shown do not take into account how many comparisons were made, nor do they reflect the effect of a particular factor after adjustment for all other factors. apparent homogeneity or heterogeneity among groups should not be over-interpreted. gastrointestinal adverse reactions patients on dabigatran etexilate capsules 150 mg had an increased incidence of gastrointestinal adverse reactions (35% vs 24% on warfarin). these were commonly dyspepsia (including abdominal pain upper, abdominal pain, abdominal discomfort, and epigastric discomfort) and gastritis-like symptoms (including gerd, esophagitis, erosive gastritis, gastric hemorrhage, hemorrhagic gastritis, hemorrhagic erosive gastritis, and gastrointestinal ulcer). hypersensitivity reactions in the re-ly study, drug hypersensitivity (including urticaria, rash, and pruritus), allergic edema, anaphylactic reaction, and anaphylactic shock were reported in <0.1% of patients receiving dabigatran etexilate capsules. treatment and reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism dabigatran etexilate capsules was studied in 4,387 patients in 4 pivotal, parallel, randomized, double-blind trials. three of these trials were active-controlled (warfarin) (re-cover, re-cover ii, and re-medy), and one study (re-sonate) was placebo-controlled. the demographic characteristics were similar among the 4 pivotal studies and between the treatment groups within these studies. approximately 60% of the treated patients were male, with a mean age of 55.1 years. the majority of the patients were white (87.7%), 10.3% were asian, and 1.9% were black with a mean crcl of 105.6 ml/min. bleeding events for the 4 pivotal studies were classified as major bleeding events if at least one of the following criteria applied: fatal bleeding, symptomatic bleeding in a critical area or organ (intraocular, intracranial, intraspinal or intramuscular with compartment syndrome, retroperitoneal bleeding, intra-articular bleeding, or pericardial bleeding), bleeding causing a fall in hemoglobin level of 2.0 g/dl (1.24 mmol/l or more, or leading to transfusion of 2 or more units of whole blood or red cells). re-cover and re-cover ii studies compared dabigatran etexilate capsules 150 mg twice daily and warfarin for the treatment of deep vein thrombosis and pulmonary embolism. patients received 5 to 10 days of an approved parenteral anticoagulant therapy followed by 6 months, with mean exposure of 164 days, of oral only treatment; warfarin was overlapped with parenteral therapy. table 4 shows the number of patients experiencing bleeding events in the pooled analysis of re-cover and re-cover ii studies during the full treatment including parenteral and oral only treatment periods after randomization. table 4 bleeding events in re-cover and re-cover ii treated patients bleeding events-full treatment period including parenteral treatment dabigatran etexilate capsules 150 mg twice daily n (%) warfarin n (%) hazard ratio (95% ci) c patients n=2,553 n=2,554 major bleeding event a 37 (1.4) 51 (2.0) 0.73 (0.48, 1.11) fatal bleeding 1 (0.04) 2 (0.1) bleeding in a critical area or organ 7 (0.3) 15 (0.6) fall in hemoglobin ≥2g/dl or transfusion ≥2 units of whole blood or packed red blood cells 32 (1.3) 38 (1.5) bleeding sites for mbe b intracranial 2 (0.1) 5 (0.2) retroperitoneal 2 (0.1) 1 (0.04) intraarticular 2 (0.1) 4 (0.2) intramuscular 2 (0.1) 6 (0.2) gastrointestinal 15 (0.6) 14 (0.5) urogenital 7 (0.3) 14 (0.5) other 8 (0.3) 8 (0.3) clinically relevant non-major bleeding 101 (4.0) 170 (6.7) 0.58 (0.46, 0.75) any bleeding 411 (16.1) 567 (22.7) 0.70 (0.61, 0.79) note: mbe can belong to more than one criterion. a patients with at least one mbe. b bleeding site based on investigator assessment. patients can have more than one site of bleeding. c confidence interval the rate of any gastrointestinal bleeds in patients receiving dabigatran etexilate capsules 150 mg in the full treatment period was 3.1% (2.4% on warfarin). the re-medy and re-sonate studies provided safety information on the use of dabigatran etexilate capsules for the reduction in the risk of recurrence of deep vein thrombosis and pulmonary embolism. re-medy was an active-controlled study (warfarin) in which 1,430 patients received dabigatran etexilate capsules 150 mg twice daily following 3 to 12 months of oral anticoagulant regimen. patients in the treatment studies who rolled over into the re-medy study had a combined treatment duration of up to more than 3 years, with mean exposure of 473 days. table 5 shows the number of patients experiencing bleeding events in the study. table 5 bleeding events in re-medy treated patients dabigatran etexilate capsules 150 mg twice daily n (%) warfarin n (%) hazard ratio (95% ci) c patients n=1,430 n=1,426 major bleeding event a 13 (0.9) 25 (1.8) 0.54 (0.25, 1.16) fatal bleeding 0 1 (0.1) bleeding in a critical area or organ 7 (0.5) 11 (0.8) fall in hemoglobin ≥2g/dl or transfusion ≥2 units of whole blood or packed red blood cells 7 (0.5) 16 (1.1) bleeding sites for mbe b intracranial 2 (0.1) 4 (0.3) intraocular 4 (0.3) 2 (0.1) retroperitoneal 0 1 (0.1) intraarticular 0 2 (0.1) intramuscular 0 4 (0.3) gastrointestinal 4 (0.3) 8 (0.6) urogenital 1 (0.1) 1 (0.1) other 2 (0.1) 4 (0.3) clinically relevant non-major bleeding 71 (5.0) 125 (8.8) 0.56 (0.42, 0.75) any bleeding 278 (19.4) 373 (26.2) 0.71 (0.61, 0.83) note: mbe can belong to more than one criterion. a patients with at least one mbe. b bleeding site based on investigator assessment. patients can have more than one site of bleeding. c confidence interval in the re-medy study, the rate of any gastrointestinal bleeds in patients receiving dabigatran etexilate capsules 150 mg was 3.1% (2.2% on warfarin). re-sonate was a placebo-controlled study in which 684 patients received dabigatran etexilate capsules 150 mg twice daily following 6 to 18 months of oral anticoagulant regimen. patients in the treatment studies who rolled over into the re-sonate study had combined treatment duration up to 9 months, with mean exposure of 165 days. table 6 shows the number of patients experiencing bleeding events in the study. table 6 bleeding events in re-sonate treated patients dabigatran etexilate capsules 150 mg twice daily n (%) placebo n (%) hazard ratio (95% ci) c patients n=684 n=659 major bleeding event a 2 (0.3) 0 bleeding in a critical area or organ 0 0 gastrointestinal b 2 (0.3) 0 clinically relevant non-major bleeding 34 (5.0) 13 (2.0) 2.54 (1.34, 4.82) any bleeding 72 (10.5) 40 (6.1) 1.77 (1.20, 2.61) note: mbe can belong to more than one criterion. a patients with at least one mbe. b bleeding site based on investigator assessment. patients can have more than one site of bleeding. c confidence interval in the re-sonate study, the rate of any gastrointestinal bleeds in patients receiving dabigatran etexilate capsules 150 mg was 0.7% (0.3% on placebo). clinical myocardial infarction events in the active-controlled vte studies, a higher rate of clinical myocardial infarction was reported in patients who received dabigatran etexilate capsules [20 (0.66 per 100 patient-years)] than in those who received warfarin [5 (0.17 per 100 patient-years)]. in the placebo-controlled study, a similar rate of nonfatal and fatal clinical myocardial infarction was reported in patients who received dabigatran etexilate capsules [1 (0.32 per 100 patient-years)] and in those who received placebo [1 (0.34 per 100 patient-years)]. gastrointestinal adverse reactions in the four pivotal studies, patients on dabigatran etexilate capsules 150 mg had a similar incidence of gastrointestinal adverse reactions (24.7% vs 22.7% on warfarin). dyspepsia (including abdominal pain upper, abdominal pain, abdominal discomfort, and epigastric discomfort) occurred in patients on dabigatran etexilate capsules 7.5% vs 5.5% on warfarin, and gastritis-like symptoms (including gastritis, gerd, esophagitis, erosive gastritis and gastric hemorrhage) occurred at 3.0% vs 1.7%, respectively. hypersensitivity reactions in the 4 pivotal studies, drug hypersensitivity (including urticaria, rash, and pruritus), allergic edema, anaphylactic reaction, and anaphylactic shock were reported in 0.1% of patients receiving dabigatran etexilate capsules. prophylaxis of deep vein thrombosis and pulmonary embolism following hip replacement surgery dabigatran etexilate capsules was studied in 5476 patients, randomized and treated in two double-blind, active-controlled non-inferiority trials (re-novate and re-novate ii). the demographic characteristics were similar across the two studies and between the treatment groups within these studies. approximately 45.3% of the treated patients were male, with a mean age of 63.2 years. the majority of the patients were white (96.1%), 3.6% were asian, and 0.3% were black with a mean crcl of 92 ml/min. bleeding events for the re-novate and re-novate ii studies were classified as major bleeding events if at least one of the following criteria applied: fatal bleeding, symptomatic bleeding in a critical area or organ (intraocular, intracranial, intraspinal or retroperitoneal bleeding), bleeding causing a fall in hemoglobin level of 2.0 g/dl (1.24 mmol/l) or more, or leading to transfusion of 2 or more units of whole blood or red cells, requiring treatment cessation or leading to re-operation. the re-novate study compared dabigatran etexilate capsules 75 mg taken orally 1-4 hours after surgery followed by 150 mg once daily, dabigatran etexilate capsules 110 mg taken orally 1-4 hours after surgery followed by 220 mg once daily and subcutaneous enoxaparin 40 mg once daily initiated the evening before surgery for the prophylaxis of deep vein thrombosis and pulmonary embolism in patients who had undergone hip replacement surgery. the re-novate ii study compared dabigatran etexilate capsules 110 mg taken orally 1-4 hours after surgery followed by 220 mg once daily and subcutaneous enoxaparin 40 mg once daily initiated the evening before surgery for the prophylaxis of deep vein thrombosis and pulmonary embolism in patients who had undergone hip replacement surgery. in the re-novate and re-novate ii studies, patients received 28 to 35 days of dabigatran etexilate capsules or enoxaparin with median exposure of 33 days. tables 7 and 8 show the number of patients experiencing bleeding events in the analysis of re-novate and re-novate ii. table 7 bleeding events in re-novate treated patients dabigatran etexilate capsules 220 mg n (%) enoxaparin n (%) patients n=1,146 n=1,154 major bleeding event 23 (2.0) 18 (1.6) clinically relevant non-major bleeding 48 (4.2) 40 (3.5) any bleeding 141 (12.3) 132 (11.4) table 8 bleeding events in re-novate ii treated patients dabigatran etexilate capsules 220 mg n (%) enoxaparin n (%) patients n=1,010 n=1,003 major bleeding event 14 (1.4) 9 (0.9) clinically relevant non-major bleeding 26 (2.6) 20 (2.0) any bleeding 98 (9.7) 83 (8.3) in the two studies, the rate of major gastrointestinal bleeds in patients receiving dabigatran etexilate capsules and enoxaparin was the same (0.1%) and for any gastrointestinal bleeds was 1.4% for dabigatran etexilate capsules 220 mg and 0.9% for enoxaparin. gastrointestinal adverse reactions in the two studies, the incidence of gastrointestinal adverse reactions for patients on dabigatran etexilate capsules 220 mg and enoxaparin was 39.5% and 39.5%, respectively. dyspepsia (including abdominal pain upper, abdominal pain, abdominal discomfort, and epigastric discomfort) occurred in patients on dabigatran etexilate capsules 220 mg in 4.1% vs. 3.8% on enoxaparin, and gastritis-like symptoms (including gastritis, gerd, esophagitis, erosive gastritis and gastric hemorrhage) occurred at 0.6% vs. 1.0%, respectively. hypersensitivity reactions in the two studies, drug hypersensitivity (such as urticaria, rash, and pruritus) was reported in 0.3% of patients receiving dabigatran etexilate capsules 220 mg. clinical myocardial infarction events in the two studies, clinical myocardial infarction was reported in 2 (0.1%) of patients who received dabigatran etexilate capsules 220 mg and 6 (0.3%) of patients who received enoxaparin. 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. dab-igatran-fig1 6.2 postmarketing experience the following adverse reactions have been identified during post approval use of dabigatran etexilate capsules. because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. the following adverse reactions have been identified during post approval use of dabigatran etexilate capsules: angioedema, thrombocytopenia, esophageal ulcer, alopecia, neutropenia, agranulocytosis.

xilate capsules to 75 mg twice daily when administered concomitantly with the p-gp inhibitors dronedarone or systemic ketoconazole. the use of the p-gp inhibitors verapamil, amiodarone, quinidine, clarithromycin, and ticagrelor does not require a dose adjustment of dabigatran etexilate capsules. these results should not be extrapolated to other p-gp inhibitors [see warnings and precautions (5.5), use in specific populations (8.6), and clinical pharmacology (12.3)] . the concomitant use of dabigatran etexilate capsules and p-gp inhibitors in patients with severe renal impairment (crcl 15 to 30 ml/min) should be avoided [see warnings and precautions (5.5), use in specific populations (8.6), and clinical pharmacology (12.3)] . 7.2 treatment and reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients avoid use of dabigatran etexilate capsules and p-gp inhibitors in patients with crcl <50 ml/min [see warnings and precautions (5.5), use in specific populations (8.6), and clinical pharmacology (12.3)] . 7.3 prophylaxis of deep vein thrombosis and pulmonary embolism in adult patients following hip replacement surgery in patients with crcl ≥50 ml/min who have concomitant administration of p-gp inhibitors such as dronedarone or systemic ketoconazole, it may be helpful to separate the timing of administration of dabigatran etexilate capsules and the p-gp inhibitor by several hours. the concomitant use of dabigatran etexilate capsules and p-gp inhibitors in patients with crcl <50 ml/min should be avoided [see warnings and precautions (5.5), use in specific populations (8.6) and clinical pharmacology (12.2, 12.3)] . 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.

rition at an exposure 2.6 times the human exposure. at a similar exposure, dabigatran decreased the number of implantations when rats were treated prior to mating and up to implantation (gestation day 6). dabigatran administered to pregnant rats and rabbits during organogenesis up to exposures 8 and 13 times the human exposure, respectively, did not induce major malformations. however, the incidence of delayed or irregular ossification of fetal skull bones and vertebrae was increased in the rat (see data) . the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. clinical considerations disease-associated maternal and/or embryo/fetal risk pregnancy confers an increased risk for thromboembolism that is higher for women with underlying thromboembolic disease and certain high-risk pregnancy conditions. published data describe that women with a previous history of venous thrombosis are at high risk for recurrence during pregnancy. fetal/neonatal adverse reaction use of anticoagulants, including dabigatran etexilate capsules, may increase the risk of bleeding in the fetus and neonate. monitor neonates for bleeding [see warnings and precautions (5.2)]. labor or delivery all patients receiving anticoagulants, including pregnant women, are at risk for bleeding. dabigatran etexilate capsules use during labor or delivery in women who are receiving neuraxial anesthesia may result in epidural or spinal hematomas. consider discontinuation or use of shorter acting anticoagulant as delivery approaches [see warnings and precautions (5.2, 5.3)]. data animal data dabigatran has been shown to decrease the number of implantations when male and female rats were treated at a dosage of 70 mg/kg (about 2.6 to 3.0 times the human exposure at mrhd of 300 mg/day based on area under the curve [auc] comparisons) prior to mating and up to implantation (gestation day 6). treatment of pregnant rats after implantation with dabigatran at the same dose increased the number of dead offspring and caused excess vaginal/uterine bleeding close to parturition. dabigatran administered to pregnant rats and rabbits during organogenesis up to maternally toxic doses of 200 mg/kg (8 and 13 times the human exposure, respectively, at a mrhd of 300 mg/day based on auc comparisons) did not induce major malformations, but increased the incidence of delayed or irregular ossification of fetal skull bones and vertebrae in the rat. death of offspring and mother rats during labor in association with uterine bleeding occurred during treatment of pregnant rats from implantation (gestation day 7) to weaning (lactation day 21) with dabigatran at a dose of 70 mg/kg (about 2.6 times the human exposure at mrhd of 300 mg/day based on auc comparisons). 8.2 lactation risk summary there are no data on the presence of dabigatran in human milk, the effects on the breastfed child, or on milk production. dabigatran and/or its metabolites were present in rat milk. breastfeeding is not recommended during treatment with dabigatran etexilate capsules. 8.3 females and males of reproductive potential females of reproductive potential requiring anticoagulation should discuss pregnancy planning with their physician. the risk of clinically significant uterine bleeding, potentially requiring gynecological surgical interventions, identified with oral anticoagulants including dabigatran should be assessed in females of reproductive potential and those with abnormal uterine bleeding. 8.4 pediatric use safety and effectiveness of dabigatran etexilate capsules have not been established in pediatric patients with non-valvular atrial fibrillation or those 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. 8.5 geriatric use of the total number of patients in the re-ly study, 82% were 65 and over, while 40% were 75 and over. the risk of stroke and bleeding increases with age, but the risk-benefit profile is favorable in all age groups [see warnings and precautions (5), adverse reactions (6.1), and clinical studies (14.1)] . 8.6 renal impairment reduction of risk of stroke and systemic embolism in non-valvular atrial fibrillation in adult patients no dose adjustment of dabigatran etexilate capsules is recommended in patients with mild or moderate renal impairment [see clinical pharmacology (12.3)] . reduce the dose of dabigatran etexilate capsules in patients with severe renal impairment (crcl 15 to 30 ml/min) [see dosage and administration (2.2, 2.4) and clinical pharmacology (12.3)] . dosing recommendations for patients with crcl <15 ml/min or on dialysis cannot be provided. adjust dose appropriately in patients with renal impairment receiving concomitant p-gp inhibitors [see warnings and precautions (5.5), drug interactions (7.1), and clinical pharmacology (12.3)]. treatment and reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients patients with severe renal impairment (crcl ≤30 ml/min) were excluded from re-cover. dosing recommendations for patients with crcl ≤30 ml/min or on dialysis cannot be provided. avoid use of dabigatran etexilate capsules with concomitant p-gp inhibitors in patients with crcl <50 ml/min [see warnings and precautions (5.5), drug interactions (7.2), and clinical pharmacology (12.3)]. prophylaxis of deep vein thrombosis and pulmonary embolism in adult patients following hip replacement surgery patients with severe renal impairment (crcl <30 ml/min) were excluded from re-novate and re-novate ii. dosing recommendations for patients with crcl <30 ml/min or on dialysis cannot be provided. avoid use of dabigatran etexilate capsules with concomitant p-gp inhibitors in patients with crcl <50 ml/min [see warnings and precautions (5.5), drug interactions (7.3) and clinical pharmacology (12.2, 12.3)]. 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.

lar ossification of fetal skull bones and vertebrae was increased in the rat (see data) . the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. clinical considerations disease-associated maternal and/or embryo/fetal risk pregnancy confers an increased risk for thromboembolism that is higher for women with underlying thromboembolic disease and certain high-risk pregnancy conditions. published data describe that women with a previous history of venous thrombosis are at high risk for recurrence during pregnancy. fetal/neonatal adverse reaction use of anticoagulants, including dabigatran etexilate capsules, may increase the risk of bleeding in the fetus and neonate. monitor neonates for bleeding [see warnings and precautions (5.2)]. labor or delivery all patients receiving anticoagulants, including pregnant women, are at risk for bleeding. dabigatran etexilate capsules use during labor or delivery in women who are receiving neuraxial anesthesia may result in epidural or spinal hematomas. consider discontinuation or use of shorter acting anticoagulant as delivery approaches [see warnings and precautions (5.2, 5.3)]. data animal data dabigatran has been shown to decrease the number of implantations when male and female rats were treated at a dosage of 70 mg/kg (about 2.6 to 3.0 times the human exposure at mrhd of 300 mg/day based on area under the curve [auc] comparisons) prior to mating and up to implantation (gestation day 6). treatment of pregnant rats after implantation with dabigatran at the same dose increased the number of dead offspring and caused excess vaginal/uterine bleeding close to parturition. dabigatran administered to pregnant rats and rabbits during organogenesis up to maternally toxic doses of 200 mg/kg (8 and 13 times the human exposure, respectively, at a mrhd of 300 mg/day based on auc comparisons) did not induce major malformations, but increased the incidence of delayed or irregular ossification of fetal skull bones and vertebrae in the rat. death of offspring and mother rats during labor in association with uterine bleeding occurred during treatment of pregnant rats from implantation (gestation day 7) to weaning (lactation day 21) with dabigatran at a dose of 70 mg/kg (about 2.6 times the human exposure at mrhd of 300 mg/day based on auc comparisons).

fidence intervals; variations should be expected when measuring aptt. while advice cannot be provided on the level of recovery of aptt needed in any particular clinical setting, the curves can be used to estimate the time to get to a particular level of recovery, even when the time since the last dose of dabigatran etexilate capsules is not precisely known. in the re-ly trial, the median (10 th to 90 th percentile) trough aptt in patients receiving the 150 mg dose was 52 (40 to 76) seconds. figure 2 average time course for effects of dabigatran on aptt, following approved dabigatran etexilate capsules dosing regimens in adult patients with various degrees of renal impairment* *simulations based on pk data from a study in subjects with renal impairment and pk/aptt relationships derived from the re-ly study; aptt prolongation in re-ly was measured centrally in citrate plasma using ptt reagent roche diagnostics gmbh, mannheim, germany. there may be quantitative differences between various established methods for aptt assessment. the degree of anticoagulant activity can also be assessed by the ecarin clotting time (ect). this test is a more specific measure of the effect of dabigatran than activated partial thromboplastin time (aptt). in the re-ly trial, the median (10 th to 90 th percentile) trough ect in patients receiving the 150 mg dose was 63 (44 to 103) seconds. in orthopedic hip surgery patients, maximum aptt response (emax) to dabigatran and baseline aptt were higher shortly after surgery than at later time points (e.g. ≥3 days after surgery). cardiac electrophysiology no prolongation of the qtc interval was observed with dabigatran etexilate at doses up to 600 mg. 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. dab-igatran-fig2 12.3 pharmacokinetics dabigatran etexilate mesylate is absorbed as the dabigatran etexilate ester. the ester is then hydrolyzed, forming dabigatran, the active moiety. dabigatran is metabolized to four different acyl glucuronides and both the glucuronides and dabigatran have similar pharmacological activity. pharmacokinetics described here refer to the sum of dabigatran and its glucuronides. dabigatran displays dose-proportional pharmacokinetics in healthy adult subjects and adult patients in the range of doses from 10 to 400 mg. given twice daily, dabigatran’s accumulation factor in adults is approximately two. absorption the absolute bioavailability of dabigatran following oral administration of dabigatran etexilate is approximately 3% to 7%. dabigatran etexilate is a substrate of the efflux transporter p-gp. after oral administration of dabigatran etexilate in healthy volunteers, cmax occurs at 1-hour post-administration in the fasted state. coadministration of dabigatran etexilate capsules with a high-fat meal delays the time to c max by approximately 2 hours but has no effect on the bioavailability of dabigatran; dabigatran etexilate capsules may be administered with or without food. the oral bioavailability of dabigatran etexilate increases by 75% when the pellets are taken without the capsule shell compared to the intact capsule formulation based on a single-dose relative bioavailability study. dabigatran etexilate capsules should therefore not be broken, chewed, or opened before administration. distribution dabigatran is approximately 35% bound to human plasma proteins. the red blood cell to plasma partitioning of dabigatran measured as total radioactivity is less than 0.3. the volume of distribution of dabigatran is 50 to 70 l. elimination dabigatran is eliminated primarily in the urine. renal clearance of dabigatran is 80% of total clearance after intravenous administration. after oral administration of radiolabeled dabigatran, 7% of radioactivity is recovered in urine and 86% in feces. the half-life of dabigatran in healthy adult subjects is 12 to 17 hours. metabolism after oral administration, dabigatran etexilate is converted to dabigatran. the cleavage of the dabigatran etexilate by esterase-catalyzed hydrolysis to the active principal dabigatran is the predominant metabolic reaction. dabigatran is not a substrate, inhibitor, or inducer of cyp450 enzymes. dabigatran is subject to conjugation, forming pharmacologically active acyl glucuronides. four positional isomers, 1-o, 2-o, 3-o, and 4-o-acylglucuronide exist, and each accounts for less than 10% of total dabigatran in plasma. specific populations renal impairment an open, parallel-group, single-center study compared dabigatran pharmacokinetics in healthy adult subjects and adult patients with mild to moderate renal impairment receiving a single dose of dabigatran etexilate capsules 150 mg. exposure to dabigatran increases with severity of renal function impairment (table 10). similar findings were observed in the re-ly, re-cover and re-novate ii trials. table 10 impact of renal impairment on dabigatran pharmacokinetics renal function crcl (ml/min) increase in auc increase in c max t 1/2 (h) normal ≥ 80 1x 1x 13 mild 50 to 80 1.5x 1.1x 15 moderate 30 to 50 3.2x 1.7x 18 severe + 15 to 30 6.3x 2.1x 27 + patients with severe renal impairment were not studied in re-ly, re-cover and re-novate ii. dosing recommendations in subjects with severe renal impairment are based on pharmacokinetic modeling [see dosage and administration (2.2, 2.4) and use in specific populations (8.6)] . hepatic impairment administration of dabigatran etexilate capsules in adult patients with moderate hepatic impairment (child-pugh b) showed a large inter-subject variability, but no evidence of a consistent change in exposure or pharmacodynamics. drug interactions a summary of the effect of coadministered drugs on dabigatran exposure in healthy adult subjects is shown in figures 3.1 and 3.2. in the orthopedic hip surgery patients, limited clinical data with p-gp inhibitors is available. figure 3.1 effect of p-gp inhibitor or inducer (rifampicin) drugs on peak and total exposure to dabigatran (cmax and auc). shown are the geometric mean ratios (ratio) and 90% confidence interval (90% ci). the perpetrator and dabigatran etexilate dose and dosing frequency are given as well as the time of perpetrator dosing in relation to dabigatran etexilate dose (time difference) figure 3.2 effect of non-p-gp inhibitor or inducer, other drugs, on peak and total exposure to dabigatran (cmax and auc). shown are the geometric mean ratios (ratio) and 90% confidence interval (90% ci). the perpetrator and dabigatran etexilate dose and dosing frequency are given as well as the time of perpetrator dosing in relation to dabigatran etexilate dose (time difference) in re-ly, dabigatran plasma samples were also collected. the concomitant use of proton pump inhibitors, h2 antagonists, and digoxin did not appreciably change the trough concentration of dabigatran. impact of dabigatran on other drugs in clinical studies exploring cyp3a4, cyp2c9, p-gp and other pathways, dabigatran did not meaningfully alter the pharmacokinetics of amiodarone, atorvastatin, clarithromycin, diclofenac, clopidogrel, digoxin, pantoprazole, or ranitidine. 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. dab-igatran-fig3-1 dab-igatran-fig3-2

late capsules with a high-fat meal delays the time to c max by approximately 2 hours but has no effect on the bioavailability of dabigatran; dabigatran etexilate capsules may be administered with or without food. the oral bioavailability of dabigatran etexilate increases by 75% when the pellets are taken without the capsule shell compared to the intact capsule formulation based on a single-dose relative bioavailability study. dabigatran etexilate capsules should therefore not be broken, chewed, or opened before administration. distribution dabigatran is approximately 35% bound to human plasma proteins. the red blood cell to plasma partitioning of dabigatran measured as total radioactivity is less than 0.3. the volume of distribution of dabigatran is 50 to 70 l. elimination dabigatran is eliminated primarily in the urine. renal clearance of dabigatran is 80% of total clearance after intravenous administration. after oral administration of radiolabeled dabigatran, 7% of radioactivity is recovered in urine and 86% in feces. the half-life of dabigatran in healthy adult subjects is 12 to 17 hours. metabolism after oral administration, dabigatran etexilate is converted to dabigatran. the cleavage of the dabigatran etexilate by esterase-catalyzed hydrolysis to the active principal dabigatran is the predominant metabolic reaction. dabigatran is not a substrate, inhibitor, or inducer of cyp450 enzymes. dabigatran is subject to conjugation, forming pharmacologically active acyl glucuronides. four positional isomers, 1-o, 2-o, 3-o, and 4-o-acylglucuronide exist, and each accounts for less than 10% of total dabigatran in plasma. specific populations renal impairment an open, parallel-group, single-center study compared dabigatran pharmacokinetics in healthy adult subjects and adult patients with mild to moderate renal impairment receiving a single dose of dabigatran etexilate capsules 150 mg. exposure to dabigatran increases with severity of renal function impairment (table 10). similar findings were observed in the re-ly, re-cover and re-novate ii trials. table 10 impact of renal impairment on dabigatran pharmacokinetics renal function crcl (ml/min) increase in auc increase in c max t 1/2 (h) normal ≥ 80 1x 1x 13 mild 50 to 80 1.5x 1.1x 15 moderate 30 to 50 3.2x 1.7x 18 severe + 15 to 30 6.3x 2.1x 27 + patients with severe renal impairment were not studied in re-ly, re-cover and re-novate ii. dosing recommendations in subjects with severe renal impairment are based on pharmacokinetic modeling [see dosage and administration (2.2, 2.4) and use in specific populations (8.6)] . hepatic impairment administration of dabigatran etexilate capsules in adult patients with moderate hepatic impairment (child-pugh b) showed a large inter-subject variability, but no evidence of a consistent change in exposure or pharmacodynamics. drug interactions a summary of the effect of coadministered drugs on dabigatran exposure in healthy adult subjects is shown in figures 3.1 and 3.2. in the orthopedic hip surgery patients, limited clinical data with p-gp inhibitors is available. figure 3.1 effect of p-gp inhibitor or inducer (rifampicin) drugs on peak and total exposure to dabigatran (cmax and auc). shown are the geometric mean ratios (ratio) and 90% confidence interval (90% ci). the perpetrator and dabigatran etexilate dose and dosing frequency are given as well as the time of perpetrator dosing in relation to dabigatran etexilate dose (time difference) figure 3.2 effect of non-p-gp inhibitor or inducer, other drugs, on peak and total exposure to dabigatran (cmax and auc). shown are the geometric mean ratios (ratio) and 90% confidence interval (90% ci). the perpetrator and dabigatran etexilate dose and dosing frequency are given as well as the time of perpetrator dosing in relation to dabigatran etexilate dose (time difference) in re-ly, dabigatran plasma samples were also collected. the concomitant use of proton pump inhibitors, h2 antagonists, and digoxin did not appreciably change the trough concentration of dabigatran. impact of dabigatran on other drugs in clinical studies exploring cyp3a4, cyp2c9, p-gp and other pathways, dabigatran did not meaningfully alter the pharmacokinetics of amiodarone, atorvastatin, clarithromycin, diclofenac, clopidogrel, digoxin, pantoprazole, or ranitidine. 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. dab-igatran-fig3-1 dab-igatran-fig3-2

decreased in females receiving 70 mg/kg, or 3 times the human exposure at mrhd based on auc comparisons.

iving 70 mg/kg, or 3 times the human exposure at mrhd based on auc comparisons.

dy was to determine if dabigatran etexilate capsules was non-inferior to warfarin in reducing the occurrence of the composite endpoint, stroke (ischemic and hemorrhagic) and systemic embolism. the study was designed to ensure that dabigatran etexilate capsules preserved more than 50% of warfarin’s effect as established by previous randomized, placebo-controlled trials of warfarin in atrial fibrillation. statistical superiority was also analyzed. a total of 18,113 patients were randomized and followed for a median of 2 years. the patients’ mean age was 71.5 years and the mean chads 2 score was 2.1. the patient population was 64% male, 70% caucasian, 16% asian, and 1% black. twenty percent of patients had a history of a stroke or tia and 50% were vitamin k antagonist (vka) naïve, defined as less than 2 months total lifetime exposure to a vka. thirty-two percent of the population had never been exposed to a vka. concomitant diseases of patients in this trial included hypertension 79%, diabetes 23%, and cad 28%. at baseline, 40% of patients were on aspirin and 6% were on clopidogrel. for patients randomized to warfarin, the mean percentage of time in therapeutic range (inr 2 to 3) was 64%. relative to warfarin and to dabigatran etexilate capsules 110 mg twice daily, dabigatran etexilate capsules 150 mg twice daily significantly reduced the primary composite endpoint of stroke and systemic embolism (see table 11 and figure 4). table 11 first occurrence of stroke or systemic embolism in the re-ly study* dabigatran etexilate capsules 150 mg twice daily dabigatran etexilate capsules 110 mg twice daily warfarin patients randomized 6,076 6,015 6,022 patients (% per yr) with events 135 (1.12%) 183 (1.54%) 203 (1.72%) hazard ratio vs warfarin (95% ci) 0.65 (0.52, 0.81) 0.89 (0.73, 1.09) p-value for superiority 0.0001 0.27 hazard ratio vs dabigatran etexilate capsules 110 mg (95% ci) 0.72 (0.58, 0.91) p-value for superiority 0.005 * randomized itt figure 4 kaplan-meier curve estimate of time to first stroke or systemic embolism the contributions of the components of the composite endpoint, including stroke by subtype, are shown in table 12. the treatment effect was primarily a reduction in stroke. dabigatran etexilate capsules 150 mg twice daily was superior in reducing ischemic and hemorrhagic strokes relative to warfarin. table 12 strokes and systemic embolism in the re-ly study dabigatran etexilate capsules 150 mg twice daily warfarin hazard ratio vs warfarin (95% ci) patients randomized 6,076 6,022 stroke 123 187 0.64 (0.51, 0.81) ischemic stroke 104 134 0.76 (0.59,0.98) hemorrhagic stroke 12 45 0.26 (0.14, 0.49) systemic embolism 13 21 0.61 (0.30, 1.21) in the re-ly trial, the rate of all-cause mortality was lower on dabigatran etexilate capsules 150 mg than on warfarin (3.6% per year versus 4.1% per year). the rate of vascular death was lower on dabigatran etexilate capsules 150 mg compared to warfarin (2.3% per year versus 2.7% per year). non-vascular death rates were similar in the treatment arms. the efficacy of dabigatran etexilate capsules 150 mg twice daily was generally consistent across major subgroups (see figure 5). figure 5 stroke and systemic embolism hazard ratios by baseline characteristics* * randomized itt note: the figure above presents effects in various subgroups all of which are baseline characteristics and all of which were pre-specified. the 95% confidence limits that are shown do not take into account how many comparisons were made, nor do they reflect the effect of a particular factor after adjustment for all other factors. apparent homogeneity or heterogeneity among groups should not be over-interpreted. in re-ly, a higher rate of clinical myocardial infarction was reported in patients who received dabigatran etexilate capsules (0.7 per 100 patient-years for 150 mg dose) than in those who received warfarin (0.6). dab-igatran-fig4 dab-igatran-fig5 14.2 treatment and reduction in the risk of recurrence of deep venous thrombosis and pulmonary embolism in adult patients in the randomized, parallel group, double-blind trials, re-cover and re-cover ii, patients with deep vein thrombosis and pulmonary embolism received dabigatran etexilate capsules 150 mg twice daily or warfarin (dosed to target inr of 2 to 3) following initial treatment with an approved parenteral anticoagulant for 5 to 10 days. in re-cover, the median treatment duration during the oral only treatment period was 174 days. a total of 2,539 patients (30.9% patients with symptomatic pe with or without dvt and 68.9% with symptomatic dvt only) were treated with a mean age of 54.7 years. the patient population was 58.4% male, 94.8% white, 2.6% asian, and 2.6% black. the concomitant diseases of patients in this trial included hypertension (35.9%), diabetes mellitus (8.3%), coronary artery disease (6.5%), active cancer (4.8%), and gastric or duodenal ulcer (4.4%). concomitant medications included agents acting on renin-angiotensin system (25.2%), vasodilators (28.4%), serum lipid-reducing agents (18.2%), nsaids (21%), beta-blockers (14.8%), calcium channel blockers (8.5%), asa (8.6%), and platelet inhibitors excluding asa (0.6%). patients randomized to warfarin had a mean percentage of time in the inr target range of 2.0 to 3.0 of 60% in re-cover study. in re-cover ii, the median treatment duration during the oral only treatment period was 174 days. a total of 2,568 patients (31.8% patients with symptomatic pe with or without dvt and 68.1% with symptomatic dvt only) were treated with a mean age of 54.9 years. the patient population was 60.6% male, 77.6% white, 20.9% asian, and 1.5% black. the concomitant diseases of patients in this trial included hypertension (35.1%), diabetes mellitus (9.8%), coronary artery disease (7.1%), active cancer (3.9%), and gastric or duodenal ulcer (3.8%). concomitant medications included agents acting on renin-angiotensin system (24.2%), vasodilators (28.6%), serum lipid-reducing agents (20.0%), nsaids (22.3%), beta-blockers (14.8%), calcium channel blockers (10.8%), asa (9.8%), and platelet inhibitors excluding asa (0.8%). patients randomized to warfarin had a mean percentage of time in the inr target range of 2.0 to 3.0 of 57% in re-cover ii study. in studies re-cover and re-cover ii, the protocol specified non-inferiority margin (2.75) for the hazard ratio was derived based on the upper limit of the 95% confidence interval of the historical warfarin effect. dabigatran etexilate capsules was demonstrated to be non-inferior to warfarin (dosed to target inr of 2 to 3) (table 13) based on the primary composite endpoint (fatal pe or symptomatic non-fatal pe and/or dvt) and retains at least 66.9% (re-cover) and 63.9% (re-cover ii) of the historical warfarin effect, respectively. table 13 primary efficacy endpoint for re-cover and re-cover ii –modified itt a population dabigatran etexilate capsules 150 mg twice daily n (%) warfarin n (%) hazard ratio vs warfarin (95% ci) re-cover n=1,274 n=1,265 primary composite endpoint b 34 (2.7) 32 (2.5) 1.05 (0.65, 1.70) fatal pe c 1 (0.1) 3 (0.2) symptomatic non-fatal pe c 16 (1.3) 8 (0.6) symptomatic recurrent dvt c 17 (1.3) 23 (1.8) re-cover ii n=1,279 n=1,289 primary composite endpoint b 34 (2.7) 30 (2.3) 1.13 (0.69, 1.85) fatal pe c 3 (0.2) 0 symptomatic non-fatal pe c 9 (0.7) 15 (1.2) symptomatic recurrent dvt c 30 (2.3) 17 (1.3) a modified itt analyses population consists of all randomized patients who received at least one dose of study medication. b number of patients with one or more event. c number of events. for patients with multiple events each event is counted independently. in the randomized, parallel-group, double-blind, pivotal trial, re-medy, patients received dabigatran etexilate capsules 150 mg twice daily or warfarin (dosed to target inr of 2 to 3) following 3 to 12 months of treatment with anticoagulation therapy for an acute vte. the median treatment duration during the treatment period was 534 days. a total of 2,856 patients were treated with a mean age of 54.6 years. the patient population was 61% male, and 90.1% white, 7.9% asian and 2.0% black. the concomitant diseases of patients in this trial included hypertension (38.6%), diabetes mellitus (9.0%), coronary artery disease (7.2%), active cancer (4.2%), and gastric or duodenal ulcer (3.8%). concomitant medications included agents acting on renin-angiotensin system (27.9%), vasodilators (26.7%), serum lipid reducing agents (20.6%), nsaids (18.3%), beta-blockers (16.3%), calcium channel blockers (11.1%), aspirin (7.7%), and platelet inhibitors excluding asa (0.9%). patients randomized to warfarin had a mean percentage of time in the inr target range of 2.0 to 3.0 of 62% in the study. in study re-medy, the protocol specified non-inferiority margin (2.85) for the hazard ratio was derived based on the point estimate of the historical warfarin effect. dabigatran etexilate capsules was demonstrated to be non-inferior to warfarin (dosed to target inr of 2 to 3) (table 14) based on the primary composite endpoint (fatal pe or symptomatic non-fatal pe and/or dvt) and retains at least 63.0% of the historical warfarin effect. if the non-inferiority margin was derived based on the 50% retention of the upper limit of the 95% confidence interval, dabigatran etexilate capsules was demonstrated to retain at least 33.4% of the historical warfarin effect based on the composite primary endpoint. table 14 primary efficacy endpoint for re-medy – modified itt a population dabigatran etexilate capsules 150 mg twice daily n=1,430 n (%) warfarin n=1,426 n (%) hazard ratio vs warfarin (95% ci) primary composite endpoint b 26 (1.8) 18 (1.3) 1.44 (0.78, 2.64) fatal pe c 1 (0.07) 1 (0.07) symptomatic non-fatal pe c 10 (0.7) 5 (0.4) symptomatic recurrent dvtc 17 (1.2) 13 (0.9) a modified itt analyses population consists of all randomized patients who received at least one dose of study medication. b number of patients with one or more event. c number of events. for patients with multiple events each event is counted independently. in a randomized, parallel-group, double-blind, pivotal trial, re-sonate, patients received dabigatran etexilate capsules 150 mg twice daily or placebo following 6 to 18 months of treatment with anticoagulation therapy for an acute vte. the median treatment duration was 182 days. a total of 1,343 patients were treated with a mean age of 55.8 years. the patient population was 55.5% male, 89.0% white, 9.3% asian, and 1.7% black. the concomitant diseases of patients in this trial included hypertension (38.8%), diabetes mellitus (8.0%), coronary artery disease (6.0%), history of cancer (6.0%), gastric or duodenal ulcer (4.5%), and heart failure (4.6%). concomitant medications included agents acting on renin-angiotensin system (28.7%), vasodilators (19.4%), beta-blockers (18.5%), serum lipid reducing agents (17.9%), nsaids (12.1%), calcium channel blockers (8.9%), aspirin (8.3%), and platelet inhibitors excluding asa (0.7%). based on the outcome of the primary composite endpoint (fatal pe, unexplained death, or symptomatic non-fatal pe and/or dvt), dabigatran etexilate capsules was superior to placebo (table 15). table 15 primary efficacy endpoint for re-sonate – modified itt a population dabigatran etexilate capsules 150 mg twice daily n=681 n (%) placebo n=662 n (%) hazard ratio vs placebo (95% ci) primary composite endpoint b 3 (0.4) 37 (5.6) 0.08 (0.02, 0.25) p-value <0.0001 fatal pe and unexplained death c 0 2 (0.3) symptomatic non-fatal pe c 1 (0.1) 14 (2.1) symptomatic recurrent dvt c 2 (0.3) 23 (3.5) a modified itt analyses population consists of all randomized patients who received at least one dose of study medication. b number of patients with one or more events. c number of events. for patients with multiple events each event is counted independently. 14.3 prophylaxis of deep vein thrombosis and pulmonary embolism in adult patients following hip replacement surgery in the randomized, parallel group, double-blind, non-inferiority trials, re-novate and re-novate ii patients received dabigatran etexilate capsules 75 mg orally 1-4 hours after surgery followed by 150 mg daily (re-novate), dabigatran etexilate capsules 110 mg orally 1-4 hours after surgery followed by 220 mg daily (re-novate and re-novate ii) or subcutaneous enoxaparin 40 mg once daily initiated the evening before surgery (re-novate and re-novate ii) for the prophylaxis of deep vein thrombosis and pulmonary embolism in patients who have undergone hip replacement surgery. overall, in re-novate and re-novate ii, the median treatment duration was 33 days for dabigatran etexilate capsules and 33 days for enoxaparin. a total of 5,428 patients were treated with a mean age of 63.2 years. the patient population was 45.3% male, 96.1% white, 3.6% asian, and 0.4 % black. the concomitant diseases of patients in these trials included hypertension (46.1%), venous insufficiency (15.4%), coronary artery disease (8.2%), diabetes mellitus (7.9%), reduced renal function (5.3%), heart failure (3.4%), gastric or duodenal ulcer (3.0%), vte (2.7%), and malignancy (0.1%). concomitant medications included cardiac therapy (69.7%), nsaids (68%), vasoprotectives (29.7%), agents acting on renin-angiotensin system (29.1%), beta-blockers (21.5%), diuretics (20.8%), lipid modifying agents (18.2%), any antithrombin/anticoagulant (16.0%), calcium channel blockers (13.6%), low molecular weight heparin (7.8%), aspirin (7.0%), platelet inhibitors excluding asa (6.9%), other antihypertensives (6.7%), and peripheral vasodilators (2.6%). for efficacy evaluation all patients were to have bilateral venography of the lower extremities at 3 days after last dose of study drug unless an endpoint event had occurred earlier in the study. in the primary efficacy analysis, dabigatran etexilate capsules 110 mg orally 1-4 hours after surgery followed by 220 mg daily was non-inferior to enoxaparin 40 mg once daily in a composite endpoint of confirmed vte (proximal or distal dvt on venogram, confirmed symptomatic dvt, or confirmed pe) and all cause death during the treatment period (tables 16 and 17). in the studies 2,628 (76.5%) patients in re-novate and 1,572 (78.9%) patients in re-novate ii had evaluable venograms at study completion. table 16 primary efficacy endpoint for re-novate dabigatran etexilate capsules 220 mg n (%) enoxaparin n (%) number of patients a n=880 n= 897 primary composite endpoint 53 (6.0) 60 (6.7) risk difference (%) vs enoxaparin (95% ci) -0.7 (-2.9, 1.6) number of patients n=909 n= 917 composite endpoint of major vte b and vte related mortality 28 (3.1) 36 (3.9) number of patients n=905 n= 914 proximal dvt 23 (2.5) 33 (3.6) number of patients n=874 n= 894 total dvt 46 (5.3) 57 (6.4) number of patients n=1,137 n= 1,142 symptomatic dvt 6 (0.5) 1 (0.1) pe 5 (0.4) 3 (0.3) death 3 (0.3) 0 a full analysis set (fas): the fas included all randomized patients who received at least one subcutaneous injection or one oral dose of study medication, underwent surgery and subjects for whom the presence or absence of an efficacy outcome at the end of the study was known, i.e., an evaluable negative venogram for both distal and proximal dvt in both legs or any of the following: positive venography in one or both legs, or confirmed symptomatic dvt, pe, or death during the treatment period. b vte is defined as proximal dvt and pe table 17 primary efficacy endpoint for re-novate ii dabigatran etexilate capsules 220 mg n (%) enoxaparin n (%) number of patients a n=792 n= 786 primary composite endpoint 61 (7.7) 69 (8.8) risk difference (%) vs enoxaparin (95% ci) -1.1 (-3.8, 1.6) number of patients n=805 n= 795 composite endpoint of major vte b and vte related mortality 18 (2.2) 33 (4.2) number of patients n=804 n= 793 proximal dvt 17 (2.1) 31 (3.9) number of patients n=791 n= 784 total dvt 60 (7.6) 67 (8.5) number of patients n=1,001 n= 992 symptomatic dvt 0 4 (0.4) pe 1 (0.1) 2 (0.2) death 0 1 (0.1) a full analysis set (fas): the fas included all randomized patients who received at least one subcutaneous injection or one oral dose of study medication, underwent surgery and subjects for whom the presence or absence of an efficacy outcome at the end of the study was known, i.e., an evaluable negative venogram for both distal and proximal dvt in both legs or any of the following: positive venography in one or both legs, or confirmed symptomatic dvt, pe, or death during the treatment period. b vte is defined as proximal dvt and pe 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.

inistration (2.5)] bleeding inform patients that they may bleed more easily, may bleed longer, and should call their healthcare provider for any signs or symptoms of bleeding [see warnings and precautions (5.2)]. instruct patients to seek emergency care right away if they have any of the following, which may be a sign or symptom of serious bleeding: unusual bruising (bruises that appear without known cause or that get bigger) pink or brown urine red or black, tarry stools coughing up blood vomiting blood, or vomit that looks like coffee grounds instruct patients to call their healthcare provider or to get prompt medical attention if they experience any signs or symptoms of bleeding: pain, swelling or discomfort in a joint headaches, dizziness, or weakness reoccurring nose bleeds unusual bleeding from gums bleeding from a cut that takes a long time to stop menstrual bleeding or vaginal bleeding that is heavier than normal if patients have had neuraxial anesthesia or spinal puncture, and particularly, if they are taking concomitant nsaids or platelet inhibitors, advise patients to watch for signs and symptoms of spinal or epidural hematoma, such as back pain, tingling, numbness (especially in the lower limbs), muscle weakness, and stool or urine incontinence. if any of these symptoms occur, advise the patient to contact his or her physician immediately [see boxed warning] . gastrointestinal adverse reactions instruct patients to call their healthcare provider if they experience any signs or symptoms of dyspepsia or gastritis: dyspepsia (upset stomach), burning, or nausea abdominal pain or discomfort epigastric discomfort, gerd (gastric indigestion) [see adverse reactions (6.1)] invasive or surgical procedures instruct patients to inform their healthcare provider that they are taking dabigatran etexilate capsules before any invasive procedure (including dental procedures) is scheduled [see dosage and administration (2.8)] . concomitant medications ask patients to list all prescription medications, over-the-counter medications, or dietary supplements they are taking or plan to take so their healthcare provider knows about other treatments that may affect bleeding risk (e.g., aspirin or nsaids) or dabigatran exposure (e.g., dronedarone or systemic ketoconazole) [see warnings and precautions (5.2, 5.5)] . prosthetic heart valves instruct patients to inform their healthcare provider if they will have or have had surgery to place a prosthetic heart valve [see warnings and precautions (5.4)] . allergic reactions advise adult patients and caregivers that some adults taking dabigatran etexilate capsules have developed symptoms of an allergic reaction. advise adult patients or caregivers to inform their healthcare provider if they develop symptoms of an allergic reaction, such as hives, rash, or itching. advise adult patients or caregivers to seek emergency medical attention if they develop chest pain or tightness, swelling of the face or tongue, trouble breathing or wheezing, or feeling dizzy or faint. pregnancy advise patients to inform their healthcare provider immediately if they become pregnant or intend to become pregnant during treatment with dabigatran etexilate capsules [see use in specific populations (8.1)]. lactation advise patients not to breastfeed if they are taking dabigatran etexilate capsules [see use in specific populations (8.2)]. 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. manufactured by: alkem laboratories ltd., india. distributed by: ascend laboratories, llc parsippany, nj 07054 revised: june, 2022