The discontinuation rate due to bleeding events was approximately 1% in the ELIQUIS-treated patients compared to 0.4% in those patients in the placebo group in the AMPLIFY-EXT study. Fatigue is found among people who take Eliquis, especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months. The safety of ELIQUIS has been evaluated in 1 Phase II and 3 Phase III studies including 5924 patients exposed to ELIQUIS 2.5 mg twice daily undergoing major orthopedic surgery of the lower limbs (elective hip replacement or elective knee replacement) treated for up to 38 days. Learn more about Eliquis (apixaban) at EverydayHealth.com. * All bleeding criteria included surgical site bleeding. Bleeding; INFREQUENT side effects. DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), bleeding from wounds or needle injections, any bleeding that will not stop; headache, dizziness, weakness, feeling like you might pass out; black or bloody stools, coughing up blood or vomit that looks like coffee grounds. Table 3: Bleeding During the Treatment Period in Patients Undergoing ARISTOTLE Study Design. None of them are perfect solutions that have not had reported side effects. Because clinical trials are conducted under widely varying conditions, adverse reaction 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. common (1% to 10%): Dizziness, headache, fatigue, syncope, Common (1% to 10%): Cataract, conjunctival hemorrhage, eye hemorrhageischemic stroke, vertigo These occur in 1-10% of patients with side effects. Table 8: Adverse Reactions Occurring in ≥1% of Patients Undergoing Extended Treatment for DVT and PE in the AMPLIFY-EXT Study. Increased risk of thrombotic events after premature discontinuation [see, Spinal/epidural anesthesia or puncture [see. My Eliquis side effects were chest pain, body aches, and fatigue. The most common reason for treatment discontinuation in both studies was for bleeding-related adverse reactions; in ARISTOTLE this occurred in 1.7% and 2.5% of patients treated with ELIQUIS and warfarin, respectively, and in AVERROES, in 1.5% and 1.3% on ELIQUIS and aspirin, respectively. Complete Blood Count (CBC): Test, Types, Ranges, and Chart. Eliquis. … And studies … Take note that if your doctor or physician prescribed you with Eliquis, he/she knows that the benefit you will get from the prescription medication is far more significant compared to the risk of side effects. All rights reserved. Eliquis(Apixaban Tablets) side effects drug center, Medical Editor: John P. Cunha, DO, FACOEP. Prolonged loss of blood, secondary to hemorrhage and internal bleed, can result in anemia, pale skin, exacerbation of shortness of breath, poor endurance, and fatigue. Our Eliquis (apixaban) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication. Figure 1: Major Bleeding Hazard Ratios by Baseline Characteristics – ARISTOTLE Study, Table 2: Bleeding Events in Patients with Nonvalvular Atrial Fibrillation in AVERROES. 1. The study uses data from the FDA. Adverse reactions occurring in ≥1% of patients undergoing hip or knee replacement surgery in the 1 Phase II study and the 3 Phase III studies are listed in Table 4. Apixaban is also used to prevent deep vein thrombosis (DVT; a blood clot, usually in the leg) and pulmonary embolism (PE; a blood clot in the lung) in people who are having hip replacement or knee replacement surgery. Eliquis side effects should be fully considered by anyone who is considering taking the medication to improve their health. You may report side effects … It is recommended that patients use the information presented as a part of a broader decision-making process. Different individuals may respond to medication in different ways. Eliquis (Apixaban) is an oral antiplatelet belonging to the class of direct factor Xa inhibitors. Adverse reactions occurring in ≥1% of patients in the AMPLIFY study are listed in Table 6. It is manufactured by Bristol-Myers Squibb and Pfizer under the trade name Eliquis. generic drugs) are not considered. I was finally switched to Savaysa (edoxaban) and those side effects … Bleeding was assessed in each study beginning with the first dose of double-blind study drug. 95,464 people reported to have side effects when taking Eliquis. The discontinuation rate due to bleeding events was 0.7% in the ELIQUIS-treated patients compared to 1.7% in enoxaparin/warfarin-treated patients in the AMPLIFY study. In total, 11% of the patients treated with ELIQUIS 2.5 mg twice daily experienced adverse reactions.
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