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Arixtra is an anticoagulant: it prevents the blood from coagulating (clotting). The active ingredient in Arixtra, fondaparinux sodium, stops one of the substances (factors) that are involved in the clotting of blood, factor Xa. When this is blocked, no thrombin (another factor) can be produced, and no clot can be formed.
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Fondaparinux injection. Fondaparinux is a medication that prevents blood clotting after knee, hip or abdominal surgery. Blood clots happen when your blood thickens. This can be dangerous when clots form in the arteries or veins. The brand name of this medication is Arixtra®.
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ARIXTRA is supplied as a sterile, preservative-free injectable solution for subcutaneous use. Each single-dose, prefilled syringe of ARIXTRA, affixed with an automatic needle protection system, contains 2.5 mg of fondaparinux sodium in 0.5 mL, 5.0 mg of fondaparinux sodium in 0.4 mL, 7.5 mg of fondaparinux sodium in 0.6 mL, or 10.0 mg of fondaparinux sodium in 0.8 mL of an isotonic solution of.
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No. Fondaparinux (Arixtra) is a lab-made version of a part of heparin, so it has a very similar structure to heparin and has similar properties as heparin. But fondaparinux (Arixtra) and heparin are two different medications. Both are injectable blood thinners that are given under the skin in the stomach, but heparin can also be given as an injection into the veins (IV) for certain situations.
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Arixtra side effects. Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.. Also seek emergency medical attention if you have symptoms of a spinal blood clot: back pain, numbness or muscle weakness in your lower body, or loss of bladder or bowel control.. Arixtra can cause you to bleed more easily.
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Prophylaxis. >50 kg: 2.5 mg SC once daily for 5-9 days or up to 10 days following abdomonal surgery; for hip replacement, 11 days recommended and a minimum 10-14 days recommended for patients undergoing total hip or knee arthroplasty, or hip fracture surgery; administered for up to 35 days in some instances.
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Arixtra was at least as effective as enoxaparin in preventing death or an ischaemic event in patients with unstable angina or myocardial infarction without ST-segment elevation, with around 5% of the patients in each group had died or had an ischaemic event after nine days. In the study of myocardial infarction with ST-segment elevation.
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Adult: 2.5 mg once daily for 30-45 days. Adult: <50 kg: 5 mg once daily; 50-100 kg: 7.5 mg once daily; >100 kg: 10 mg once daily. Treatment duration: 5-9 days, or until oral anticoagulation is established. Adult: 2.5 mg once daily, starting 6-8 hr after surgery, continue for at least 5-9 days. In high-risk patients, 6-14 days or up to 32 days.
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Penggunaan injeksi Arixtra mungkin akan menimbulkan reaksi alergi pada beberapa orang seperti: Ruam dan gatal pada area bekas suntikan. Nyeri otot. Sulit bernafas. Pembengkakan pada wajah, bibir, lidah. Efek samping yang bisa saja timbul selama penggunaan Arixtra, yaitu: Demam.
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In patients with acute symptomatic DVT and in patients with acute symptomatic PE, the recommended dose of ARIXTRA is 5 mg (body weight <50 kg), 7.5 mg (body weight 50 to 100 kg), or 10 mg (body weight >100 kg) by subcutaneous injection once daily (ARIXTRA treatment regimen). Initiate concomitant treatment with warfarin sodium as soon as.
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Arixtra injeksi 7.5 mg/0.6 mL, 2 × 1's (Rp690,000/pak) Apa Nama Perusahaan Produsen Arixtra? Produsen obat (perusahaan farmasi) adalah suatu perusahaan atau badan usaha yang melakukan kegiatan produksi, penelitian, pengembangan produk obat maupun produk farmasi lainnya. Obat yang diproduksi bisa merupakan obat generik maupun obat bermerek.
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ST segment elevation MI 2.5 mg once daily w/ 1st dose administered IV & subsequent doses administered SC. Initiate treatment as soon as possible following diagnosis & continued for up to 8 days or until hospital discharge. DVT & PE >100 kg 10 mg SC once daily, 50-100 kg 7.5 mg SC once daily, <50 kg 5 mg SC once daily.
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ARIXTRA Injection is providedin a single-dose, prefilled syringe affixed with an automatic needle protection system. ARIXTRA is administered by subcutaneous injection. It must not be administered by intramuscular injection. ARIXTRA is intended for use under a physician's guidance.
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Menggunakan obat ini dengan dosis yang berlebihan dapat menyebabkan berbagai efek samping pada kesehatan. Arixtra dapat memicu munculnya reaksi alergi, seperti kesulitan bernapas dan pembengkakan pada beberapa bagian tubuh, seperti bibir, wajah, lidah, hingga tenggorokan. Kamu juga disarankan untuk segera mengunjungi rumah sakit dan lakukan.