FONDAPARINUX PACKAGE INSERT PDF

The recommended dose of fondaparinux is mg once daily administered .. Instruction for self-administration is mentioned in the Package Leaflet. The needle. Mylan manufactures ARIXTRA®* (fondaparinux sodium) Injection, Solution ( Arixtra) in strengths of 25 mg05 mL 5 mgmL5 Category: Human Prescription Drug. Each pre-filled automatic safety syringe contains mg of fondaparinux .. 72 hours after the first study drug administration and continued for 90 ± 7 days, with regular .. Insert the full length of the needle perpendicularly (at an angle of.

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If you are not sure whether you should start using Arixtra, talk to your doctor or pharmacist. Arixtra contains the medication fondaparinux sodium, a synthetic compound which helps prevent blood clots forming in blood vessels.

The CMI and the CMI Search are not intended to be used by consumers to diagnose, treat, cure or prevent any disease or for any therapeutic purpose. Information and interactions contained in this Web site are for information purposes only and are not intended to be used to diagnose, treat, cure or prevent any disease.

Treatment and Prevention of Heparin Induced Thrombocytopenia: If you are about to be started on any new medicine, tell your doctor, dentist or pharmacist that you are using Arixtra. However, they are also known to cause clinically relevant side effects, or adverse drug events, such as bleeding including hemorrhagic stroke, gastrointestinal bleeding, osteoporosis long-term usepriapism, and fodaparinux from inhibition of aldosterone synthesis.

Dietary clues to a healthy microbiome. The effects of low molecular weight and standard heparin on calcium loss from fetal rat calvaria. If you use this medicine after the expiry date has passed, it may not work as well as it should. If you have not told your doctor or pharmacist about any of the above, tell them before you start using Arixtra. The incidence of HIT is greatest in unfractionated heparin use beyond 4 packags at therapeutic doses.

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Arixtra is not recommended for use during pregnancy, unless you and your doctor or pharmacist have discussed the risks and benefits involved.

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It is not known whether Arixtra passes into human breast milk. Arixtra is used to prevent blood clots forming in patients who are recovering from orthopaedic or abdominal surgery.

The use of anticoagulants, such as unfractionated heparin UFH and low-molecular weight heparin LMWH have significantly improved patient oriented outcomes for medical conditions related to thrombotic events. Further, the accuracy, currency and completeness of the information available on this Web site cannot be guaranteed. All medicines have risks and benefits.

You may need urgent medical attention. Antibodies to macromolecular platelet factor 4-heparin complexes in heparin-induced thrombocytopenia: Do not use Arixtra if you are breast-feeding or plan to breast-feed. Fondaparinux Arixtra is an anticoagulant that shares the same pentasaccharide sequence as UFH and LMWH for the binding to antithrombin, however it has no extra chain and thus, is not considered a heparin product.

Do not use Arixtra to treat any other complaints unless your doctor or pharmacist tells you to.

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CMI is supplied by the relevant pharmaceutical company for each consumer medical product. If you get any side effects, do not stop using Arixtra without first talking to your doctor or pharmacist.

Explanation The use of anticoagulants, such as unfractionated heparin UFH and low-molecular weight heparin LMWH have significantly improved patient oriented outcomes for medical conditions related to thrombotic events. Do not be alarmed by this list of possible side effects. Symptoms of an allergic reaction to Arixtra may include skin rash, itchiness, shortness of breath, or difficulty breathing.

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Fondaparinux (Arixtra)

Tell your doctor or pharmacist if you are elderly or have a low body weight less than 50 kg as you may be at increased risk of fonvaparinux if you are given Arixtra. Iinsert injection should be kept at room temperature less than 25 degrees C. Do not use Arixtra after the expiry date EXP printed on the pack. Serious side effects are rare. Treatment and prevention of heparin-induced thrombocytopenia: You may not experience any of them.

Please enter text to search. As noted above, the length of the chain which influences the molecular weight contributes, in part, to heparin’s ability to bind to PF4 that triggers the immune mediated response seen in HIT. Arixtra may be given for up to 31 days.

Arixtra Solution for injection –

Some medicines and Arixtra may interfere with each other. Instructions on how to use the Arixtra syringe are contained in the package insert in each Arixtra carton.

Arixtra is given to you as a subcutaneous injection an injection just under the skin. Sometimes they are serious, most of ffondaparinux time they are not. It is recommended that your doctor monitor’s your fondalarinux platelets at the beginning and end of your treatment with Arixtra. Tell your doctor or pharmacist if you notice anything that is making you feel unwell.

Linkins LA et al. Ask your doctor or pharmacist if you have any concerns. Arixtra should not be given as an intramuscular injection an injection into the muscle.

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