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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Arixtra should not be given fondparinux an intramuscular injection an injection into the muscle. Do not use Arixtra to treat any other complaints flndaparinux your doctor or pharmacist tells you to. 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. Ask your doctor if you have any questions about why Arixtra has been prescribed for you. Treatment and prevention of heparin-induced thrombocytopenia: Do not use Arixtra after the expiry date EXP printed on the pack. Arixtra is supplied in Australia by: The incidence of HIT is greatest in unfractionated heparin use beyond 4 days at therapeutic doses.
It is not known whether Arixtra passes into human breast milk. For example, it is known that unfractionated heparin use, especially beyond 4 days of treatment, is known to have a greater risk for causing HIT when compared to LMWH dalteparin, enoxaparin, and tinzaparin.
This web site is intended for Australian residents and is not a substitute for independent professional advice. Surf therapy can help depression and PTSD. 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 fonfaparinux injection just fondapparinux the skin. New cancer test is as good as gold. There are number of risk factors associated with increasing the chance for a patient to develop HIT, one of which is the type of anticoagulant used.
Symptoms of an allergic reaction to Arixtra may include packqge rash, itchiness, shortness of breath, or difficulty breathing. You may need urgent medical attention. Your doctor or pharmacist may have more information on medicines to be careful with or to avoid while using Arixtra.
Arixtra may be given for up to 31 days. You may need medical treatment if you get some of the side effects. 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.
While low-molecular weight heparins LMWH can also cause HIT, the incidence is much lower and appears to be related, in part, to the molecular weight. MIMS Australia uses its best endeavours to ensure that at the time of publishing, as indicated on the publishing date for each resource e.
The effects of low molecular weight and standard heparin on calcium loss from fetal rat calvaria. Your doctor or pharmacist will discuss the possible risks and benefits of using Arixtra during pregnancy.
If you have not told your doctor or pharmacist about any of the above, tell them before you start using Arixtra. Your doctor or pharmacist will discuss the possible risks and benefits of using Arixtra during breast-feeding.
Arixtra Solution for injection –
Do not use Arixtra if you are pregnant or intend to become pregnant. Please enter text to search. If your doctor or pharmacist tells you to stop using Arixtra or the injections have passed inxert expiry date, ask your pharmacist what to do with any that are left over.
Other side effects not listed above may occur in some patients. It is recommended that your doctor monitor’s your blood platelets at the beginning and end of your treatment with Arixtra.
Further, the accuracy, currency and completeness of the information available on this Web site cannot be guaranteed. Treatment and Prevention of Heparin Induced Thrombocytopenia: CMI is supplied by the relevant pharmaceutical company for each consumer medical product.
Your doctor or pharmacist has weighed the risks of you using Arixtra against the benefits they expect it will have for you.
Research Triangle Park, NC. All copyright and responsibility for CMI is that of the relevant pharmaceutical company.
Fondaparinux (Arixtra) | – A Hematology Oncology Wiki
These may be signs of serious side effects. Serious side effects are rare. Arixtra is also used to treat blood clots once they have formed. You may wish to keep it to read again. Arixtra will normally be stored in the pharmacy or on the hospital ward.
You may also like. The reference to the chain is related to the part of the heparin molecule attached to the pentasaccharide sequence that is used in binding to antithrombin when exerting imsert antithrombotic effect. Consumers should be aware that the information provided by the Consumer Medicines Information CMI search CMI Search is for information purposes only and consumers should continue to obtain professional advice from a qualified healthcare professional regarding any condition for which they have searched for CMI.
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 bleeding if you are given Arixtra.
Information and interactions contained in this Web site are for information purposes only fondaparimux are not intended to be used to diagnose, treat, cure or prevent any disease. Linkins LA et al.
The usual dose of Arixtra is 2. If you have epidural or spinal anaesthesia a pain killing injection around the spinal cordtell your doctor or nurse immediately if you have back pain, numbness or weakness in the legs, or fondaparinjx with bowel or bladder function.