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About ARIXTRA 7.5MG INJECTION
ARIXTRA 7.5MG INJECTION belongs to a class of drugs called anticoagulants (blood thinner) primarily used to prevent/treat deep vein thrombosis (blood clots in leg veins), pulmonary embolism (blood clots in the lung), heart attack, and severe angina. It also reduces the risk of blood clots after orthopedic (such as hip or knee surgery), or abdominal surgery. ARIXTRA 7.5MG INJECTION prevents blood clot formation during and shortly after restricted movement because of an acute illness. Deep vein thrombosis is a medical condition in which blood clots form in deep veins, usually in the legs. Pulmonary embolism is a condition in which a blood clot blocks the arteries in the lungs.
ARIXTRA 7.5MG INJECTION contains ‘Fondaparinux sodium’ that works by inhibiting the action of clotting factors (a natural substance in the blood that causes clotting). Thereby preventing the conversion of fibrinogen to fibrin (a protein that binds platelets together and forms a clot) and helping prevent blood clot formation. It eases blood flow through the veins, making it less likely to develop a severe blood clot.
ARIXTRA 7.5MG INJECTION will be administered by a trained healthcare professional; hence do not self-administer. Some people may experience unusual bleeding, anemia (low number of red blood cells), bruising or swelling. Most of these side effects of ARIXTRA 7.5MG INJECTION do not require medical attention and gradually resolve over time. However, if the side effects persist or worsen, please consult your doctor.
If you are pregnant or breastfeeding, it is advised to consult a doctor before using ARIXTRA 7.5MG INJECTION. ARIXTRA 7.5MG INJECTION is not recommended for children below 17 years of age. ARIXTRA 7.5MG INJECTION should be used with caution in the elderly above 60, as they may be at high risk of bleeding. If you have a stomach ulcer, kidney or liver problems, high blood pressure, or bleeding problems, inform your doctor before receiving ARIXTRA 7.5MG INJECTION. If you are about to undergo surgery, inform your doctor about the treatment with ARIXTRA 7.5MG INJECTION. Keep your doctor informed about your health condition and medications to rule out any interactions.
Uses of ARIXTRA 7.5MG INJECTION
Directions for Use
Medicinal Benefits
ARIXTRA 7.5MG INJECTION belongs to a class of drugs known as anticoagulants or blood thinners. ARIXTRA 7.5MG INJECTION contains ‘Fondaparinux sodium’ used to prevent deep vein thrombosis (blood clot in the blood vessels of legs) and pulmonary embolism (blood clot in the blood vessels lungs). It also reduces the risk of blood clots during orthopedic (such as hip or knee surgery), abdominal surgery, or restricted movement because of an acute illness. ARIXTRA 7.5MG INJECTION works by stopping the action of clotting factor Xa (a natural substance in the blood that causes clotting). This inhibits fibrin production (a protein that binds platelets together and forms a clot), preventing blood clot formation. ARIXTRA 7.5MG INJECTION is also used to treat certain types of heart attack and chest pain called unstable angina.
How ARIXTRA 7.5MG INJECTION Works
Storage
What if I have taken an overdose of ARIXTRA 7.5MG INJECTION
Drug Warnings
Do not receive ARIXTRA 7.5MG INJECTION if you are allergic to any of the contents; if you are bleeding excessively, have a bacterial heart infection, or have very severe kidney disease. If you are pregnant or breastfeeding, it is advised to consult a doctor before using ARIXTRA 7.5MG INJECTION. ARIXTRA 7.5MG INJECTION is not recommended for children as safety and effectiveness have not been established. ARIXTRA 7.5MG INJECTION should be used with caution in the elderly above 65, as they may be at high risk of bleeding. If you are about to undergo any surgery, inform your doctor that you are receiving ARIXTRA 7.5MG INJECTION. If you notice bleeding gums, blood in urine, coughing up blood or vomit that looks like coffee grounds, pain, swelling, dizziness, weakness, unusual bruising, nose bleeds, abnormal vaginal bleeding or heavy menstrual periods, bloody or tarry stools, please consult a doctor immediately. Avoid alcohol consumption during treatment with ARIXTRA 7.5MG INJECTION as it may increase the risk of stomach bleeding. Inform your doctor before receiving ARIXTRA 7.5MG INJECTION if you have a stomach ulcer, kidney or liver problems, high blood pressure, bleeding problems, are 75 years or older, or weigh less than 50kg. Do not discontinue using ARIXTRA 7.5MG INJECTION without consulting your doctor, as this may increase your chances of having another heart attack or stroke.
Drug-Drug Interactions
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Drug-Food Interactions
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Diet & Lifestyle Advise
Habit Forming
Therapeutic Class
Product Substitutes
Alcohol
Unsafe
You are recommended to avoid consuming alcohol with ARIXTRA 7.5MG INJECTION as it may increase the risk of bleeding.
Pregnancy
Caution
Please inform your doctor if you are pregnant or planning pregnancy. Your doctor will prescribe only if it is clearly necessary.
Breast Feeding
Caution
Breastfeeding is not recommended during treatment with ARIXTRA 7.5MG INJECTION. If you are a nursing mother, inform your doctor before receiving this injection.
Driving
Caution
It is unknown if ARIXTRA 7.5MG INJECTION affects your ability to drive or operate machinery. Therefore, drive or operate machinery only if you are alert.
Liver
Caution
ARIXTRA 7.5MG INJECTION should be used with caution, especially if you have a history of liver diseases. Your doctor may adjust the dose if required based on your condition.
Kidney
Caution
ARIXTRA 7.5MG INJECTION should be administered with caution if you have a history of kidney diseases. Your doctor may adjust the dose if required based on your condition. This medicine is not recommended for patients with severe kidney disease.
Children
Caution
ARIXTRA 7.5MG INJECTION is not recommended for children below 17 years of age as safety and effectiveness have not been established.
Have a query?
ARIXTRA 7.5MG INJECTION belongs to a class of drugs called anticoagulants (blood thinner) primarily used to prevent/treat deep vein thrombosis (blood clots in leg veins), pulmonary embolism (blood clots in the lung), heart attack, and severe angina. It also reduces the risk of blood clots after orthopedic (such as hip or knee surgery), or abdominal surgery. ARIXTRA 7.5MG INJECTION prevents blood clot formation during and shortly after restricted movement because of an acute illness.
ARIXTRA 7.5MG INJECTION stops the action of clotting factors. This prevents the formation of unwanted blood clots (thrombosis) in the blood vessels.
If you have diabetes, inform your doctor before receiving ARIXTRA 7.5MG INJECTION. ARIXTRA 7.5MG INJECTION should be used with caution in diabetic patients as they may be at increased risk of bleeding. Regular blood tests are advised to monitor blood clotting time while receiving ARIXTRA 7.5MG INJECTION.
You are not recommended to take aspirin with ARIXTRA 7.5MG INJECTION as co-administration of these two medicines may increase the risk of haemorrhage. However, please consult a doctor immediately if you notice blood in urine or stools, dizziness, unusual bleeding or bruising, vomiting, weakness or headache. If you are supposed to use these medicines together, you are advised to contact your doctor so that the dose may be adjusted appropriately.
Yes, ARIXTRA 7.5MG INJECTION may increase the risk of bleeding, and the effects of ARIXTRA 7.5MG INJECTION may last for four days even after discontinuation. Always be careful while doing activities that may cause injury or bleeding. Please inform your doctor immediately if you notice purple spots on the skin, unusual bruising, blood in urine, black tarry stools, or unusual bleeding from the gums or nose.
Tests such as platelet count, factor V assay, fibrinogen level test, prothrombin time test (PT or PT-INR), and the INR (international normalized ratio) are used to determine blood clotting time.
You are usually not advised to have a tattoo or body piercing while receiving ARIXTRA 7.5MG INJECTION as it may increase the risk of bleeding and infection. If you still wish to proceed further, contact your doctor to adjust the dose, or any antibiotics may be prescribed. Let the piercer or tattooist know in advance that you are on treatment with a blood thinner.
Please consult your doctor if you are due to undergo any surgery. The doctor might stop the administration of ARIXTRA 7.5MG INJECTION a few days before surgery as it can cause an increased risk of bleeding during surgery.
No, you should not take ARIXTRA 7.5MG INJECTION with OTC painkillers as it may cause interactions. Consult the doctor if you have any odd pain.
No, you should not self-administer ARIXTRA 7.5MG INJECTION because some people may experience anemia (low number of red blood cells), unusual bleeding, bruising or swelling. It should be administered by the doctor or nurse to prevent adverse effects.
Excessive menstrual bleeding while taking ARIXTRA 7.5MG INJECTION may be concerning, as this medication increases the risk of bleeding due to its anticoagulant effect. It’s important to consult the doctor if you have excessive bleeding, as they may need to evaluate your condition and adjust your treatment to ensure your safety.
The long-term use of ARIXTRA 7.5MG INJECTION will be based on your specific clotting disorder and risk factors. The doctor will assess the risks and benefits and determine how long the treatment should be continued. Consult the doctor if you have any concerns.
Yes, ARIXTRA 7.5MG INJECTION may increase the risk of bleeding, with its effects lasting up to four days after discontinuing the medication. Take extra caution during activities that might cause injury or bleeding.
The side effects of ARIXTRA 7.5MG INJECTION include anaemia (low number of red blood cells), unusual bleeding, bruising or swelling. Consult the doctor if any of these symptoms persist or worsen.
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