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Octanate 500 IU/10 ml is a Product of the Generic Human Coagulation Factor VIII

Octanate 500 IU/10 ml belongs to the generic category of Human Coagulation Factor VIII. This medicine should be used according to a doctor's advice. We have provided detailed information about the uses, dosage, effectiveness, side effects, precautions, drug interactions, storage conditions, and other important details of Octanate 500 IU/10 ml. Our goal is to present essential medicine information in one place for patients, caregivers, and healthcare professionals. To better understand Human Coagulation Factor VIII and ensure the safe use of this medicine, please read the information below carefully and consult a healthcare professional when necessary.

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Octanate 500 IU/10 ml

City Overseas Ltd. (Mfg. by: Octapharma S.A.S., France) · IV Infusion

Generic

Human Coagulation Factor VIII

Strength500 IU/10 ml
Unit Price
11000

/ 500 IU vial

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Description of Octanate 500 IU/10 ml

Octanate 500 IU/10 ml may be available as a prescription or over-the-counter medicine, depending on local regulations and medical recommendations. It is used for the treatment and management of specific conditions or symptoms. The way this medicine is used may vary depending on the patient's condition and the advice of a healthcare provider. Detailed information about the approved uses, therapeutic applications, and other relevant details of Octanate 500 IU/10 ml is provided below to help users gain a clear understanding of this medicine.

What Is Octanate 500 IU/10 ml Indications and Uses?

Octanate belongs to a group of medicines called clotting factors and contains human blood coagulation factor VIII. This is a special protein involved in blood clotting. Octanate is used to treat and prevent bleeding in patients with haemophilia A. This is a condition in which bleeding can go on for longer than expected. It is due to an hereditary lack of coagulation factor VIII in the blood.


Dosage And Administration of Octanate 500 IU/10 ml

Dosage for the prevention of bleeding: If you suffer from severe haemophilia A you should inject 20 to 40 IU of factor VIII per kg body weight every two or three days for long-term prevention. Your dosage should be adjusted according to your response. In some cases shorter dosage intervals or higher dosages may be necessary.Dosage calculation: Always use Octanate exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure. Factor VIII activity refers to the amount of factor VIII present in the plasma. It is expressed either as a percentage (relative to normal human blood plasma) or in International Units (IU). The dosage of factor VIII is expressed in IU. One IU of factor VIII activity is equivalent to the amount of factor VIII in one ml of normal human blood plasma. One IU of factor VIII per kg body weight raises the plasma factor VIII activity by 1.5%-2% of normal activity. To calculate your dosage, the level of factor VIII activity in your blood plasma is measured. This will indicate by how much the activity needs to be increased. Please consult your doctor if you are uncertain how much your factor VIII activity has to be increased or how to calculate your dosage.


Drug Interactions of Octanate 500 IU/10 ml

No interactions of Moroctocog alfa (AF-CC) (r-DNA origin) with other medicinal products have been reported.


Side Effects of Octanate 500 IU/10 ml

Like all medicines, this medicine can cause side effects, although not everybody gets them. Even though rare (may affect up to 1 in 1,000 people), hypersensitivity or allergic reactions have been observed in patients treated with factor VIII containing products. Contact your doctor if you suffer from the symptoms: being sick (vomiting), burning and stinging at the infusion site, chest tightness, chills, faster heart beat (tachycardia), feeling sick (nausea), feeling of pins and needles (tingling), flushing, headache, hives (urticaria), low blood pressure (hypotension), rash, restlessness, swelling of the face, lips, mouth, tongue or throat which may cause difficulty in swallowing or breathing (angioedema), tiredness (lethargy), wheezing. In very rare (may affect up to 1 in 10,000 people) cases, this hypersensitivity may lead to a severe life-threatening allergic reaction called anaphylaxis, which may include shock, as well as some or all of the symptoms described above. In this case please contact your doctor immediately or call for an ambulance.


Use During Pregnancy and Lactation

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.


Precautions And Warnings for Octanate 500 IU/10 ml

In order to improve traceability of biological medicinal products, the name and the batch number of the administered product should be clearly recorded. It is strongly recommended that every time Moroctocog alfa (AF-CC) (r-DNA origin) is administered to a patient, the name on the carton and batch number of the product are recorded in order to maintain a link between the patient and the batch number of the medicinal product. Patients can affix one of the peel-off labels found on the vial or prefilled syringe to document the batch number in their diary or for reporting any side effects


Therapeutic Class

Anti-fibrinolytic drugs


Storage Conditions of It

Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date, which is stated on the label. The expiry date refers to the last day of that month. Store at 2°C-8°C. Do not freeze. Keep the vials in the outer carton in order to protect from light. Use the reconstituted solution immediately and for single use only. Do not use this medicine if you notice cloudy or incompletely dissolved solutions. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help to protect the environment.

Data Source: Data source of Indications and Usages, Pharmacology, Dosage & Administration, Drug Interactions, Side Effects, Use during Pregnancy & Lactation, Precautions & Warnings, Use in Special Populations, Therapeutic Class, and Storage Conditions is the concerned medicine company or respective organization.

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The information provided on All Samadhan is intended for general informational purposes only and is prepared based on our best practices. It is not a substitute for professional medical advice, diagnosis, or treatment. While we strive to keep the information accurate and up to date, we do not guarantee its completeness or accuracy. The absence of specific information or warnings about any medicine or service should not be considered as an assurance or endorsement by All Samadhan. All Samadhan shall not be held responsible for any consequences arising from the use of this information. We strongly recommend consulting a qualified healthcare professional or physician for any medical concerns, questions, or clarifications.All Samadhan is a digital healthcare software platform operated by MS Genius Experts. We provide technology solutions for pharmacies and healthcare providers; we are not a direct seller or dispenser of prescription medicines

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