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Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml is a Product of the Generic Fondaparinux Sodium

Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml belongs to the generic category of Fondaparinux Sodium. 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 Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml. Our goal is to present essential medicine information in one place for patients, caregivers, and healthcare professionals. To better understand Fondaparinux Sodium 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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Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml

Square Pharmaceuticals PLC. · Ophthalmic Solution

Generic

Fondaparinux Sodium

Strength2.5 mg/0.5 ml
Unit Price
৳ 800

/ 0.5 ml pre-filled syringe

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Description of Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml

Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 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 Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml is provided below to help users gain a clear understanding of this medicine.

What Is Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml Indications and Uses?

Fonidel is a Factor Xa inhibitor (anticoagulant) indicated for: Prophylaxis of deep vein thrombosis (DVT) in patients undergoing- hip fracture surgery (including extended prophylaxis) hip replacement surgery knee replacement surgery or abdominal surgery. Treatment of Prophylaxis of deep vein thrombosis (DVT) or acute pulmonary embolism (PE) when administered in conjunction with warfarin.


Pharmacology (Source, Chemical and Physical Composition) Of Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml

The antithrombotic activity of Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml (Fondaparinux Sodium) is the result of selective inhibition of Factor Xa. By selectively binding to antithrombin III (ATIII), Fondaparinux Sodium potentiates (about 300 times) the innate neutralization of Factor Xa by ATIII. Neutralization of Factor Xa interrupts the blood coagulation cascade and thus inhibits thrombin formation and thrombus development. Fondaparinux Sodium does not inactivate thrombin (activated Factor II) and has no known effect on platelet function. At the recommended dose, Fondaparinux Sodium does not affect fibrinolytic activity or bleeding time.


Dosage And Administration of Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml

Prophylaxis of deep vein thrombosis : Fondaparinux 2.5 mg subcutaneously once daily after hemostasis has been established. The initial dose should be given no earlier than 6 to 8 hours after surgery and continued for 5 to 9 days. For patients undergoing hip fracture surgery, extended prophylaxis up to 24 additional days is recommended. Treatment of deep vein thrombosis and pulmonary embolism : Fondaparinux 5 mg (body weight <50 kg) Fondaparinux 7.5 mg (50 to 100 kg) or Fondaparinux 10 mg (>100 kg) subcutaneously once daily. Treatment should continue for at least 5 days until INR 2 to 3 achieved with warfarin sodium. Pediatric Use : Safety and effectiveness of Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml (Fondaparinux Sodium) in pediatric patients have not been established. Geriatric Use : In clinical trials, the efficacy of Fondaparinux Sodium in the elderly (65 years or older) was similar to that seen in patients younger than 65 years; however, serious adverse events increased with age. Use in renal or hepatic impairment : The risk of bleeding is increased with reduced renal or hepatic function.


Drug Interactions of Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml

Discontinue agents that may enhance the risk of hemorrhage prior to initiation of therapy with Fonidel unless essential. If co-administration is necessary, monitor patients closely for hemorrhage.


Side Effects of Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml

The most common adverse reactions associated with the use of Fonidel are-bleeding complications, mild local irritation (injection site bleeding, rash and pruritus) following subcutaneous injection, anemia, insomnia, hypokalemia, dizziness, hypotension, confusion, bullous eruption, hematoma & post-operative hemorrhage.


Precautions And Warnings for Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml

Use with caution in patients who have conditions or are taking concomitant medications that increase risk of hemorrhage Bleeding risk is increased in renal impairment and in patients with low body weight <50 kg Consider the potential risks and benefits before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis Thrombocytopenia can occur with administration of Fonidel Periodic routine complete blood counts (including platelet counts), serum creatinine level and stool occult blood tests are recommended


Use During Pregnancy and Lactation

Pregnancy Category B. It is not known whether Fonidel Ophthalmic Solution Eye Drop 2.5 mg/0.5 ml (Fondaparinux Sodium) is excreted in human milk. Caution should be exercised when Fondaparinux Sodium is administered to a nursing woman.


Therapeutic Class

Parenteral anti-coagulants


Storage Conditions of It

Store below 25° C. Do not freeze. Keep the medicine out of reach of children. Pack Image: Fonidel 2.5 mg/0.5 ml Eye Drop Thanks for using MedEx! How would you rate your experience so far?


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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N.B.: 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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