CEPROTIN® is a brand-name medication that contains Protein C Concentrate (Human). It is a specialized blood product used in the treatment of individuals with severe congenital protein C deficiency, a rare genetic disorder that can lead to blood clotting problems. CEPROTIN® is a concentrated form of human protein C, a natural anticoagulant protein found in the blood. It is used to replace deficient or absent protein C in individuals with severe congenital protein C deficiency. This deficiency can lead to an increased risk of thrombosis (blood clots) and other complications.
Indications and Uses
CEPROTIN® is indicated for the following purposes:
Treatment and prevention of venous thrombosis and purpura fulminans in individuals with severe congenital protein C deficiency.
It is used to replace missing or deficient protein C, which helps regulate blood clotting.
Dosage and Administration
The dosage of CEPROTIN® is determined by a healthcare provider and is individualized based on the patient's specific protein C levels and clinical condition. The medication is administered intravenously. The dose and frequency of administration will vary depending on the severity of the protein C deficiency and the clinical situation.
Contraindications
CEPROTIN® should not be used in individuals with known hypersensitivity to human protein C concentrate or any of its components. It is essential to discuss any allergies or potential reactions with a healthcare provider.
Adverse Effects and Side Effects
Adverse effects with CEPROTIN® are rare but may include:
Allergic reactions, which can manifest as hives, difficulty breathing, and swelling of the face, lips, or tongue.
Blood clots, which can be a concern if the dose is excessive or if the individual's risk factors for thrombosis are not adequately managed.
It is crucial to report any adverse effects or unusual reactions to your healthcare provider.
Storage and Shelf Life:
Store CEPROTIN® at room temperature (2-25°C or 36-77°F). Protect it from freezing and excessive heat. Do not use CEPROTIN® after the expiration date.
Packaging and Presentation
CEPROTIN® is available in vials or vials with transfer devices, and it is intended for intravenous administration.
Regulatory Information
CEPROTIN® is subject to regulation by health authorities to ensure its safety and efficacy. It is essential to use this medication as directed by a healthcare professional and in accordance with local regulations.
References
Always consult with your healthcare provider and refer to the official prescribing information and product labeling for the most up-to-date and comprehensive information on CEPROTIN®. Your healthcare provider will guide you in the proper use of this medication, monitor your progress, and tailor the treatment to your specific medical condition.
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