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Highly Regulated (List I)Translated

ELOCTA

3000 UI/Powder for Injectable Sol./EFMOROCTOCOG
SEWEDISH ORPHAN BIOVITRUM
ManufacturerVerified lab

SEWEDISH ORPHAN BIOVITRUM

Public retail price
N/ADZD

Identification

Active ingredient (INN)
EFMOROCTOCOG
Internal code
12 J 212
Country of Origin
Sweden
Pharmaceutical form
Powder for Injectable Sol.
Prescription List
Highly Regulated (List I)
Packaging
b/1 seringue
ELOCTA
Clinical View
Highly Regulated (List I)

DAWA Clinical Workbench v2.0

Information may not be accurate. Always consult a physician, pharmacist, or specialist before acting on any data shown here.

Indications

Used to prevent, treat and reduce the incidence of hemophilia a.

Associated Conditions

Use under medical supervision: pregnancy and breastfeeding, given the possibility of adverse effect on the foetus.

The body may produce anti-warming objects as an immune reaction, thereby reducing the therapeutic effect of the drug.

The patient must be monitored if symptoms of the formation of these antibodies, such as the non-highness of the eighth factor in the blood or the continuation of the bleeding after the medication is given, are present.

Mechanism of Action

He's a copy of the eighth clotting agent, produced by the remodelled DNA technology.

He activates the tenth clotting agent in collaboration with the activated ninth clotting agent and then the tenth activated clotting agent converts prothrombin to thrombin, which converts phenogen to febrin, and with the thirteenth clotting agent, it is a constant clot.

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