| ID | 392 |
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| No | 392 |
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| Brand Name | KEDRIALB |
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| Ingredients | HUMAN ALBUMIN 200 G/L |
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| Dosage Form | SOLUTION FOR INFUSION |
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| Primary Packaging | VIAL |
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| Storage | DO NOT STORE THE PRODUCT ABOVE 30'C |
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| Shelf Life | 36 MONTHS FROM THE MANUFACTURING DATE |
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| Pack Size | BOX OF 1 VIAL 50 ML |
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| Dispensing Category | Prescription only |
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| ATC Classification | XX |
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| Pharmaceutical Class | ALBUMIN |
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| Indications | RESTORATION AND MAINTENANCE OF CIRCULATING BLOOD VOLUME WHERE VOLUME DEFICIENCY HAS BEEN DEMONSTRATED, AND USE OF A COLLOID IS APPROPRIATE. THE CHOICE OF ALBUMIN RATHER THAN ARTIFICIAL COLLOID WILL DEPEND ON THE CLINICAL SITUATION OF THE INDIVIDUAL PATIENT |
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| Contraindications | HYPERSENSITIVITY TO ALBUMIN PREPARATIONS OR TO ANY OF THE EXCIPIENTS. |
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| Side Effects | MILD REACTIONS SUCH AS FLUSH, URTICARIA, FEVER, AND NAUSEA OCCUR RARELY, THESE RESCTIONS NORMALLY DISAPPEEAR. |
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| Unit Price | - |
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| EDL |
Yes |
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| Description | A CLEAR, SLIGHTLY VISCOUS LIQUID, IT IS ALMOST COLOURLESS, YELLOW, AMBER OR GREEN |
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| Note | |
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| License Owner | DAOVI PHARMA IMPORT-EXPORT SOLE CO.,LTD |
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| Manufacturer | KEDRION S.P.A |
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| Country | ITALY |
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| Import Registration No | 21111024 |
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| Import Registration Date | 2010-06-02 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2021-05-31 |
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| FDD Registration No | 11 I 4334/17 |
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| FDD Registration Date | 2022-05-17 |
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| Expiry Date | 2025-05-16 |
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