| ID | 419 |
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| No | 419 |
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| Brand Name | ARICEPT EVESS 10 MG |
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| Ingredients | DONEPEZIL HYDROCHLORIDE 10 MG EQ.TO DONEPEZIL FREE BASE 9.12 MG |
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| Dosage Form | TABLET |
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| Primary Packaging | BLISTERPACK |
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| Storage | DO NOT STORE ABOVE 30'C |
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| Shelf Life | 3 YEARS |
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| Pack Size | BOX OF 28,30,56,60,98 OR 120 TABLETS. |
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| Dispensing Category | Prescription only |
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| ATC Classification | N06DA02 |
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| Pharmaceutical Class | DEMENTIA |
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| Indications | SYMPTOMATIC TREATMENT OF MILD, MODERATELY SEVERE AND SEVERE DEMENTIA OF THE ALZHEIMER'S TYPE, VASCULAR DEMENTIA ( DEMENTIA ASSOCIATED WITH CEREBROVASCULAR DISEASE), DEMENTIA WITH LEWY BODIES( DLB). |
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| Contraindications | ARICEPT IS CONTRAINDICATED IN PATIENTS WITH A KNOW HYPERSENSITIVITY TO DONPEZIL HYDROCHLORIDE, PIPERIDINE DERIVATIVE. |
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| Side Effects | THE MOST COMMON ADVERSE EVENTS ARE DIARRHOEA,MUSCLE CRAMPS, FATIGUE, NAUSEA, VOMITING AND INSOMNIA. |
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| Unit Price | - |
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| EDL |
No |
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| Description | YELLOW, ROUND TABLETS DEBOSSED ARICEPT ON ONE SIDE AND 10 ON THE OTHER SIDE |
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| Note | |
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| License Owner | DKSH LAOS COMPANY LIMITED |
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| Manufacturer | BUSHU PHARMACEUTICALS LTD. MISATO FACTORY |
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| Country | THAILAND |
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| Import Registration No | 1B 6/52 (N ) |
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| Import Registration Date | 2009-11-27 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 09-ARP-2022 |
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| FDD Registration No | 03 I 3780/12 |
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| FDD Registration Date | 2022-09-14 |
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| Expiry Date | 2025-09-13 |
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