This brand name is authorized in Austria, Ecuador, Spain, Finland, France, Hong Kong, Ireland, Malta, New Zealand, Poland, Romania, United Kingdom
The drug JAYDESS contains one active pharmaceutical ingredient (API):
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1
Levonorgestrel
UNII 5W7SIA7YZW - LEVONORGESTREL
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The precise mode of action of levonorgestrel as an emergency contraceptive is not known. At the recommended regimen, levonorgestrel is thought to work mainly by preventing ovulation and fertilisation if intercourse has taken place in the preovulatory phase, when the likelihood of fertilisation is the highest. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| JAYDESS Intrauterine delivery system | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| G02BA03 | Plastic IUD with progestogen | G Genito urinary system and sex hormones → G02 Other gynecologicals → G02B Contraceptives for topical use → G02BA Intrauterine contraceptives |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | Identifier(s): 24-MEE-0114 |
| Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 77169 |
| Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 102958 |
| Country: FR | Base de données publique des médicaments | Identifier(s): 63905960 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 243798 |
| Country: HK | Department of Health Drug Office | Identifier(s): 64965 |
| Country: IE | Health Products Regulatory Authority | Identifier(s): 33478 |
| Country: MT | Medicines Authority | Identifier(s): MA639/02101 |
| Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 16172 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100297416, 100361500 |
| Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W64048001, W64048002 |
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