This brand name is authorized in Australia, Cyprus, Estonia, Spain, France, Croatia, Ireland, New Zealand, Poland, Romania, United Kingdom
The drug SEVREDOL contains one active pharmaceutical ingredient (API):
1
Morphine
UNII 76I7G6D29C - MORPHINE
|
Morphine is a narcotic analgesic obtained from opium. Morphine acts as an agonist at opiate receptors in the CNS particularly Mu and to a lesser extent Kappa receptors. Mu receptors are thought to mediate supraspinal analgesia, respiratory depression and euphoria, and Kappa receptors, spinal analgesia, miosis and sedation. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
SEVREDOL Film-coated tablet | 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 |
---|---|---|
N02AA01 | Morphine | N Nervous system → N02 Analgesics → N02A Opioids → N02AA Natural opium alkaloids |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: AU | Pharmaceutical Benefits Scheme | Identifier(s): 5393W, 5394X, 8669G, 8670H |
Country: EE | Ravimiamet | Identifier(s): 1042805, 1042816, 1080470, 1080492, 1382273, 1382284, 1382295, 1382307 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 59655, 59656 |
Country: FR | Base de données publique des médicaments | Identifier(s): 60907447, 67233047 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 28987, 30782, 30795 |
Country: HR | Agencija za lijekove i medicinske proizvode | Identifier(s): HR-H-915182609, HR-H-932315368 |
Country: IE | Health Products Regulatory Authority | Identifier(s): 45683, 45748, 68549 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 4147, 4148 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100102513 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W59251001, W59251002, W59251003, W59252001, W59252002, W59252003 |
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