SEVREDOL

This brand name is authorized in Australia, Cyprus, Estonia, Spain, France, Croatia, Ireland, New Zealand, Poland, Romania, United Kingdom

Active ingredients

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.

Read about Morphine

Medication package inserts

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

Medicine classification

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
Discover more medicines within N02AA01

Authorization and marketing

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: 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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