This brand name is authorized in Austria, Cyprus, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Poland, Romania, United Kingdom, United States, South Africa
The drug OPTISON contains one active pharmaceutical ingredient (API):
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1
Perflutren
UNII T8C6W1N6NW - HUMAN ALBUMIN MICROSPHERES
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When used in conjunction with diagnostic ultrasound, perflutren provides opacification of cardiac chambers, improvement in delineation of endocardial borders, enhancement of the Doppler signal, and visualisation of wall motion and blood flow within the heart. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| OPTISON Dispersion for injection | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| V08DA01 | V Various → V08 Contrast media → V08D Ultrasound contrast media → V08DA Ultrasound contrast media | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: EE | Ravimiamet | Identifier(s): 1203051, 1203062 |
| Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 98065002 |
| Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 010529 |
| Country: FR | Base de données publique des médicaments | Identifier(s): 67461741 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 342677 |
| Country: IT | Agenzia del Farmaco | Identifier(s): 034650010, 034650022 |
| Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1030336, 1030337 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100172034 |
| Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W51612001, W51612002 |
| Country: US | FDA, National Drug Code | Identifier(s): 0407-2707 |
| Country: ZA | Health Products Regulatory Authority | Identifier(s): 34/28/0075 |
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