This brand name is authorized in Austria, Croatia, Ecuador, Estonia, Finland, Ireland, Lithuania, Malta, New Zealand, Poland, Romania, South Africa, Tunisia.
The drug RHESONATIV contains one active pharmaceutical ingredient (API):
1
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UNII
RX2MM64U68 - HUMAN IMMUNOGLOBULINS
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Human anti-D immunoglobulin contains specific antibodies (IgG) against the Rh(D) antigen of human erythrocytes. It can also contain antibodies to other Rh antigens, e.g. anti-Rh C antibodies. The mechanism by which anti-D immunoglobulin suppresses immunisation to Rh(D) positive red cells is not known. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| RHESONATIV Solution for injection | MPI, EU: SmPC | Health Products Regulatory Authority (IE) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J06BB01 | Anti-D (rh) immunoglobulin | J Antiinfectives for systemic use → J06 Immune sera and immunoglobulins → J06B Immunoglobulins → J06BB Specific immunoglobulins |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | 146-MBE-1119 |
| EE | Ravimiamet | 1295782, 1295816, 1295827, 1584828 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 063818 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-584583753 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1025648, 1025649, 1031947 |
| MT | Medicines Authority | MA1219/01001, MA1219/01002 |
| NZ | Medicines and Medical Devices Safety Authority | 12509, 12510 |
| PL | Rejestru Produktów Leczniczych | 100193540, 100375949 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W65901001, W65901002, W65901003, W65902001, W65902002, W65902003 |
| TN | Direction de la Pharmacie et du Médicament | 2103021 |
| ZA | Health Products Regulatory Authority | 51/30.1/0996 |
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