The World Health Organization's ATC classification organizes medical drugs based on therapeutic properties, chemical composition, and anatomy. It helps make essential medicines readily available globally and is widely used in the pharmaceutical industry.
Level | Code | Title | |
---|---|---|---|
1 | J | Antiinfectives for systemic use | |
2 | J06 | Immune sera and immunoglobulins | |
3 | J06B | Immunoglobulins |
Code | Title | |
---|---|---|
J06BA | Immunoglobulins, normal human | |
J06BB | Specific immunoglobulins | |
J06BC | Antibacterial monoclonal antibodies | |
J06BD | Antiviral monoclonal antibodies |
Active Ingredient | Description | |
---|---|---|
Ansuvimab |
Ansuvimab is a recombinant human monoclonal antibody with antiviral activity against Zaire ebolavirus. |
|
Anthrax immunoglobulin |
Anthrax immuneglobulin is a human immune globulin that is used in combination with antibiotics to treat anthrax. Anthrax immunoglobulin binds to protective antigen (PA) to prevent PA mediated cellular entry of anthrax edema factor and lethal factor. |
|
Anti-D (rh) immunoglobulin |
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. |
|
Bezlotoxumab |
Bezlotoxumab is a human monoclonal antitoxin antibody that binds with high affinity to C. difficile toxin B and neutralizes its activity. Bezlotoxumab prevents CDI recurrence by providing passive immunity against toxin produced by the outgrowth of persistent or newly-acquired C. difficile spores. |
|
Casirivimab and imdevimab |
Casirivimab (IgG1Îș) and imdevimab (IgG1λ) are two recombinant human monoclonal antibodies which are unmodified in the Fc regions. Casirivimab and imdevimab bind to non-overlapping epitopes of the spike protein receptor binding domain (RBD) of SARS-CoV-2. This prevents RBD binding to the human ACE2 receptor, so preventing virus entry into cells. |
|
Cytomegalovirus immunoglobulin |
Cytomegalovirus immunoglobulin is used as a CMV-specific polyclonal immunoglobulin preparation that binds to CMV surface antigens thereby neutralizing the potential of CMV from entering host cells and presenting the CMV particle for phagocytosis. Furthermore, cytomegalovirus immunoglobulin can activate CMV-reactive immune cells for long-lasting CMV-specific immune responses. |
|
Human hepatitis B immunoglobulin |
Human hepatitis B immunoglobulin solution for infusion contains mainly immunoglobulin G (IgG) with a specifically high content of antibodies against hepatitis B virus surface antigen (HBs). It is used for the immunoprophylaxis of hepatitis B and the prevention of hepatitis B virus re-infection after liver transplantation for hepatitis B induced liver failure. |
|
Human antimeasles immunoglobulin |
|
|
Human normal immunoglobulin G |
Human normal immunoglobulin contains mainly immunoglobulin G (IgG) with a broad spectrum of antibodies against infectious agents. Human normal immunoglobulin contains the IgG antibodies present in the normal population. It is usually prepared from pooled plasma from not fewer than 1000 donors. |
|
Human rabies immunoglobulin |
Human rabies immunoglobulin contains mainly immunoglobulin G (IgG) with a specifically high content of antibodies against rabies virus. Human Rabies Immunoglobulin must always be used in combination with a rabies vaccine. |
|
Human varicela zoster immunoglobulin |
Human varicella zoster immunoglobulin contains mainly immunoglobulin G (IgG) with a specifically high content of antibodies against varicella-zoster virus. It is used for prophylaxis against varicella zoster virus (VZV) infection. |
|
Immunoglobulins, normal human, IV |
Human normal immunoglobulin contains mainly immunoglobulin G (IgG) with a broad spectrum of antibodies against infectious agents. The mechanism of action in indications other than replacement therapy is not fully elucidated, but includes immunomodulatory effects. |
|
Nirsevimab |
Nirsevimab is a recombinant neutralising human IgG1Äž long-acting monoclonal antibody to the prefusion conformation of the RSV F protein which has been modified with a triple amino acid substitution (YTE) in the Fc region to extend serum half-life. Nirsevimab inhibits the essential membrane fusion step in the viral entry process, neutralising the virus and blocking cell-to-cell fusion. |
|
Obiltoxaximab |
Obiltoxaximab is a monoclonal antibody that binds the protective antigen (PA) of B. anthracis. Obiltoxaximab inhibits the binding of PA to its cellular receptors, preventing the intracellular entry of the anthrax lethal factor and oedema factor, the enzymatic toxin components responsible for the pathogenic effects of anthrax toxin. |
|
Palivizumab |
Palivizumab is a humanised IgG1Îș monoclonal antibody directed to an epitope in the A antigenic site of the fusion protein of respiratory syncytial virus (RSV). This humanised monoclonal antibody is composed of human (95%) and murine (5%) antibody sequences. It has potent neutralising and fusion-inhibitory activity against both RSV subtype A and B strains. |
|
Pertussis filamentous hemagglutinin |
|
|
Regdanvimab |
Regdanvimab is a recombinant human IgG1 monoclonal antibody that binds to the receptor binding domain (RBD) of the spike(s) protein of SARS-CoV-2 consequently blocking cellular entry and SARS-CoV-2 infection. |
|
Sotrovimab |
Sotrovimab is a dual action, engineered human IgG1 mAb that binds to a conserved epitope on the spike protein receptor binding domain of SARS-CoV-2. It is used for the treatment of symptomatic adults and adolescents with acute covid-19 infection who do not require oxygen supplementation and who are at increased risk of progressing to severe covid infection. |
|
Tetanus immunoglobulin |
Human tetanus immunoglobulin contains mainly immunoglobulin G (IgG) with a specifically high content of antibodies against the toxin produced by the bacteria clostridium tetanus. |
|
Tixagevimab and Cilgavimab |
Tixagevimab and cilgavimab are two recombinant human IgG1 monoclonal antibodies, with amino acid substitutions in the Fc regions, to extend antibody half-life and to reduce antibody effector function and potential risk of antibody-dependent enhancement of disease. Tixagevimab and cilgavimab can simultaneously bind to non-overlapping regions of the spike protein receptor binding domain (RBD) of SARS-CoV-2. Tixagevimab, cilgavimab and their combination bind to spike blocking its interaction with the human ACE2 receptor, resulting in a blockade of virus entry. |
|
Vaccinia immunoglobulin |
Vaccinia immunoglobulin provides passive immunity for individuals with complications to vaccinia virus vaccination. The exact mechanism of action is not known. |
Title | Information Source | Document Type | |
---|---|---|---|
BEYFORTUS Solution for injection | European Medicines Agency (EU) | MPI, EU: SmPC | |
CUTAQUIG Solution for infusion | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
CUVITRU Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
CYTOGAM Solution for infusion | FDA, National Drug Code (US) | MPI, US: SPL/Old | |
CYTOTECT CP BIOTEST Solution for infusion | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
EBANGA Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
EVUSHELD Solution for injection | European Medicines Agency (EU) | MPI, EU: SmPC | |
FLEBOGAMMA DIF Solution for infusion | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
GAMASTAN Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
GAMMANORM Solution for injection | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
GAMMAPLEX Solution for infusion | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
GAMUNEX Solution for infusion | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
GAMUNEX-C Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
HEPAGAM B Solution for infusion | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
HEPATECT CP Solution for infusion | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
HIZENTRA Solution for injection | European Medicines Agency (EU) | MPI, EU: SmPC | |
HYPERHEP B Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/Old | |
HYPERRAB Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
HYPERRHO S/D FULL DOSE Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/Old | |
HYPERTET Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/Old | |
INTRAGAM Solution for infusion | Medicines and Medical Devices Safety Authority (NZ) | MPI, EU: SmPC | |
KIOVIG Solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
NYXTHRACIS Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
PANZYGA Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
REGKIRONA Concentrate for solution for infusion | MPI, EU: SmPC | ||
REGKIRONA Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
RHESONATIV Solution for injection | Health Products Regulatory Authority (IE) | MPI, EU: SmPC | |
RHOPHYLAC Solution for injection | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
RONAPREVE Solution for injection/infusion | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
SYNAGIS Solution for injection | European Medicines Agency (EU) | MPI, EU: SmPC | |
TETAGAM-P Solution for injection | Health Products Regulatory Authority (IE) | MPI, EU: SmPC | |
VARIZIG Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
WINRHO SDF Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/PLR | |
XEVUDY Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
ZINPLAVA Concentrate for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
ZUTECTRA Solution for injection | European Medicines Agency (EU) | MPI, EU: SmPC |