ATC code J
| : Antiinfectives for systemic use |
|---|
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| Human only |
| ATCvet only |
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| Other ATC codes |
ATC code J Antiinfectives for systemic use is a section of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products.[1][2][3][4]
Codes for veterinary use (ATCvet codes) can be created by placing the letter Q in front of the human ATC code: for example, QJ.[5] ATCvet codes without corresponding human ATC codes are cited with the leading Q in the following list.
National versions of the ATC classification may include additional codes not present in this list, which follows the WHO version.
See also
- Immune sera, immunoglobulins and vaccines for veterinary use are in the ATCvet group QI.
References
- ^ "ATC (Anatomical Therapeutic Chemical Classification System) – Synopsis". National Institutes of Health. Retrieved 1 February 2020.
- ^ "Anatomical Therapeutic Chemical (ATC) Classification". World Health Organization. Retrieved 3 January 2022.
- ^ "Structure and principles". WHO Collaborating Centre for Drug Statistics Methodology. 15 February 2018. Retrieved 3 January 2022.
- ^ "ATC/DDD Index 2022: code J". WHO Collaborating Centre for Drug Statistics Methodology.
- ^ "ATCvet Index 2022: code QJ". WHO Collaborating Centre for Drug Statistics Methodology.
Major chemical drug groups – based upon the Anatomical Therapeutic Chemical Classification System | |
|---|---|
| gastrointestinal tract / metabolism (A) | |
| blood and blood forming organs (B) | |
| cardiovascular system (C) | |
| skin (D) | |
| genitourinary system (G) | |
| endocrine system (H) | |
| infections and infestations (, P, QI) | |
| malignant disease (L01–L02) | |
| immune disease (L03–L04) | |
| muscles, bones, and joints (M) | |
| brain and nervous system (N) |
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| respiratory system (R) | |
| sensory organs (S) | |
| other ATC (V) | |
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| 30S |
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| 50S |
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| Antifolates (inhibit bacterial purine metabolism, thereby inhibiting DNA and RNA synthesis) |
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| Quinolones (inhibit bacterial topoisomerase and/or DNA gyrase, thereby inhibiting DNA replication) |
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| Anaerobic DNA inhibitors |
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| RNA synthesis |
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| Glycopeptides Lipoglycopeptides | |
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| Polymyxins | |
| Steroid antibacterials | |
| Imidazole derivatives | |
| Pleuromutilins | |
| Nitrofuran derivatives | |
| Other antibacterials | |
| Wall/ membrane |
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| Intracellular |
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| Others |
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| Nucleic acid inhibitor |
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| Protein synthesis inhibitor |
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| Cell envelope antibiotic |
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| Other/unknown | |||||||||
| Combinations | |||||||||
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| Baltimore I |
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| Hepatitis B (VII) | |||||||||||||||||||||
| Multiple/general |
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| Hepatitis C |
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| Hepatitis D | |||||||||
| Picornavirus | |||||||||
| Anti-influenza agents | |||||||||
| Multiple/general |
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| Capsid inhibitors | |||||||||||||
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| Entry/fusion inhibitors (Discovery and development) | |||||||||||||
| Integrase inhibitors (Integrase strand transfer inhibitors (INSTI)) | |||||||||||||
| Maturation inhibitors | |||||||||||||
| Protease Inhibitors (PI) (Discovery and development) |
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| Reverse-transcriptase inhibitors (RTIs) |
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| Combined formulations |
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| Pharmacokinetic boosters | |||||||||||||
| Experimental agents |
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Immune sera and immunoglobulins (J06) | |||||
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| Polyclonal antibodies |
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| Monoclonal antibodies | |||||
| Development | |||||||||||
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| Classes | |||||||||||
| Administration | |||||||||||
| Vaccines |
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| Inventors/ researchers | |||||||||||
| Controversy | |||||||||||
| Related | |||||||||||
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