ATC code J
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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 issues of the ATC classification may include additional codes not present in this list, which follows the WHO version.
See also
[edit]- Immune sera, immunoglobulins and vaccines for veterinary use are in the ATCvet group QI.
References
[edit]- ^ "ATC (Anatomical Therapeutic Chemical Classification System) – Synopsis". National Institutes of Health. Retrieved 1 February 2020.
- ^ World Health Organization. "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 | |
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gastrointestinal tract / metabolism (A) | |
blood and blood forming organs (B) | |
cardiovascular system (C) | |
skin (D) | |
genitourinary system (G) | |
endocrine system (H) | |
infections and infestations (J, 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) | |
30S |
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50S | |||||||||||||||
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β-lactams (inhibit synthesis of peptidoglycan layer of bacterial cell wall by binding to and inhibiting PBPs, a group of D-alanyl-D-alanine transpeptidases) |
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Polypeptides |
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Intracellular |
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Other |
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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 |
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Administration | |||||||||||
Vaccines |
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Related | |||||||||||
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