| ATC code C: Cardiovascular system |
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| Other ATC codes |
ATC code C Cardiovascular system 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, QC.[5]
National issues of the ATC classification may include additional codes not present in this list, which follows the WHO version.
References
- ↑ "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 C". WHO Collaborating Centre for Drug Statistics Methodology.
- ↑ "ATCvet Index 2022: code QC". 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) | |
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| Bufadienolides |
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| Cardenolides |
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| Channel blockers |
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| Receptor agonists and antagonists |
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| Ion transporters |
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Cardiac stimulants excluding cardiac glycosides (C01C) | |||||||||||||||
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| Adrenergic and dopaminergic agents |
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| Phosphodiesterase inhibitors (PDE3I) | |||||||||||||||
| Other cardiac stimulants | |||||||||||||||
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| Nitrovasodilators | |
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| Quinolone vasodilators | |
| Others | |
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| Sympatholytics (antagonize α-adrenergic vasoconstriction) | |||||
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| Other antagonists |
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| Nitrovasodilator (arterioles and venules) | |
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| Hydrazinophthalazines (arterioles) | |
| Potassium channel openers (arterioles) | |
| Calcium channel blockers (arterioles) |
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| Sulfonamides (and etacrynic acid) |
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| Potassium-sparing (at CD) |
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| Osmotic diuretics (PT, DL) | |||||||||
| Vasopressin receptor inhibitors (DCT and CD) | |||||||||
| Other | |||||||||
| Combination products | |||||||||
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| Phenylethanolamine derivatives | |
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| Alpha blockers |
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| Niacin and derivatives | |
| Purine derivatives | |
| Ergot alkaloids | |
| Other peripheral vasodilators | |
| Antihemorrhoidals for topical use |
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| Antivaricose therapy |
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| Capillary stabilising agents |
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| β, non-selective | |
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| β1-selective | |
| β2-selective | |
| α1- + β-selective | |
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| Calcium |
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| Potassium |
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| Sodium |
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| Chloride |
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| Others |
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See also: Receptor/signaling modulators • Transient receptor potential channel modulators | |||||||||||||||||||||||||
| ACE inhibitors ("-pril") |
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| AIIRAs ("-sartan") | |
| Renin inhibitors ("-kiren") | |
| Dual ACE/NEP inhibitors |
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| Neprilysin inhibitors | |
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| GI tract |
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| Liver |
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| Blood vessels |
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| Combinations | |||||||||||||
| Other | |||||||||||||
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