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This template's documentation is missing, inadequate, or does not accurately describe its functionality or the parameters in its code. Please help to expand and improve it . Editors can experiment in this template's sandbox ( create | mirror ) and testcases ( create ) pages.
[[Category:Drug templates by structure]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Drug templates by structure]]</noinclude> to the end of the template code, making sure it starts on the same line as the code's last character.
If the template has a separate documentation page (usually called "Template:template name/doc"), add [[Category:Drug templates by ATC]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Drug templates by ATC]]</noinclude>
[[Category:Drug templates]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Drug templates]]</noinclude> to the end of the template code, making sure it starts on the same line as the code's last character.
Name of the drug, medication, or vaccine, including combination drugs. The article title will be used if this is left blank. String: suggested: type: type: Drug type, can be left <blank> (for single chemical), "vaccine", "combo" (combination of drugs), and "mab" (monoclonal antibody) Example combo: String: suggested: IUPAC_name: IUPAC_name ...
The template does not at the current time include summary information about the drug class itself. Instead, it contains a consistent interface to other sources that provide information about the drug class. Don't worry about trying to fill in all the fields – even if you can only get one or two, that still can be useful.
{{Drug use | state = expanded}} will show the template expanded, i.e. fully visible. {{Drug use | state = autocollapse}} will show the template autocollapsed, i.e. if there is another collapsible item on the page (a navbox, sidebar, or table with the collapsible attribute), it is hidden apart from its title bar, but if not, it is fully visible.
The phrase "drug design" is similar to ligand design (i.e., design of a molecule that will bind tightly to its target). [6] Although design techniques for prediction of binding affinity are reasonably successful, there are many other properties, such as bioavailability, metabolic half-life, and side effects, that first must be optimized before a ligand can become a safe and effictive drug.