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1.
Nucleic Acids Res ; 51(D1): D1276-D1287, 2023 01 06.
Article in English | MEDLINE | ID: covidwho-2189411

ABSTRACT

DrugCentral monitors new drug approvals and standardizes drug information. The current update contains 285 drugs (131 for human use). New additions include: (i) the integration of veterinary drugs (154 for animal use only), (ii) the addition of 66 documented off-label uses and iii) the identification of adverse drug events from pharmacovigilance data for pediatric and geriatric patients. Additional enhancements include chemical substructure searching using SMILES and 'Target Cards' based on UniProt accession codes. Statistics of interests include the following: (i) 60% of the covered drugs are on-market drugs with expired patent and exclusivity coverage, 17% are off-market, and 23% are on-market drugs with active patents and exclusivity coverage; (ii) 59% of the drugs are oral, 33% are parenteral and 18% topical, at the level of the active ingredients; (iii) only 3% of all drugs are for animal use only; however, 61% of the veterinary drugs are also approved for human use; (iv) dogs, cats and horses are by far the most represented target species for veterinary drugs; (v) the physicochemical property profile of animal drugs is very similar to that of human drugs. Use cases include azaperone, the only sedative approved for swine, and ruxolitinib, a Janus kinase inhibitor.


Subject(s)
Drug Approval , Drug-Related Side Effects and Adverse Reactions , Veterinary Drugs , Animals , Humans , Drug-Related Side Effects and Adverse Reactions/veterinary , Veterinary Drugs/administration & dosage , Veterinary Drugs/adverse effects , Off-Label Use/veterinary
3.
Nucleic Acids Res ; 49(D1): D1160-D1169, 2021 01 08.
Article in English | MEDLINE | ID: covidwho-910390

ABSTRACT

DrugCentral is a public resource (http://drugcentral.org) that serves the scientific community by providing up-to-date drug information, as described in previous papers. The current release includes 109 newly approved (October 2018 through March 2020) active pharmaceutical ingredients in the US, Europe, Japan and other countries; and two molecular entities (e.g. mefuparib) of interest for COVID19. New additions include a set of pharmacokinetic properties for ∼1000 drugs, and a sex-based separation of side effects, processed from FAERS (FDA Adverse Event Reporting System); as well as a drug repositioning prioritization scheme based on the market availability and intellectual property rights forFDA approved drugs. In the context of the COVID19 pandemic, we also incorporated REDIAL-2020, a machine learning platform that estimates anti-SARS-CoV-2 activities, as well as the 'drugs in news' feature offers a brief enumeration of the most interesting drugs at the present moment. The full database dump and data files are available for download from the DrugCentral web portal.


Subject(s)
Antiviral Agents/therapeutic use , COVID-19 Drug Treatment , Databases, Pharmaceutical/statistics & numerical data , Drug Approval/statistics & numerical data , Drug Discovery/statistics & numerical data , Drug Repositioning/statistics & numerical data , SARS-CoV-2/drug effects , Antiviral Agents/adverse effects , Antiviral Agents/pharmacokinetics , COVID-19/epidemiology , COVID-19/virology , Drug Approval/methods , Drug Discovery/methods , Drug Repositioning/methods , Epidemics , Europe , Humans , Information Storage and Retrieval/methods , Internet , Japan , SARS-CoV-2/physiology , United States
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