In the realm of medical information, the accuracy and reliability of sources are paramount. At rxreasoner.com, we prioritize the delivery of well-founded and up-to-date content by meticulously curating information from official sources. Our commitment to providing accurate and trustworthy medical information is reflected in our sourcing practices, which involve intergovernmental organizations, goverment departments, established healthcare organizations and authoritative regulatory agencies. This ensures that our audience receives information that is not only informative but also rooted in the latest advancements and consensus within the medical community.
The World Health Organization (WHO) is a specialized agency of the United Nations responsible for international public health. The primary goal of the WHO is to promote and protect global health, monitor and respond to health emergencies, provide leadership on international health issues, and set and monitor health standards and guidelines. WHO is made up of member states, and it collaborates with governments, international organizations, and non-governmental organizations to achieve its mission of ensuring that people around the world attain the highest possible level of health.
The Food and Drug Administration (FDA) is a federal agency of the United States Department of Health and Human Services (HHS). The FDA is responsible for protecting and promoting public health by regulating and supervising various products, including food, drugs, medical devices, biologics, and cosmetics. Its primary mission is to ensure the safety, effectiveness, and quality of these products. The FDA plays a critical role in evaluating and approving new drugs and medical devices, ensuring the safety of the food supply, and monitoring and addressing public health concerns.
European Medicines Agency (EMA) is responsible for the scientific evaluation, supervision, and safety monitoring of medicines in the EU. The EMA plays a crucial role in the approval and regulation of pharmaceutical products, including human and veterinary medicines. It assesses the quality, safety, and efficacy of drugs and provides recommendations for their approval and use within the EU member states. The agency also monitors the safety of medicines once they are on the market and provides scientific guidance to healthcare professionals and the pharmaceutical industry.
SNOMED International is a not-for-profit organization responsible for the management and development of SNOMED CT (Systematized Nomenclature of Medicine - Clinical Terms). SNOMED CT is a comprehensive and multilingual clinical terminology system used in healthcare and medical informatics to standardize and encode clinical information. It serves as a global standard for clinical terminology, facilitating the exchange of health information and enhancing interoperability among healthcare systems and electronic health records. It is widely used in healthcare settings to encode and exchange clinical information, making it a valuable tool for improving patient care, supporting clinical research, and enhancing the interoperability of health information systems globally.
The International Committee on Taxonomy of Viruses (ICTV) is a scientific organization responsible for classifying and naming viruses. The ICTV operates under the International Union of Microbiological Societies (IUMS). Its primary mission is to standardize and systematize the nomenclature and classification of viruses, ensuring consistency and clarity in the field of virology. The work of the International Committee on Taxonomy of Viruses is essential for the scientific community, as it allows researchers to communicate effectively about viruses, compare research findings, and advance our understanding of these infectious agents. By providing a standardized framework for virus classification and naming, the ICTV contributes to the organization and coherence of virological knowledge.
DailyMed is a comprehensive, publicly accessible, and online resource provided by the U.S. National Library of Medicine (NLM), which is a part of the National Institutes of Health (NIH). DailyMed is designed to offer information about medications, including prescription and over-the-counter drugs, to healthcare professionals, patients, and the general public. DailyMed is an important resource for healthcare professionals, as it allows them to access the most current and authoritative information about medications. Researchers and scientists can rely on DailyMed for data related to pharmaceuticals and pharmacovigilance.
The Electronic Medicines Compendium (eMC) is a digital resource that provides comprehensive and up-to-date information on medicines and medical products available in the United Kingdom. It serves as an authoritative reference for healthcare professionals, patients, and the general public to access detailed information about medicines, including prescription drugs, over-the-counter products, and other healthcare products. The Electronic Medicines Compendium is a valuable resource for healthcare professionals to ensure safe and effective medication administration, and it also empowers patients and caregivers to make informed decisions about their health and the medications they take. It plays a critical role in promoting transparency and knowledge sharing in the field of pharmaceuticals.
The Health Canada Drug Product Database (DPD) is a comprehensive, publicly accessible online database that provides information on drug products approved for use in Canada. This database serves as a valuable resource for healthcare professionals, researchers, and the general public to access information about medications available in the Canadian market. The Health Canada Drug Product Database is an essential resource to ensure transparency and provide access to reliable information about drug products available in Canada. It helps healthcare providers make informed decisions, patients understand their medications, and researchers access data for various purposes, including pharmacovigilance and clinical research.
Medsinfo.com.au is the centralised source of approved Australian medicine information for consumers and health professionals. This online resource provides information about medications, healthcare, or pharmaceutical products (prescription drugs, over-the-counter medications) in Australia. Medsinfo.com.au supports Australia’s national strategy for the Quality Use of Medicines, whose goal is to make the best possible use of medicines to improve health outcomes for all Australians.
The Australian Register of Therapeutic Goods (ARTG) is a regulatory database and system maintained by the Therapeutic Goods Administration (TGA), which is part of the Australian Government Department of Health. The ARTG serves as a comprehensive listing of therapeutic goods that are approved for sale and use in Australia. Therapeutic goods include pharmaceuticals, medical devices, complementary medicines, and other healthcare products. The Australian Register of Therapeutic Goods is a fundamental component of the TGA's efforts to ensure that therapeutic goods in Australia meet the necessary quality and safety standards, promoting public health and safety in the country.
The Austrian Medicinal Product Index (Österreichischer Arzneimittelindex) is an official publication in Austria that serves as a reference for authorized medicinal products available in the country. It is maintained and published by the Austrian Federal Office for Safety in Health Care (Bundesamt für Sicherheit im Gesundheitswesen or BASG). The Austrian Medicinal Product Index includes information about pharmaceutical drugs and other medicinal products approved for use in Austria. It typically provides details about these products, including their trade names, active ingredients, dosage forms, strengths, marketing authorization holders, and other relevant information. This index is a valuable resource for healthcare professionals, regulatory authorities, and the pharmaceutical industry in Austria, as it helps ensure transparency and accessibility to information about authorized medicinal products within the country.
The Health Sciences Authority (HSA) in Singapore is a statutory board under the Ministry of Health (MOH) that plays a vital role in regulating and ensuring the safety, quality, and efficacy of health products, including pharmaceuticals, medical devices, and complementary health products in Singapore. It was established to safeguard public health and ensure the proper regulation of healthcare products. The Health Sciences Authority in Singapore plays a critical role in maintaining the high standards of healthcare products available in the country, thereby ensuring the safety and well-being of the population. It collaborates with various stakeholders, including healthcare professionals, industry partners, and international regulatory agencies, to fulfill its mission of protecting public health in Singapore.
The HPRA (Health Products Regulatory Authority) is the regulatory agency responsible for the oversight and regulation of health products in Ireland. The HPRA ensures that medicines, medical devices, healthcare products, and cosmetics in Ireland meet the necessary standards for safety, quality, and efficacy. The HPRA is dedicated to protecting the health and safety of the Irish population by ensuring that health products are safe, effective, and of high quality. It also collaborates with other international regulatory agencies and organizations to promote best practices and regulatory alignment. The HPRA plays a pivotal role in the regulation of health products within the Irish healthcare system.
The SAHPRA (South African Health Products Regulatory Authority) repository is an electronic database and information resource provided by SAHPRA, the regulatory agency responsible for overseeing the safety, quality, and efficacy of health products in South Africa. The repository contains various documents and information related to health products, including pharmaceuticals, medical devices, and complementary medicines, which are regulated by SAHPRA. The SAHPRA repository contributes to transparency and access to regulatory information, helping healthcare professionals, industry stakeholders, and the public make informed decisions and understand the regulatory landscape in South Africa.
Web application for performing searchings with different criteria, so that different information level details of medicines are available. Displays medical information resources and makes reference to medicine availability in community services and/or pharmacy services, as well as details of the authorisation and marketing status and other medicine characteristics associated to the medicinal product. The information is displayed along with the leaflet, summary of product characteristics (SPCs) and the rest of necessary information of a medicine.