42 milliards de dollars US par an: cout mondial estime des erreurs de medication.
MediSafe organizes your clinical base, cross-checks alerts and shows a visual traffic light before a problem catches you off guard.
Before issuing its result, MediSafe can integrate the medical information already stored in LifeQR and expand it with medical history, studies, lab work, imaging and clinical notes. It then contrasts medication and clinical context against clinical engines, official regulatory databases and pharmacovigilance sources to generate a clearer, portable and multilingual output.
Especially useful for tourists, workers in transit, older adults while traveling or children: the medical base can be prepared in the language of the country where the user is located, whether medication was entered by brand name or active ingredient.
Plus de 1,5 million de passages aux urgences par an et pres de 500 000 hospitalisations dues a des evenements indesiables lies aux medicaments aux Etats-Unis.
Plus de 40% des erreurs de medication sont liees a une mauvaise conciliation a l'admission, lors des transferts et a la sortie; pres de 20% de ces erreurs provoquent un dommage.
Ce que fait MediSafe
MediSafe contrasts the medication already stored in the LifeQR profile with clinical engines, official regulatory databases and pharmacovigilance sources before issuing its traffic-light result. It can also organize medical history, studies, lab work, imaging and reports, and review every drug by brand name or active ingredient to support clearer clinical reading in any country.
This is an informational and clinical collaboration tool. In its medication safety materials, the WHO indicates that patient tools should be used in collaboration with healthcare professionals.
Pourquoi c'est utile
Medication errors and incomplete treatment information remain a major cause of preventable harm. That is why a tool that gathers medication, allergies, history, studies, lab work and imaging in a portable format can help reduce exposure to avoidable admissions, duplicated work and delays when the person is far from their usual health system or facing a language change.
Travel, transfers and environments where every minute matters
For tourists, workers in transit, older adults while traveling, children and field teams, the value becomes even clearer: when someone is far from their usual system, faces a language change or needs a faster response, carrying medication, studies, history and alerts in a multilingual base helps preserve continuity of care.
Comment MediSafe valide avant d'emettre le feu tricolore
Whenever a new drug is added or the medical history changes, MediSafe runs an exhaustive review of the profile. It does not stop at a brand name: it normalizes medication, recognizes active ingredients and equivalents, reevaluates background, studies, lab work and imaging, contrasts the combination with specialized clinical engines, verifies current regulatory labeling and prepares the base to be shown in the local language where it is needed.
Normalisation et interoperabilite
- RxNorm: normalizes clinical names and links vocabularies used by pharmacy and interaction software, including First Databank, Micromedex, Multum and Gold Standard.
- MED-RT: reference pharmacologic terminology and successor to NDF-RT for drug classifications and clinical relationships.
- RxClass: connects pharmacologic classes with RxNorm members and lets you navigate classes sourced from ATC, MED-RT, FDA/SPL and others.
- ATC: can be used as an additional layer to group therapeutic families and evaluate class-level duplication or conflicts.
Moteurs cliniques d'interactions et de screening
- FDB MedKnowledge: moteur sous licence pour detecter des interactions cliniquement significatives; inclut les medicaments sur ordonnance, OTC, therapies alternatives et même certains ingredients inactifs.
- Medi-Span Clinical Screening: depistage des interactions medicament-medicament, medicament-aliment et medicament-alcool, avec severite, documentation, conduite a tenir, debut et contexte clinique comme l'age, la grossesse ou l'allaitement.
- DrugBank: fournit des interactions medicament-medicament, medicament-categorie et categorie-categorie avec severite structuree.
- Micromedex: reference clinique fondee sur les preuves avec fonctions d'interactions, compatibilite IV, identification et comparaison des medicaments, mise Á jour quotidiennement.
- UpToDate Lexidrug / Facts & Comparisons: permet de vérifiér interactions medicament-medicament, allergies, grossesse, allaitement, maladies, aliments, alcool et duplication therapeutique, avec echelles de risque.
- Oracle Health Multum: base de reference pharmacologique utilisee par Oracle Health EHR pour descriptions de medicaments, interactions et aide a la revue d'utilisation.
- BNF Interactions: permet de rechercher des interactions et affiche la severite ainsi que le type de preuve.
- Gold Standard Drug Database / Clinical Pharmacology: solutions integrables d'information pharmacologique pour le support a la decision therapeutique.
Regulatory sources and official labeling
- DailyMed: NLM database with the latest labeling submitted to the FDA and currently in use.
- openFDA Drug Label API: public SPL label API for prescription and OTC drugs.
- Drugs@FDA: includes most products approved since 1939 and states that it updates daily.
- FDA NDC Directory: NDC code directory with daily updates for products listed with the FDA.
- GSRS / UNII: unique ingredient identifiers generated by FDA and used in electronic listings such as DailyMed.
- EMA ePI: authorized electronic product information in the European Union, focused on accessibility, searchability and multilingual capacity.
- emc (UK): updated, approved and regulated information for medicines authorized in the United Kingdom.
- CIMA (AEMPS, Spain): official information updated daily for medicines authorized in Spain.
- Health Canada Drug Product Database: authorized medicines database for Canada, with nightly updates and access to product monographs.
- TGA Product Information / ARTG: TGA-approved information on quality, safety and efficacy, plus the public register of therapeutic goods legally supplied in Australia.
- ANMAT National Medicines Formulary: official free-access database with medicines registered and marketed in Argentina.
Couches speciales
- MedlinePlus Herbs and Supplements: adds effectiveness, usual dose and interaction information for herbs and supplements.
- LactMed: peer-reviewed database on drugs and other substances during breastfeeding, with milk levels, potential effects and therapeutic alternatives.
Pharmacovigilance and safety signals
- FAERS / openFDA: repository of adverse events and medication errors submitted to the FDA; useful as a post-marketing signal, although the FDA clarifies that it does not prove causality or allow incidence calculation.
- EudraVigilance: EMA system for managing and analyzing suspected adverse reactions in the EEA.
- VigiBase: global database of adverse event reports for medicines and vaccines under the WHO monitoring program, administered by UMC.
LifeQR can add automatic alerts and exact GPS location during an emergency
Beyond MediSafe's clinical and multilingual analysis, LifeQR can automatically notify emergency contacts and share the exact GPS location where the event happened. This adds an extra protection layer when the person cannot explain their situation by themselves.
Feu tricolore MediSafe
Vert
Vert: avec les informations disponibles et les sources consultees au moment de l'analyse, aucune alerte pertinente n'a ete detectee pour la combinaison saisie.
Jaune
Jaune: une interaction possible, un doublon, une precaution ou un conflit a ete detecte et merite d'etre vérifié avant de poursuivre.
Rouge
Rouge: une interaction majeure possible, une contre-indication ou un avertissement a haut risque a ete detecte et justifie une verification prioritaire avec un médecin ou un pharmacien.
The visual traffic light logic is consistent with risk and severity modules used by tools such as Facts & Comparisons, DrugBank and BNF.
Avis important
MediSafe is an informational tool that supports clinical communication. It does not diagnose, prescribe or replace the evaluation of physicians, pharmacists, emergency services or other health professionals. The traffic light expresses guidance alerts based on the information entered, active integrations, available licenses and sources consulted at the time of analysis. Pharmacovigilance and regulatory labeling data may contribute relevant signals, but by themselves they do not equal a diagnosis or prove clinical causality in an individual case.
Data sources and reference frameworks
WHO, CDC, NLM/NIH, FDA, EMA, AEMPS, Health Canada, TGA, ANMAT, UMC/WHO Programme for International Drug Monitoring, in addition to clinical and regulatory engines such as RxNorm, MED-RT, RxClass, FDB MedKnowledge, Medi-Span, DrugBank, Micromedex, UpToDate Lexidrug, Facts & Comparisons, Oracle Health Multum, BNF, Gold Standard Drug Database, Clinical Pharmacology, DailyMed, openFDA, Drugs@FDA, NDC Directory, GSRS/UNII, EMA ePI, emc, CIMA, Canada's Drug Product Database, TGA Product Information, ANMAT's national formulary, MedlinePlus Herbs & Supplements, LactMed, FAERS, EudraVigilance and VigiBase.
Activez MediSafe pour cette fiche
MediSafe adds a clinical layer for medication, medical history, studies, lab work and imaging, with a clearer output designed for multilingual and mobility contexts.