AI ee Badbaadada Dawooyinka iyo Kediska Feejignaanta Dawooyinka

Jawaabaha iyo sharraxaadaha waxay soo baxayaan markaad qaadanayso kediska.

1. Waa maxay yoolka koowaad ee ka feejignaanta farmasiga?
   • Ogaanshaha, qiimaynta, iyo ka hortagga waxyeelada daawooyinka ka dib marka la isticmaalo
   • Suuqgeynta daawooyinka cusub ee dhakhaatiirta
   • Dejinta qiimaha tafaariiqda daawooyinka
   • Naqshadeynta baakooyinka kiniinka
2. In the published n2c2 clinical NLP system, what information did the system extract from narrative notes?
   • Only patients’ handwritten signatures
   • Medication and adverse-event concepts and their relations
   • Only final regulatory decisions
   • Only medicine prices
3. Waa maxay falanqaynta isku dheelitir la'aanta ayaa lagu ogaadaa xogta dhacdooyinka xun?
   • Farqiga qiimaha u dhexeeya summada iyo dawooyinka guud
   • Isbitaalkee ayaa soo gudbiyay warbixinadii ugu badnaa
   • Lamaanayaasha dhacdada maandooriyaha ah ayaa la soo sheegay in ka badan intii la saadaaliyay fursadaha tirakoobka
   • Taariikhaha ay dhacayaan dawooyinka
4. What is VigiBase, according to Uppsala Monitoring Centre?
   • A database of randomized clinical-trial efficacy results only
   • A list of confirmed causal side effects for every medicine
   • A commercial catalogue of approved drug prices
   • The WHO global database of reported adverse events for medicines and vaccines
5. Waa maxay MedDRA loo isticmaalo dhuumaha ilaalinta farmasiga?
   • Kalmado caafimaad oo habaysan oo loogu talagalay habaynta falcelinta iyo xaaladaha
   • Nooca baakadaha daawada
   • App-ka jadwalka dhakhaatiirta
   • Nooc ka mid ah iskaanka MRI
6. Which sequence does UMC describe in its signal-management process?
   • Diagnosis, prescription, dispensing, billing and discharge
   • Detection, validation, prioritisation, assessment and communication
   • Data collection, automatic causality decision, recall and litigation
   • Model training, deployment, billing and marketing
7. How should a high disproportionality score in a spontaneous-report database be interpreted?
   • As a population incidence rate for all patients
   • As a confirmed causal adverse reaction
   • As a statistical signal for further assessment, not proof that the drug caused the event
   • As proof that no other factor contributed
8. Which four elements satisfy the minimum ICSR criteria in ICH E2D(R1)?
   • A confirmed causal link, a batch number, a prescriber signature, and a laboratory result
   • A product label, a randomized trial, a treatment response, and a safety committee vote
   • A hospital admission, a known dose, a genetic profile, and a published case report
   • An adverse event or other observation, a suspect or interacting product, an identifiable patient, and an identifiable reporter