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. 2018 May 29;7:243. Originally published 2018 Feb 28. [Version 2] doi: 10.12688/f1000research.13694.2

Box 2. WHO–UMC causality categories.

Causality term Assessment criteria
Certain • Event or laboratory test abnormality, with plausible time relationship to drug intake
• Cannot be explained by disease or other drugs
• Response to withdrawal plausible (pharmacologically, pathologically)
• Event definitive pharmacologically or phenomenologically (i.e. an objective and specific medical disorder or a
recognised pharmacological phenomenon)
• Rechallenge satisfactory, if necessary
Probable/Likely • Event or laboratory test abnormality, with reasonable time relationship to drug intake, Unlikely to be attributed to
disease or other drugs
• Response to withdrawal clinically reasonable
• Rechallenge not required
Possible • Event or laboratory test abnormality, with reasonable time relationship to drug intake
• Could also be explained by disease or other drugs
• Information on drug withdrawal may be lacking or unclear
Unlikely • Event or laboratory test abnormality, with a time to drug intake that makes a relationship improbable (but not
impossible)
• Disease or other drugs provide plausible explanations
Conditional/
Unclassified
• Event or laboratory test abnormality
• More data for proper assessment needed, or
• Additional data under examination
Unassessable/
Unclassifiable
• Report suggesting an adverse reaction
• Cannot be judged because information is insufficient or Contradictory
• Data cannot be supplemented or verified

Reference The Uppsala Monitoring Center. The use of the WHO-UMC system for standardised case causality assessment. Reproduced with permission of Uppsala monitoring centre. Available at https://www.who-umc.org/media/2768/standardised-case-causality-assessment.pdf