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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
A A A+ A- A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 AA AB AC AD AE AF AG AH AI AJ AK AL AM AN AO AP AQ AR AS AT AU AV AW AX AY AZ
AD AD ADA ADB ADC ADD ADE ADF ADH ADI ADJ ADL ADM ADN ADO ADP ADR ADS ADT ADU ADV

Adverse Event Attribution to Product or Procedure

[A specific identifiable level (defined qualitatively or quantitatively) of probability of adverse event being caused or associated with the product or procedure administration to a patient. ( NCI )]
UMLS (NCI) C1510821
 
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