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. 2017 Jun 8;18:44. doi: 10.1186/s40360-017-0153-6

Table 2.

Drugs grouped by Anatomical Therapeutic Chemical (ATC) classification code and their relative distribution in clusters C1–C4 based on the similarity of their predicted adverse drug reactions induced by synergistic drug-drug interactions (ADRs)

ATC code Classification All drugs C1
%
C2
%
C3
%
C4
%
ADR
N %
A Alimentary tract and metabolism 64 10 12 14 10 8 ~
B Blood and blood forming organs 12 2 2 1 1 4 ~
C Cardiovascular system 88 14 22 24 11 8 + +
D Dermatologicals 19 3 2 0 4 5
G Genito/urinary system and sex hormones 28 5 0 4 6 7
H Systemic hormonal preparations 9 1 0 1 <1 4
J Anti-infectives for systemic use 34 6 6 7 5 5 ~
L Antineoplastic and immune-modulating agents 61 10 1 1 11 20 – –
M Musculo-skeletal system 45 7 16 7 4 5 + +
N Nervous system 167 27 29 28 31 21 ~
P Anti-parasitic products, insecticides, and repellents 10 2 0 0 2 3
R Respiratory system 49 8 6 11 8 7 ~
S Sensory organs 11 2 2 1 2 2 ~
V Various 16 3 3 2 3 2 ~

Only drugs that have an ATC classification are included. The last column indicates the propensity of ADRs to be preferentially associated with compounds in clusters C1 and C2 (+ +), have no preferential association with drugs in any cluster (~), or be preferentially associated with compounds in clusters C3 and C4 (– or – –), respectively. Each column sums to 100% and the values indicate the distribution of drugs among the ATC classification for each cluster. The number of DDI-induced ADRs for each drug was highly variable, indicating no systematic variation of DDI-induced ADRs on a per drug basis among the ATC drug classes