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Table 6 Classification of DRP (N = 191)

From: Drug-related problems in type 2 diabetes mellitus patients with dyslipidemia

Code

Detailed classification

n (%)

P1

Adverse reactions

31 (7.6)

P1.1

Side-effect suffered (non-allergic)

27 (6.6)

P1.2

Side-effect suffered (allergic)

4 (1.0)

P2

Drug choice problem

106 (26.1)

P2.1

Inappropriate drug (not most appropriate for indication)

27 (6.7)

P2.2

Inappropriate drug form (not most appropriate for indication)

1 (0.2)

P2.3

Inappropriate duplication of therapeutic group or active ingredient

9 (2.2)

P2.4

Contra-indication for drug (incl. Pregnancy/breast feeding)

15 (3.7)

P2.5

No clear indication for drug use

8 (2.0)

P2.6

No drug prescribed but clear indication

46 (11.3)

P3

Dosing problem

58 (14.3)

P3.1

Drug dose too low or dosage regime not frequent enough

41 (10.1)

P3.2

Drug dose too high or dosage regime too frequent

10 (2.5)

P3.3

Duration of treatment too short

6 (1.5)

P3.4

Duration of treatment too long

1 (0.2)

P4

Drug use problem

58 (14.3)

P4.1

Drug not taken/administered at all

58 (14.3)

P5

Interactions

73 (18.0)

P5.1

Potential interaction

73 (18.0)

P6

Others

80 (19.7)

P6.1

Patient dissatisfied with therapy despite taking drug(s) correctly

23 (5.7)

P6.2

Insufficient awareness of health and diseases (possibly leading to future problems)

48 (11.8)

P6.3

Unclear complaints. Further clarification necessary

2 (0.5)

P6.4

Therapy failure (reason unknown)

7 (1.7)

Total

 

*406 (100.0)

  1. *A patient may have one or more DRP. DRPs of code P1.3 (toxic effect suffered), P4.2 (wrong drug taken/administered at all) and P5.2 (manifest interaction) were not listed in the table as none of the patients experienced these problems.