Classification

for Drug related

problems
V8.02
© 2003-2017 Pharmaceutical Care Network Europe Foundation
This classification can freely be used in Pharmaceutical Care Research and practice, as long as the
PCNE association is informed of its use and results of validations. The classification is available
both as a Word document and a PDF document.
Contact: [email protected]

This classification should be referred to as ‘The PCNE Classification V 8.02’

This version is not directly backwards compatible with versions before V8.0.

PCNE classification 1 15-6-2017 V8.02

Introduction

During the working conference of the Pharmaceutical Care Network Europe in January 1999, a
classification scheme was constructed for drug related problems (DRPs). The classification is part of
a total set of instruments. The set consists of the classification scheme, reporting forms and cases for
training or validation. The classification system is validated and adapted regularly. The current
version is V8, which has been developed during an expert workshop in February 2016 and a
subsequent specialist meeting in April 2017. It is no longer compatible with previous versions because
a number of major sections have been revised. In V 8.01, a necessary code C3.5 (which had dropped
out) is re-added.
The classification is for use in research into the nature, prevalence, and incidence of DRPs and also
as a process indicator in experimental studies of Pharmaceutical Care outcomes. It is also meant to
help health care professionals to document DRP-information in the pharmaceutical care process.
Throughout the classification the word ‘drug’ is used, where others might use the term ‘medicine’.
The hierarchical classification is based upon similar work in the field, but it differs from existing
systems because it separates the problems from the causes. Quality experts will recognise that the
causes are often named ‘Medication Errors’ by others.
The following official PCNE-DRP definition is the basis for the classification:

A Drug-Related Problem is an event or circumstance involving drug therapy that actually or

potentially interferes with desired health outcomes.

The basic classification now has 3 primary domains for problems, 8 primary domains for causes and
5 primary domains for Interventions. In V7 a new section, called ‘Acceptance of the Intervention
Proposals’ was added, including 3 domains.
However, on a more detailed level there are 7 grouped sub domains for problems, 35 grouped sub
domains for causes and 16 grouped sub domains for interventions, and 10 subdomains for intervention
acceptance. Those sub-domains can be seen as explanatory for the principal domains.
In 2003 a scale has been added to indicate if or to what extend the problem has been solved, containing
4 primary domains and 7 sub domains.

J.W.Foppe van Mil/ Nejc Horvat / Tommy Westerlund

Zuidlaren, April/May/June/October 2017

Changes between V8.01 and 8.02

The confusing term ‘Therapy failure’ has been removed from P1.1.
An omission has been corrected: C6.6 Administration via wrong route, cause code added.

Changes between V8.0 and 8.01

An omission has been corrected Code C3.5 had dropped out of the tables, and has been reinserted.

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The basic classification

Code Primary domains

V8.01
Problems P1 Treatment effectiveness
(also potential) There is a (potential) problem with the (lack of) effect of
the pharmacotherapy
P2 Treatment safety
Patient suffers, or could suffer, from an adverse drug event
P3 Others
Causes C1 Drug selection
(including possible causes The cause of the DRP can be related to the selection of the
for potential problems) drug
C2 Drug form
The cause of the DRP is related to the selection of the drug
form
C3 Dose selection
The cause of the DRP can be related to the selection of the
dosage schedule
C4 Treatment duration
The cause of the DRP is related to the duration of treatment
C5 Dispensing
The cause of the DRP can be related to the logistics of the
prescribing and dispensing process
C6 Drug use/ process
The cause of the DRP is related to the way the patient gets
the drug administered by a health professional or carer, in
spite of proper instructions (on the label)
C7 Patient related
The cause of the DRP can be related to the patient and his
behaviour (intentional or non-intentional)
C8 Other
Planned Interventions I0 No intervention
I1 At prescriber level
I2 At patient level
I3 At drug level
I4 Other
Intervention Acceptance A1 Intervention accepted
A2 Intervention not accepted
A3 Other
Status of the DRP O0 Problem status unknown
O1 Problem solved
O2 Problem partially solved
O3 Problem not solved

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The Problems

Primary Domain Code Problem

V8.01
1.Treatment effectiveness P1.1 No effect of drug treatment
There is a (potential) problem P1.2 Effect of drug treatment not optimal
with the (lack of) effect of P1.3 Untreated symptoms or indication
the pharmacotherapy
2. Treatment safety P2.1 Adverse drug event (possibly) occurring
Patient suffers, or could
suffer, from an adverse drug
event
3. Others P3.1 Problem with cost-effectiveness of the treatment
P3.2 Unnecessary drug-treatment
P3.3 Unclear problem/complaint. Further clarification
necessary (please use as escape only)

 Potential Problem

 Manifest Problem

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The Causes (including possible causes for potential problems)
N.B. One problem can have more causes

Primary Domain Code Cause

V8.01
1. Drug selection C1.1 Inappropriate drug according to guidelines/formulary
The cause of the (potential) C1.2 Inappropriate drug (within guidelines but otherwise
DRP is related to the selection contra-indicated)
of the drug
C1.3 No indication for drug
C1.4 Inappropriate combination of drugs or drugs and herbal
medication
C1.5 Inappropriate duplication of therapeutic group or active
ingredient
Prescribing

C1.6 No drug treatment in spite of existing indication

C1.7 Too many drugs prescribed for indication
2. Drug form C2.1 Inappropriate drug form (for this patient)
The cause of the DRP is related
to the selection of the drug form
3. Dose selection C3.1 Drug dose too low
The cause of the DRP is related C3.2 Drug dose too high
to the selection of the dose or
C3.3 Dosage regimen not frequent enough
dosage
C3.4 Dosage regimen too frequent
C3.5 Dose timing instructions wrong, unclear or missing
4. Treatment duration C4.1 Duration of treatment too short
The cause of the DRP is related C4.2 Duration of treatment too long
to the duration of treatment
5. Dispensing C5.1 Prescribed drug not available
The cause of the DRP is related
Disp

C5.2 Necessary information not provided

to the logistics of the
C5.3 Wrong drug, strength or dosage advised (OTC)
prescribing and dispensing
process C5.4 Wrong drug or strength dispensed
6. Drug use process C6.1 Inappropriate timing of administration and/or dosing
The cause of the DRP is related intervals
to the way the patient gets the C6.2 Drug under-administered
drug administered by a health
professional or carer, despite C6.3 Drug over-administered
proper dosage instructions (on C6.4 Drug not administered at all
the label) C6.5 Wrong drug administered
C6.6 Drug administered via wrong route
7. Patient related C7.1 Patient uses/takes less drug than prescribed or does not
The cause of the DRP is related take the drug at all
to the patient and his behaviour C7.2 Patient uses/takes more drug than prescribed
Use

(intentional or non-intentional)
C7.3 Patient abuses drug (unregulated overuse)
C7.4 Patient uses unnecessary drug
C7.5 Patient takes food that interacts
C7.6 Patient stores drug inappropriately
C7.7 Inappropriate timing or dosing intervals
C7.8 Patient administers/uses the drug in a wrong way
C7.9 Patient unable to use drug/form as directed
8. Other C8.1 No or inappropriate outcome monitoring (incl. TDM)
C8.2 Other cause; specify
C8.3 No obvious cause
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The Planned Interventions

N.B. One problem can lead to more interventions
Primary Domain Code Intervention
V8.01
No intervention I0.1 No Intervention
1. At prescriber level I1.1 Prescriber informed only
I1.2 Prescriber asked for information
I1.3 Intervention proposed to prescriber
I1.4 Intervention discussed with prescriber
2. At patient level I2.1 Patient (drug) counselling
I2.2 Written information provided (only)
I2.3 Patient referred to prescriber
I2.4 Spoken to family member/caregiver
3. At drug level I3.1 Drug changed to ….
I3.2 Dosage changed to ….
I3.3 Formulation changed to …..
I3.4 Instructions for use changed to …..
I3.5 Drug stopped
I3.6 New drug started
4. Other intervention or I4.1 Other intervention (specify)
activity I4.2 Side effect reported to authorities

Acceptance of the Intervention proposals

N.B. One level of acceptance per intervention proposal

Primary domain Code Implementation

V8.01
1. Intervention accepted A1.1 Intervention accepted and fully implemented
(by prescriber or patient) A1.2 Intervention accepted, partially implemented
A1.3 Intervention accepted but not implemented
A1.4 Intervention accepted, implementation unknown
2. Intervention not A2.1 Intervention not accepted: not feasible
accepted A2.2 Intervention not accepted: no agreement
(by prescriber or patient) A2.3 Intervention not accepted: other reason (specify)
A2.4 Intervention not accepted: unknown reason
3. Other (no information on A3.1 Intervention proposed, acceptance unknown
acceptance) A3.2 Intervention not proposed

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Status of the DRP

N.B. This domain depicts the outcome of the intervention. One problem (or the combination of
interventions) can only lead to one level of solving the problem
Primary Domain Code Outcome of intervention
V8.01
0. Not known O0.1 Problem status unknown
1. Solved O1.1 Problem totally solved
2. Partially solved O2.1 Problem partially solved
3. Not solved O3.1 Problem not solved, lack of cooperation of patient
O3.2 Problem not solved, lack of cooperation of prescriber
O3.3 Problem not solved, intervention not effective
O3.4 No need or possibility to solve problem

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 PCNE
Classification
for Drug
related
problems
Help

V8.02
© 2003-2017 Pharmaceutical Care Network Europe Foundation
This classification can freely be used in Pharmaceutical Care Research and practice, as long as
the Foundation is informed of its use and results of validations. The classification is available
both as a Word document and a PDF document.
Contact: [email protected]

This help document is related to as ‘Help to the PCNE Classification V 8.02

PCNE classification Help 8 15-6-2017 V8.02

Finding or selecting codes in the PCNE classification

A Drug-Related Problem is an event or circumstance involving drug therapy that actually or

potentially interferes with desired health outcomes.

For the use of the PCNE classification it is important to separate the real (or potential) problem
(that affects or is going to affect the outcome) from its cause(s). Often such problems are caused
by a certain type of error e.g. prescribing errors or drug-use or administration errors. But there
might be no error at all involved. Also, a medication error does not necessarily have to lead to a
drug-related problem, there can be no problem or the problem is potential. The cause is usually
the behaviour that has caused (or will cause) the problem, and most often that is a medication
error. A cause or a combination of causes and a problem together, will usually lead to one or
more interventions.
The classification can be used in two ways, depending on the level of information needed.
If only the main domains are used, there is in general enough information for research purposes.
If the system is used for documenting pharmaceutical care activities in practice, the sub domains
can be useful.

Problem section
Basically, the problem is defined as ‘the expected or unexpected event or circumstance that is,
or might be wrong, in therapy with drugs’. (the P-codes)
There are 3 major domains in the problem section. The following descriptions could help to find
the right problem domain:

The clinical effect of the treatment is not as expected or there is no treatment See P1
The patient suffers from an ADR at normal dose or from a toxic reaction See P2
Nothing seems wrong in the treatment, but there is another problem. See P3

Causes section
Each (potential) problem has a cause. The cause is the action (or lack of action) that leads up to
the occurrence of a potential or real problem. There may be more (potential) causes for a
problem. (The C-code)

The cause of the DRP is related to the selection of the drug See C1
The cause of the DRP is related to the selection of the drug form See C2
The cause of the DRP is related to the selection of a dose or dosage schedule See C3
The cause of the DRP is related to the duration of the therapy See C4
The cause of the DRP is related to the logistics of the prescribing or dispensing See C5
process
The cause of the DRP is related to the way the patient gets the drug administered by See C6
a health professional or carer, despite proper dosage instructions (on the label).
(principally used for hospital or home-care by caregivers)
The cause of the DRP is related to the personality or the behaviour of the patient See C7
Other See C8

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Planned Intervention section

The problem will usually lead to one or more in interventions to correct the cause of the problem.
(The I-code)

There is or can be no intervention See I0

Intervention through the prescriber See I1
Intervention through the patient, his carers or relatives See I2
Intervention directly by changing drug or indicating change in drug use See I3
Other intervention See I4

Level of acceptance of intervention proposals

In this section you can indicate if the suggestion for the intervention to patient or prescriber has
been accepted.

Intervention accepted (by prescriber or patient) See A1

Intervention not accepted (by prescriber or patient) See A2
No intervention proposed or acceptance unknown (no information) See A3

Status of the DRP

Previously called Outcome’, this section can be used to document if a problem has been solved.
For evaluation purposes it is desirable to indicate if the problem has been solved by a specific
intervention (the I-code), that has been not, partially or fully accepted by the prescriber and
patient (the A code).

Problem totally solved See O1

Problem partially solved See O2
Problem not solved See O3

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