Survey of unlicensed and off label drug use in paediatric wards in European countriesBMJ 2000; 320 doi: https://doi.org/10.1136/bmj.320.7227.79 (Published 08 January 2000) Cite this as: BMJ 2000;320:79
- Sharon Conroy, lecturer in paediatric clinical pharmacologya,
- Imti Choonara, professor ()a,
- Piero Impicciatore, research fellowa,
- Angelika Mohn, research fellowa,
- Henrik Arnell, research fellowb,
- Anders Rane, professor of clinical pharmacologyb,
- Carmen Knoeppel, medical studentc,
- Hannsjoerg Seyberth, professor of paediatricsc,
- Chiara Pandolfini, research fellowd,
- Maria Pia Raffaelli, hospital pharmacistd,
- Francesca Rocchi, research fellowd,
- Maurizio Bonati, head of unitd,
- Geert't Jong, research fellowe,
- Matthijs de Hoog, consultant in paediatric critical caree,
- John van den Anker, professor in paediatrics and neonatology on behalf of the European Network for Drug Investigation in Childrene
- a Academic Division of Child Health (University of Nottingham), Derbyshire Children's Hospital, Derby DE22 3NE
- b University Hospital, Uppsala, Sweden
- c University Children's Hospital, Marburg, Germany
- d Mario Negri Institute, Milan, Italy
- e Department of Paediatrics (Erasmus University Rotterdam), Sophia Children's Hospital, Rotterdam, Netherlands
- Correspondence to: I Choonara
- Accepted 1 November 1999
Objective: To determine the extent of use of unlicensed and off label drugs in children in hospital in five European countries.
Design: Prospective study of drugs administered to children in general paediatric medical wards over four weeks.
Setting: Children's wards in five hospitals (one each in the United Kingdom, Sweden, Germany, Italy, and the Netherlands).
Subjects: Children aged 4 days to 16 years admitted to general paediatric medical wards.
Main outcome measure: Proportion of drugs that were used in an unlicensed or off label manner.
Results: 2262 drug prescriptions were administered to 624 children in the five hospitals. Almost half of all drug prescriptions (1036; 46%) were either unlicensed or off label. Of these 1036, 872 were off label and 164 were unlicensed. Over half of the patients (421; 67%) received an unlicensed or off label drug prescription.
Conclusions: Use of off label or unlicensed drugs to treat children is widespread. This problem is likely to affect children throughout Europe and requires European action.
Many drugs are not tested in children, which means that they are not specifically licensed for use in children
Licensed drugs are often prescribed outside the terms of the product license (off label) in relation to age, indication, dose of frequency, route of administration, or formulation
Over two thirds (67%) of 624 children admitted to wards in five European hospitals received drugs prescribed in an unlicensed or off label manner
39% of the 2262 drug prescriptions given to children were off label
The problem of off label and unlicensed drug prescribing in children is a European problem that requires European action
Many drugs used to treat children in hospital are either not licensed for use in children or are prescribed outside the terms of their product license (off label prescribing). 1 2 Examples of use of off label drugs include diazepam rectal solution in children under 1 year (not licensed for age group), amiloride tablets in any children (formulation), or rectal injection of lorazepam for a child with an acute seizure (route). An example of unlicensed use is the preparation of a suspension from a tablet by the hospital pharmacy.
Considerable concern exists within Europe3 and the United States 4 5 about the use of unlicensed and off label drugs in children. There is, however, little information available on the extent to which these types of treatments are used. The extent of use of unlicensed and off label drugs in the United Kingdom has been reported in a paediatric intensive care unit,6 paediatric medical and surgical wards,2 and a neonatal intensive care unit.7 We wished to determine the extent of unlicensed and off label drug use in several countries within the European Union. This is important in view of the new European guidance on the clinical investigation of medicinal products in children.8
We studied a paediatric medical ward in each of the participating centres (Derby, United Kingdom; Uppsala, Sweden; Marburg, Germany; Bergamo, Italy; Rotterdam, Netherlands) prospectively for four consecutive weeks during 1998. The wards in Derby and Bergamo admitted mainly general paediatric patients, with Derby including children who had had surgery. The wards in Marburg and Uppsala had a mixture of general paediatric and respiratory cases (including cystic fibrosis). The ward in Rotterdam had the fewest general paediatric cases, containing children with cardiac, oncological, renal, and respiratory disease. Data on all patients admitted to the ward were collected by the investigator in each centre. The child's age, date of birth, weight, and diagnosis were recorded as well as details of all drugs administered (route of administration, dose, and indication for use). We did not include standard intravenous replacement solutions, flushes of 0.9% sodium chloride or heparin, blood products, oxygen, or drugs in clinical trials.
We assessed all drugs administered to determine if their use was unlicensed and off label using a previously described classification system. 1 2 Categories of unlicensed use were modification of licensed drugs (such as crushing tablets to prepare a suspension); drugs that are licensed but the formulation is manufactured under a special licence (such as a liquid preparation of a drug that is licensed only in tablet form); new drugs available under a special manufacturing licence (such as caffeine injections for apnoea of prematurity); use of chemicals as drugs when no pharmaceutical grade preparation is available; drugs used before a licence has been granted; and imported drugs (drugs imported from a country where they are licensed). Off label use included use of a drug in situations not covered by the product licence or the summary of product characteristics—that is, at a different dose or frequency, in different clinical indications, in different age groups, administration by an alternative route, or in a formulation not approved for use in children.
The primary reference sources for determining licensed indications were the Association of the British Pharmaceutical Industry's Data Sheet Compendium in the United Kingdom; the Swedish Physician's Desk Reference 1998 in Sweden; the Rote Liste 1996 and FachInfo compact disc (1997) in Germany; the Informatore Farmaceutico 1998 (national formulary) and technical leaflets in Italy; and the Repertorium 98/99 and Farmacotherapeutisch Kompas 1998 in the Netherlands.
A total of 624 children were admitted to the general paediatric wards in the five participating centres and received 2262 drug prescriptions (table 1). The prescribing habits in the five centres differed greatly. Paracetamol was the most widely prescribed drug and analgesic in four of the five centres. Dipyrone was frequently used in Italy only. Salbutamol and cefuroxime were both widely used (table 2). Almost half of all drug prescriptions (1036) were either unlicensed or off label (table 1). Many more prescriptions were off label (872) than unlicensed (164). The results were remarkably similar in Derby, Uppsala, and Marburg. Use of unlicensed and off label drugs was greatest in Bergamo and Rotterdam, with Bergamo having the highest percentage of off label prescriptions (66%) and Rotterdam the highest percentage of unlicensed prescriptions (14%).
Over half of the children (421; 67%) received an unlicensed or off label drug prescription during their stay in hospital. Analgesics and bronchodilators were among the five most frequently prescribed off label drugs in four centres (table 3). The commonest category of off label drug use was dose and frequency in three centres (Uppsala, Marburg, and Bergamo), accounting for more than half of off label use. In the other two centres (Derby and Rotterdam) dose and frequency accounted for 31-32% of off label drug use. The main category for off label drug use in Rotterdam was formulation. Formulation was also an important category in Bergamo but not in the other centres. Age was the commonest category of off label drug use in Derby (table 4). Table 5 shows examples of off label drug use. In Bergamo 53% of the children who received beclometasone were under 12 months old, although it is licensed only for children aged 2 years and over in Italy.
The drug use in the five paediatric wards differed. This is not surprising as each of the wards had different subspecialty interest and prescribing habits are different within each country.9 Unlicensed drug use was highest in Rotterdam, which had the highest number of patients with complex diseases. Many of these children received drugs that are not available in a paediatric formulation and therefore had to be modified by the pharmacy department to make them suitable for administration to children. Stability data are rarely available for such products, which are rendered unlicensed by this modification. Dipyrone is no longer available in many European countries because of the risk of agranulocytosis.10 It is, however, widely used in Italy. About half of the children in each of the five countries received drugs that are either unlicensed or off label.
It is concerning that most bronchodilator drug prescriptions for children in hospital with asthma are off label, since this is a common condition for which there has been considerable research. The efficacy of bronchodilators in children under the age of 2 years is variable, especially in infants under the age of 12 months. A particular problem was the widespread use of inhaled corticosteroids in children under the age of 2 years (off label for age and dose); few data exist on the effect of inhaled corticosteroids on growth suppression in this age group. Studies are required to determine whether the off label use of bronchodilators is justified by good scientific evidence.
The most common reasons for off label use were that the medicine was prescribed at a different dose or frequency, in a different formulation, or in an age group for which it had not been licensed. There were also some children who received the drug for a different indication or by an alternative route. It is ironic that it is children who are most likely to receive medicines that are either unlicensed or used off label since the regulations for the licensing of medicines were introduced after cases of drug toxicity in the developing fetus (thalidomide) and newborn infant (chloramphenicol induced grey baby syndrome).3
Not all off label drug use is inappropriate. Drug toxicity is more likely with aminoglycosides if they are used in neonates as recommended by the manufacturers at intervals of 8–12 hours rather than at longer intervals. In many cases, however, the risk of off label drug use is not known because there are inadequate data. A recent study has shown that adverse drug reactions are an important problem in children after unlicensed or off label drug prescriptions.11
Reducing the risk
The new European guidance on the clinical investigation of medicinal products in children encourages pharmaceutical companies that wish to introduce new products to investigate these in children when clinically appropriate. Changes have also been made in the United States to encourage pharmaceutical companies to carry out clinical trials in children. These changes in regulations may improve knowledge for new products, although a recent study found little improvement in new drugs licensed in Europe.12 However, a major problem remains with many existing drugs commonly used in children. Health professionals concerned about the lack of information regarding the use of drugs in children are in a difficult situation. They need to raise awareness of the problem in society as a whole without causing undue anxiety among parents.
To ensure that children are not exposed to unnecessary risks, controlled clinical trials are required to determine the most appropriate dose in children of different ages. A mechanism and infrastructure needs to be established to determine who will fund these trials. The European Network for Drug Investigation in Children has been established to try to improve this situation.13 We feel that the European Union, national departments of health, and politicians as well as the European Medicines Evaluation Agency must take a more proactive role in getting drugs tested in children. If they fail to do so, children will continue to be denied the same rights as adults in relation to receiving treatment with drugs that have been fully tested.
Contributors: IC initiated and designed the study, supervised the collection of data, analysed the data, and was involved in writing the paper. SC designed the data collection forms, coordinated and was involved in collecting and analysing the data, and was involved in writing the paper. AM, MPR, FR, GJ, and MH were involved in analysis of the data and in writing the paper. PI, HA, AR, CK, HS, CP, MB, and JA were involved in the design of the study, helped collect the data, analysed the data, and were involved in writing the paper.
Competing interests IC, AR, HS, and JA attended a round table meeting of experts on the use of new medicines in children organised by EMEA in 1997. IC has a grant from the Medicines Control Agency in the United Kingdom in relation to drug reaction surveillance in children.