Implementing Ecopharmacovigilance in Practice: Challenges and Potential Opportunities
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Tracking environmental risks after launch of the product, via literature monitoring for emerging data on exposure and effects
Using Environmental Risk Management Plans (ERMPs) as a centralized resource to assess and manage the risks of a drug throughout its life cycle
Further research, testing or monitoring in the environment when a risk is identified
Keeping a global EPV perspective
Increasing transparency and availability of environmental data for medicinal products.
In recent years concern has been expressed over the potential impact of pharmaceuticals in the environment (PIE) and consequently a comprehensive Environmental Risk Assessment (ERA) is now a regulatory requirement prior to launch of any new drug. However, there is no formal framework or mechanism to review the ERA, or to monitor for potential adverse effects in the environment, once a product has been launched.
Within Europe, the Pharmacovigilance Framework  includes a reference to the pollution of waters and soils with pharmaceutical residues and states that “Member states should consider measures to monitor and evaluate the risk of environmental effects, including those which may have an impact on public health”. This suggests that a kind of PV for the environment, or ecopharmacovigilance (EPV), should be explored.
The aim of this article is to explore what EPV might mean in practice and to discuss some of the challenges and potential opportunities that need to be faced when trying to implement EPV procedures. We also describe our approach to developing Environmental Risk Management Plans (ERMPs), which start to address some of the challenges of EPV.
2 What is Ecopharmacovigilance (EPV)?
Before introducing the EPV concept, some background is necessary on PIE and the ERA of pharmaceuticals.
2.1 Pharmaceuticals in the Environment
In recent years, human pharmaceuticals from numerous therapeutic classes have increasingly been detected in the environment, typically at ng/L to low μg/L in surface waters [2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17]. The potential routes of environmental entry have been extensively reviewed. These include (i) patient excretion either as parent compound or metabolites via the sewer system, (ii) direct release into the waste water system from manufacturing, hospitals or disposal via toilets/sinks, and (iii) terrestrial depositions, for example via sludge application to land, leaching from solid waste landfills, or irrigation with treated or untreated wastewaters [4, 13, 16, 18, 19].
It is generally accepted that excretion of pharmaceuticals after human and veterinary therapeutic use dominates the global input of pharmaceuticals into the environment. Manufacturing effluent discharges and the disposal of unused drugs make a relatively small contribution to the overall environmental load [8, 16, 20, 21]. Nevertheless, localized elevated drug concentrations can occur adjacent to discharges from hospitals  and manufacturing sites if emissions are not properly treated and controlled [23, 24, 25]. Proactive initiatives to manage pharmaceutical manufacturing and formulation wastes have been described elsewhere [26, 27]. Similarly, disposal of unused drugs is a very specific issue that can be managed effectively if the appropriate preventative methods are put in place. This may include guidance for patients, take-back schemes and disposal practices . Pharmaceutical residues in the environment associated with human excretion are an inevitable consequence of patient drug use, and unlike manufacturing-related releases and unused drugs, it is a much more difficult source to control. The level of effective sewage treatment in a particular region may reduce the resulting concentrations, but there will still be some residues remaining, so the question remains as to whether or not such residues present any significant risk, and what level of residues is acceptable. This question is routinely addressed for new drugs by undertaking an ERA as part of the regulatory approval process.
2.2 Environmental Risk Assessment of Pharmaceuticals
In both Europe and North America, there are regulatory requirements governing the ERA of human pharmaceuticals [28, 29]. It is widely accepted that the European Union (EU) regulations are currently the most demanding and data intensive. In most cases, a new regulatory submission or line extension has to be accompanied by an ERA, which requires environmental fate and effects tests to be undertaken.
ERA is addressed through the generation of a risk quotient, i.e. the ratio of the predicted environmental concentration (PEC) to the predicted no-effect concentration (PNEC) ratio (PEC:PNEC). The PEC provides an estimate of the maximum concentration anticipated to occur in the environment, resulting from patient use and subsequent excretion into the wastewater system. The PNEC is derived from ecotoxicological tests, normally on algae, daphnids and fish (representing three trophic levels), together with an assessment factor that accounts for interspecies differences in toxicity. Typically, worst-case assumptions are initially made in deriving the PEC (e.g., 100 % excretion by patients, no removal during sewage treatment), and generally if the PEC:PNEC is <1 no further information is required. Conversely, if PEC:PNEC is >1 then additional testing is generally needed to refine the PEC or PNEC. If this fails to refine the risk quotient to <1 then appropriate risk management measures may need to be put in place.
The ERA must normally be in place prior to approval of a new drug in the EU, and if an environmental risk is identified, “specific arrangements to limit it should be envisaged” . However, there is no requirement for an ERA to be updated or reviewed once a new drug has been approved.
2.3 Definition of EPV
The term ‘ecopharmacovigilance’ was first coined by Velo . However, a number of other articles have proposed terms to describe this newly emerging field: ecopharmacology , environmental pharmacology , pharmacoenvironmentology , pharmacovigilance [21, 34] and ecopharmacostewardship . Whilst these articles introduce the concept of EPV, and some approaches to EPV, they tend to cover a much broader scope that captures all areas of sustainable pharmacy, such as green drug design, green chemistry in process development, minimization of manufacturing emissions, improved prescribing practices and the management of unused drugs. In addition, many of the EPV approaches that have been advocated to date have been largely preventative in nature and have assumed that the presence of pharmaceuticals in the environment will inevitably result in an adverse impact without any consideration of likelihood of impact or risk. As such many of the approaches advocated under EPV are simply designed to reduce the environmental concentrations of pharmaceuticals. In taking this preventative approach, EPV could be in danger of failing to relate field-based observations to the environmental risk assessments, or to understanding whether pharmaceuticals actually result in adverse environmental impacts, and, if so, how. It also fails to consider the relative impact that pharmaceuticals have on ecosystems versus other environmental stimuli.
PV has been defined by the World Health Organisation (WHO) as “the science and activities relating to the detection, assessment understanding and prevention of adverse effects or any other possible drug related problems” [36, 37]. Thus, a reasonable starting point for EPV is to take this definition and directly apply it to the environment. In doing so, EPV would describe the science and activities associated with the detection, evaluation, understanding and prevention of adverse effects of pharmaceuticals in the environment. This definition of EPV reflects the approach communicated at the International Society of Pharmacovigilance annual meeting in Ghana in November 2010 , and that endorsed by Velo and Moretti .
2.4 Comparison of Pharmacovigilance (PV) with EPV
Both PV and EPV aim to monitor the adverse effects of pharmaceuticals, PV in patients and EPV in the environment but potentially also in humans through indirect non-therapeutic exposure. Exposure to drugs in humans is well defined through clinical trials by knowing the dose given and measuring plasma levels, which can in turn in some instances be correlated to adverse drug reactions (ADRs). Conversely, whilst drugs and their metabolites can be detected in the environment and their concentrations measured or predicted, apart from a limited number of studies [40, 41], actual exposure in wildlife is generally not known. Drugs prescribed to patients are monitored, and ADRs identified, discussed and clarified as necessary through the PV process. In contrast, species in the environment are not routinely monitored (unless there is a specific reason to do so) and there is no equivalent to the doctor-patient interaction that is so important for identifying ADRs in patients.
PV is highly regulated in most countries around the world [29, 37] with pharmaceutical companies subject to inspection and dissuasive disciplinary measures in cases of non-compliance. In contrast, EPV is a new concept and an emerging science that is not regulated.
Summary of some of the similarities and differences between ecopharmacovigilance (EPV) and pharmacovigilance (PV)
Similarities between EPV and PV
Differences between EPV and PV
Aims to identify any adverse environmental impacts including the indirect impact on humans
Identifies the nature and frequency of ADRs in patients
Not subject to regulation
Adverse environmental impact may be missed as ERA is conducted in highly controlled exposures in the laboratory, to a limited range of species that act as surrogates for all wildlife
ADRs in the wider patient populations may be missed as preclinical safety assessment is conducted within a limited range of species with defined endpoints and clinical trials represent selected patient populations under controlled conditions
Potentially all species in all environmental compartments could be exposed. This includes indirect exposure to humans
Exposure of prescribed drugs is restricted to identifiable individuals and a target population (human or veterinary)
EPV is captured in the ERMPs
PV is captured in the RMPs
Dose is unknown but environmental concentrations can be predicted or measured. Actual exposure levels are unknown without sophisticated biological monitoring work
Dose is known and defined by medication regimen. Exposure levels can be measured.
EPV issues identified for any drug are documented within the ERMP and action plans are agreed within AstraZeneca
RMPs ensure a robust assessment of the potential risks with a response plan to minimize or mitigate them for patients using AstraZeneca products
No routine monitoring is in place; however, some fish plasma levels are being monitored for scientific studies
Exposed populations are under regular supervision and routine monitoring could be in place
ERA procedures can learn from EPV and be refined to increase future levels of environmental protection.
PV updates the drug development programme and safety assessments
Not possible to identify adverse environmental impacts directly through discussion with the species of concern. Human intervention is required to assess impacts on the environment
In most cases it is possible to discuss and clarify issues with the patient directly.
If adverse environmental impacts are seen it is difficult to attribute these to one particular cause.
May or may not be easy to attribute ADR to one particular drug or a sub-population of patients
2.5 Determining a Relationship between Cause and Effect in the Environment
Unlike many other chemicals that enter the environment, human drugs are designed to have highly specific interactions with their intended biochemical target in their intended target species . It is these unique properties that raised questions over the potential impact of pharmaceuticals in the environment, in terms of their potential interaction with aquatic life, higher predators and humans . Despite the widespread detection of pharmaceuticals in the environment and the potential for effects in wildlife species, there is only one identified case in which an adverse environmental impact in the field has been solely attributed to a pharmaceutical. Diclofenac, a non-steroidal anti-inflammatory drug, is the only well documented example where a pharmaceutical has resulted in an adverse population-level impact on non-target populations in the wild . This was through its veterinary application in South-East Asia to treat inflammation and fever in domestic livestock. Vultures ingested diclofenac when feeding on the carcasses of livestock that had been treated with high doses shortly before their deaths. It is estimated that somewhere between 10 and 40 million vultures have been poisoned, and that three species of Gyps vultures are now critically endangered . Gyps vultures are extremely sensitive to diclofenac and exposure to the drug causes abdominal gout and acute kidney failure. The lethal dose for renal failure is of the order of 0.1–0.2 mg/kg [46, 47]. Acute effects have also been observed in the African white-backed vulture (Gyps africanus) and the Eurasian griffon vulture (Gyps fulvus)  as a result of diclofenac exposure. However, the North American species of vulture such as Cathartes aura appear to be less sensitive than Gyps vultures by exposure to diclofenac . Rapid population declines have also been observed in non-Gyps vulture populations in South America and Asia , but the cause of these declines has not yet been established. A key factor that facilitated the link between the population decline in vultures with diclofenac exposure was the scale of the population decline and the acute impact the diclofenac had. However, it is extremely unlikely that any other human pharmaceuticals will cause such obvious acute effects on wildlife and, consequently, it may prove extremely challenging to link chronic adverse impacts on wildlife with a specific pharmaceutical or group of pharmaceuticals with the same mechanism of action .
A classic example is the case of ethinylestradiol (EE2), a known potent endocrinally active pharmaceutical that has been shown to affect the sexual development of male fish in extremely low concentrations in the laboratory [51, 52, 53]. Comprehensive field surveys have also shown that intersex fish are widespread in British rivers [54, 55]. From an environmental risk assessment perspective, EE2 is without doubt the most extensively studied human pharmaceutical on the market. Nevertheless, it is very difficult to attribute the appearance of feminized male fish in the environment to the presence of EE2 alone since the observed effects can result from the exposure of fish to many other stressors in the environment that are also known to have endocrine-disrupting effects. These include other estrogen-like and anti-androgen-like chemicals such as the nonylphenol and octylphenol ethoxylate surfactants and their degradation products , bisphenol A , phthalates [56, 58], phytoestrogens such as genistein and equol  and endogenous estrogen excreted from women [60, 61]. Population level impacts have been reported in the experimental lake studies by Kidd et al.  as a result of EE2 exposure albeit at levels significantly above those found in rivers. This illustrates the complexity associated with linking cause and effect where several natural and synthetic chemicals are implicated, and the body of scientific data is continuing to grow and the full picture may not yet be clear.
3 EPV in Practice
It is clear that there are several differences between PV and EPV and several challenges that need to be overcome if EPV is to be effective in practice, particularly with respect to relating cause and effect. Nevertheless, whilst EPV is very much a developing concept, we have identified some things that can be done to ensure that risk assessments and scientific understanding of pharmaceuticals in the environment remain as up to date as possible.
3.1 Environmental Risk Management Plans (ERMPs)
3.2 Ongoing Research to Improve Scientific Understanding of Pharmaceuticals in the Environment and Environmental Risk Assessment
ERAs are by definition predictive assessments of potential risks, normally based on experimental laboratory studies. As scientific understanding increases, ERA practice and associated regulatory guidance can be developed accordingly. In many ways, the development of the current EU ERA guideline  demonstrated some of the principles of EPV in that it applied the scientific knowledge and understanding available at the time. Consequently, the current ERA guideline reflects that patient use and excretion result in a widespread continuous emission of low levels of pharmaceuticals to the environment, and as such longer term chronic studies with sublethal endpoints were required to indicate the potential for population level effects. It was also recognized that specific classes of drugs, or particular modes of action (e.g. compounds that are designed to interact with endocrine systems), may require additional evaluation.
One area of current interest is whether it may be possible to predict potential effects on environmental species from knowledge of the preclinical and clinical data for a compound, since many of the biological receptors and metabolic pathways present in humans are also present in environmental species . Winter et al.  have reviewed some of the concepts and challenges faced in using preclinical data, and knowledge of mode of action, from drug discovery and development to aid in the design of more ‘intelligent’ ERA. Such knowledge can help identify potentially sensitive species or sensitive life-stages that should be considered when designing appropriate testing strategies . Similarly, the physicochemical properties, metabolism, stability and adsorption data for a compound can help to identify relevant environmental compartments where it may be expected to be present, which in turn can help to focus further testing. There would seem little point in conducting tests on species that are unlikely to be exposed, for example.
There are many examples of individual and collaborative research between industry, academia and government acting in a proactive manner to improve the scientific understanding of PIE and ERA, to ensure that ERA guidance is offering adequate levels of environmental protection. The European Commission (EC) has funded a number of specific projects in the area. These include KNAPPE (Knowledge and Need Assessment on Pharmaceutical Products in Environmental Waters) , ERAPharm , Pharmas  and Cytothreat . These projects have assessed and are currently assessing the environmental risks associated with β-blockers, selective serotonin reuptake inhibitors, antibiotics and cytotoxic drugs. In addition, the EC  (DG SANCO, DG Environment and the Executive Agency for Health and Consumers; EAHC) is currently reviewing data on PIE and the potential impact on the environment and public health, including a review of the current legislation for human and veterinary drugs. Similarly there have been some important national initiatives around the world that have helped to inform the PIE debate, for example the recent work undertaken by the United Kingdom Water Industry Research (UKWIR) , which investigated in detail the occurrence and removal of several micropollutants, including some pharmaceuticals, in UK wastewaters. Another example is the academia-based PIE project MistraPharma , which aims to identify human pharmaceuticals that are likely to be of concern to aquatic ecosystems, and to address the risk for promotion of antibiotic resistance in the environment.
In addition, partial and full fish life-cycle studies have been conducted to address concerns that the acute to chronic ratios used in risk assessment were not protective enough for all modes of actions. These include studies on EE2 , tamoxifen , propranolol , atenolol [74, 75], anastrozole and bicalutamide , and levonorgestrel and drospirenone .
Studies have also been conducted that demonstrate that the antiviral drug oseltamivir (Tamiflu®) is unlikely to have an impact on the environment as a result of widespread consumption due to the global bird flu pandemic , and seasonal influenza and pandemic-use conditions .
Antibiotics represent a class of drugs that are receiving particular attention as the increasing prevalence of antimicrobial resistance (AMR) in clinically important pathogens is undermining their efficacy. WHO has identified options for action to combat the evolving threat of antimicrobial resistance . Many of the control measures identified are focused on reducing the use of antibiotics and increasing surveillance to track antimicrobial use and resistance; they do not appear to look at natural reservoirs of resistance and the impact that other chemical co-selectors may have on the increased burden and transmission of AMR. At a recent AMR workshop hosted by the Canadian Society of Microbiology it was agreed that an increasing body of data exists that demonstrates that the genes encoding for resistance in clinically relevant bacteria appear to be recruited from environmental bacteria [81, 82, 83]. Therefore more research is required to determine whether environmental input of human and veterinary antibiotics, antibiotic-resistant bacteria, biocides and metals (e.g. copper and zinc) from various activities promotes an increase in the abundance of antibiotic-resistant bacteria in clinically important pathogens.
Finally, the Society of Environmental Toxicology and Chemistry (SETAC) has recently published the outcomes of a collaborative workshop that identified the top 20 questions related to PIE . The workshop was attended by experts from academia, governments and industry from around the world and provides an important summary of current knowledge gaps and future research needs. Some of the key recommendations for further research work were to (i) conduct a comparative assessment between pharmaceuticals and other environmental stressors to determine their relative impact on human and environmental health, (ii) determine whether environmental exposure to antibiotic residues results in adverse human health outcomes through the spread of antimicrobial resistance to clinically important pathogens, and (iii) link mode of action-based biomarker responses to ecologically important adverse outcome pathways.
These examples highlight just some of the proactive and collaborative approaches to product stewardship and research on PIE. They also demonstrate that all interested stakeholders from regulatory agencies, academia, non-governmental organizations and industry are actively engaged in the debate. Such initiatives demonstrate many of the principles of EPV and are essential for improving our understanding of the science of PIE. The outcomes ultimately may lead to improvements in ERA practices and can help to inform the revisions of future ERA regulation.
3.3 Literature Monitoring and ERA/ERMP Refinement
Within AstraZeneca, alongside our research activities we routinely monitor the literature for any newly published information relating to our products. Depending on the significance of any findings, such data may then be used to refine the ERA assumptions, and update the ERMPs as appropriate. In practice this generally requires identifying and assessing any relevant published ecotoxicological information that could impact the PNEC and any information on fate and exposure that might impact on the PEC. This includes any data on the occurrence of the APIs in the environment and deciding how such findings should be interpreted, for example whether measured concentrations relate to manufacturing or hospital discharges or whether they are indicative of more widespread concentrations associated with normal patient use and excretion into domestic wastewater. To be used in ERA directly, any published information, including non-standard data, needs to be sufficiently robust, for example following the criteria laid out by Klimisch et al. , Kϋster et al.  and Ågerstrand et al. . If relevant information is identified, and if there is an established link between the endpoint and an adverse population effect , this can then be used to refine the ERA assumptions as appropriate, and options for further risk refinement, risk management or further research can then be considered in the ERMP. It is also important to recognise that publications of biomarker endpoints can also be useful to direct future research activities , but it is equally important that such studies include sufficient supporting information so that the data may be interpreted appropriately.
3.4 Refining ERAs when the Ratio of the Predicted Environmental Concentration to the Predicted No-Effect Concentration is >1
If the PEC:PNEC is >1, further refinement of the risk assessment is generally appropriate. This might require additional targeted testing to refine the PEC or the PNEC. Another option might be to undertake targeted monitoring of concentrations in the environment in order to confirm whether the PEC calculations are reasonable. The choice of follow-up measure adopted is likely to be decided on a case-by-case basis, reflecting the nature of the risks identified and the data available for the specific compound in question.
For drugs that are relatively data rich, species sensitivity distributions have been generated with all the environmental effects data to provide more confidence in the effects and risk assessment. Two examples of such an approach are the work of Caldwell et al.  for EE2, and the deterministic and probabilistic risk assessment of naproxen by Straub and Stewart . Further refinement in the PEC values for EE2 have been made based on the results from the PhATE (Pharmaceutical Assessment and Transport Evaluation) and GREAT-ER (Geography Referenced Regional Exposure Assessment Tool for European Rivers) models to identify the 90th-percentile low-flow PECs in surface water for EE2 in the USA and Europe, respectively .
3.5 Keeping a Global EPV Perspective
Current ERA practices largely reflect EU and US pharmaceutical use patterns and the potential risks associated with drugs in those regions. Just as PV addresses regional differences, so too should ERAs be designed to ensure protection in any region where the drug will be used. Whilst many areas of the European Medicines Agency (EMA) ERA guideline have global relevance, there may be some inherent assumptions that are not applicable in other regions. For example, the EMA guideline does not consider irrigation as a potential route to the terrestrial environment, whilst this is normal practice in some parts of the world, particularly in water-stressed areas. Similarly, disease prevalence, cultural practices and climate are different in different parts of the world, so the risk profile associated with a pharmaceutical agent may also be different. The challenge is to identify what region-specific exposure scenarios may need to be considered, recognizing that this may not always be straightforward, especially when considering uses such as for example the veterinary use of diclofenac in cattle. A major reason for the unanticipated impact of diclofenac on vulture populations was the sensitivity of certain raptors to diclofenac and a failure of the risk assessment to recognise this exposure route. Secondary poisoning of raptors has previously been recognised and mitigated against. For example, bald and golden eagles, other wildlife and domestic dogs have been intoxicated or killed after ingestion of pentobarbital residues present in tissues of euthanized carcasses that have been disposed of inadequately . In order to control these risks, disposal procedures were tightened (e.g., incineration of euthanized carcasses or immediate deep burial) and penalties for the violation of appropriate disposal were developed. Thus, it is certainly relevant, and arguably the essence of EPV, to ask the question whether the vulture decline could have been detected earlier if this exposure route had been identified before employing widespread use in cattle. As pointed out by Winter et al. , if this exposure route had been considered, then this might have triggered targeted effects testing on carrion-feeding birds. This underlines the importance of consideration of the patterns of compound usage, local cultural and agricultural practices, and ecology of the species assessed, in order to explain the patterns of contamination observed.
3.6 Transparency with Data
One of the ways to encourage effective EPV practices is to ensure that relevant environmental information is shared between government, academia, industry and other interested stakeholders. For several years environmental data have been made publically available in the Swedish Prescribing guide , which includes environmental risk information of the API, based on the PEC/PNEC ratio, as well as information about degradation and bioaccumulation, and results from environmental studies. Environmental data for AstraZeneca products are now also available on their corporate responsibility webpages . The information available on AstraZeneca.com is slightly different to that on Fass.se in that it considers an EU-wide risk assessment, rather than a Swedish-based one; however, both systems are based on the total API volume used in all products, from all companies, containing the same active ingredient. It is hoped that this transparency will contribute to the scientific knowledge about environmental properties of API. It is notable that the EMA has recently made significant changes to its policy on data transparency . It is not yet clear how this will work in practice but it is likely that much of the ERA information that is provided as part of the regulatory submission will be more publically accessible in future.
3.7 Identifying Adverse Environmental Impacts
One of the key challenges for EPV is that any observations of ecological trends or adverse effect in the environment will almost certainly not (at least initially) be identified as being associated with any one particular cause. It took several years to identify the cause of the vulture decline due to diclofenac poisoning. Similarly, research into the causes and consequences of intersex in fish is now well into its second decade, with no single cause having been identified. Whether there is a long-term population-level impact is also still uncertain and is dependent on the severity of feminized males [103, 104]. Another key challenge for EPV is that in the environment there are many different species that may be potentially exposed; however, it is simply not possible to monitor all of them. In contrast, with PV, it is usually possible to monitor all patients who are taking a particular drug.
Biological monitoring studies of species, species assemblages and ecosystems are being undertaken all the time by a range of researchers in many parts of the world. These may identify adverse or unexpected effects of unknown cause and such observations may (or may not) subsequently be included in reports or scientific publications. However, even if the observations are reported they are, in effect, randomly distributed throughout the literature and there is currently no worldwide process, other than serendipity, whereby connections might be made and restorative action initiated.
In the EU, this type of monitoring activity already forms the central core of the Water Framework Directive (WFD), and requires that every watercourse within the EU27 has to be monitored periodically to determine its ecological status. Those that do not comply with the conditions for “good ecological” status must be subjected to further investigation to determine the reason for their non-compliance. Once the reasons have been established, plans then need to be drawn up and implemented to remedy the deficiency.
In terms of pharmaceuticals, it would be expected that any adverse impact in the aquatic environment would occur where the environmental residue concentration was highest, for example in the vicinity of outfalls from large wastewater treatment plants. Consequently, within the EU any such adverse impacts could emerge from the ecological monitoring being undertaken for the WFD, although attribution of cause and effect is still likely to be extremely difficult unless there is a very substance-specific effect. In addition, potential adverse environmental impacts in species living in the terrestrial or atmospheric environment would be unlikely to be identified from the activities within the WFD. It should also be noted that ecological monitoring is undertaken at a local level with no formal mechanism for sharing data on adverse impacts either between or even within member states.
The above sections highlight some of the challenges associated with EPV and some of the practical measures that can be undertaken to ensure that the ERA understanding of a drug remains up to date and globally relevant throughout the life of a new drug.
Most of the pro-active measures proposed here often form part of the research activities that are already undertaken by pharmaceutical companies, academics and governments, sometimes collaboratively, and are not part of any regulatory requirement. However, it is also clear in the EU Medicines Directive that if a risk is identified in the ERA follow-up work is required to refine the ERA or identify appropriate “specific arrangements to limit it”. Thus, in principle the mechanism exists in the EU to manage risks effectively for new medicinal products and line extensions, providing those risks are identified before approval.
One additional challenge for EPV is that many older established drugs pre-date current regulatory requirements for environmental risk assessment. Of approximately 4,000 APIs on the market today only about 10 % have sufficient data to enable a PEC:PNEC value to be calculated . For these drugs there is typically considerably more information on their occurrence in the environment than there is on their effects. Thus, the significance of trace levels of these drugs in the environment is often poorly understood. The challenge is to identify which of these APIs should be prioritized for further evaluation.
In an attempt to address this challenge, Roos et al.  have used nine prioritization schemes to prioritize and rank 582 human drugs based on environmental hazard and risk. Due to the availability of data, not all these drugs could be assessed. The authors favoured risk-based approaches over hazard-based systems, as environmental risk reflects both exposure and impact, and recommended that hazard-based approaches should only be applied for human drugs where insufficient exposure data exist. Using the traditional PEC:PNEC prioritization approach on 196 human drugs, for which robust data were available, they identified seven with a PEC:PNEC >1, indicating that, where sufficient data exist for analysis, the majority of pharmaceuticals pose no significant risk to the environment.
5 Summary and Conclusions
In this article we have accepted the definition of EPV based upon the WHO definition of PV:
Ecopharmacovigilance is the science and activities associated with the detection, evaluation, understanding and prevention of adverse effects of pharmaceuticals in the environment.
We have presented some ideas on what EPV might mean in practice, together with some challenges and opportunities for implementing EPV procedures. We suggest that the main focus of EPV should be after launch of a drug, which will help to identify any possible risks throughout the life of the product. It should be emphasized that EPV is a developing science, still very much in its infancy, and there is therefore room for further debate and research before any formalized approach to EPV is established.
We have identified that there are many similarities between EPV and PV, but also some important differences that have implications for any practical implementation of EPV. In particular, to determine a causal relationship between a drug and an ADR is not straightforward in terms of a patient, but nowhere near as difficult as attributing adverse impacts in environmental species to a single drug.
Tracking environmental risks after launch of the product, via literature monitoring for emerging data, and by use of Environmental Risk Management Plans
Further research, testing or monitoring in the environment when a risk is identified
Keeping a global EPV perspective
Increasing transparency and availability of environmental data for medicinal products.
These measures will help to ensure that any issues associated with PIE are identified in a timely way, and can be managed appropriately. In addition, research in this area will continue, and the SETAC 20 questions publication  has provided a comprehensive summary of the current state of science of PIE and has identified clear areas where future research is needed.
Sarah Barrett, Nigel Budgen, Claire Coleman, Paul Robinson and Alan Sharpe are acknowledged for their valuable input into the establishing of ecopharmacovigilance principles in AstraZeneca. In addition support from the AstraZeneca Safety, Health and Environment Strategy is acknowledged.
Conflict of interest
The authors have no conflicts of interest that are directly relevant to the content of this paper.
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