E2e step 4 pharmacovigilance planning (pvp)

ICH Step 4
November 2003
November 2003
December 2004
June 2005
7 Westferry Circus, Canary Wharf, London, E14 4HB, UK Tel. (44-20) 74 18 85 75 Fax (44-20) 75 23 70 40 E-mail: mail@emea.eu.int http://www.emea.eu.int EMEA 2004 Reproduction and/or distribution of this document is authorised for non commercial purposes only provided the EMEA is acknowledged PHARMACOVIGILANCE PLANNING: PLANNING OF PHARMACOVIGILANCE
Table of Content
2.1.1 Non-clinical.5 2.1.2 Clinical .5 a. Limitations of the human safety database .5 b. Populations not studied in the pre-approval phase .6 c. Adverse events (AEs) / Adverse drug reactions (ADRs) .6 Identified risks that require further evaluation.6 Potential risks that require further evaluation .6 d. Identified and potential interactions, including food-drug and drug-drug interactions e. Epidemiology.6 f. Pharmacological class effects .7 3. PHARMACOVIGILANCE PLAN .7
3.1 STRUCTURE OF THE PHARMACOVIGILANCE PLAN.7 3.1.1 Summary of ongoing safety issues.7 3.1.2 Routine pharmacovigilance practices .8 3.1.3 Action plan for safety issues.8 3.1.4 Summary of actions to be completed, including milestones .8 3.2.1 Design and Conduct of Observational Studies .9 4. REFERENCES .9
Pharmacovigilance planning: planning of pharmacovigilance activities

1. Introduction
1.1 Objective
This guideline is intended to aid in planning pharmacovigilance activities, especially in
preparation for the early postmarketing period of a new drug (in this guideline, the term
“drug” denotes chemical entities, biotechnology-derived products, and vaccines). The main
focus of this guideline is on a Safety Specification and Pharmacovigilance Plan that might be
submitted at the time of licence application. The guideline can be used by sponsors to develop
a stand-alone document for regions that prefer this approach or to provide guidance on
incorporation of elements of the Safety Specification and Pharmacovigilance Plan into the
Common Technical Document (CTD).
The guideline describes a method for summarising the important identified risks of a drug,
important potential risks, and important missing information, including the potentially at-risk
populations and situations where the product is likely to be used that have not been studied
pre-approval. It proposes a structure for a Pharmacovigilance Plan and sets out principles of
good practice for the design and conduct of observational studies. It does not describe other
methods to reduce risks from drugs, such as risk communication. The guideline takes into
consideration ongoing work in the three regions and beyond on these issues.
This guideline does not cover the entire scope of pharmacovigilance. It uses the WHO
definition of the term ‘pharmacovigilance’ as “the science and activities relating to the
detection, assessment, understanding and prevention of adverse effects or any other drug
related problems.” This definition encompasses the use of pharmacoepidemiological studies.
1.2 Background
The decision to approve a drug is based on its having a satisfactory balance of benefits and
risks within the conditions specified in the product labeling. This decision is based on the
information available at the time of approval. The knowledge related to the safety profile of
the product can change over time through expanded use in terms of patient characteristics and
the number of patients exposed. In particular, during the early postmarketing period the
product might be used in settings different from clinical trials and a much larger population
might be exposed in a relatively short timeframe.
Once a product is marketed, new information will be generated, which can have an impact on
the benefits or risks of the product; evaluation of this information should be a continuing
process, in consultation with regulatory authorities. Detailed evaluation of the information
generated through pharmacovigilance activities is important for all products to ensure their
safe use. The benefit-risk balance can be improved by reducing risks to patients through
effective pharmacovigilance that can enable information feedback to the users of medicines in
a timely manner.
Industry and regulators have identified the need for better and earlier planning of
pharmacovigilance activities before a product is approved or a license is granted. This ICH
guideline has been developed to encourage harmonisation and consistency, to prevent
duplication of effort, and could be of benefit to public health programs throughout the world
as they consider new drugs in their countries.

1.3 Scope
The guideline could be most useful for new chemical entities, biotechnology-derived
products, and vaccines, as well as for significant changes in established products (e.g., new
dosage form, new route of administration, or new manufacturing process for a
biotechnologically-derived product) and for established products that are to be introduced to
new populations or in significant new indications or where a new major safety concern has
The purpose of this guideline is to propose a structure for a Pharmacovigilance Plan, and a
Safety Specification that summarises the identified and potential risks of the product to be
addressed in the Plan. The guideline is divided into the following sections:
• Safety Specification
• Annex – Pharmacovigilance Methods. It is recommended that company pharmacovigilance experts get involved early in product development. Planning and dialogue with regulators should also start long before license application. A Safety Specification and Pharmacovigilance Plan can also be developed for products already on the market (e.g., new indication or major new safety concern). The Plan could be used as the basis for discussion of pharmacovigilance activities with regulators in the different ICH regions and beyond. For products with important identified risks, important potential risks or important missing information, the Pharmacovigilance Plan should include additional actions designed to address these concerns. For products for which no special concerns have arisen, routine pharmacovigilance as described in section 3.1.2 should be sufficient for post-approval safety monitoring, without the need for additional actions (e.g., safety studies). During the course of implementing the various components of the Plan, any important emerging benefit or risk information should be discussed and used to revise the Plan. The following principles underpin this guideline: • Planning of pharmacovigilance activities throughout the product life-cycle • Science-based approach to risk documentation • Effective collaboration between regulators and industry • Applicability of the Pharmacovigilance Plan across the three ICH regions.
2. Safety Specification

The Safety Specification should be a summary of the important identified risks of a drug,
important potential risks, and important missing information. It should also address the
populations potentially at-risk (where the product is likely to be used), and outstanding safety
questions which warrant further investigation to refine understanding of the benefit-risk
profile during the post-approval period. This Safety Specification is intended to help industry
and regulators identify any need for specific data collection and also to facilitate the
construction of the Pharmacovigilance Plan. The Safety Specification can be built initially
during the pre-marketing phase and, at the time approval is sought, it should reflect the status
of issues that were being followed during development.

The Common Technical Document (CTD), especially the Overview of Safety [2.5.5],
Benefits and Risks Conclusions [2.5.6], and the Summary of Clinical Safety [2.7.4] sections,
includes information relating to the safety of the product, and should be the basis of the safety
issues identified in the Safety Specification. Sponsors should support the Safety Specification
with references to specific pages of the CTD or other relevant documents. The Safety
Specification can be a stand-alone document, usually in conjunction with the
Pharmacovigilance Plan, but elements can also be incorporated into the CTD. The length of
the document will generally depend on the product and its development program. Appendices
can be added if it is considered important to provide a more detailed explanation of important
risks or analyses.

2.1 Elements of the Specification
It is recommended that sponsors follow the structure of elements provided below when
compiling the Safety Specification. The elements of the Safety Specification that are included
are only a guide. The Safety Specification can include additional elements, depending on the
nature of the product and its development program. Conversely, for products already on the
market with emerging new safety concerns, only a subset of the elements might be relevant.
The focus of the Safety Specification should be on the identified risks, important potential
risks, and important missing information. The following elements should be considered for
2.1.1 Non-clinical
Within the Specification, this section should present non-clinical safety findings that have not
been adequately addressed by clinical data, for example:
• Toxicity (including repeat-dose toxicity, reproductive/developmental toxicity,
nephrotoxicity, hepatotoxicity, genotoxicity, carcinogenicity etc.) • General pharmacology (cardiovascular, including QT interval prolongation; nervous • Other toxicity-related information or data. If the product is intended for use in special populations, consideration should be given to whether specific non-clinical data needs exist. 2.1.2 Clinical A. LIMITATIONS OF THE HUMAN SAFETY DATABASE
Limitations of the safety database (e.g., related to the size of the study population, study inclusion/exclusion criteria) should be considered, and the implications of such limitations with respect to predicting the safety of the product in the marketplace should be explicitly discussed. Particular reference should be made to populations likely to be exposed during the intended or expected use of the product in medical practice. The world-wide experience should be briefly discussed, including: Any new or different safety issues identified Any regulatory actions related to safety. B. POPULATIONS NOT STUDIED IN THE PRE-APPROVAL PHASE
The Specification should discuss which populations have not been studied or have only been studied to a limited degree in the pre-approval phase. The implications of this with respect to predicting the safety of the product in the marketplace should be explicitly discussed (CTD 2.5.5). Populations to be considered should include (but might not be limited to): • Patients with relevant co-morbidity such as hepatic or renal disorders • Patients with disease severity different from that studied in clinical trials • Sub-populations carrying known and relevant genetic polymorphism • Patients of different racial and/or ethnic origins. C. ADVERSE EVENTS (AES) / ADVERSE DRUG REACTIONS (ADRS)
This section should list the important identified and potential risks that require further characterisation or evaluation. Specific references should be made to guide a reviewer to where clinical safety data are presented (e.g., relevant sections of the CTD 2.5.5 and 2.7.4). Discussion of risk factors and potential mechanisms that apply to identified AEs/ADRs should draw on information from any part of the CTD (non-clinical and clinical) and other relevant information, such as other drug labels, scientific literature, and post-marketing experience. Identified risks that require further evaluation More detailed information should be included on the most important identified AEs/ADRs, which would include those that are serious or frequent and that also might have an impact on the balance of benefits and risks of the product. This information should include evidence bearing on a causal relationship, severity, seriousness, frequency, reversibility and at-risk groups, if available. Risk factors and potential mechanisms should be discussed. These AEs/ADRs should usually call for further evaluation as part of the Pharmacovigilance Plan (e.g., frequency in normal conditions of use, severity, outcome, at-risk groups, etc.). Potential risks that require further evaluation Important potential risks should be described in this section. The evidence that led to the conclusion that there was a potential risk should be presented. It is anticipated that for any important potential risk, there should be further evaluation to characterise the association. D. IDENTIFIED AND POTENTIAL INTERACTIONS, INCLUDING FOOD-DRUG AND DRUG-DRUG
Identified and potential pharmacokinetic and pharmacodynamic interactions should be discussed. For each, the evidence supporting the interaction and possible mechanism should be summarised, and the potential health risks posed for the different indications and in the different populations should be discussed. E. EPIDEMIOLOGY
The epidemiology of the indication(s) should be discussed. This discussion should include incidence, prevalence, mortality and relevant co-morbidity, and should take into account whenever possible stratification by age, sex, and racial and/or ethnic origin. Differences in the epidemiology in the different regions should be discussed (because the epidemiology of the indication(s) may vary across regions), if this information is available. In addition, for important adverse events that may require further investigation, it is useful to review the incidence rates of these events among patients in whom the drug is indicated (i.e., the background incidence rates). For example, if condition X is an important adverse event in patients who are treated with drug Y for disease Z, then it is useful to review the incidence of condition X in patients with disease Z who are not treated with drug Y; this is the background rate of condition X among patients with disease Z. Information on risk factors for an adverse event (condition X) would also be useful to include, if available. F. PHARMACOLOGICAL CLASS EFFECTS
The Safety Specification should identify risks believed to be common to the pharmacological
2.2 Summary
At the end of the Safety Specification a summary should be provided of the:
• Important identified risks
• Important missing information.
Sponsors are encouraged to summarise specific ongoing safety issues on an issue-by-issue
basis, including both non-clinical and clinical data that are pertinent to the problem.
3. Pharmacovigilance Plan

This section gives guidance on the structure of a Pharmacovigilance Plan. The
Pharmacovigilance Plan should be based on the Safety Specification. The Specification and
Plan can be written as two parts of the same document. The Plan would normally be
developed by the sponsor and can be discussed with regulators during product development,
prior to approval (i.e., when the marketing application is submitted) of a new product, or
when a safety concern arises post-marketing. It can be a stand-alone document but elements
could also be incorporated into the CTD.
For products for which no special concerns have arisen, routine pharmacovigilance as
described in section 3.1.2 should be sufficient for post-approval safety monitoring, without
the need for additional actions (e.g., safety studies). However, for products with important
identified risks, important potential risks, or important missing information, additional actions
designed to address these concerns should be considered.
The length of the document will likely depend on the product and its development program.
The Pharmacovigilance Plan should be updated as important information on safety becomes
available and milestones are reached.
3.1 Structure of the Pharmacovigilance Plan
Outlined below is a suggested structure for the Pharmacovigilance Plan. The structure can be
varied depending on the product in question and the issues identified in the Safety
3.1.1 Summary of ongoing safety issues
At the beginning of the Pharmacovigilance Plan a summary should be provided of the:
• Important identified risks
This is important if the Pharmacovigilance Plan is a separate document from the Safety Specification. 3.1.2 Routine pharmacovigilance practices Routine pharmacovigilance should be conducted for all medicinal products, regardless of whether or not additional actions are appropriate as part of a Pharmacovigilance Plan. This routine pharmacovigilance should include the following: • Systems and processes that ensure that information about all suspected adverse reactions that are reported to the personnel of the company are collected and collated in an accessible manner • The preparation of reports for regulatory authorities: o Expedited adverse drug reaction (ADR) reports o Periodic Safety Update Reports (PSURs) • Continuous monitoring of the safety profile of approved products including signal detection, issue evaluation, updating of labeling, and liaison with regulatory authorities • Other requirements, as defined by local regulations. In some ICH regions, there might be a regulatory requirement to present within the Pharmacovigilance Plan an overview of the company’s organisation and practices for conducting pharmacovigilance. In the absence of such a requirement, a statement that the company’s routine pharmacovigilance practices include the elements outlined in the bulleted list above should be sufficient. 3.1.3 Action plan for safety issues The Plan for each important safety issue should be presented and justified according to the following structure: • Safety issue • Monitoring by the sponsor for safety issue and proposed action(s) • Milestones for evaluation and reporting. Any protocols for specific studies can be provided in the CTD section Other Clinical Study Reports or other sections as appropriate (e.g., Module 4 if the study is a non-clinical study). 3.1.4 Summary of actions to be completed, including milestones An overall Pharmacovigilance Plan for the product bringing together the actions for all individual safety issues should be presented. Whereas section 3.1.3 suggests presenting an action plan by ongoing safety issue, for this section the Pharmacovigilance Plan for the product should be organised in terms of the actions to be undertaken and their milestones. The reason for this is that one proposed action (e.g., a prospective safety cohort study) could address more than one of the identified issues. It is recommended that milestones for completion of studies and other evaluations, and for submission of safety results, be included in the Pharmacovigilance Plan. In developing these milestones one should consider when: • Exposure to the product will have reached a level sufficient to allow potential identification/characterisation of the AEs/ADRs of concern or resolution of a particular concern, and/or • The results of ongoing or proposed safety studies are expected to be available. These milestones might be aligned with regulatory milestones (e.g., PSURs, annual
reassessment and license renewals) and used to revise the Pharmacovigilance Plan.

3.2 Pharmacovigilance methods
The best method to address a specific situation can vary depending on the product, the
indication, the population being treated and the issue to be addressed. The method chosen can
also depend on whether an identified risk, potential risk or missing information is the issue
and whether signal detection, evaluation or safety demonstration is the main objective of
further study. When choosing a method to address a safety concern, sponsors should employ
the most appropriate design. The Annex provides a summary of the key methods used in
pharmacovigilance. This is provided to aid sponsors considering possible methods to address
specific issues identified by the Safety Specification. This list is not all-inclusive, and
sponsors should use the most up-to-date methods that are relevant and applicable.
3.2.1 Design and Conduct of Observational Studies
Carefully designed and conducted pharmacoepidemiological studies, specifically
observational (non-interventional, non-experimental) studies, are important tools in
pharmacovigilance. In observational studies, the investigator “observes and evaluates results
of ongoing medical care without 'controlling' the therapy beyond normal medical practice.”1
Before the observational study that is part of a Pharmacovigilance Plan commences, a
protocol should be finalised. Experts from relevant disciplines (e.g., pharmacovigilance
experts, pharmacoepidemiologists and biostatisticians) should be consulted. It is
recommended that the protocol be discussed with the regulatory authorities before the study
starts. It is also suggested that the circumstances in which a study should be terminated early
be discussed with regulatory authorities and documented in advance. A study report after
completion, and interim reports if appropriate, should be submitted to the authorities
according to the milestones within the Pharmacovigilance Plan.
Study protocols should, as a minimum, include the study aims and objectives, the methods to
be used, and the plan for analysis. The final study report should accurately and completely
present the study objectives, methods, results, and the principal investigator’s interpretation of
the findings.
It is recommended that the sponsor follow good epidemiological practice for observational
studies and also internationally accepted guidelines, such as the guidelines endorsed by the
International Society for Pharmacoepidemiology.2 In some of the ICH regions, local laws and
guidelines also apply to the design and conduct of observational studies and should be
The highest possible standards of professional conduct and confidentiality should always be
maintained and any relevant national legislation on data protection followed.
4. References
1) CIOMS, Current Challenges in Pharmacovigilance: Pragmatic Approaches. Report of
CIOMS Working Group V. Geneva; World Health Organization (WHO), 2001. 2) Guidelines for Good Pharmacoepidemiology Practices (GPP), International Society for Pharmacoepidemiology, http://www.pharmacoepi.org/resources/guidelines_08027.cfm, August 2004.
ANNEX - Pharmacovigilance Methods
I. Passive

A spontaneous report is an unsolicited communication by healthcare professionals
or consumers to a company, regulatory authority or other organisation (e.g., WHO,
Regional Centres, Poison Control Centre) that describes one or more adverse drug
reactions in a patient who was given one or more medicinal products and that does
not derive from a study or any organised data collection scheme.1
Spontaneous reports play a major role in the identification of safety signals once a
drug is marketed. In many instances, a company can be alerted to rare adverse
events that were not detected in earlier clinical trials or other pre-marketing
studies. Spontaneous reports can also provide important information on at-risk
groups, risk factors, and clinical features of known serious adverse drug reactions.
Caution should be exercised in evaluating spontaneous reports, especially when
comparing drugs. The data accompanying spontaneous reports are often
incomplete, and the rate at which cases are reported is dependent on many factors
including the time since launch, pharmacovigilance-related regulatory activity,
media attention, and the indication for use of the drug.2,3,4,5
Systematic methods for the evaluation of spontaneous reports
More recently, systematic methods for the detection of safety signals from
spontaneous reports have been used. Many of these techniques are still in
development and their usefulness for identifying safety signals is being evaluated.
These methods include the calculation of the proportional reporting ratio, as well
as the use of Bayesian and other techniques for signal detection6,7,8. Data mining
techniques have also been used to examine drug-drug interactions9. Data mining
techniques should always be used in conjunction with, and not in place of,
analyses of single case reports. Data mining techniques facilitate the evaluation of
spontaneous reports by using statistical methods to detect potential signals for
further evaluation. This tool does not quantify the magnitude of risk, and caution
should be exercised when comparing drugs. Further, when using data mining
techniques, consideration should be given to the threshold established for detecting
signals, since this will have implications for the sensitivity and specificity of the
method (a high threshold is associated with high specificity and low sensitivity).
Confounding factors that influence spontaneous adverse event reporting are not
removed by data mining. Results of data mining should be interpreted with the
knowledge of the weaknesses of the spontaneous reporting system and, more
specifically, the large differences in the ADR reporting rate among different drugs
and the many potential biases inherent in spontaneous reporting. All signals should
be evaluated recognising the possibility of false positives. In addition, the absence
of a signal does not mean that a problem does not exist.
Series of case reports can provide evidence of an association between a drug and an adverse event, but they are generally more useful for generating hypotheses than for verifying an association between drug exposure and outcome. There are certain distinct adverse events known to be associated more frequently with drug therapy, such as anaphylaxis, aplastic anemia, toxic epidermal necrolysis and Stevens-Johnson Syndrome10,11. Therefore, when events such as these are spontaneously reported, sponsors should place more emphasis on these reports for detailed and rapid follow-up. Several methods have been used to encourage and facilitate reporting by health professionals in specific situations (e.g., in-hospital settings) for new products or for limited time periods12. Such methods include on-line reporting of adverse events and systematic stimulation of reporting of adverse events based on a pre-designed method. Although these methods have been shown to improve reporting, they are not devoid of the limitations of passive surveillance, especially selective reporting and incomplete information. During the early post-marketing phase, companies might actively provide health professionals with safety information, and at the same time encourage cautious use of new products and the submission of spontaneous reports when an adverse event is identified. A plan can be developed before the product is launched (e.g., through site visits by company representatives, by direct mailings or faxes, etc.). Stimulated adverse event reporting in the early post-marketing phase can lead companies to notify healthcare professionals of new therapies and provide safety information early in use by the general population (e.g., Early Post-marketing Phase Vigilance, EPPV in Japan). This should be regarded as a form of spontaneous event reporting, and thus data obtained from stimulated reporting cannot be used to generate accurate incidence rates, but reporting rates can be estimated. Active surveillance, in contrast to passive surveillance, seeks to ascertain completely the number of adverse events via a continuous pre-organised process. An example of active surveillance is the follow-up of patients treated with a particular drug through a risk management program. Patients who fill a prescription for this drug may be asked to complete a brief survey form and give permission for later contact13. In general, it is more feasible to get comprehensive data on individual adverse event reports through an active surveillance system than through a passive reporting system. Active surveillance can be achieved by reviewing medical records or interviewing patients and/or physicians in a sample of sentinel sites to ensure complete and accurate data on reported adverse events from these sites. The selected sites can provide information, such as data from specific patient subgroups, that would not be available in a passive spontaneous reporting system. Further, information on the use of a drug, such as abuse, can be targeted at selected sentinel sites14. Some of the major weaknesses of sentinel sites are problems with selection bias, small numbers of patients, and increased costs. Active surveillance with sentinel sites is most efficient for those drugs used mainly in institutional settings such as hospitals, nursing homes, haemodialysis centres, etc. Institutional settings can have a greater frequency of use for certain drug products and can provide an infrastructure for dedicated reporting. In addition, automatic detection of abnormal laboratory values from computerized laboratory reports in certain clinical settings can provide an efficient active surveillance system. Intensive monitoring of sentinel sites can also be helpful in identifying risks among patients taking orphan drugs. Drug event monitoring is a method of active pharmacovigilance surveillance. In drug event monitoring, patients might be identified from electronic prescription data or automated health insurance claims. A follow-up questionnaire can then be sent to each prescribing physician or patient at pre-specified intervals to obtain outcome information. Information on patient demographics, indication for treatment, duration of therapy (including start dates), dosage, clinical events, and reasons for discontinuation can be included in the questionnaire12,15,16,17. Limitations of drug event monitoring can include poor physician and patient response rates and the unfocused nature of data collection, which can obscure important signals. In addition, maintenance of patient confidentiality might be a concern. On the other hand, more detailed information on adverse events from a large number of physicians and/or patients might be collected. A registry is a list of patients presenting with the same characteristic(s). This characteristic can be a disease (disease registry) or a specific exposure (drug registry). Both types of registries, which only differ by the type of patient data of interest, can collect a battery of information using standardised questionnaires in a prospective fashion. Disease registries, such as registries for blood dyscrasias, severe cutaneous reactions, or congenital malformations can help collect data on drug exposure and other factors associated with a clinical condition. A disease registry might also be used as a base for a case-control study comparing the drug exposure of cases identified from the registry and controls selected from either patients with another condition within the registry, or patients outside the registry. Exposure (drug) registries address populations exposed to drugs of interest (e.g., registry of rheumatoid arthritis patients exposed to biological therapies) to determine if a drug has a special impact on this group of patients. Some exposure (drug) registries address drug exposures in specific populations, such as pregnant women. Patients can be followed over time and included in a cohort study to collect data on adverse events using standardised questionnaires. Single cohort studies can measure incidence, but, without a comparison group, cannot provide proof of association. However, they can be useful for signal amplification, particularly for rare outcomes. This type of registry can be very valuable when examining the safety of an orphan drug indicated for a specific condition. Traditional epidemiologic methods are a key component in the evaluation of adverse events. There are a number of observational study designs that are useful in validating signals from spontaneous reports or case series. Major types of these designs are cross-sectional studies, case-control studies, and cohort studies (both retrospective and prospective)12,15. Data collected on a population of patients at a single point in time (or interval of time) regardless of exposure or disease status constitute a cross-sectional study. These types of studies are primarily used to gather data for surveys or for ecological analyses. The major drawback of cross-sectional studies is that the temporal relationship between exposure and outcome cannot be directly addressed. These studies are best used to examine the prevalence of a disease at one time point or to examine trends over time, when data for serial time points can be captured. These studies can also be used to examine the crude association between exposure and outcome in ecologic analyses. Cross-sectional studies are best utilised when exposures do not change over time. In a case-control study, cases of disease (or events) are identified. Controls, or patients without the disease or event of interest, are then selected from the source population that gave rise to the cases. The controls should be selected in such a way that the prevalence of exposure among the controls represents the prevalence of exposure in the source population. The exposure status of the two groups is then compared using the odds ratio, which is an estimate of the relative risk of disease in the two groups. Patients can be identified from an existing database or using data collected specifically for the purpose of the study of interest. If safety information is sought for special populations, the cases and controls can be stratified according to the population of interest (the elderly, children, pregnant women, etc.). For rare adverse events, existing large population-based databases are a useful and efficient means of providing needed drug exposure and medical outcome data in a relatively short period of time. Case-control studies are particularly useful when the goal is to investigate whether there is an association between a drug (or drugs) and one specific rare adverse event, as well as to identify risk factors for adverse events. Risk factors can include conditions such as renal and hepatic dysfunction, that might modify the relationship between the drug exposure and the adverse event. Under specific conditions, a case-control study can provide the absolute incidence rate of the event. If all cases of interest (or a well-defined fraction of cases) in the catchment area are captured and the fraction of controls from the source population is known, an incidence rate can be calculated. In a cohort study, a population-at-risk for the disease (or event) is followed over time for the occurrence of the disease (or event). Information on exposure status is known throughout the follow-up period for each patient. A patient might be exposed to a drug at one time during follow-up, but non-exposed at another time point. Since the population exposure during follow-up is known, incidence rates can be calculated. In many cohort studies involving drug exposure, comparison cohorts of interest are selected on the basis of drug use and followed over time. Cohort studies are useful when there is a need to know the incidence rates of adverse events in addition to the relative risks of adverse events. Multiple adverse events can also be investigated using the same data source in a cohort study. However, it can be difficult to recruit sufficient numbers of patients who are exposed to a drug of interest (such as an orphan drug) or to study very rare outcomes. Like case-control studies, the identification of patients for cohort studies can come from large automated databases or from data collected specifically for the study at hand. In addition, cohort studies can be used to examine safety issues in special populations (the elderly, children, patients with co-morbid conditions, pregnant women) through over-sampling of these patients or by stratifying the cohort if sufficient numbers of patients exist. There are several automated databases available for pharmacoepidemiologic studies12,15,18. They include databases which contain automated medical records or automated accounting/billing systems. Databases that are created from accounting/billing systems might be linked to pharmacy claims and medical claims databases. These datasets might include millions of patients. Since they are created for administrative or billing purposes, they might not have the detailed and accurate information needed for some research, such as validated diagnostic information or laboratory data. Although medical records can be used to ascertain and validate test results and medical diagnoses, one should be cognizant of the privacy and confidentiality regulations that apply to patient medical records. When significant risks are identified from pre-approval clinical trials, further clinical studies might be called for to evaluate the mechanism of action for the adverse reaction. In some instances, pharmacodynamic and pharmacokinetic studies might be conducted to determine whether a particular dosing instruction can put patients at an increased risk of adverse events. Genetic testing can also provide clues about which group of patients might be at an increased risk of adverse reactions. Furthermore, based on the pharmacological properties and the expected use of the drug in general practice, conducting specific studies to investigate potential drug-drug interactions and food-drug interactions might be called for. These studies can include population pharmacokinetic studies and drug concentration monitoring in patients and normal volunteers. Sometimes, potential risks or unforeseen benefits in special populations might be identified from pre-approval clinical trials, but cannot be fully quantified due to small sample sizes or the exclusion of subpopulations of patients from these clinical studies. These populations might include the elderly, children, or patients with renal or hepatic disorder. Children, the elderly, and patients with co-morbid conditions might metabolise drugs differently than patients typically enrolled in clinical trials. Further clinical trials might be used to determine and to quantify the magnitude of the risk (or benefit) in such populations. To elucidate the benefit-risk profile of a drug outside of the formal/traditional clinical trial setting and/or to fully quantify the risk of a critical but relatively rare adverse event, a large simplified trial might be conducted. Patients enrolled in a large simplified trial are usually randomized to avoid selection bias. In this type of trial, though, the event of interest will be focused to ensure a convenient and practical study. One limitation of this method is that the outcome measure might be too simplified and this might have an impact on the quality and ultimate usefulness of the trial. Large, simplified trials are also resource-intensive. Descriptive studies are an important component of pharmacovigilance, although not for the detection or verification of adverse events associated with drug exposures. These studies are primarily used to obtain the background rate of outcome events and/or establish the prevalence of the use of drugs in specified populations. The science of epidemiology originally focused on the natural history of disease, including the characteristics of diseased patients and the distribution of disease in selected populations, as well as estimating the incidence and prevalence of potential outcomes of interest. These outcomes of interest now include a description of disease treatment patterns and adverse events. Studies that examine specific aspects of adverse events, such as the background incidence rate of or risk factors for the adverse event of interest, can be used to assist in putting spontaneous reports into perspective15. For example, an epidemiologic study can be conducted using a disease registry to understand the frequency at which the event of interest might occur in specific subgroups, such as patients with concomitant illnesses. Drug utilisation studies (DUS) describe how a drug is marketed, prescribed, and used in a population, and how these factors influence outcomes, including clinical, social, and economic outcomes12. These studies provide data on specific populations, such as the elderly, children, or patients with hepatic or renal dysfunction, often stratified by age, gender, concomitant medication, and other characteristics. DUS can be used to determine if a product is being used in these populations. From these studies denominator data can be developed for use in determining rates of adverse drug reactions. DUS have been used to describe the effect of regulatory actions and media attention on the use of drugs, as well as to develop estimates of the economic burden of the cost of drugs. DUS can be used to examine the relationship between recommended and actual clinical practice. These studies can help to determine whether a drug has the potential for drug abuse by examining whether patients are taking escalating dose regimens or whether there is evidence of inappropriate repeat prescribing. Important limitations of these studies can include a lack of clinical outcome data or information of the indication for use of a product. REFERENCES 1. ICH Guideline E2D; Post-approval Safety Data Management: Definitions and Standards for Expedited Reporting, 3.1.1 Spontaneous Reports. 2. Pinkston V, Swain EJ. Management of adverse drug reactions and adverse event data through collection, storage, and retrieval. In Stephens MDB, Talbot JCC, and Routledge PA, eds. Detection of New Adverse Drug Reactions. 4th ed. 1998;MacMillan Reference Ltd, London. p282. 3. Faich GA, U.S. adverse drug reaction surveillance 1989 – 1994. Pharmacoepidemiology 4. Goldman SA, Limitations and strengths of spontaneous reports data. Clinical Therapeutics 5. Hartmann K, Doser AK, Kuhn M, Postmarketing safety information: How useful are spontaneous reports. Pharmacoepidemiology and Drug Safety 1999;8:S65-S71. 6. ‘Responding to Signals’ Waller PC and Arlett PA, in Pharmacovigilance, Editor Mann 7. DuMouchel W., Bayesian data mining in large frequency tables, with an application to the FDA Spontaneous Reporting system. Am Stat 1999;53:177-190. 8. Bate A, Lindquist M, Edwards IR, A Bayesian neural network method for adverse drug reaction signal generation. Eur J Clin Pharmacology 1998;54:315-321. 9. Van Puijenbroek E, Egberts ACG, Heerdink ER, Leufkens HGM, Detecting drug-drug interactions using a database for spontaneous adverse drug reactions: An example with diuretics and non-steroidal anti-inflammatory drugs. Eur J Clin Pharmacol 2000;56:733-738. 10. Venning GR, Identification of adverse reactions to new drugs. III: Alerting processes and early warning systems. BMJ 1983;286:458-460. 11. Edwards IR, The management of adverse drug reactions: From diagnosis to signal. 12. In Strom BL (ed.). Pharmacoepidemiology, 3rd ed. 2002; John Wiley and Sons, Ltd, New 13. Mitchell AA, Van Bennekom CM, Louik C. A pregnancy-prevention program in women of childbearing age receiving isotretinoin. N Engl J Med (1995 Jul 13); 333(2):101-6. 14. Task Force on Risk Management. Report to the FDA Commissioner. Managing the risks from medical product use: Creating a risk management framework. Part 3. How does FDA conduct postmarketing surveillance and risk assessment. May 1999. 15. In Mann RD and Andrews EB (eds.) Pharmacovigilance 2002, John Wiley and Sons, Ltd, 16. Coulter DM, The New Zealand intensive medicines monitoring programme in pro-active safety surveillance. Pharmacoepidemiology and Drug Safety 2000;9:273-280. 17. Mackay FJ, Post-marketing studies. The work of the Drug Safety Research Unit. Drug 18. Garcia Rodriguez LA, Perez Gutthann S, Use of the UK General Practice Research Database for Pharmacoepidemiology. Br. J Clin Pharmacol 1998;45:419-425.

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