- Research article
- Open Access
- Open Peer Review
Post-marketing withdrawal of 462 medicinal products because of adverse drug reactions: a systematic review of the world literature
© Onakpoya et al. 2016
- Received: 15 December 2015
- Accepted: 7 January 2016
- Published: 4 February 2016
The Correction to this article has been published in BMC Medicine 2019 17:56
There have been no studies of the patterns of post-marketing withdrawals of medicinal products to which adverse reactions have been attributed. We identified medicinal products that were withdrawn because of adverse drug reactions, examined the evidence to support such withdrawals, and explored the pattern of withdrawals across countries.
We searched PubMed, Google Scholar, the WHO’s database of drugs, the websites of drug regulatory authorities, and textbooks. We included medicinal products withdrawn between 1950 and 2014 and assessed the levels of evidence used in making withdrawal decisions using the criteria of the Oxford Centre for Evidence Based Medicine.
We identified 462 medicinal products that were withdrawn from the market between 1953 and 2013, the most common reason being hepatotoxicity. The supporting evidence in 72 % of cases consisted of anecdotal reports. Only 43 (9.34 %) drugs were withdrawn worldwide and 179 (39 %) were withdrawn in one country only. Withdrawal was significantly less likely in Africa than in other continents (Europe, the Americas, Asia, and Australasia and Oceania). The median interval between the first reported adverse reaction and the year of first withdrawal was 6 years (IQR, 1–15) and the interval did not consistently shorten over time.
There are discrepancies in the patterns of withdrawal of medicinal products from the market when adverse reactions are suspected, and withdrawals are inconsistent across countries. Greater co-ordination among drug regulatory authorities and increased transparency in reporting suspected adverse drug reactions would help improve current decision-making processes.
- Adverse drug reaction
- Drug withdrawal
- Systematic review
- Voluntary recall
Drug regulatory authorities award marketing authorizations that license pharmaceutical companies to market medicinal products when there is sufficient evidence that the product has a favourable benefit-to-harm balance . If a new adverse drug reaction is suspected after approval, several courses of action can be taken by the regulator and/or manufacturer, including adding a new product label with specific warnings , adding a new contraindication , issuing a Direct Healthcare Professional Communication , allowing patients to decide whether they will take the drug , and in the most serious cases, withdrawal or revocation of the licence .
Post-approval withdrawal of medicinal products because of adverse drug reactions can be triggered by evidence obtained from various sources – anecdotal reports, observational studies, clinical trials, systematic reviews, or animal data. The removal of previously approved products from the market can result in loss of confidence in medicines by the public, loss of effective compounds (i.e. effective for treating the specific indication, but for which the benefit-to-harm balance was considered unfavourable), and loss of revenue for drug manufacturers. When there is no concrete evidence linking drug use with a suspected adverse reaction, such withdrawals can be contentious.
We have previously reported inconsistencies in the pattern of withdrawals of 95 medicines to which deaths were attributed . To date, there has been no comprehensive and systematic review of medicinal products that have been withdrawn because of adverse drug reactions in general. In addition, there is a paucity of data about the evidence on which such withdrawal decisions are based. Furthermore, the pattern of post-approval withdrawals across geographical regions worldwide has never been examined. Therefore, we performed a systematic review to identify medicinal products that have been withdrawn after approval because of any kinds of adverse drug reactions; to assess the types of evidence on which the withdrawal decisions were based; to identify the types of attributed adverse drug reactions responsible; to examine the patterns of withdrawal across geographical regions; to examine the intervals between launch dates and (1) the times of the first reports of adverse reactions and (2) the first dates of withdrawal; and to examine the intervals between the first reports of adverse drug reactions and the first withdrawals.
the World Health Organization’s (WHO’s) database of Consolidated List of Products whose consumption and/or sale have been banned, withdrawn, severely restricted, or not approved by governments (Issues 6, 8, 12, and 14, and the updated version of issue 14)
the WHO’s Drug Information (Volumes 1–28)
the WHO’s Pharmaceuticals Newsletter (1997–2014)
Meyler’s Side Effects of Drugs: The International Encyclopaedia of Adverse Drug Reactions and Interactions, volumes 1–8 and editions 9–15, and the Side Effects of Drugs Annuals 1–36
Stephens’ Detection of New Adverse Drug Reactions, 5th edition 
the Pharmaceutical Manufacturing Encyclopedia, 3rd edition 
The Merck Index, 15th Edition 
the website of the UK Medicines and Healthcare products Regulatory Agency
the website of the US Food and Drug Administration (FDA)
the database of withdrawn drugs of the European Medicines Agency
Health Canada Drug Product Database
the website of the Indian Central Drugs Standard Control Organization
the website of the Australian Therapeutic Goods Administration
the website of the Nigeria National Agency for Food and Drug Administration and Control
the website of the Ghana Food and Drugs Authority
the website of the South Africa Medicines Control Council
Please see Additional file 1: Web 1 for full list of drug regulatory websites assessed.
For each medicinal product withdrawn, we then searched PubMed, Medline, and Google Scholar for the first reported adverse drug reaction.
Search terms used included “drug withdrawal”, “fatal*”, “death(s)”, “side effect”, “adverse effect”, “adverse reaction”, “adverse event”, “poison”, “toxicity”, “voluntary recall”, “suspension”, “prohibition”, “banned”, “remov*”, “revoke*”, “discontinued” (a Medline search strategy is included as a Additional file 2: Web 2). If we could not find information for a medicinal product using its chemical name for searches, we used the trade name or code name. We also searched the references of retrieved full texts for any earlier dates of reports of suspected adverse reactions. If an article had evidence of an earlier reported date, that date was chosen as the first adverse reaction date. If a drug was withdrawn because of two or more adverse reactions, we used the first reported date of any such reactions.
To determine the accuracy of launch dates, we compared the information on the WHO database of Consolidated List of Products with the information in the Merck index, the Pharmaceutical Manufacturing Manual, and a newly developed database for withdrawn and discontinued products . To determine the dates of first withdrawal and countries of withdrawal, we cross-checked WHO data with the database for withdrawn products; if the information was not found in that database, we compared the dates with the results of searches in PubMed and Google Scholar.
We define a medicinal product as “Any substance or combination of substances which may be used in, or administered to, human beings, either with a view to restoring, correcting or modifying physiological functions by exerting a pharmacological, immunological or metabolic action, or to making a medical diagnosis” . For the purpose of our review, such applications could be via oral, intravenous, intramuscular, sublingual, inhalational, rectal, or topical routes. To be included in the review, a product must have been withdrawn from the market because of reports of a suspected adverse reaction or reactions, or problems related to hazards or harms. We included medicinal products that had previously been withdrawn (by regulatory authorities and/or drug manufacturers) because of adverse reactions but had been re-introduced or made available in other, safer, formulations. When only one formulation of a product was withdrawn, the product was included in the list, and the formulation was noted; however, if all formulations of the product were subsequently withdrawn, we used the earliest date, irrespective of formulation, as the year of first withdrawal. We did not exclude products based on routes of administration. We excluded medicines for which there was documented regulatory evidence that they had been voluntarily withdrawn by marketing authorization holders solely for commercial reasons, or withdrawn based on contamination of the active ingredient by other agents (such as organisms and active or toxic compounds). We also excluded herbal products, non-human medicines, and non-prescription medicines.
Assessing the types of evidence
We documented the highest level of available evidence before the year of first withdrawal of products, based on the Oxford Centre for Evidence-based Medicine (OCEBM) criteria  rating the levels of evidence of harms as follows: Level 5, mechanism-based reasoning (lowest); Level 4, case-series or case-control studies; Level 3, non-randomized, cohort, or follow-up studies; Level 2, randomized clinical trials; and Level 1, systematic reviews (highest). One reviewer (IJO) documented the levels of evidence, which were independently verified by a second reviewer (JKA). Discrepancies were resolved through discussion.
For each withdrawn product, we extracted data on the date of marketing authorization, the launch date, or the date of first recorded use; the drug class and therapeutic indication ; the year in which an adverse drug reaction related to the reason for withdrawal was first reported; the year of first withdrawal; the country or countries of withdrawal; and the reported organ or system that was affected by the drug. When the exact launch date of a product was not available (16 cases), we used the first date of reported use in humans by cross-checking references on PubMed with Medline. If two or more adverse reactions were reported as reasons for withdrawal, we used the date of the first reported reaction.
One reviewer (IJO) extracted the data and a second reviewer (JKA) verified them independently. When there were discrepancies in the attributed dates, the reviewers re-checked the dates together and arrived at a consensus by discussion.
We used summary tables to document the intervals between launch year and the year of first reports of adverse drug reactions, the interval between launch year and the year of first withdrawal, and the interval between the first report of an adverse drug reaction and the year of first withdrawal. Because these intervals were skewed, we used medians and interquartile ranges (IQR) as measures of central dispersion.
We used scatter plots to explore the relationships between launch dates and times to first reports of adverse drug reactions and withdrawals.
Because drug regulatory systems in most African countries are not well developed [15–17], we compared withdrawal rates in Africa with five other continents. We computed the relative rates (RR) and 95 % confidence intervals (CI) of withdrawals per country in Africa versus the other five continents. A P value <0.05 was considered statistically significant.
Levels of evidence used for drug withdrawals
Levels of evidence used to justify post-marketing withdrawal of medicinal products
Level of evidencea
Number (%) of withdrawals
All marketed drugs (n = 462)
Marketed drugs launched since 1950 (n = 286)
Level 1: Systematic reviews
Level 2: Randomized studies
Level 3: Non-randomized studies
Level 4: Case reports
Level 5: Mechanism-based reasoning
Types of adverse drug reactions
Hepatotoxicity (81 cases; 18 %) was the most commonly reported adverse drug reaction that led to withdrawal (Additional file 3: Table S1), followed by immune-related reactions (79 cases; 17 %), cardiotoxicity (63 cases; 14 %), neurotoxicity (76 cases; 16 %), haematological toxicity (53 cases; 11 %), carcinogenicity (61 cases; 13 %), and drug abuse and dependence (52 cases; 11 %). Deaths were associated with withdrawals in 114 cases (25 %).
Patterns of withdrawals
Post-marketing withdrawal of medicinal products because of adverse drug reactions in different continents
No. of countries
Total population (millions)
No. of withdrawn products
Rate of withdrawals/million population
Rates of withdrawal/country
RR of withdrawal per country versus Africa (95 % CI)a
a P value versus Africa
Australasia & Oceania
1.59 ( 1.32–1.90)
Interval between launch year and first reported adverse drug reaction
The median interval between launch year and the year in which an adverse reaction was first reported was 8 years (IQR, 2–20) for all the drugs and 4 years (IQR, 1–10) for drugs launched after 1960.
Interval between launch year and first withdrawal
Interval between the first reported adverse drug reaction and the first withdrawal
Relation between time of launch to first adverse drug reaction report versus the interval between the first adverse drug reaction report and the first withdrawal
We have identified 462 medicinal products withdrawn because of adverse drug reactions between 1953 and 2013. Hepatotoxicity and immune-mediated reactions were responsible for over 30 % of withdrawals, and death was attributed as among the reasons for withdrawal in 25 % of instances. Withdrawals were significantly less common in Africa than in Asia, Europe, and North and South America.
Evidence for withdrawal
Case reports were most often used as evidence on which withdrawal decisions were based, being used in 71 % of all the products, 70 % of those launched after 1950, and 66 % of those launched after 1960. This corroborates our previous finding that case reports were most commonly used as evidence for withdrawal of 95 medicinal products because of drug-attributed deaths , and confirms that formal studies are often not conducted when adverse drug reactions are reported anecdotally . However, the frequency with which anecdotal reports have provided the dominant source of information has reduced with time, from 85 % in the 1950s to 64 % in the 1990s; since 2000, the frequency has fallen even further, to 35 %, but the number of products affected during the last few years is relatively small.
Patterns of withdrawal
There were significantly fewer withdrawals in Africa than in the other five continents. This suggests that there is better co-ordination among drug regulatory authorities in those geographical regions than in Africa. Furthermore, the delays between the first report of an adverse reaction and first withdrawal were more often than not longer in African countries than in Europe or North America, which were not significantly different from each other. Thus, harmful drugs are likely to stay on the market for longer in Africa.
There was a lower rate of withdrawal in African countries than elsewhere. Factors that can affect withdrawals include the strength of a local regulatory agency, and the availability of proper monitoring facilities or preventive strategies. According to the WHO, only 4 % of African nations have moderately developed pharmacovigilance systems and 39 % lack adequate regulatory capacity . Furthermore, the ability of a country to restrict access to harmful drugs is related to per capita gross national product , and this contributes to the so-called medical poverty trap (increases in overall out-of-pocket expenses for health care in families who are already poor) .
Delays between launch dates and reports of adverse drug reactions
The interval between first launch and first report of adverse reactions has shortened over time (Fig. 2). This is probably largely due to improved pharmacovigilance, better methods of signal detection, and better reporting of suspected adverse drug reactions. However, at least 5 years elapsed before the first report of an adverse drug reaction in 31 % of instances for products launched after 1960, suggesting that detection of adverse reactions to approved medicinal products has improved with developments in drug regulation, but the improvements have not been substantial. This may be attributable to a variety of factors, such as selective reporting of benefits and harms in clinical trials  and flawed regulatory assessment procedures , which have led to calls for changes to current drug adverse event monitoring strategies [24, 25].
Regulatory assessment of clinical trials data of medicinal products is seldom conducted in many African countries, where the drug regulatory processes are geared to grant marketing licences for imported products that have been assessed in other places and populations.
Under-reporting of adverse drug reactions
Under-reporting of adverse drug reactions could cause delays in making withdrawal decisions. There is evidence that clinicians selectively report adverse drug reactions [26, 27], and the authors of a review of hospital admissions due to adverse drug reactions concluded that physicians seldom report such events when they occur . A low rate of reporting among health-care professionals could be due to poor knowledge of how to use the spontaneous reporting systems , conflicts of interest , forgetfulness, lack of time, and uncertainty about causal relationships between drugs and adverse events . Proactive measures to encourage physicians to report suspected adverse drug reactions have been suggested . Indeed, provision of economic incentives and/or educational activities improves the reporting of adverse drug reactions among hospital clinicians [33–37]. Patients are also likely to under-report suspected adverse reactions to medications , and empowerment of patients has been advocated [39, 40].
Delays to withdrawals after reports of adverse drug reactions
Frequency of withdrawals compared with overall new drug approvals
The number of withdrawn medicinal products is probably only a small fraction of overall approvals. As examples, less than 2 % of new drug approvals by the FDA between 1950 and 2011  and 3 % of approved products in Canada and the USA between 1992 and 2011 were withdrawn , suggesting that drug regulatory authorities have made considerable efforts at ensuring that harmful drugs are not marketed.
Comparison with previous studies
We have confirmed and extended the result of previous studies, all of which have been considerably smaller and of more limited time spans. We have also documented the levels of evidence used for making the withdrawal decisions, analysed time courses, and included data from African countries, not previously reported.
For example, an analysis of 19 medicinal products withdrawn between 2002 and 2011 showed that case reports were commonly used to justify withdrawal decisions, but less so with time . A review of 121 withdrawn products showed that hepatotoxicity, cardiotoxicity, and carcinogenicity were the most common reasons for withdrawals between 1960 and 1999 . There were inconsistencies in the patterns of withdrawal of 26 products between 1971 and 1992 in the UK and the USA , and in drug withdrawal policies across countries , although an earlier study of 24 products suggested consistency in withdrawal patterns between the UK and USA from 1964 to 1983 . In a study of 22 products withdrawn in Canada between 1990 and 2009 , the median interval between approval and withdrawal was 3.5 years (IQR, 1.9–7.9); our data, analysed over the same period, show a value of 3 years (IQR, 1–6; n = 72). Our results are consistent with all of these findings.
Strengths and limitations
We used robust methods to search for medicinal products withdrawn because of adverse reactions and documented the evidence on which the withdrawal decisions were based. In addition, we accessed data from a variety of sources. However, we recognize some limitations. We do not have information on the delay between the actual occurrence of an adverse drug reaction due to a medicinal product and the date it first appeared in the literature. Nevertheless, such delays are unlikely to have significantly influenced the results. We do not have data from countries in Africa that are blighted by armed conflict, e.g. Burundi, the Central African Republic, and Somalia; indeed, we did not identify any information on withdrawn medicinal products from these countries in the WHO drug lists. Furthermore, as of 2009, over half of all African countries did not have a drug regulatory website . We did not access data from non-English drug regulatory websites; however, we do not think that the information from such sites would significantly alter our results, since a majority of such countries report their data to the WHO. In addition, the accuracy of the information from the databases used to document launch and withdrawal dates has not been assessed, but we did use information from other selected texts to check for any inconsistencies. Furthermore, we do not have data on countries in which withdrawn drugs were approved by regulatory authorities, where such exist; this difficulty has previously been reported by other authors .
We may not have identified all medicinal products withdrawn in association with adverse drug reactions because of the possibility of negative publication bias, and we do not know how many patients in all were affected by adverse reactions. This could also have influenced the speed with which regulatory decisions were taken. Some medicines are available only on prescription in some regions and may be available over the counter elsewhere. For example, antibiotics are generally available as prescription-only medicines in the UK ; in contrast, the results of surveys in Nigeria showed that self-medication with antibiotics and antimalarial drugs was common both in the general public and among healthcare workers [52, 53].
Universal guidelines for determining when a drug should be withdrawn when serious adverse drug reactions are suspected should be developed and promoted.
More efforts should be made towards strengthening drug monitoring systems in low- and middle-income economies, especially in Africa; the proposal by the WHO in collaboration with African Union countries to establish an African Medicines Agency by 2018 is a welcome development.
Regulatory authorities and drug manufacturers should expedite action when adverse drug reactions are suspected; formal studies to test for such associations should be conducted sooner rather than later; temporary suspensions or restrictions could be considered.
There should be more transparency in reporting adverse events observed during clinical trials; access to clinical study reports should be a priority for future drug regulation.
More active engagement of health professionals and patients in reporting suspected adverse drug reactions should be encouraged.
The interval between launch date and reports of adverse drug reactions has shortened over the past few decades, perhaps because of better reporting of suspected adverse reactions or stricter regulation. In addition, increasing numbers of individuals may have been exposed to the withdrawn products in recent years, leading to quicker detection of adverse reactions. However, withdrawal of products following reports of suspected adverse reactions, sufficiently serious to warrant withdrawal, has not improved consistently over the last 60 years. In addition, harmful drugs are less likely to be withdrawn in African countries. Greater co-ordination among drug regulatory authorities and increased transparency in the reporting of suspected adverse drug reactions would help improve decision-making processes.
IJO receives scholarship funding from the Clarendon Fund for the DPhil programme in Primary Care at the University of Oxford. CJH is supported by the National Institute for Health Research School for Primary Care Research.
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