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R E V I E W

Drug and Alcohol Review (July 2010), 29, 426–436
DOI: 10.1111/j.1465-3362.2009.00140.x

REVIEW

Unrecorded consumption, quality of alcohol and
health consequences
dar_140

426..436

JÜRGEN REHM1,2,3*, FOTIS KANTERES1 & DIRK W. LACHENMEIER4*
1

CAMH—Centre for Addiction and Mental Health,Toronto, Canada, 2Dalla Lana School of Public Health, Faculty of
Medicine, University of Toronto,Toronto, Canada, 3Technische Universität Dresden, Klinische Psychologie and Psychotherapie,
Dresden, German, and 4Chemisches undVeterinäruntersuchungsamt (CVUA) Karlsruhe, Karlsruhe, Germany

Abstract
Issues. This contribution aims to examine systematically the evidence on the impact of the quality of unrecorded alcohol
products on health consequences. Approach. Systematic computer assisted review of the literature. Key Findings.There are
a number of pathways related to alcohol quality that may lead to acute or chronic health problems.The following constituents
and contaminants of alcoholic beverages were identified as likely contributors to these problems: (i) toxic metals (e.g. lead) from
contaminated water sources or unsuitable distillation equipment; (ii) volatile constituents, such as acetaldehyde or higher
alcohols, which may be produced in significant amounts due to faults in production technology or microbiological spoilage; (iii)
ethyl carbamate (urethane), a carcinogenic contaminant with major occurrence in certain fruit and sugarcane spirits; (iv)
biologically active flavour compounds (e.g. coumarin in cosmetics used as non-beverage alcohol); (v) toxic compounds used to
denature alcohol (e.g. methanol or diethyl phthalate). In addition, the often higher ethanol content may have detrimental health
effects. These pathways should not be assumed as present for all subcategories of unrecorded alcohol, but are more relevant to
certain types and geographic regions. Implications.A health impact of unrecorded alcohol over and above the effect of ethanol
cannot be excluded. More research is urgently needed, especially with respect to liver disease and alcohol poisoning as endpoints.
Conclusion.A feasible approach for new research on the effects of unrecorded alcohol could be based on a representative sample
from low socioeconomic regions with high prevalence of unrecorded consumption. [Rehm J, Kanteres F, Lachenmeier DW.
Unrecorded consumption, quality of alcohol and health consequences. Drug Alcohol Rev 2010;29;426–436]
Key words: alcohol, unrecorded alcohol, quality of alcoholic beverages, alcohol poisoning, liver disease.
Issues
Alcohol has been identified as a major risk factor for the
global burden of disease [1]. According to the International Classification of Disease, it has a detrimental
impact on more than 50 different major disease and
injury categories [2,3]. Alcohol-attributable health
burden is particularly high in Central and Eastern
Europe, Central and South America, and countries of
the former Soviet Union [4]. In the year 2000, 30% of
global alcohol consumption was estimated to be unrecorded [5,6]; a high proportion of this was found to

come from both countries of lower to middle income
and the former Soviet Union. ‘Unrecorded’ is an overview category for any kind of alcohol that is not taxed as
beverage alcohol or registered in the jurisdiction where
it is consumed [7]. Due to the relatively limited information and difficulties in measuring this category, its
public health consequences are not clear.
Currently the main determinants of alcohol-related
public health consequences considered by agencies,
such as the World Health Organization (WHO), are
volume and patterns of consumption, particularly
heavy drinking occasions [8]; these two dimensions are

*Both authors contributed equally to this work and share the responsibility as principal author.
Jürgen Rehm PhD, Professor (CAMH—Centre for Addiction and Mental Health), Fotis Kanteres BSc (Hons), Research Analyst (CAMH—
Centre for Addiction and Mental Health), Dirk W. Lachenmeier PhD, Food Chemist and Toxicologist [Chemisches und Veterinäruntersuchungsamt (CVUA) Karlsruhe].
Correspondence to Prof Dr Jürgen Rehm, CAMH—Centre for Addiction and Mental Health, 33 Russell Street, room 2035B, Toronto, ON,
Canada, M5S 2S1. Tel: +1 416 535 8501 ext 6907; Fax: +1 416 260 4156; E-mail: jtrehm@aol.com
Received 11 October 2009; accepted for publication 9 August 2009.
© 2010 Australasian Professional Society on Alcohol and other Drugs

Unrecorded alcohol and health

the only ones included in the alcohol portion of the
Comparative Risk Assessment for the Global Burden of
Disease Study [1,4]. In the estimation and monitoring
of consequences and risk factors of alcohol, unrecorded
and recorded consumption are treated equivalently.
However, product quality, especially for, but not
restricted to, certain categories of unrecorded alcohol,
may have an important additional impact on health.
This article systematically reviews the literature on the
different categories of unrecorded alcohol and health
outcomes, in order to determine whether this kind of
alcohol carries a health risk over and above that associated with ethanol.
Approach

427

selected articles.This was accompanied by a hand search
of the reference lists of all selected articles for any
relevant studies not included in the databases, which
resulted in 91 selected articles and five books. In total, we
retained 140 articles and five books for the current
evaluation of the health impact of unrecorded alcohol.
English was the main language of the electronic databases; however, there were no language restrictions and
authors were able to review articles in English, French,
Spanish, Portuguese, German, Russian, Polish and
Chinese. The references, including abstracts, were
imported into Reference Manager V.12 (Thomson
Reuters, Carlsbad, CA, USA) and the relevant articles
were manually identified and obtained in full text.
Key findings

A computer-assisted literature search was conducted
using a combination of the key words: alcohol, unrecorded, homemade, illegal, illicit, clandestine and surrogate. The criteria for inclusion/exclusion were that the
literature contain information on morbidity or mortality
related to unrecorded consumption (as defined in [7];
see below), including animal studies testing the effects of
components of unrecorded alcohol products (e.g. acetaldehyde). Literature that focused solely on consumption
or drinking patterns and not on health effects, while used
to aid the search on the whole, was not included in the
final evaluation. The search resulted in 234 abstracts in
OVID (MEDLINE) of which 19 articles were selected,
317 references in Pubmed of which three additional
articles were selected (16 overlapped), and 221 in
ETOH (database of the National Institute for Alcohol
Abuse and Alcoholism) of which additional 27 were
selected (five overlapped); resulting in a total of 49

The classification and global presence of unrecorded
alcohol products
The last systematic attempt to assess the amount of
unrecorded consumption was for the year 2002 [9],
based on information systematically collected by the
Global Information System on Alcohol And Health
(GISAH) of the WHO [10]. Information about unrecorded consumption was obtained from key informants
via a questionnaire distributed to all governments by
the WHO; in addition, specific surveys and other systematic empirical studies on unrecorded consumption
were included [11]. The results are summarised in
Table 1. As can be seen, the prevalence for unrecorded
consumption is generally proportional to a country’s
level of income, with lower-income countries having a
higher percentage of consumption that is unrecorded.
Overall, there is a high potential measurement bias in

Table 1. Estimates of recorded and unrecorded per capita adult (15+) alcohol consumption 2002 ([9], based on GISAH)

WHO regions
Africa
America A: Canada and United States
Central and South America
Eastern Mediterranean
Western Europe (Europe A)
European B: Central and Eastern Europe
European C: Russia and surrounding countries
South East Asia (including India)
Western Pacific A: Australia, Japan, and New Zealand
Western Pacific B: China and Pacific
World

Adult per capita
recordeda + unrecorded
alcohol consumption (in
litres of pure alcohol)

Adult per capita
unrecorded alcohol
consumption (in litres
of pure alcohol)

Percentage of
unrecorded
consumption to
total consumption

7.0
9.4
8.0
0.7
12.2
7.5
14.9
2.0
9.4
6.0
6.2

2.5
1.1
2.5
0.5
1.3
2.8
6.1
1.5
1.7
1.1
1.7

35
12
32
74
11
38
41
74
18
19
28

a

Recorded consumption for 2002 was calculated as an average of recorded per capita alcohol consumption 2001–2003.
GISAH, Global Information System on Alcohol And Health [10]; WHO, World Health Organization.
© 2010 Australasian Professional Society on Alcohol and other Drugs

428

J. Rehm et al.

estimating unrecorded consumption, including the possibility of double counting between countries (e.g.
unrecorded alcohol produced in country x and
smuggled to y may be counted in both countries).
Within the overview category of unrecorded alcohol
products four main categories can be distinguished [7]:

• Unrecorded legal alcohol products (e.g. home•



made alcohol in jurisdictions where home production is legal);
Unrecorded illegal alcohol products (e.g. either
from illegal production or from smuggling);
Surrogate alcohol not officially made for human
consumption, but in many instances produced and
distributed with clear intent for this exact purpose
(e.g. cosmetics, medicinal alcohol);
Recorded alcohol from different jurisdiction (e.g.
cross-border shopping).

While there is no adequate global data on the distribution of unrecorded consumption across these categories, there are good indications that it varies across
regions [12]. Significant proportions of ‘traditional’
homebrew have been found in Sub Sahara Africa
[13–23] and Latin America [24–29]. It should be noted
that legality can vary in terms of local legislature [30],
thus similar alcohol products may fall on different sides
of the legal divide. As such, alcohol may be produced
and distributed in a purported ‘traditional’ manner, yet
be classified as illegal by authorities [31].
McKee et al. found surrogate alcohol in Russia to
include medicinal compounds (e.g. tinctures) and
‘other’ spirits (mainly sold as aftershaves) [32]. This
form of alcohol product and its consumption have been
most notably reported in Russia [32–38] and countries
of Central and Eastern Europe [7,38–41]. However,
the Nordic countries of Europe have also historically
reported impact of surrogate alcohol [42]. Limited use
of surrogate alcohol, especially by people with alcohol
use disorders, is suspected in many countries.
In India, a recent article estimated 2/3 of the alcohol
consumed in the country as unrecorded [43]. Most of
the illicit consumption is so-called ‘country liquor’,
spirit made from locally available cheap raw material,
such as sugarcane, rice, palm, coconut and cheap
grains, with an alcohol content between 25% and 45%,
which appears in both recorded and unrecorded forms
[12]. Illegal country liquor is mostly produced clandestinely in small production units, and with no legal
quality control checks, alcohol concentration of this
liquor varies greatly (up to 56%). Adulteration is quite
frequent, with industrial methylated spirit previously
identified as a common adulterant, and as having
caused incidents, such as mass poisonings with consumers losing lives and suffering irreversible damage to
© 2010 Australasian Professional Society on Alcohol and other Drugs

their eyes (see below). Cheaper than licensed country
liquor, illicit liquor is popular among the poorer sections of the population ([12]; for an ethnographic
report [44]). While India has high rates of abstinence
[43], those who drink often have a pattern of heavy
drinking occasions, and this patterns also holds for
country liquor consumption (e.g [45]).
Higher income regions (North America, Western
Europe) have relatively high alcohol consumption, and
have generally provided the most overall information
and scientific literature on the topic. While data on
unrecorded alcohol are sparse, there have been some
significant studies in the Nordic countries (Norway,
Sweden, Finland) [42,46–50] and the Netherlands
[51]. The main area of concern in these works is home
production, smuggling and untaxed trade/traveller’s
items, and not health issues specifically related to unrecorded alcohol. In North America, literature has also
been limited, mainly focused on production and consumption [52–55].
Globally, cross-border shopping is of minimal relevance: this can be easily illustrated when one compares
the volume and sources of unrecorded alcohol in different parts of the world.The overwhelming majority of
unrecorded consumption stems from India, Africa,
South America and the countries of the former Soviet
Union, where cross-border shopping plays only a
minimal role (see above for overviews on the respective
sources). While cross-border shopping may be important in some parts of Europe (e.g. Nordic countries
[42,49–51,56]). In terms of quality and potential health
consequences over and above those of recorded
alcohol: this form of alcohol is recorded and quality
controlled in the jurisdiction it originates and thus
should not have any additional health consequences. As
such, the following paragraphs will only be relevant for
other forms of unrecorded consumption.
Chemical composition of unrecorded alcohol
Table 2 gives an overview of the main potential components in unrecorded alcohol. This is only a selection,
as alcohol may contain more than 1000 different components [113]; most of the components listed may also
appear in recorded alcohol.
From all compounds that are potentially present in
unrecorded alcohol, methanol appears to have the
highest potency for acute toxic effects. The problems
associated with methanol intoxication were previously
discussed in detail [65]. We found that the incidence of
methanol poisoning was relatively infrequent, yet as
the consequences of such instances were often severe,
the few outbreaks received high media exposure. The
problem appears to be on the decline of late, as most
jurisdictions have abolished the practice of using

Contamination of water source.

Residues on or contamination of
raw materials (e.g. grain) for
alcohol production.

Nitrate, water
quality

Pesticides/
mycotoxins

WHO, World Health Organization.

Natural occurrence due to certain
ingredients (herbs), addition for
flavouring, ingredient in cosmetic
alcohol.

Contaminant due to food-contact
materials.

Lead

Biologically
active flavourings

Process-derived contaminant may
be formed from hydrocyanic acid
or other precursors.

Ethyl carbamate

Denaturing agent in certain
jurisdictions. May also occur as
ingredient in cosmetic alcohol.

Natural by-product of alcohol
fermentation, higher
concentrations due to
microbiological spoilage, enriched
in the first fractions of distillation.

Acetaldehyde

Diethyl
phthalate

Natural by-product of alcohol
fermentation, in pure form as
‘surrogate alcohol’ (e.g. windshield
washer).

Higher alcohols
(e.g. propanol,
butanol, etc.)

Contaminants due to food-contact
materials.

Natural by-product of alcohol
production in low concentrations,
in criminal cases addition of spirits
denatured with methanol or even
addition of pure methanol.

Methanol

Metals

Natural fermentation and/or
addition of neutral or denatured
alcohol.

Sources

Ethanol

Compound

Different effects including
carcinogenicity [91].

No guidelines for alcohol, limits for raw
materials in certain jurisdictions

No international maximum levels for
alcohol. EU or WHO drinking water levels
can be used as guideline [106,107].

International limits available (e.g. from
Codex Alimentarius or EU) [110,111].

Different effects (e.g.,
hepatotoxicity of coumarin [109]).

Nitrate, ingested under conditions
that result in endogenous
nitrosation, is an IARC group 2A
carcinogen [91].

Tolerable daily intake of 5 mg/kg body
weight [108].

No systematic data available. However, highly unlikely to occur in
any alcohol due to degradation during fermentation as well as
separation during distillation.

No systematic data available.

Single cases, for example, coumarin in surrogate alcohol from
Lithuania [7]. Anecdotal evidence on nitro musk compounds in some
eau-de-colognes in Russia [112].

No systematic data available. Detected in some unrecorded samples
from Russia [62].

Metals (e.g. lead, arsenic, antimony, cadmium, copper, zinc) may be
found in unrecorded alcohol due to deficiencies in production
technology No systematic current data available. Metal
contaminations were especially described in moonshine from the
USA [65]. (see lead above)

Lead intoxications were commonly described in consumers of
American moonshine. Moonshine is typically produced in ground
stills using barrels, automobile radiators, and multiple copper tube
units sealed with solder as condensers. During the production of
moonshine, the leaching of lead from solder or other lead-containing
materials in the radiators can result in lead contamination
[52,98–105].

Lead Maximum Level in Wine: 200 mg L-1
[97].

No international maximum levels for
alcohol (besides for lead). EU or WHO
drinking water levels can be used as
guideline [106,107].

No systematic studies available. Found in some unrecorded alcohols
from Hungary [7], Poland [41], and Brazil [95]. Relatively low or
undetectable concentrations in Guatemala and Mexico [96].

No systematic studies available. Found in some unrecorded alcohols
from Guatemala [31]. Limited evidence points to public health risk
[90]. Russian samogons may contain higher levels of acetaldehyde
than recorded beverages (vodka) [60].

Limited and contradictory evidence [32,39,60–63,87,88] Own
research shows that the content of higher alcohols in unrecorded
alcohol is very similar to recorded distilled beverages (e.g. fruit
spirits, rum) [7,86]. The preliminary maximum level is seldom
exceeded.

Several methanol poisoning outbreaks associated with unrecorded
alcohol [68–85].

Unrecorded alcohol often contains higher ethanol concentrations.
This was consistently shown in a number of countries
[7,32,36,60–63].

Incidence in unrecorded alcohol

No harmonised international limits.
Canadian upper limit for distilled spirits:
0.15 mg L-1 [94].

Limited epidemiological evidence [92,93].
Margin of Exposure in Health Relevant
Ranges [90].

Higher alcohols have been speculated as
cause for unrecorded alcohol toxicity in
Eastern Europe. However, no
epidemiological evidence. Limited evidence
from animal experiments. Preliminary
maximum level 1000 g hl-1 of pure alcohol
for the sum of all higher alcohols [86].

Methanol has been described to be the
most common cause for surrogate alcohol
toxicity [65,66]. Maximum tolerable
concentration: 2%/vol [66]. EU provides
limits for certain spirits [67].

No safe level. Drinking guidelines for
‘low-risk’ drinking [58,59].

Toxicological Evaluation

Hepatic effects and reproductive
toxicity in animal experiments
[108].

Toxic and/or carcinogenic effects.

Poisoning as well as chronic toxic
effects (IARC group 2B [91]).

Typical carcinogenic contaminant
of alcoholic beverages (IARC
group 2A [91]).

Acetaldehyde may contribute to
the carcinogenicity of alcoholic
beverages [89,90] (IARC group
2B [91]).

Similar to effects of ethanol.
Potency may increase with chain
length [86].

Fatal poisoning, blindness [64].

Acute intoxication and poisoning,
as well as over 50 different major
disease conditions including some
cancer types such as oesophageal
cancer [4,57].

Major toxic effects

Table 2. Chemical composition of unrecorded alcohol

Unrecorded alcohol and health
429

© 2010 Australasian Professional Society on Alcohol and other Drugs

430

J. Rehm et al.

methanol to denature alcohol (which therefore cannot
lead to problems if ingested as surrogate alcohol).
However, there are still spectacular outbreaks, such as
the recent ‘toxic alcohol episode’ in Gujarat, a dry
Indian state, in which over 100 people were killed and
hundreds hospitalised [114].
Thus far, the largest study on the chemical composition of unrecorded alcohol was conducted by Nuzhnyi
[60], which predominantly consisted of samples from
Russia (n = 81), as well as different African countries,
India and Mexico (n < 10 for each country). The
general conclusion was that the samples of unrecorded
alcohol did not pose a toxic hazard, and were even
considered to be of high quality in terms of taste.
In our own research we have studied the general
composition of unrecorded alcohol from Nigeria [19],
Lithuania and Hungary [7], Poland [41], Guatemala
[31] and Vietnam [115]. More specific studies on ethyl
carbamate contamination were conducted in Guatemala and Mexico [96], and Brazil [95].
In general, we are in agreement with Nuzhnyi [60], as
the alcohols we studied were in most cases, of a relatively high quality and regarded to be safe according to
international food standards (see rationale for toxicological evaluation in Table 2). Only single samples were
suspicious, for example, surrogate alcohols from
Lithuania with coumarin contents [7], or artisanally
produced samples from Guatemala with very high
acetaldehyde contamination [31]. Ethyl carbamate contamination was detected in samples from Hungary,
Poland and Brazil [7,41,95].
For all other compounds (e.g. metals, diethyl phthalate, flavourings, etc.), we have only very old and apparently outdated information (e.g. regarding lead in
American moonshine), or literature that lacks systematic data.
In sum, while there have been a number of recent
small scale studies undertaken in different parts of the
world, the exact chemical composition of unrecorded
alcohol is generally unknown. Due to its nature, there is
no labelling of content as well as no systematic controls
by authorities for major parts of unrecorded consumption, such as homemade, illegal and surrogate alcohol.
The category of surrogate alcohol may be quality controlled, but only with the original use in mind (e.g.
cosmetic use, etc.) and not for human consumption.
The available knowledge from small scale studies points
to relatively little contamination, but more systematic
and larger studies are needed before we can draw better
conclusions.
Health consequences of low-quality alcohol
Listed in Table 2 is a selection of the most relevant
components and contaminants of low-quality alcohol
© 2010 Australasian Professional Society on Alcohol and other Drugs

and their hypothesised health impacts. If we look at the
potential of chronic toxic effects that are anecdotally
associated with unrecorded consumption (e.g. liver cirrhosis), there is only one consistent finding: unrecorded
alcohols often contain higher ethanol concentrations
than recorded alcohols [7,32,36,60–63].
In addition to ethanol, over 1000 different components, usually at trace levels, may occur in alcoholic
beverages [113]. Although the health effects of these
constituents have been demonstrated in animals as well
as at the human level, many countries generally lack
data regarding their presence in alcoholic beverages and
public health consequences over time. As mentioned,
while relatively uncommon and certainly not comparable with the overall health impact of alcohol [3,5],
instances of methanol-attributable deaths or blindness
receive a disproportionate amount of exposure in the
press and scientific literature [65]. Conversely, there are
almost no data on more long-term consequences, such
as chronic diseases, which may stem specifically from
unrecorded consumption. This is partially due to the
fact that few people consume only unrecorded alcohol
over time. Consider the example of a person who died
of alcoholic liver cirrhosis in Russia, and had been
mainly consuming unrecorded alcohol products in his
final years. Typically they would have been drinking
only recorded alcohol for some time, and when drinking more and more heavily, switched to surrogate
alcohol for economic reasons [36].With this switch and
subsequent exposure to ‘other’ alcohol, there are three
possible impacts:

• The



alcoholic liver cirrhosis would have taken
exactly the same course, if, ceteris paribus, this
person had consumed recorded alcohol only.
The alcoholic liver cirrhosis would have taken a
different course, for example, later onset, longer
duration, or no fatal outcome, if, ceteris paribus,
this person had consumed recorded alcohol only.
The alcoholic liver cirrhosis would not have
occurred with recorded consumption.

It is extremely difficult to show that unrecorded consumption or mainly unrecorded consumption is causal
in the onset of a chronic disease, that is, that the components which differ between recorded and unrecorded
alcohol consumption cause certain health consequences [116]. As a result, there are not many studies
investigating whether unrecorded consumption causes
health consequences over and above those of recorded.
Notably, such a study was conducted in India [117],
wherein the authors concluded that unrecorded consumption (country liquor) was associated with a
general risk of alcoholic liver disease, particularly alcoholic liver cirrhosis, despite having relatively lower

Unrecorded alcohol and health

alcohol concentrations than the local recorded type.
However, this study was not well controlled, and confounding by social status and other factors can thus not
be excluded.
For the most part, evidence on the health impact of
unrecorded alcohol is indirect, leaving alternative explanations for the significant, proportionally high levels of
disease. For instance, data on the rates (levels and
trends) of liver cirrhosis morbidity and mortality differ
dramatically between European countries, including
instances of a difference of more than a factor of 10
between countries with similar levels of drinking [118].
On a wider regional basis, the South Eastern European
countries and countries of the former Soviet Union had
at least threefold liver cirrhosis mortality rates compared
with Mediterranean and other EU countries, for both
men and women, even though their overall volume of
drinking did not differ [119]. Therefore, while the
volume of alcohol consumption has been shown to be
strongly related to liver cirrhosis rates, neither this sole
variable nor its association with hepatitis C virus rates
are capable of explaining these differences. As hypothesised by Szücs and colleagues [39], product quality may
be an important contributing cause. These authors
found significantly higher concentrations of methanol,
isobutanol, 1-propanol and isoamyl alcohol in illicitly
distilled spirits in Hungary, and argued that this may
cause hepatic damage in various ways, subsequently
contributing to the high level of alcohol-induced liver
cirrhosis in the country. However, current toxicological
evaluations [86] cast doubt on this hypothesis. This is
compounded by the fact that many recorded alcohol
products contain the same levels of higher alcohols as
unrecorded alcohols [7,86]. More recently, Solodun and
colleagues presented evidence that unrecorded alcohol
was specifically hepatotoxic and, among other components, identified polyhexamethylenguanidine hydrochloride, which is part of medicinal alcohol, as a
potential cause [116]. These findings still have to be
corroborated by other researchers.
In Central Mexico, another region with extremely
high liver cirrhosis rates [12], pulque mixed with contaminated water at the retail levels has been speculated
to be the cause [120]. In Africa, iron overload from the
consumption of large volumes of traditional beer that is
home-brewed in iron pots or drums has been associated
with liver fibrosis, cirrhosis and hepatocellular carcinoma [121]. Overall, these observations have led to the
hypothesis that unrecorded consumption has an effect
on liver disease over and above that of ethanol, but the
evidence is not conclusive.
Another aspect of this health concern is that poisoning, and alcohol poisoning in particular, are especially
prevalent in countries with significant unrecorded consumption, namely surrogate alcohol consumption. In

431

2002, the rate of poisoning of men in countries of the
Former Soviet Union (Russia, Belarus, and Ukraine)
and Baltic countries was almost 17-fold and eightfold
higher, respectively, when compared with the other EU
countries (own calculations based on WHO mortality
data; see also [119]). We hypothesise that high ethanol
concentrations and product quality may play an important role. As mentioned above, unrecorded products are
generally higher in alcohol concentration, but especially
for countries of the former Soviet Union (see Table 2).
For other aspects of product quality, Solodun et al.
provide some hypotheses, which mainly rely on acute
liver toxicity related to several chemicals found in
typical products [116]. Nevertheless, coding practices
and drinking patterns cannot be ruled out as alternative
explanations. However, recent research has shown that
there is very substantial under-reporting of alcohol poisoning deaths in Russia, suggesting that the above differences may be even greater [122,123].
Recently, Leon and colleagues [34] presented data
suggesting that the ceteris paribus consumption of nonbeverage alcohol accounted for more than 30% of mortality among men between the ages of 25 and 54 in the
Russian town of Izhevsk (proportion calculated by
Lachenmeier et al. [65]). Notably, the mortality impact
went beyond poisoning and liver disease, and included
problems, such as cardiovascular disease. However, the
cause of these high levels was not clear, and could have
simply been the result of the ethanol per se, a component in addition to alcohol, or of the interaction of
ethanol with lower socioeconomic status [124].
Given the lack of evidence for unrecorded alcohol
containing substantially toxic components over and
above recorded alcohol, other variables may be considered for an alternative explanation for the apparent
ecological differences in rates of liver cirrhosis and
other health outcomes between countries. For instance,
higher alcohol content, problematic drinking patterns,
lower socioeconomic status and poor health status may
all play a role, including in combination, and the interaction effect of these factors may well be even greater
than the sum of its parts. This phenomenon is exemplified for several cancers where drinking and smoking
occur together [125].
In summation, there are health phenomena, especially in regards to high rates of liver, and alcohol poisoning and mortality, where the quality of alcohol
products cannot be ruled out as having an effect over
and above that of ethanol. However, the evidence is far
from conclusive.
Implications
Our review has revealed that unrecorded consumption
is widespread and we cannot exclude that it may have
© 2010 Australasian Professional Society on Alcohol and other Drugs

432

J. Rehm et al.

detrimental health consequences over and above the
impact of ethanol alone.

• First, we do not have sufficient information on the






extent of unrecorded consumption. Many of the
current estimates of unrecorded alcohol are based
on expert judgments, including government estimates. We need to develop more standardised
methods to quantify the extent of unrecorded consumption empirically, including the quantification
of different subcategories, as they may be relevant
for public health.
Second, there has been no systematic controlled
research on comparing health consequences for
recorded versus unrecorded consumption. While
such research is methodologically challenging, it
has to be established to increase our understanding of the consequences of unrecorded consumption. Given the current knowledge and
consumption data, unrecorded consumption is
public health relevant even if it has little or no
health effects over and above those of ethanol. If
such effects exist, their systematic examination
would be even more pertinent. Below we propose
a first strategy to screen for potentially health relevant compounds of recorded and unrecorded
alcohol. This step has to be complemented by
carefully controlled epidemiological studies, which
compare the effects of recorded versus unrecorded
consumption on health outcomes mentioned
above.
Third, even while developing better methods, the
level of unrecorded consumption should be monitored with current methodology.
Fourth, where potential problems with the quality
of alcohol have been identified (e.g. high acetaldehyde concentrations in Cuxa in Guatemala [31]),
measures should be taken. A number of different
measures are possible. These range from trying to
legalise unrecorded consumption with subsequent
quality control to teaching the producers of unrecorded products how to avoid the quality problems detected. In the example of high
acetaldehyde concentrations, one way would be to
instruct the producers to discard the first
acetaldehyde-rich fractions during distillation.

Conclusion
Given the high level of alcohol-attributable burden of
disease, a recent expert committee to the WHO on
problems related to alcohol consumption [126] recommended the establishment of a monitoring system for
alcohol consumption and alcohol-related harm indicators, which could aid in advancing the current WHO
© 2010 Australasian Professional Society on Alcohol and other Drugs

GISAH [10]. Currently, none of the indicators in the
GISAH, which are used for regular global status
reports, are designed to measure the product quality of
alcohol beverages and other consumed alcohol products, such as composition, including the concentrations
of different compounds. Quality has the potential to
impact health and it may thus account for a significant
part of the high level of alcohol-attributable burden of
disease in low- and middle-income countries in Central
and Eastern Europe, as well as the Americas. Considering the potential public health importance, the
quality of alcohol should be analysed more systematically. This should include, but not be limited to, unrecorded alcohol products. The reasoning for this can be
seen in the relatively high proportion of recorded
alcohol samples with problems. For example, in the
German Federal State Baden-Württemberg in 2007,
dependent on spirit type, up to 28% of commercial
samples analysed had problems with alcohol quality
[127].
Low product quality of alcoholic beverages, as
defined above, may impact health and account for a
sizable proportion of alcohol-attributable disease
burden in low- to middle-income countries, over and
above the volume of alcohol consumption and patterns
of drinking. Research on alcohol quality can and should
be undertaken to investigate potential health impact
and contribute to health policy interventions [128].
Alcohol quality can be primarily tested by the chemical
analysis of representative samples of regularly consumed alcohol in areas with high liver cirrhosis rates
and alcohol poisoning, with methods routinely available
in every alcohol test laboratory (e.g. see the European
Union’s reference methods [129]). The major challenge, however, is the procurement of samples in a
quantity sufficient enough to enable researchers to
draw conclusions about the public health impact of
alcohol quality.
We suggest the following sampling strategy. Because
unrecorded consumption, liver cirrhosis and alcohol
poisoning disproportionately affect people of lower
socioeconomic status (SES) [65], representative
samples should be drawn from lower SES areas (e.g.
random walk samples). Next, participants should be
asked about their alcohol consumption, including how
they purchase and get access to alcohol. A random
subset of these participants should be asked to provide
samples for chemical analysis or to identify their suppliers for sampling. We are well aware of the potential
problems of such a strategy. People may fear identifying
illegal material and activities. However, field experiences in Guatemala [31] and the recent WHO study on
unrecorded consumption in Brazil, China, India and
Russia (unpublished; see [130] for Indian results)
provide relatively optimistic predictions: people are

Unrecorded alcohol and health

willing to identify unrecorded products, especially in
countries or regions, where unrecorded alcohol is
highly prevalent. In addition, or alternatively, alcohol
outlets that sell unrecorded alcohol products may also
be included for sampling in the study area [31]. In any
case, we need good regional feasibility studies before
we can conduct such full scale studies in different
countries.
Depending on the area, the alcohol consumed may or
may not primarily concern unrecorded alcohol. As
there may also be problems with recorded consumption, all sources should be subjected to chemical analysis. Regarding postulated outcomes, case–control (with
respect to liver cirrhosis and alcohol poisoning) and
additional case-crossover studies in emergency rooms
(with respect to alcohol poisoning) could be conducted,
with chemical analyses integrated into both designs.
This would allow for a more direct way to test the
hypothesis that certain compounds are causally relevant
for the above outcomes.
References
[1] Ezzati M, Lopez AD, Rodgers A, Vander Hoorn S, Murray
CJL, Comparative Risk Assessment Collaborating Group.
Selected major risk factors and global and regional burden
of disease. Lancet 2002;360:1347–60.
[2] Rehm J, Room R, Graham K, Monteiro M, Gmel G,
Sempos CT. The relationship of average volume of alcohol
consumption and patterns of drinking to burden of
disease: an overview. Addiction 2003;98:1209–28.
[3] Rehm J, Mathers C, Popova S, Thavorncharoensap M,
Teerawattananon Y, Patra J. Global burden of disease and
injury and economic cost attributable to alcohol use and
alcohol use disorders. Lancet 2009;373:2223–33.
[4] Rehm J, Room R, Monteiro M, et al. Alcohol as a risk
factor for global burden of disease. Eur Addict Res
2003;9:157–64.
[5] Room R, Babor T, Rehm J. Alcohol and public health.
Lancet 2005;365:519–30.
[6] Rehm J, Rehn N, Room R, et al. The global distribution of
average volume of alcohol consumption and patterns of
drinking. Eur Addict Res 2003;9:147–56.
[7] Lachenmeier DW, Sarsh B, Rehm J. The composition of
alcohol products from markets in Lithuania and Hungary,
and potential health consequences: a pilot study. Alcohol
Alcohol 2009;44:93–102.
[8] World Health Organization. The world health report
2002: reducing risks, promoting healthy life. Geneva, Switzerland: WHO, 2002.
[9] Rehm J, Patra J, Baliunas D, Popova S, Roerecke M,
Taylor B. Alcohol, the burden of disease of. In: Heggenhougen K, Quah S, eds. International encyclopedia of
public health, vol. 1. San Diego, CA: Academic Press,
2008:135–51.
[10] World Health Organization. Global Information System on
Alcohol and Health. 2010. Available at: http://apps.who.int/
globalatlas/default.asp (accessed 1 January 2010).
[11] Rehm J, Klotsche J, Patra J. Comparative quantification of
alcohol exposure as risk factor for global burden of disease.
Int J Methods Psychiatr Res 2007;16:66–76.

433

[12] World Health Organization. Global Status Report on
Alcohol. Geneva: World Health Organization, 2004.
[13] Obot IS. The measurement of drinking patterns and
alcohol problems in Nigeria. J Subst Abuse 2000;12:169–
81.
[14] Pitso JMN. Field tales of hazardoues home brewed alcoholic beverages: the case of Selebi Phikwe, Botswana. Afr J
Drug Alcohol Stud 2007;6:89–103.
[15] Heap S. Transport and liquor in colonial Nigeria. J Trans
Hist 2000;21:28–53.
[16] Heap S. We think prohibition is a farce: drinking in the
alcohol-prohibited zone of colonial northern Nigeria. Int J
Afr Hist Stud 1998;31:23–52.
[17] Obot IS. Nigeria: alcohol and society today. Addiction
2007;102:519–22.
[18] Haworth A, Simpson R. Moonshine markets. Issues in
unrecorded alcohol beverage production and consumption. New York: Brunner-Routledge, 2004.
[19] Ejim OS, Brands B, Rehm J, Lachenmeier DW. Composition of surrogate alcohol from South-Eastern Nigeria.
Afr J Drug Alcohol Stud 2007;6:65–74.
[20] Papas RK, Sidle JE, Wamalwa ES, et al. Estimating alcohol
content of traditional brew in Western Kenya using culturally relevant methods: the case for cost over volume. AIDS
Behav 2009; DOI: 10.1007/s10461-008-9492-z.
[21] Willis J. Potent Brews: a social history of alcohol in East
Africa 1850–1999. Athens, OH: Ohio University Press,
2002.
[22] Bryceson D. Alcohol in Africa: mixing business, pleasure
and politics. Portsmouth, NH: Heinmann, 2002.
[23] Camara PA. Alcoolisation au koutoukou en Côte d’Ivoire:
constat et propositions [Koutoukou abuse in the Ivory
Coast. Findings and proposals]. Alcoologie et Addictologie 2002;24:319–28.
[24] Bourke JG. Primitive distillation among the tarascoes. Am
Anthropol 1893;6:65–70.
[25] Bruman HJ. The Asiatic origin of the Huichol Still. Geogr
Rev 1944;34:418–27.
[26] Ramirez JF, Sanchez-Marroquin A, Alvarez MM, Valyasevi R. Industrialization of Mexican pulque. In:
Steinkraus KH, ed. Industrialization of indigenous fermented foods, 2nd edn. New York, Basel: Marcel Dekker,
2004.
[27] Zizumbo-Villarreal D, Colunga-GarcíaMarín P. Early
coconut distillation and the origins of mezcal and tequila
spirits in west-central Mexico. Genet Resour Crop Evol
2008;55:493–510.
[28] Miranda MB, Martins NGS, Belluco AES, Horii J,
Alcarde AR. Chemical quality of Brazilian sugarcane
spirits. Cienc Tecnol Aliment 2007;27:897–901.
[29] Garcia M, Alarcón M, Duk S, Weigert G. Induction of
micronuclei in mice bone marrow cells by home made
aguardientes collected in southern Chile and their incidence in gastric cancer. Bull Environ Contam Toxicol
1992;49:866–70.
[30] Haworth A. Local alcohol issues in Zambia. In: Haworth
A, Simpson R, eds. Moonshine Markets. Issues in unrecorded alcohol beverage production and consumption.
New York: Brunner-Routledge, 2004:41–66.
[31] Kanteres F, Lachenmeier DW, Rehm J. Alcohol in Mayan
Guatemala: consumption, distribution, production and
composition of cuxa. Addiction 2009;104:752–9.
[32] McKee M, Suzcs S, Sarvary A, et al. The composition of
surrogate alcohols consumed in Russia. Alcohol Clin Exp
Res 2005;29:1884–8.
© 2010 Australasian Professional Society on Alcohol and other Drugs

434

J. Rehm et al.

[33] Popova S, Rehm J, Patra J, Zatonski W. Comparing alcohol
consumption in central and eastern Europe to other European countries. Alcohol Alcohol 2007;42:465–73.
[34] Leon DA, Saburova L, Tomkins S, et al. Hazardous alcohol
drinking and premature mortality in Russia: a population
based case-control study. Lancet 2007;369:2001–9.
[35] Leon DA, Chenet L, Shkolnikov VM, et al. Huge variation
in Russian mortality rates 1984–94: artefact, alcohol, or
what? Lancet 1997;350:383–8.
[36] Gil A, Polikina O, Koroleva N, McKee M, Tomkins S,
Leon DA. Availability and characteristics of nonbeverage
alcohols sold in 17 Russian cities in 2007. Alcohol Clin
Exp Res 2009;33:79–85.
[37] Khaltourina DA, Korotayev AV. Potential for alcohol
policy to decrease the mortality crisis in Russia. Eval
Health Prof 2008;31:272–81.
[38] Razvodovsky YE. Noncommercial alcohol in central and
eastern Europe. ICAP Review 3. In: International Center
for Alcohol Policies, ed. Noncommercial alcohol in three
regions. Washington, DC: International Center for
Alcohol Policies, 2008:17–23.
[39] Szücs S, Sárváry A, McKee M, Ádány R. Could the high
level of cirrhosis in central and eastern Europe be due
partly to the quality of alcohol consumed? An exploratory
investigation. Addiction 2005;100:536–42.
[40] Pärna K, Lang K, Raju K, Väli M, McKee M. A rapid
situation assessment of the market for surrogate and illegal
alcohols in Tallinn, Estonia. Int J Public Health 2007;52:
402–10.
[41] Lachenmeier DW, Ganss S, Rychlak B, et al. Association
between quality of cheap and unrecorded alcohol products
and public health consequences in Poland. Alcohol Clin
Exp Res 2009;33:1757–69.
[42] Nordlund S, Österberg E. Unrecorded alcohol consumption: its economics and its effects on alcohol control in the
Nordic countries. Addiction 2000;95:S551–S564.
[43] Prasad R. Alcohol use on the rise in India. Lancet
2009;373:17–18.
[44] Chowdhury AN, Ramakrishna J, Chakraborty AK, Weiss
MG. Cultural context and impact of alcohol use in the
Sundarban Delta, West Bengal, India. Soc Sci Med 2006;
63:722–31.
[45] Gupta PC, Saxena S, Pednekar MS, Maulik PK. Alcohol
consumption among middle-aged and elderly men: a community study from western India. Alcohol Alcohol
2003;38:327–31.
[46] Mäkelä K. The changing nature of unrecorded alcohol
consumption in Finland in the postwar period. Contemp
Drug Probl 1981;10:103–44.
[47] Norström T. Estimating changes in unrecorded alcohol
consumption in Norway using indicators of harm. Addiction 1998;93:1531–8.
[48] Österberg E. Unrecorded alcohol consumption in
Finland in the 1990s. Contemp Drug Probl 2000;27:271–
99.
[49] Leifman H, Österberg E, Ramstedt M. Alcohol in postwar
Europe: a discussion of indicators on consumption and
alcohol-related harm. Stockholm: European Comparative
Alcohol Study, 2002.
[50] Leifman H. Estimations of unrecorded alcohol consumption levels and trends in 14 European countries. Nord
Alkohol Narkotika Tidskr 2001;18 (English Supplement):
54–70.
[51] Lemmens PH. Unrecorded alcohol consumption in the
Netherlands: legal, semi-legal and illegal production and
© 2010 Australasian Professional Society on Alcohol and other Drugs

[52]

[53]

[54]

[55]

[56]

[57]

[58]

[59]

[60]

[61]

[62]

[63]

[64]
[65]

[66]

[67]

[68]

trade in alcoholic beverages. Contemp Drug Probl
2000;27:301–13.
Morgan BW, Parramore CS, Ethridge M. Lead contaminated moonshine: a report of Bureau of Alcohol, Tobacco
and Firearms analyzed samples. Vet Hum Toxicol
2004;46:89–90.
Meyer MG, Toborg MA, Denham SA, Mande MJ. Cultural perspectives concerning adolescent use of tobacco
and alcohol in the Appalachian mountain region. J Rural
Health 2008;24:67–74.
Single E, Giesbrecht N. The 16% solution and other mysteries concerning the accuracy of alcohol consumption
estimates based on sales data. Br J Addict 1979;74:165–
73.
MacDonald S, Wells S, Giesbrecht N. Unrecorded alcohol
consumption in Ontario, Canada: estimation procedures
and research implications. Drug Alcohol Rev 1999;18:
21–9.
Österberg E. Unrecorded alcohol consumption in Finland
1998. Helsinki: National Research and Development
Centre for Welfare and Health, 2003.
Rehm J, Sulkowska U, Manczuk M, et al. Alcohol accounts
for a high proportion of premature mortality in central and
eastern Europe. Int J Epidemiol 2007;36:458–67.
Bondy SJ, Rehm J, Ashley MJ, Walsh G, Single E, Room
R. Low-risk drinking guidelines: the scientific evidence.
Can J Public Health 1999;90:264–70.
Rehm J, Room R, Taylor B. Method for moderation: measuring lifetime risk of alcohol-attributable mortality as a
basis for drinking guidelines. Int J Methods Psychiatr Res
2008;17:141–51.
Nuzhnyi V. Chemical composition, toxic, and organoleptic
properties of noncommercial alcohol samples. In:
Haworth A, Simpson R, eds. Moonshine markets. Issues in
unrecorded alcohol beverage production and consumption. New York: Brunner-Routledge, 2004:177–99.
Lang K, Vali M, Szücs S, Adany R, McKee M. The composition of surrogate and illegal alcohol products in
Estonia. Alcohol Alcohol 2006;41:446–50.
Savchuk SA, Nuzhnyi VP, Kolesov GM. Factors affecting
the accuracy of the determination of diethyl phthalate in
vodka, ethanol, and samples of illegal alcoholic products. J
Anal Chem 2006;61:1198–203.
Huckenbeck W, Freudenstein P, Jeszenszky E, Scheil HG.
Congeners in spirits produced by moonshine distillers.
Blutalkohol 2003;40:294–301.
Kruse JA. Methanol poisoning. Intensive Care Med
1992;18:391–7.
Lachenmeier DW, Rehm J, Gmel G. Surrogate alcohol:
what do we know and where do we go? Alcohol Clin Exp
Res 2007;31:1613–24.
Paine AJ, Dayan AD. Defining a tolerable concentration of
methanol in alcoholic drinks. Hum Exp Toxicol 2001;20:
563–8.
European Parliament and Council. Regulation (EC) No
110/2008 of the European Parliament and of the Council
of 15 January 2008 on the definition, description,
presentation, labelling and the protection of geographical
indications of spirit drinks and repealing Council Regulation (EEC) No 1576/89. Off J Europ Union 2008;L39:16–
54.
Bennett IL, Jr, Cary FH, Mitchell GL Jr, Cooper MN.
Acute methyl alcohol poisoning: a review based on experiences in an outbreak of 323 cases. Medicine 1953;32:
431–63.

Unrecorded alcohol and health

[69] Tonning DJ, Brooks DW, Harlow CM. Acute methyl
alcohol poisoning in 49 naval ratings. Can Med Assoc J
1956;74:20–7.
[70] Krishnamurthi MV, Natarajan AR, Shanmugasundaram
K, Padmanabhan K, Nityanandan K. Acute methyl
alcohol poisoning. (A review of an outbreak of 89 cases). J
Assoc Physicians India 1968;16:801–5.
[71] Kane RL, Talbert W, Harlan J, Sizemore G, Cataland S. A
methanol poisoning outbreak in Kentucky. A clinical epidemiologic study. Arch Environ Health 1968;17:119–29.
[72] Seng NT. Methyl alcohol poisoning: a report of 20 cases.
Med J Malaysia 1978;33:13–16.
[73] Naraqi S, Dethlefs RF, Slobodniuk RA, Sairere JS. An
outbreak of acute methyl alcohol intoxication. Aust N Z J
Med 1979;9:65–8.
[74] Mittal BV, Desai AP, Khade KR. Methyl alcohol poisoning: an autopsy study of 28 cases. J Postgrad Med
1991;37:9–13.
[75] Laranjerai R, Dunn J. Death by methanol poisoning in
Brazil. Addiction 1998;93:1103–4.
[76] Liu JJ, Daya MR, Mann NC. Methanol-related deaths in
Ontario. J Toxicol Clin Toxicol 1999;37:69–73.
[77] Meyer RJ, Beard ME, Ardagh MW, Henderson S. Methanol poisoning. N Z Med J 2000;113:11–13.
[78] Davis LE, Hudson D, Benson BE, Jones Easom LA,
Coleman JK. Methanol poisoning exposures in the United
States: 1993–1998. J Toxicol Clin Toxicol 2002;40:499–
505.
[79] Swartz RD, Millman RP, Billi JE, et al. Epidemic methanol poisoning: clinical and biochemical analysis of a recent
episode. Medicine 1981;60:373–82.
[80] Duman E, Akgür SA, ÖZTÜrk P, Sen F. Fatal poisonings
in the Aegean region of Turkey. Vet Hum Toxicol
2003;45:106–8.
[81] Kalkan S, Cevik AA, Cavdar C, et al. Acute methanol
poisonings reported to the Drug and Poison Information
Center in Izmir, Turkey. Vet Hum Toxicol 2003;45:334–7.
[82] Yayci N, Agritmis H, Turla A, Koc S. Fatalities due to
methyl alcohol intoxication in Turkey: an 8-year study.
Forensic Sci Int 2003;131:36–41.
[83] Gülmen MK, Meral D, Hilal A, Akcan R, Çekin N.
Methanol intoxications in Adana, Turkey. Toxicol Mech
Methods 2006;16:353–7.
[84] Azmak D. Methanol related deaths in Edirne. Leg Med
2006;8:39–42.
[85] Hovda KE, Hunderi OH, Tafjord AB, Dunlop O, Rudberg
N, Jacobsen D. Methanol outbreak in Norway 2002-2004:
epidemiology, clinical features and prognostic signs. J
Intern Med 2005;258:181–90.
[86] Lachenmeier DW, Haupt S, Schulz K. Defining maximum
levels of higher alcohols in alcoholic beverages and surrogate alcohol products. Regul Toxicol Pharmacol
2008;50:313–21.
[87] Savchuk SA, Kolesov GM, Nuzhnyi VP. Chromatographic
study of the chemical composition and potential toxicity of
spirits and alcoholic beverages. J Anal Chem 2007;62:
575–82.
[88] Mosha D, Wangabo J, Mhinzi G. African traditional
brews: how safe are they? Food Chem 1996;57:205–9.
[89] Lachenmeier DW, Sohnius E-M. The role of acetaldehyde
outside ethanol metabolism in the carcinogenicity of alcoholic beverages: evidence from a large chemical survey.
Food Chem Toxicol 2008;46:2903–11.
[90] Lachenmeier DW, Kanteres F, Rehm J. Carcinogenicity of
acetaldehyde in alcoholic beverages: risk assessment

[91]

[92]

[93]

[94]
[95]

[96]

[97]

[98]

[99]

[100]

[101]

[102]

[103]

[104]

[105]

[106]
[107]

[108]

[109]

435

outside ethanol metabolism. Addiction 2009;104:533–
50.
International Agency for Research on Cancer. IARC
monographs on the evaluation of carcinogenic risks to
humans. 2009. Available at: http://monographs.iarc.fr
(accessed July 2009).
Linderborg K, Joly JP, Visapää JP, Salaspuro M. Potential
mechanism for Calvados-related oesophageal cancer.
Food Chem Toxicol 2008;46:476–9.
Yokoyama A, Ohmori T, Muramatsu T, et al. Cancer
screening of upper aerodigestive tract in Japanese alcoholics with reference to drinking and smoking habits and
aldehyde dehydrogenase-2 genotype. Int J Cancer 1996;
68:313–16.
EFSA. Ethyl carbamate and hydrocyanic acid in food and
beverages. EFSA J 2007;551:1–44.
Lachenmeier DW, Kuballa T, Lima MCP, et al. Ethyl
carbamate analysis in German fruit spirits and Brazilian
sugarcane spirits (cachaça): improved sample cleanup with
automated parallel evaporation. Deut Lebensm Rundsch
2009;105:507–12.
Lachenmeier DW, Kanteres F, Kuballa T, López MG,
Rehm J. Ethyl Carbamate in alcoholic beverages from
Mexico (Tequila, Mezcal, Bacanora, Sotol) and Guatemala (Cuxa): market survey and risk assessment. Int J
Environ Res Public Health 2009;6:349–60.
Codex Alimentarius. Maximum levels for lead (CODEX
STAN 230-2001, Rev. 1-2003). 2003. Available at: http://
www.codexalimentarius.net (accessed November 2007).
Ellis T, Lacy R. Illicit alcohol (moonshine) consumption
in West Alabama revisited. South Med J 1998;91:858–
60.
Anon. Elevated blood lead levels associated with illicitly
distilled alcohol—Alabama, 1990–1991. MMWR Morb
Mortal Wkly Rep 1992;41:294–5.
Reynolds PP, Knapp MJ, Baraf HS, Holmes EW.
Moonshine and lead. Relationship to the pathogenesis of
hyperuricemia in gout. Arthritis Rheum 1983;26:1057–
64.
Morgan BW, Barnes L, Parramore CS, Kaufmann RB.
Elevated blood lead levels associated with the consumption of moonshine among emergency department patients
in Atlanta, Georgia. Ann Emerg Med 2003;42:351–8.
Pegues DA, Hughes BJ, Woernle CH. Elevated blood lead
levels associated with illegally distilled alcohol. Arch Intern
Med 1993;153:1501–4.
Kaufmann RB, Staes CJ, Matte TD. Deaths related to lead
poisoning in the United States, 1979–1998. Environ Res
2003;91:78–84.
Staes C, Matte T, Staeling N, Rosenblum L, Binder S.
Lead poisoning deaths in the United States, 1979 through
1988. JAMA 1995;273:847–8.
Holstege CP, Ferguson JD, Wolf CE, Baer AB, Poklis A.
Analysis of moonshine for contaminants. J Toxicol Clin
Toxicol 2004;42:597–601.
World Health Organization. Guidelines for drinking-water
quality. Geneva: World Health Organization, 2006.
European Council. Council Directive 98/83/EC on the
quality of water intended for human consumption. Off J
Europ Comm 1998;L330:32–54.
Sekizawa J, Dobson S, Touch RJ. Diethyl phthalate
(Concise International Chemical Assessment Document
52). Geneva: World Health Organization, 2003.
Felter SP, Vassallo JD, Carlton BD, Daston GP.
A safety assessment of coumarin taking into account
© 2010 Australasian Professional Society on Alcohol and other Drugs

436

[110]

[111]

[112]

[113]

[114]

[115]

[116]

[117]

[118]

[119]

J. Rehm et al.

species-specificity of toxicokinetics. Food Chem Toxicol
2006;44:462–75.
European Council. Council Directive (EEC) No 88/388
on the approximation of the laws of the Member States
relating to flavourings for use in foodstuffs and to source
materials for their production. Off J Europ Comm
1988;L184:61–6.
Codex Alimentarius. General requirements for natural flavourings (CAC/GL 29.1987). 1985. Available at: http://
www.codexalimentarius.net (accessed July 2008).
Lachenmeier DW, Kanteres F, Rehm J. Unrecorded
alcohol in Russia: is there more to it than just ethanol?
Alcohol Clin Exp Res 2009;33:759–60.
IARC. IARC monographs on the evaluation of carcinogenic risks to humans, Vol. 44. Alcohol Drinking. Lyon,
France: 1988.
CNN-IBN. Investigation Cops Hand-in-Glove with Guj
Hooch Mafia. 2009.Available at: http://ibnlive.in.com/
news/investigation-cops-handinglove-with-guj-hoochmafia/96991-3.html (accessed July 2009).
Lachenmeier DW, Anh PTH, Popova S, Rehm J. The
quality of alcohol products in Vietnam and its implications
for public health. Int J Environ Res Public Health
2009;6:2090–101.
Solodun YV, Klevno VA, Lelyukh TD, et al. Forensicmedical evaluation of toxic hepatitis associated with
surrogate alcohol poisoning. Sud Med Ekspert
2008;51:23–8.
Narawane NM, Bhatia S, Abraham P, Sanghani S, Sawant
SS. Consumption of ‘country liquor’ and its relation to
alcoholic liver disease in Mumbai. J Assoc Physicians India
1998;46:510–13.
Zatonski W, Sulkowska U, Manczuk M, Rehm J, Boffetta
P, La Vecchia C. Liver cirrhosis mortality in Europe.
Warsaw: The Maria Sklodowska-Curie Memorial Cancer
Center and Institute of Oncology, 2007.
Zatonski W, Manczuk M, Sulkowska U, HEM project
team, eds. Closing the health gap in the European Union.
Warsaw: Cancer Epidemiology and Prevention Division.
The Maria Sklodowska-Curie Memorial Cancer Center
and Institute of Oncology, 2008. Available at: http://
hem.waw.pl/index.php?idm=87,139&cmd=1.

© 2010 Australasian Professional Society on Alcohol and other Drugs

[120] Room R, Jernigan D, Carlini-Marlatt B, et al. Alcohol in
developing societies: a public health approach. Helsinki:
Finnish Foundation for Alcohol Studies in collaboration
with World Health Organization, 2002.
[121] Kew MC, Asare GA. Dietary iron overload in the African
and hepatocellular carcinoma. Liver Int 2007;27:735–41.
[122] Zaridze D, Maximovitch D, Lazarev A, et al. Alcohol
poisoning is a main determinant of recent mortality trends
in Russia: evidence from a detailed analysis of mortality
statistics and autopsies. Int J Epidemiol 2009;38:143–
53.
[123] Rehm J. Commentary: alcohol poisoning in Russia: implications for monitoring and comparative risk factor assessment. Int J Epidemiol 2009;38:154–5.
[124] Rehm J, Gmel G. Alcohol consumption and public health
in Russia. Lancet 2007;369:1975–6.
[125] Taylor B, Rehm J. When risk factors combine: the interaction between alcohol and smoking for aerodigestive
cancer, coronary heart disease, and traffic and fire injury.
Addict Behav 2006;31:1522–35.
[126] WHO Expert Committee on Problems Related to Alcohol
Consumption. 2009. Available at: http://www.who.int/
substance_abuse/expert_committee_alcohol/en/ (accessed
July 2009).
[127] Baden-Württemberg. Jahresbericht 2007. Überwachung
von Lebensmitteln, Bedarfsgegenständen, Kosmetika und
Futtermitteln. Stuttgart, Germany. 2008. Available at:
http://www.untersuchungsaemter-bw.de Ministerium für
Ernährung und Ländlichen Raum Baden-Württemberg
(accessed 1 January 2010).
[128] Lachenmeier DW. Reducing harm from alcohol: what
about unrecorded products? Lancet 2009;374:977.
[129] European Commission. Commission Regulation (EC) No
2870/2000 laying down Community reference methods
for the analysis of spirits drinks. Off J Europ Comm
2000;L333:20–46.
[130] Benegal V, Gururaj G, Murthy P. WHO Collaborative
Project on Unrecorded consumption of Alcohol. Karnataka, India. Bangalore, India. 2003. Available at: http://
www.nimhans.kar.nic.in/deaddiction/Publications.html
National Institute of Mental Health and Neurosciences
(accessed 1 January 2010).















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