Keywords
homoeoprophylaxis - immunisation - effectiveness - infectious diseases - SARS-CoV-2
Introduction
From Hahnemann's use in 1799 of Belladonna 30 to prevent scarlet fever[1] to the prevention of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
in 2023, appropriate dosing with appropriately 'similar' remedies have been used to
prevent targeted infectious diseases. This method has been known as homoeoprophylaxis (HP) since Burnett's use of the term in 1884.[2]
Potentised medicines past 12C are non-toxic. They still can cause reactions (a fact
that troubles sceptics – 'nothing' causing something), but there is no point in prescribing
a medicine that is safe if it does not work. So, it is necessary to ask – what evidence
do we have of the effectiveness of HP over the past 223 years, including effectiveness
against SARS-CoV-2?
We know that almost all the early evidence of the effectiveness of HP was contained
in clinic reports and essays on the subject. One of the earliest statistical measures
of the effectiveness of HP was by Dr Charles Eaton in 1907.[3] The formal database of HP evidence has been steadily expanding since the 1970s,
especially in India, Cuba, and Brazil where governments have supported the use of
HP.
However, recent data from 2020, 2021 and 2022 suggests that the effectiveness of HP
remedies against SARS-CoV-2 is lower than expected.
The purpose of this article is to examine available evidence and suggest possible
explanations for the emerging difference and solutions to improve the effectiveness
of HP against SARS-CoV-2.
Method
To determine the effectiveness of HP against SARS-CoV-2 compared with other infectious
diseases, an attempt has been made to quantify a measure of effectiveness in both
groups using data from India, Cuba, and Brazil where homeopathy enjoys different levels
of Government support, and from Australia where it does not.
These reviews are NOT formal meta-analyses which are not possible due to the heterogeneous
nature of the evidence. Nor are they reviews of every HP intervention undertaken.
In 2019, one author (I.G.) published two related reports outlining the results of
studies where over 247,000,000 doses of HP remedies were given between 1974 and 2014
to more than 50,000,000 individuals. Most of the dosing was directed by government
authorities in India, Cuba, and Brazil. This record is but a modest part of the entire
use of HP since 1799 but supports the claim that properly prescribed potencies of
'similar' HP remedies confer an average effectiveness of around 88%.[4]
[5] New material was added to the [Table 2] below and one study was withdrawn.
The interventions studied provided a variety of either numerical assessments of effectiveness,
or descriptive assessments.
This data is compared with evidence of the effectiveness of HP against SARS-CoV-2.
Initially, a literature search involving 13 journals was undertaken which suggested
13 articles may be of use. Further analysis reduced the list to 6 articles, and they
were analysed to show their measures of effectiveness. This was then compared with
data collected by the authors in surveys undertaken in Australia in 2021 and 2022.
The 2021 survey was published in 2022[6] and the 2022 survey was published in 2023.[7]
A summary of relevant data from both surveys is presented in two parts in the following
text.
Results
PART A: Evidence supporting HP effectiveness against non-coronavirus disease 2019
(COVID-19) infectious diseases.
A summary of the evidence describing the use of over 247,000,000 doses of HP medicines
against a range of infectious diseases from 1974 to 2014 suggested an average effectiveness
just under 90%.
The interventions studied provided a variety of either numerical assessments of effectiveness
or descriptive assessments. This made the task of preparing a normal meta-analysis
nearly impossible, although an attempt to compare several published studies was made
elsewhere and noted below.
[Table 1] shows the codes used to describe the type of study where a statistical measure of
effectiveness was supplied, and the classification of the result where the study was
descriptive. [Table 2] presents a summary of the results of some HP interventions in three countries from
1974 to 2012.
Table 1
Classification of effectiveness
|
Code
|
Description
|
|
Statistical
|
|
|
A
|
Direct control group
|
|
B
|
Indirect control group[8]
|
|
C
|
Simple % of cohort studied
|
|
D
|
Historical trend of actual reports
|
|
E
|
Fall factor analysis[9]
|
|
F
|
No control or historical trend
|
|
Descriptive
|
|
|
G
|
Clearly positive result
|
|
H
|
Somewhat positive result
|
|
I
|
Unclear result
|
|
J
|
Negative result
|
Table 2
Summary of results of HP interventions in three countries from 1974 to 2014
|
Year
|
Disease
|
Numbers of people
|
Government
directed
|
Type/dose
|
Effectiveness (%)
|
|
Cuba[10]
|
25,020,000
|
|
|
|
|
2007
|
Leptospirosis
|
2.2 million
|
Yes
|
N
|
B. G
|
|
2007
|
Hepatitis A
|
1 million
|
Yes
|
N
|
D. G
|
|
2008
|
Leptospirosis
|
2.2 million
|
Yes
|
N
|
B. G
|
|
2009
|
Dengue fever
|
20,000
|
Yes
|
N + GE
|
A. 74.1–100.0%
|
|
2010
|
Swine flu
|
9.8 million
|
Yes
|
N + GE
|
D. G
|
|
2010
|
Pneumococcal
|
9.8 million
|
Yes
|
N + GE
|
D. G
|
|
India
|
222,238,197
|
|
|
|
|
1989, 91, 93
|
Japanese encephalitis[11]
|
322,812
|
Yes
|
GE
|
99.96% C
|
|
1996
|
Dengue[12]
|
> 39,200
|
Yes
|
GE
|
99.97% C
|
|
1999
to 2009
|
Japanese encephalitis[13]
|
20,000,000
per annum
|
Yes
|
GE + N
+constitutional
|
B, D G
|
|
2006
|
Chikungunya[14]
|
1061
|
No, GP at Uni.
|
GE
|
75.7% A 82.19% C
|
|
2007
|
Epidemic fever[15]
|
1,855,374
|
Yes
|
GE
|
63.9% A 73.83% C
|
|
2014
|
Chikungunya[16]
|
19,750
|
Yes
|
GE
|
19.0%
|
|
Brazil
|
870,698
|
|
|
|
|
1974
|
Meningococcal[17]
|
18,640
|
No, private GPs
|
N. 1 dose
|
95% A
|
|
1998
|
Meningococcal[18]
|
65,826
|
Yes
|
N
|
95% 6 months to
91% 12 months A
|
|
2001
|
Dengue[19]
|
Doses 1,959
|
No, private doctors
|
GE 30
|
81.5% B, E
Inferred rate
|
|
2007
|
Dengue16
|
7,300 people
20,000 doses
|
Yes
|
GE complex
|
G
|
|
2007
|
Dengue[20]
|
[a]216,000
|
Yes
|
GE complex
|
86.7% B Inferred rate
|
|
2007–12
|
Dengue[21]
|
[b]1,085,917
|
Yes
|
GE complex
|
89.4% B Inferred rate
|
Abbreviations: GE, genus Epidemicus; GP, general practitioner; HP, homoeoprophylaxis.
a Not included in analysis as also included in the '2007-12' reference.
b The number of persons who used HP in the 5 years from 2008 to 2012 is estimated to
be 628,273 using the ratio of doses to people shown in the 2007 intervention.
In [Table 2], 'N' refers to the use of nosodes, and 'GE' refers to the use of genus Epidemicus
remedies.
There is a degree of consistency across the HP interventions shown in [Table 2], with a range of effectiveness between 63 and 99% (the survey showing 19% is clearly
an aberrant figure). An earlier analysis calculated weighted averages between 86.1
and 89.95% depending on the methodology chosen.[22]
These findings are generally analysing short-term interventions in epidemic conditions
but are consistent with one author's (I.G.) study of long-term HP use from 1986 to
2002 where the effectiveness of HP was 90.4% (95% confidence interval; 87.6–93.2%).[23] However, it should be noted that the substantial Indian interventions against Japanese
encephalitis involved giving annual doses of three remedies within 1 month which were
highly effective in preventing the disease. This is similar to the author's (IG) use
of annual doses in his Australian HP program against targeted endemic diseases.
PART B: Evidence supporting HP effectiveness against SARS-CoV-2
[Table 3] summarises the results of the limited literature review of HP interventions against
SARS-CoV-2.
Table 3
Interventions against SARS-CoV-2
|
Year
|
Country
|
Numbers
|
Remedies
|
Results
|
Comments
|
Study
|
|
2020
|
Cuba
|
45,914 +
|
Complex
|
Insufficient data
|
Positive but insufficient data
|
7
|
|
2022
|
India
|
2,233
|
6 remedies
|
Mixed results
|
2 of the 6 groups positive
|
3
|
|
2022
|
Brazil
|
Treated: 405
Control: 876 / 361
Total: 2,518
|
Arsen 30
|
98.9%
|
Study performed in a specific cluster (close population). Heterogenous comparison
groups exposed to different risks. Much less CV in active group
|
2
|
|
2022
|
India
|
Treated: 172
Control: 169
Total: 341
|
Arsen 30
|
51.5%
|
Low numbers. Incorrectly claimed 83%
|
11
|
|
2022
|
India
|
Treated: 892
Control: 1,549
Total: 2,441
|
Tub + GEx3
|
No clear idea of results
|
Insufficient data, no accurate measure of effectiveness possible
|
10
|
|
2022
|
India
|
Treated: 22,693
Control: 9,493
Total: 32,186
|
Arsen 30
|
68.2% using RT-PCR confirmed cases. 80.2% considering suspected/probable cases
|
Laboratory confirmed vs not laboratory confirmed. Multicentre randomised clustered
study
|
5
|
|
2022
|
India
|
Total
584,980
|
Arsen 30
|
Stable COVID-19 incidence on the treated population over 6 months, while the country's
incidence increased steadily
|
Larger dataset collected over 6 months but using a cut off for 3 weeks after treatment
for individuals to be included in the data. No follow-up after 3 weeks. No reference
or control group so difficult to assess effectiveness
|
6
|
Abbreviations: COVID-19, coronavirus disease 2019; RT-PCR, reverse transcription polymerase
chain reaction; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.
[Tables 4] and [5] present a summary of relevant results for the authors' 2021 and 2022 in-clinic surveys
of patients using a variety of homeopathic prevention and treatment remedies to deal
with COVID-19 and related vaccines and vaccine shedding.
Table 4
Remedy composition of 2021VPN and 2022DOV
|
2021VPN
|
2022DOV
|
|
Nosodes
|
|
JPV2 200 (Omicron strain)
|
|
JPV 200 (Delta strain)
|
JPV 200 (Delta strain)
|
|
Influenzinum Triple Nosode M
|
Influenzinum Triple Nosode M
|
|
Genus Epidemicus
|
Arsenicum album 200
|
Gelsemium 200
|
|
Bryonia 200
|
Bryonia 200
|
|
Phosphorous 200
|
Phosphorous 200
|
|
Justicia 200
|
Pulsatilla 200
|
|
Mercury Sol 200
|
Rhus tox 200
|
|
Antimonium tartaricum 200
|
Antimonium tartaricum 200
|
Abbreviations: VPN; Virus Prevention Nosodes, DOV; Delta and Omicron Variants.
Table 5
A comparative summary of results from surveys of HP users in 2021 and 2022
|
|
2021 survey
|
2022 survey
|
|
Details
|
|
No.
|
%
|
No.
|
%
|
|
Total respondents
|
|
1,912
|
|
349
|
|
|
Used 2021VPN/2022DOV
|
|
1,643
|
85.9
|
264
|
75.6
|
|
Used VPN/DOV and exposed to the disease
|
|
402
|
24.5
|
192
|
72.7
|
|
Used VPN/DOV and exposed to disease and diagnosed with disease
|
|
56
|
13.9
|
88
|
45.8
|
|
Used VPN/DOV and exposed to disease and NOT diagnosed with disease
|
|
346
|
86.1
|
104
|
54.2
|
|
… AND Taken remedy before disease
|
|
[a]
|
|
58
|
30.2
|
|
Used VPN/DOV before diagnosis, and exposed to disease and NOT diagnosed with the disease
|
|
|
|
|
69.8
|
|
How serious were the symptoms? In the 56 respondents who used VPN, the 58 respondents
who used DOV, AND were exposed to disease and diagnosed with SARS-CoV-2
|
Nil
|
4
|
7.1
|
2
|
3.5
|
|
Low
|
27
|
48.2
|
31
|
53.5
|
|
Medium
|
23
|
41.1
|
23
|
39.7
|
|
High
|
2
|
3.6
|
2
|
3.5
|
|
How long did symptoms last? (Q.31)
|
|
Av. 2.03 weeks
|
Av. 1.22 weeks
|
Abbreviation: HP, homoeoprophylaxis; SARS-CoV-2, severe acute respiratory syndrome
coronavirus 2.
a The 2021 survey asked whether the remedy was taken before the disease, but only 19/1,912
people responded meaning the resulting measure of effectiveness (96.3%) was unreliable
Thus, a range of effectiveness from 69.8 to 86.1% is suggested. This may reflect differences
in effectiveness for the Delta and Omicron strains, and/or the difference may be due
to the much smaller number of respondents in the 2022 survey. It is possible that
a figure in the low 70% range is more generally realistic.
[Table 4] describes the contents of the two HP remedies studied. One author (I.G.) decided
in February 2020 to use the Cuban approach against SARS-CoV-2 which combined similar
nosodes and GE remedies.[24] The formulas were changed when new nosodes became available and as treatment remedies
changed with the changing variants. 2021VPN was the third version and 2022DOV the
fourth version of the author's (IG) COVID-19 HP remedy. The sixth version of the COVID-19
HP remedy was released in March 2023.
The combination remedies were prepared by obtaining individual remedies from licensed
homeopathic pharmacies in Australia and the United Kingdom, which were then combined
in equal proportions.
[Table 5] focuses on attempts to assess the effectiveness of the COVID-19 HP remedies 2021VPN
and 2022DOV by measuring cases in patients who believed they had been exposed to the
disease, who had taken the remedy before exposure, and who either did or did not contract
the disease.
The results are biased – both selection bias and observer bias are present. For example,
all respondents chose to use one or both remedies for themselves and/or for their
children, some respondents who reported that they were exposed may not have been,
and some respondents who were exposed but did not develop symptoms did not realise
that they were exposed and did not reported exposure. The reader must judge which
is more likely to be the larger group.
The reason for introducing possible exposure into the analysis is because IF this
is not done, the results will overestimate the effectiveness of the HP remedies. The
approach adopted here is more likely to underestimate effectiveness, although the
respondent numbers involved are modest meaning there could be a wider fluctuation
of results.
Discussion
The authors acknowledge that the lack of homogeneous data means that a conventional
meta-analysis is not possible. Some will argue that unless a survey such as this is
conducted along strictly conventional lines it will have no value. We disagree.
There exists considerable evidence regarding the effect and effectiveness of vaccines,
some of which is questioned by independent researchers. There is considerable evidence
regarding the effect and effectiveness of HP over 220+ years, much of which is difficult
to access and much of which is 'unconventional'. We believe that any reasoned and
unbiased attempt to draw comparisons both within HP and with vaccination is worthwhile.
It is suggested that the difference between the average effectiveness of HP averages
against established infectious diseases and an estimate of the effectiveness against
SARS-CoV-2 could have been expected.
On the one hand, most of the infectious diseases that have been studied previously,
and certainly those in most national vaccination programs are relatively stable, whereas
there continue to be regularly emerging variants of SARS-CoV-2. Further, the symptom
picture of the different SARS-CoV-2 variants can be quite different and/or the same
variant can exhibit different symptoms in different countries. The symptom pictures
of many established infectious diseases are relatively stable.
In addition, the GE remedies for established infectious diseases are usually well
known and readily available. This is not always the case with remedies for SARS-CoV-2.
Finally, nosodes of established infectious diseases are known and usually available.
Once again, this is not always the case with the different variants of SARS-CoV-2.
In fact, probably the major reason why the SARS-CoV-2 HP effectiveness figures are
not higher is because high-quality and reliable nosodes of the prevailing variants
were not readily available to pharmacies and clinicians.
In that regard, the quality of the nosodes, and particularly the raw material used
in their preparation, was almost certainly a significant factor leading to the high
effectiveness of the Cuban interventions from 2007 to 2015. For example, the formulations
used in the leptospirosis interventions in 2007 and 2008 were prepared from fresh
cultures of the circulating strains that were isolated in the intervention region.
After culturing, the culture media was removed and adjusted bacteria suspensions were
used as a raw material for nosode preparation.
In this case, the presence of the infectious pathogen in the sample was not inferred
but controlled and confirmed by laboratory analysis. The same approach was used in
all Cuban HP interventions involving nosodes.
Unfortunately, this has not been the case for most SARS-CoV2 nosodes since access
to high-quality viral preparations was not possible, i.e., only samples from infected
persons where the presence of the virus was inferred by potentially unreliable polymerase
chain reaction and rapid antigen tests were available from which to prepare the nosodes,
and high-quality laboratory tests and isolation methods were not generally available.
The one exception could be shown in reference [25] where a high-quality nosode prepared by Dr Shah was used.
These factors are summarised in [Table 6] and offer reasons why the effectiveness of established HP remedies should be greater
than the effectiveness of HP remedies for SARS-CoV-2.
Table 6
Summary of characteristics of infectious diseases in general and SARS-CoV-2
|
Characteristics
|
Established diseases in general
|
SARS-CoV-2
|
|
Stability of organism
|
Relatively stable
|
Steadily changing variants
|
|
Stability of symptom picture
|
Stable across different variants
|
Changeable
|
|
Timely availability of GE remedies
|
Generally good
|
Variable
|
|
Timely availability of appropriate nosodes of different variants
|
Good
|
Difficult
|
Abbreviations: GE, genus Epidemicus; SARS-CoV-2, severe acute respiratory syndrome
coronavirus 2.
The effectiveness of HP compared with current vaccines in both circumstances is also
important.
A significant problem in making this comparison is due to the fact that there is very
little and largely insufficient data to assess vaccine effectiveness on preventing
the infection or transmission of SARS-CoV-2. Initial reports and messages suggested
that new vaccines were over 90% effective in preventing the severe disease and death.
Before too long that had been lowered below 70%. Then we were told that they were
not very effective at preventing the disease but would keep infected individuals out
of hospital. Then, as hospitalisation rates between the vaccinated and the unvaccinated
narrowed, that message was modified again.
Even vaccine advocate Gates acknowledged in late 2021 that 'We didn't have vaccines
that block transmission. We got vaccines that help you with your health, but they
only slightly reduce the transmission. So, we need a new way of doing the vaccines.[25]
More recently we have been told that new bivalent vaccine boosters (protecting against
more than one variant) are the way to go, but they have been found wanting. For example,
on 23 February, 2023 the New England Journal of Medicine published correspondence
showing effectiveness of the new boosters was 58.7% against severe infection resulting
in hospitalisation and 61.8% against severe infection resulting in hospitalisation
or death. Effectiveness to prevent simple infection would be much less. And the study
authors noted 'Booster effectiveness peaked at approximately 4 weeks and waned afterward'.[26]
Well-known vaccine advocate Dr Paul Offit admitted 'Omicron-targeting bivalent boosters
likely conferred no extra protection against COVID-19 over the original mRNA products
due to immune imprinting'.[27]
So, even though HP protection against SARS-CoV-2 is less than HP against traditional
infectious diseases, with expected HP effectiveness against SARS-CoV-2 above 70% and
with no safety issues, HP offers a genuine alternative.
Conclusion
Appropriate HP offers an option which appears to be comparably effective to vaccination,
and in the case of COVID-19 vaccines, superior to what is currently being offered,
without any risk of toxic damage. Given its low cost, ability to quickly respond to
new variants and ease of distribution HP remains an option that objective scientists
and politicians should consider.
The overall effectiveness of HP against SARS-CoV-2 would be maximised if high-quality
viral samples become available to licensed homeopathic pharmacies and manufactures,
which would also allow rapid HP remedy changes to respond to changing variants.
What Is Known
Appropriately dispensed HP remedies can prevent many unimmunised people who are exposed
to a targeted infectious disease from presenting with symptoms of the disease. An
average effectiveness of around 88% has been based on numerous interventions in tens
of millions of people.
What Is New
The average effectiveness of HP against SARS-CoV-2 appears to be clearly less than
the average effectiveness of HP against other infectious diseases. Reasons for this
are discussed and appear to explain the difference. In particular, the lack of availability
of high-quality laboratory confirmed viral isolates appears to be a major factor in
the difference.