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Covishield vs Covaxin comparison:
1. Biological Components:
Covishield is a viral vector vaccine. It uses
a weakened, non-replicating strain of Chimpanzee cold virus (adenovirus) to carry genetic material of the spike
protein of SARS-CoV-2 into human cells.
Covaxin contains an inactivated SARS-CoV-2 (Strain: NIV-2020-770) which is disabled for replication. However, the proteins are intact which are able to provoke immunity of the host.
2.
Chemical Ingredients:
Covishield |
Covaxin |
L-Histidine Ethanol L-Histidine Hydrochloride Monohydrate Magnesium Chloride Hexahydrate Polysorbate 80* Sucrose Sodium Chloride Disodium Edetate Dihydrate (EDTA) Water
for injection |
Aluminum Hydroxide gel Imidazoquinolinone
# (TLR 7/8 agonist) 2-Phenoxyethanol Phosphate buffer saline |
*Polysorbate 80 which is an
ingredient of Covishield is known
to cause anaphylactic reactions in patients
as can be read here whereas Covaxin has
no such component. |
#Also
known as Algel-IMDG which is an adjuvant
required for Covaxin but not for Covishield. |
Storage Conditions:
Both vaccines can be stored at 2 to 8 degrees Celsius
making them convenient to store and transport.
3.
Mechanism of Immunization:
Covishield – This vaccine produces antibodies against only a specific region of
the virus. It contains a portion of
the DNA that codes for the spike protein (S-protein). Once inside the cells, the DNA part first needs to enter
the nucleus to create its mirror image (complementary RNA). Then this RNA comes
out in the cytoplasm as a messenger and starts making
S-protein through a machine
available for this purpose called ribosome.
Since it is S-protein that provokes
immunity it may not be as close to natural immunity as created by Covaxin. If
there are any long-term side effects of the DNA material remaining
inside the nucleus
(e.g. integration in human
DNA) is not yet known. So far, DNA vaccines were only being tried out for treating cancer patients and never
used for preventing infections in
normal subjects.
Covaxin – This vaccine can
produce antibodies against many regions of the complete virus. Since this vaccine contains a full
inactivated virus with all its 29 proteins intact, the immunity provoked by it will be more comprehensive
and closer to natural immunity arising out of an infection. This does not contain any genetic material that can
either replicate or go inside the nucleus
but provokes the immunity against virulent proteins other than S-protein as
well. This uses a tried and tested technology platform used by other vaccines
like polio vaccine.
However, these vaccines require an adjuvant to provoke immunity. For
this purpose, alum is commonly used
which mainly provokes Th-2 type immunity which also leads to more side effects.
Hence, Bharat Biotech
has used an alternative adjuvant
“Algel-IMDG (Imidazoquinolinone)” which stimulates Th-1 type immunity
that is also generated by mRNA/DNA
vaccines.
4.
Clinical Development:
Covishield has been developed by AstraZeneca
with Oxford university in the UK and is being
manufactured by the Serum Institute India (SII) in Pune. Covishield has
completed phase 3 trials in S.
Africa, Brazil and UK. 90% of the subjects in these studies were under the age
of 55 making the efficacy and safety
data applicable to this age group. The company has presented bridging study results in Indian population to the
regulatory authorities based on which the approval was granted by DCGI.
This data is not yet available in the public
domain.
Covaxin has been developed by Hyderabad based
Bharat Biotech along with the Indian Council
of Medical Research (ICMR) and National Institute of Virology (NIV) in Pune.
5.
Dosage Regimen:
Covishield has been recommended to be taken in
2 doses. Observation of data from the UK shows improved
protection with a gap of 12 weeks
between 2 doses;
though currently the
expert committee set up by the Drug Controller General of India (DCGI) has recommended a gap of 4 weeks.
Covaxin has been recommended to be taken
in 2 doses 4 weeks apart.
6.
Efficacy:
Covishield has an average efficacy of 70% when
2 doses are administered 4 weeks apart. This
data is from a meta-analysis (pooled analysis of multiple studies) of 4
Covishield trials in 11,636
patients out of which 3 trials were single blind and one double blind in 3 different countries. The efficacy of Covishield was published in The Lancet (link to the article). Observation of data has shown that the
efficacy improves as the gap between the 2 doses is increased reaching a reported efficacy
of 82.4% with a 12-week
gap. Since, the phase-3 trials
were conducted with a 4-week interval,
it has become the standard.
Covaxin phase-3 interim results show an
efficacy of 81%. This data is from one double blind study of 28,500 patients in India. Thus, from efficacy angle,
Covaxin scores higher than Covishield
with more robust and coherent data in Indian subjects.
7.
Protection against
Mutations:
Preliminary research shows both vaccines are effective
against the variant of the novel coronavirus
first detected in the UK but there is no data on their efficacy against the
mutants found in South Africa and
Brazil. Data against these 2 variants is yet to be generated for both these
vaccines.
8.
Side Effects:
Based on the fact-sheets
released by both manufacturers:
Side Effects |
Covishield |
Covaxin |
Anaphylaxis |
ü |
û |
Tenderness, pain, warmth, redness, itching,
swelling or bruising at the
injection site, generally feeling unwell |
ü |
ü |
Stiffness in
upper arm |
û |
ü |
Fever |
ü |
ü |
Fatigue / Malaise
/ Weakness |
ü |
ü |
Headache |
ü |
ü |
Nausea / Vomiting |
ü |
ü |
Joint pain / Muscle
ache |
ü |
û |
Bodyache |
û |
ü |
Feeling dizzy,
decreased appetite, abdominal pain |
ü |
û |
Enlarged lymph nodes |
ü |
û |
Excessive sweating, itchy skin |
ü |
û |
Rashes |
ü |
ü |
9.
Precaution and Contraindications:
Based on the fact-sheets released by both
manufacturers:
Covishield |
Covaxin |
||
What should you mention to your healthcare provider before vaccination? (HCP
to decide on whether to vaccinate or not in such conditions) |
Who
should not get the vaccine? |
What should you mention to your healthcare provider before vaccination? (It is
advisable not to take the vaccine
in any of these conditions) |
Who should not get the
vaccine? |
Any history of allergies |
Has a severe allergic reaction after a
previous dose of this vaccine |
Any history of allergies |
Any history of allergies |
Fever |
Has a severe allergic reaction to an
ingredient of this vaccine |
Fever |
Has fever |
A bleeding disorder or if you are
on a blood thinner |
|
Bleeding disorder or if you are on a blood thinner |
Has a bleeding disorder or is on a blood
thinner |
Immunocompromised
or on a medicine that affects the immune system |
|
Immunocompromise d
or on a medicine that affects the immune system |
Is immunocompromised or
is on a medicine that affects the immune system |
Pregnant / Breastfeeding |
|
Pregnant / Breastfeeding |
Pregnant / Breastfeeding |
Received another Covid-19 vaccine |
|
Received another Covid-19 vaccine |
Has received another COVID-19
vaccine |
Any other serious
health related issues, as determined by the vaccinator/officer |
|
|
Has any other serious health
related issues, as determined by the vaccinator/officer |
10. Consent:
Covishield does not require any consent form as it has completed the phase-3 clinical trials
Covaxin – Since it was approved by the Indian regulatory authorities before phase 3 results were available, it is being administered to people in a large clinical trial setting. This is being termed as “clinical trial mode”. Such use is similar to some of the anti-cancer drugs which have been used on compassionate basis before it’s formal approval. This requires pre-informed consent of the patient who is explained that it is not yet approved and he provides his consent for the same. This form states that the beneficiaries will be provided care in government authorized hospitals if they faced side-effects from the vaccine. They will also reportedly get compensated if they face adverse effects from the vaccine. Now that the phase 3 efficacy data is available, once it is presented to the authorities and restricted emergency use is granted the need for informed consent will be removed.
11. Price
While the vaccine is being given for free at the
government institutions, the price at private
institutions has been capped at ₹250 per dose.
Currently, the person does not get to choose which
vaccine he/she would receive. It is likely that
once the vaccines are available for private market sale, choice of brand will
be given to the people.
Recommendation:
At the face value, the stellar reputation of Oxford
University, AstraZeneca and Serum Institute of
India is daunting enough to prefer Covishield if a choice is given to
you. However, an objective comparison
of properties, attributes and available information indicates that Covaxin is
better placed to receive our recommendation for the following
reasons: Higher efficacy
of Covaxin comes
out of robust data from one double blind controlled clinical trial as
compared to lower efficacy of Covishield
with results pooled from multiple studies that were not blinded and were
dissimilar. Covaxin also seems to
have distinct safety advantage with the lack of anaphylaxis and potential for neurological adverse events with
Covishield. Two cases of transverse myelitis in the UK had stalled
the clinical trial for
some time but resumed once the
safety was reconfirmed.
On the regulatory front, Covishield (its original codename of AZD1222) seems to have an advantage over Covaxin being approved in European countries and Australia whereas Covaxin has been approved in India and Zimbabwe so far. Also, by now millions of doses have been used in India and Europe without any major concern. Covishield may therefore be a natural choice for those who value external endorsement (in this case UK, EU, Australia). However, without extraneous considerations on the strength of head-to-head comparison shown above Covaxin is a compelling choice. for details www.drbadevshl.com
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