सिद्धार्थ Profile picture
Mar 18, 2021 24 tweets 15 min read Read on X
Pause of AZD1222 vaccine by some EU countries (Germany, Denmark, etc.) when UK has not raised any concerns, is relevant for India because > 85% of vaccine currently being admin in India is COVISHIELD (SII's AZD1222).

Thread on safety data from MHRA,UK

\1
Up to 28 Feb 2021:

1st doses of COVID19 vaccines administered by UK

- 10.7 million of BNT162b2

- 9.7 million of AZD1222

& ~ 0.8 million 2nd doses mostly of BNT162b2.

AEFIs reported via Yellow card:

- 94809 of BNT162b2

- 201622 of AZD1222

- 843 unspecified

\2 Image
Up to Feb 28, 2021 in UK:

~10.1 million received Pfizer/BioNTech's mRNA vaccine, whereas 9.7 million received AZ/Oxford vaccine

Deaths reported via Yellow card:

- 251* of BNT162b2

- 275* of AZD1222

- 6 unspecified

% of deaths in vaccine recipients: AZD1222 > BNT162b2

\3 ImageImageImage
Blood disorders: 1098 @ AZD1222, 2294 @ BNT162b2

where, Thrombocytopenias: 35 @ AZD1222, 22 in BNT162b2

- Immune Thrombocytopenia: 22 (1 death) @ AZD1222, 9 @ BNT162b2

- Thrombocytopenia: 12 @ AZD1222, 13 (1 death) @ BNT162b2

- Thrombocytopenic purpura: 1 in AZD1222

\4 ImageImage
Cardiac disorders: 1922 (39 death) @ AZD1222, 1153 (26 death) @ BNT162b2

Deaths from

- Myocardial infarction: 12 @ AZD1222, 6 @ BNT162b2

- Myocardial ischaemia: 3 in AZD1222

- Heart failures NEC: 5 @ AZD1222, 2 @ BNT162b2

- Cardiac arrest: 13 @ AZD1222, 15 @ BNT162b2

\5 ImageImageImageImage
Eye disorders: 2150 @ AZD1222, 1398 @ BNT162b2

Gastrointestinal disorders: 22336 (5 deaths) @ AZD122, 10534 (12 deaths) @ BNT162b2

General disorders: 71732 (153 death) @ AZD122, 128915 (114 death) @ BNT162b2

Infections: 3839 (38 death) @ AZD122, 2059 (38 death) @ BNT162b2

\6 ImageImage
Immune system disorders: 542 @ AZD122, 528 @ BNT162b2

Metabolic disorders: 2644 (1 death) @ AZD122, 587 (1 death) @ BNT162b2

Muscle & tissue disorders: 24631 @ AZD122, 12823 @ BNT162b2

Nervous system disorders: 43951 (19 deaths) @ AZD122, 18059 (17 deaths) @ BNT162b2

\7 ImageImage
Psychiatric disorders: 3554 @ AZD122, 1409 @ BNT162b2

Reproductive & breast disorders: 297 @ AZD122, 389 (1 death) @ BNT162b2

Respiratory disorders: 5323 (11 death) @ AZD122, 3986 (14 death) @ BNT162b2

\8
------------------

Yellow card reports: gov.uk/government/pub… ImageImage
👉A comprehensive summary of key points from European Medical Agency's assessment of Thromobocytopenia.

Key confirmation from EMA's safety committee:

1. Benefits of AZD1222 (COVISHIELD) still outweigh the risks despite possible link to rare blood clots with low blood platelets. ImageImage
2. No evidence of a problem related to specific batches of the vaccine or to particular mfg sites.

3. the vaccine may be associated w/ very rare cases of blood clots associated w/ thrombocytopenia, i.e. low levels of blood platelets (elements in the blood that help it toclot) w/ Image
or w/o bleeding, including rare cases of clots in vessels draining blood from the brain (CVST).

~20 million people in UK & EEA had got vaccine as of 16 March & EMA had reviewed only 7 cases of blood clots in multiple blood vessels (disseminated intravascular coagulation, DIC) & Image
18 cases of CVST. A causal link w/ thevaccine is not proven, but is possible and deserves further analysis.

9 of DIC & CVST cases from member states resulted in deaths. Most of these occurred in people < 55 years & majority were women👩.

Difficult to look at background rate. Image
However, based on pre-COVID figures it was calculated
that < 1 reported case of DIC might have been expected by 16 March among people < 50 w/in 14 days of receiving vaccine, whereas 5 cases had been reported. Similarly, on avg 1.35 cases of CVST might have been expected among Image
this age group whereas by the same cut-off date there had been 12.

Press brief on EMA assessment here: ema.europa.eu/en/news/covid-…



Information for vaccine recipients (left pic) and health professionals (right pic): ImageImage
🚨 (Amended) Product Information of AstraZeneca/Oxford COVID19 vaccine (COVISHIELD if mfg by SII, India) as approved by CHMP, @EMA_News on 19 March 2021, pending endorsement by @EU_Commission: ema.europa.eu/en/documents/p…

Product Info of COVISHIELD in India also needs to be updated. ImageImage
Seek immediate medical attention if AEFI like

- shortness of breath, chest pain, leg swelling, or
persistent abdominal pain

- severe or persistent headaches or blurred vision, or experience skin bruising or pinpoint round spots beyond site of jab which appears after a few days ImageImageImage
Based on clinical/laboratory features of 9 patients in Germany & Austria, a study finds: AZD1222 is associated w/ development of prothrombotic disorder that clinically resembles heparin-induced thrombocytopenia but which shows different serological profile researchsquare.com/article/rs-362… Image
At least 4 cases in India of thrombocytopenia post COVISHIELD, includes-

33yr/F (vaccine: 22 Jan, death: 3 Feb) w/ death cause earlier reported as "cerebral thrombosis" after post-mortem

80yr/M: AEFI- low platelets initially, later intracranial bleeding
ImageImageImage
Bijwerkingencentrum Lareb, Netherlands has received 5 reports of extensive thrombosis w/ a low platelet count following vaccination with Vaxzevria (COVISHIELD). It occurred 7 to 10 days after vaccination. These are women between 25 & 65 years old. lareb.nl/news/meldingen… Image
Vaxzevria (COVISHIELD): As of 4 April 2021, 169 cases of CVST & 53 cases of splanchnic vein thrombosis reported to EudraVigilance.

🚨EMA has concluded that unusual blood clots w/ low blood platelets should be listed as very rare side effects of Vaxzevria.
ema.europa.eu/en/news/astraz… ImageImage
A short commentary on @MHRAgovuk assessment of reported very rare AEFI: specific blood clots (thrombosis) with low platelets count (thrombocytopenia) associated w/ Vaxzevria (COVISHIELD).

1. Benefits of vaccine outweighs risk for vast majority of people. By 31 March, 20 million
doses have been give. MHRA had 79 case reports upto & including 31st March, 19 people died. All cases post 1st dose. Cases occurred in 51 women and 28 men, all in age group 18 to 79 years.

2. Risk of this rare blood clot about 4 people in a million. Among deceased, 3 out of 19
under 30 years. 4 out of 19 were of cerebral venous sinus thrombosis w/ low platelets, and 5 were other kinds of thrombosis in major veins.

3. Balance of benefits to risk is very favorable in older people & more finely balanced in younger people. Advise on how to minimize risk.
4. Anyone w/ symptoms 4 or more days post vaccination should seek prompt medical advice, new onset of a severe or persistent headache or blurred vision, shortness of breathe, chest pain, leg swelling, persistent abdominal pain, or indeed unusual skin bruising or pinpoint spots.

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More from @das_seed

Jul 2, 2021
Phase 3 trial results for COVAXIN (a double-blind, randomised, placebo-controlled trial). Thread.

medrxiv.org/content/10.110… 2 July 2021.

1. Vaccine efficacy against

● Symptomatic COVID19+ve: 77.8% (95% CI: 65.2–86.4) w/ 130 cases (24 COVAXIN, 106 placebo) Image
● Severe symptomatic COVID-19+ve: 93·4% (57·1–99·8) w/ 16 cases (1 COVAXIN, 15 placebo)

● Symptomatic COVID19+ve in age 18–59 yrs: 79·4% (66–88·2) w/ 109 cases (19 COVAXIN, 90 placebo)

● Asymptomatic COVID19+ve: 63·6% (29🤔–82·4) w/ 47(?) cases (13 COVAXIN+33 placebo=46🤦) ImageImage
2. Vaccine efficacy against symptomatic COVID19+ve

● B.1.617.2 (Delta): 65·2% (33·1–83·0) w/ 50 cases (13 COVAXIN, 37 placebo)

● B.1.617.1 (Kappa): 90·1% (30·4–99·8) w/ 11 cases (1 COVAXIN, 10 placebo)

3. Total 79 variants (VOIs or VOCs) detected in 130 cases analyzed for Image
Read 21 tweets
Jul 2, 2021
Based on recommendations from NTAGI, @MoHFW_INDIA on 2 July 2021 approved the vaccination of pregnant women against COVID-19.

Decision allows pregnant women to make an informed choice on taking COVID vaccination.

Decision communicated to the states/UTs.
pib.gov.in/PressReleasePa…
FAQ by @MoHFW_INDIA circulated among designated health practitioners before approval to allow COVID19 vaccination in pregnant women.

NTAGI had recommended studies to monitor safety of COVID19 vaccine in pregnant to be put in place immediately. Any update?
@MoHFW_INDIA says that pregnant woman opting for vaccination can get COVID19 vaccinated available in India any time during pregnancy.🤦‍♀️

(Not all vaccines have same safety profile. NTAGI had noted concerns along w/ recommendation to allow COVID19 vaccination for pregnant).
Read 6 tweets
Jul 2, 2021
Should Indians be concerned about commercial COVAXIN deals by @BharatBiotech?

@ICMRDELHI & @BharatBiotech have MoU on COVAXIN and also share Intellectual Property rights.

ICMR gets 5% on net sales of COVAXIN as royalty from BBIL.

Partial COVAXIN trials & mfg support from
Indian govt.

Not to forget super-extraordinary regulatory authorization to COVAXIN w/o Phase 3 trial data that allowed BBIL to opened door for early sales of COVAXIN in India & some other nations.

During early days, COVAXIN consignments only had BBIL's logo but not of ICMR.
However, there're COVAXIN consignments featuring logos of both developers, ICMR & BBIL, from March.

Commercial supply of 2 lakh COVAXIN doses to Mauritius on 19 March had logos of ICMR & BBIL w/ sign of #VaccineMaitri by Indian govt.

Was ICMR logo because of int'l shipment? No.
Read 8 tweets
Jul 1, 2021
What do we know about ZyCoV-D, a plasmid DNA vaccine candidate against symptomatic COVID19 by Zydus Cadila? Thread.

1. Results of pre-clinical studies on animals before July 2020 put in public domain in 2021:
biorxiv.org/content/10.110… 26 Jan 2021
biorxiv.org/content/10.110… 3 Feb 2021
2. Permission granted by DCGI on 2 Jun 2021 to initiate human trials adaptive Phases I & II.

Safety profile of 7 days after 1st dose of ZyCoV-D needed to be reviewed by DSMB & CDSCO before go ahead for Phase 2.

Some issues w/ these permissions are:
a) ZyCoV-D needs 3 doses for
completion (at day 0, day 28, day 56).

b) Vaccine candidate platform/tech is new for humans. 7 days for such a new vaccine candidate is too short period for monitoring. SAEs could occur based on dosages as well & some type of events may take longer to manifest.

c) Phase I trial
Read 26 tweets
May 24, 2021
A short note on dosing regimen of COVISHIELD for complete vaccination.

We've 3 different set of trials:

1. UK/Brazil trials
This trial was open-label, w/ scandalous error in dosing regimen ("half-dose" error), had multiple major amendments in protocol when trial was undergoing Image
w/ minimum gap b/w 2 doses set to be 4 weeks.

COVISHIELD was initially supposed to be a single dose vaccine, but in middle of trial they realized that booster dose was required for higher efficacy compared to just single dose.

In the process, due to mfg/supply delay, intended Image
interval of 4 weeks was not achieved & got prolonged.

Attached are intended & extrapolated sub-group analysis that was carried out by PIs as part of protocol, w/ different dosing levels & intervals.

*extrapolated analyses were not part of protocol hypothesis but in response to ImageImage
Read 17 tweets
Apr 11, 2021
A thread on recent updates (24 March- 9 April 2021) on Vaxzevria, a COVID19 vaccine mfg by AstraZeneca (called COVISHIELD if the same product is mfg by @SerumInstIndia).

1. Summary of productcharacteristics updated by @AstraZeneca after @EU_Commission's decision. Importantly, ImageImageImage
a) Thromobocytopenia is listed as common (≥1/100 to <1/10) adverse reaction

b) Thrombosis in combination w/ thrombocytopenia is listed as very rare (<1/10,000) adverse reaction

c) Currently available trial data do not allow an estimate of vaccine efficacy in 55+ yrs age group. Image
d) Asks healthcare professionals to be on alert for signs & symptoms of thromboembolism &/or thrombocytopenia. Instructs vaccinated people to seek immediate medical attention if they develop symptoms such as shortness of breath, chest pain, leg swelling, persistent abdominal pain ImageImage
Read 16 tweets

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