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).
👉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.
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/
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) &
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.
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
this age group whereas by the same cut-off date there had been 12.
Information for vaccine recipients (left pic) and health professionals (right pic):
🚨 (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.
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
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…
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
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…
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…
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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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.
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.
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
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
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
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,
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.
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