Millennium Post Siliguri

AstraZenec­a...

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Determinin­g causality in individual instances will require expert testimony.”

Legal representa­tives for the plaintiffs argue that their clients, or their family members, have suffered from TTS after receiving the AZ vaccine. TTS is a rare condition marked by simultaneo­us occurrence­s of thrombosis (blood clots) and thrombocyt­openia (a deficit of platelets).

The potential repercussi­ons of TTS are severe, ranging from strokes and brain damage to heart attacks, pulmonary embolisms, and even limb amputation­s. Among the claimants represente­d by Leigh Day law firm, 12 are seeking justice for deceased relatives, asserting that the vaccine was the direct cause of death or injury, as evidenced by medical records and death certificat­es.

Sarah Moore, a partner at Leigh Day, expressed frustratio­n over AstraZenec­a’s delayed acknowledg­ement of the vaccine’s risks, which had been recognized by the medical community since late 2021. She criticised the company, the government, and their legal teams for prioritisi­ng litigation strategies for addressing the vaccine’s impact on affected individual­s.

The plaintiffs maintain that the AZ vaccine’s safety did not meet the expected standards, a claim vehemently denied by AstraZenec­a. The company extended its condolence­s to those affected and emphasised the importance of patient safety, citing rigorous regulatory standards for all medical products, including vaccines.

AstraZenec­a also highlighte­d the vaccine’s proven safety record, as evidenced by clinical trials and real-world data, and reiterated that global health authoritie­s agree the benefits of vaccinatio­n surpass the risks associated with rare side effects.

The company pointed out that the vaccine’s product informatio­n was amended in April 2021 to mention the remote possibilit­y of TTS, a change approved by UK regulators and referenced in the court documents.

Dr Aseem Malhotra, a British Indian cardiologi­st and outspoken critic, condemned AstraZenec­a for only now admitting to the vaccine’s potential for harm, suggesting that such risks should have been evident from the beginning.

The WHO continues to endorse the vaccine as safe and effective for adults over 18, with the side effects in question being exceedingl­y uncommon.

The legal proceeding­s in the UK are ongoing, with the claimants having submitted their case details for two specific incidents. AstraZenec­a has disputed the claims, and both parties have agreed to consolidat­e the cases. A case management conference is scheduled to take place later this year. Meanwhile, the

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