A 40-year-old trial volunteer claims he suffered serious ‘neurological and psychological’ symptoms but the vaccine company dismisses his allegations.
The Indian Council of Medical Research (ICMR) is assisting an inquiry into an alleged adverse reaction during AstraZeneca’s COVID-19 vaccine trial but has found no reason to recommend halting it, a senior official at the regulator said.
A 40-year-old man said in a complaint seen by Reuters news agency that he had suffered serious “neurological and psychological” symptoms after receiving the vaccine in a trial being run by the British drugmaker’s partner, the Serum Institute of India (SII).
“There was no immediate cause of concern at this stage,” Samiran Panda, head of Epidemiology and Communicable Diseases at the ICMR, the research body involved in trials, told Reuters.
“It doesn’t mean that long term assessment will not happen, it is still happening. I am aware of the activity,” Panda said.
AstraZeneca did not respond to a request for comment.
Law firm NGR Prasad & R Rajaram Advocates sent the complaint by the unnamed volunteer, who is seeking 50 million rupees ($676,288) in compensation and a suspension of testing, manufacturing and distribution of the vaccine, to ICMR, SII, AstraZeneca and the Drugs Controller General of India.
Read More: India investigates alleged AstraZeneca vaccine ‘adverse reaction’