The top court impleaded all the States on March 8 and issued notice on the plea filed by the Child Rights Trust and a Bengaluru resident seeking directions for the protection of the fundamental rights of migrant children amidst the COVID-19 pandemic.
The poll panel said it had received a complaint from All-India Trinamool Congress MP Derek O’Brien about the speech that was “an open threat” to Bengal and its people. Referring to the Central forces firing on a mob on polling day on April 10 in Sitalkuchi, Mr. Ghosh said the incident would be the start.
The internal debate is also prompted by the party’s experience in Tamil Nadu, where Mr. Kishor’s organisation, the Indian Political Action Committee or I-PAC, advised the DMK, which heads an alliance in which the Congress is a junior partner. Congress insiders claim they were witnesses to a “sense of disquiet” among senior DMK leaders as “core political activities” were decided by the external agency.
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On Tuesday, the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention called for a pause in the use of Johnson & Johnson’s COVID-19 vaccine “out of an abundance of caution” so the agencies can review “extremely rare” blood clots.
Six recipients of the one-dose vaccine all in relatively young women developed blood clots within two weeks of receiving the shot, The New York Times reported. One died; one is currently hospitalized.
The government is expected to pause administration of the vaccine at all of its federally run vaccination sites, The New York Times also reported, and expects that state health officials will follow its cue and do the same.
KOAA Survey: Does the pausing of the J&J vaccine change your plans?
KOAA
and last updated 2021-04-13 11:09:01-04
The Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) recommended a pause in the use of Johnson & Johnson s COVID-19 vaccine out of an abundance of caution on Tuesday.
In a series of tweets Tuesday morning, the FDA said it was recommending a pause after receiving reports that six people developed rare and severe blood clots after receiving the vaccine. So far, nearly 7 million Americans have received a dose of the Johnson & Johnson vaccine.
During Tuesday morning s press conference, acting FDA commissioner Dr. Janet Woodcock said the review would take a matter of days but could extend longer depending on what we learn. Dr. Anne Schuchat, the principal director of CDC, added that the pause was taking place in order to better prepare the health system in the event more patients experience clotting.