- It appears the use of Johnson & Johnson's COVID-19 vaccine may be suspended in the United States
- This came on the heels of a woman losing her life and other people developing a rare blood-clotting disorder after taking the vaccine
- People who experienced side effects are all women between the ages of 18 and 48
Six people who developed a rare disorder involving blood clots are the latest cases of the after-effects of the Johnson & Johnson COVID-19 vaccine.
The rare disorder has already left one woman dead and another in critical condition in Nebraska.
Following these rather disturbing developments, U.S federal health agencies on Tuesday, April 13, called for the suspension of the use of the vaccine.
Reuters reports all six cases involved women between the ages of 18 and 48. The symptoms occurred 6 to 13 days after they took Johnson & Johnson's vaccine.
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NBC News also reports that the Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) in a statement recommended a pause out of caution.
Johnson & Johnson on its part said there has been no clear causal relationship between these cases and the shot made by its Janssen unit.
Meanwhile, Legit.ng reported that Australian health authorities on Sunday, March 7, suspended the use of the AstraZeneca COVID-19 vaccine following after-effects of the jab.
The nation's federal office for safety in healthcare in a statement revealed that two women, who are actually nurses, took the same batch of the vaccine in one clinic.
In a related development, the federal government has said it will continue to administer AstraZeneca COVID-19 vaccines amid reported cases of possible side effects.
This was made known by Dr. Mukhtar Mohammed, national incident manager of Presidential Task Force (PTF) on COVID-19, while speaking on Channels Television breakfast show, Sunrise Daily.
According to Dr. Mohammed, documentation has so far shown that AstraZeneca's jab is safe to use.