The Food and Drug Administration announced on Tuesday that older individuals and those with weakened immune systems are eligible for another dose of the updated COVID-19 booster. According to the FDA’s announcement, most people who received a single dose of the booster
Spring chicken! Watch this boy transform himself Young Cale Martin of Missouri decided to make a costume out of a giant chicken stuffed animal. After purchasing the stuffed animal from the local supermarket, he took out the stuffing, put it on —
The U.S. Food and Drug Administration (FDA) has authorized a single booster dose of the Pfizer-BioNTech COVID-19 vaccine bivalent for children six months old through four years of age. At least two months prior to getting this booster, children must have completed
People suffering from migraines will soon have access to pain relief in the form of a nasal spray. The U.S. Food and Drug Administration (FDA) has approved the first calcitonin gene-related peptide (CGRP) receptor antagonist nasal spray intended to treat migraines in
Mammogram facilities will need to follow some new rules soon. The U.S. Food and Drug Administration (FDA) on Thursday released updated regulations that require mammogram providers to notify patients about the density of their breast tissue. The updates apparently will give the
Feds look to fight flesh-destroying drug ‘tranq’ Fox News national correspondent Alexis McAdams has the latest on the FDA restricting imports of animal tranquilizer Xylazine, also known as ‘tranq,’ in an effort to curb overdose deaths on ‘America Reports.’ The Food and
People will soon be able to self-test for both flu and COVID-19 in one fell swoop — without leaving their homes. The Food and Drug Administration (FDA) has authorized the first over-the-counter (OTC) home test that can detect both influenza A and
Comment on this story Comment The debate between dairy devotees and oat-latte lovers over what to call plant-based milk products may soon reach some sort of denouement after the Food and Drug Administration released draft guidelines proposing that companies can continue using
The U.S. Food and Drug Administration (FDA) has warned against using an eye drop made in India that has been linked to the outbreak of a drug-resistant bacteria leading to adverse events in at least 55 patients in the United States including
The Food and Drug Administration (FDA) has just proposed treating COVID-19 vaccines in the same way in which many Americans receive the annual flu shot — in order to protect people against mutations of the virus. Not everyone is jumping up and