Conservative public interest advocacy group Defending the Republic (DTR) has obtained almost 15,000 pages of Moderna’s COVID-19 vaccine clinical trial data, claiming the data show an “utter lack of thoroughness” of the trials and calls the vaccine’s safety into “serious doubt.” As a result of successful Freedom of Information Act (FOIA) litigation against the U.S….

During a recent Labour Board hearing, a senior Health Canada official defended her department’s decision to recommend against using ivermectin to treat COVID-19, while public service employees fighting the vaccination mandate said its use could have saved lives and billions of dollars. A key argument among those who opposed mandatory COVID vaccination was that alternative…

The Secret Service has wrapped up its investigation into the recent cocaine discovery at the White House due to a lack of evidence, and no suspect was identified. President Joe Biden is sounding bullish on Ukraine’s chances of beating back Russia. What did he say in Finland as he concluded his trip to Europe? Regarding…

U.S. officials have approved the first over-the-counter birth control pill, which will let people purchase contraceptive drugs from the same store aisles as Tylenol and aspirin as the birth rate in the United States continues to drop. On Thursday, the Food and Drug Administration (FDA) said that it cleared Perrigo’s once-a-day Opill to be sold without a…

WASHINGTON—U.S. officials granted full approval to a closely watched Alzheimer’s drug on Thursday, clearing the way for Medicare and other insurance plans to begin covering the treatment for people with the brain-robbing disease. The Food and Drug Administration endorsed the IV drug, Leqembi, for patients with mild dementia and other symptoms caused by early Alzheimer’s…

The first cellular therapy for type 1 diabetes, called Lantidra, was approved by the Food and Drug Administration (FDA) for use in the United States. This is potentially good news for the 1.9 million people in the United States living with type 1 diabetes. The FDA approved the drug on June 28, after two clinical…

Public health officials say the United States needs a plan and infrastructure to avoid the fragmented response to a new disease that marked its response to the COVID pandemic. “We don’t have a systemic approach to medical product testing,” said Dr. Janet Woodcock, principal deputy commissioner for the U.S. Food and Drug Administration (FDA). Dr….

The U.S. health regulator has granted accelerated approval to Sarepta Therapeutics’ first-of-its-kind gene therapy for Duchenne muscular dystrophy (DMD), an inherited progressive muscle-wasting disorder that almost always affects young boys. Sarepta said on Thursday the Food and Drug Administration had approved the treatment for children aged between 4 and 5 years who can walk. It…

Frozen fruit from sliced strawberries to mango cubes sold at Target, Walmart, Whole Foods, Aldi, and Trader Joe’s are being recalled for a possible bacterial contamination, according to a notice posted by the U.S. Food and Drug Administration (FDA), announcing an expansion of a previous recall. The FDA-backed notice that SunOpta Inc’s subsidiary, Sunrise Growers Inc.,…

Ivermectin, the anti-parasitic medicine, was seen by most of the world as a medical miracle prior to the year 2020.   However, since the start of the COVID pandemic, Ivermectin has become a third rail topic—something that’s completely taboo to discuss openly. If you talked about it on mainstream media, you would likely be labeled…