By Vandana Rambaran | Fox News
Police in Portland, Ore. declared a “civil disturbance” Saturday evening as members of far-right groups and far-left members of Antifa continued to skirmish hours after conducted dueling demonstrations in the center of the city.
Just after 4:30 p.m, Portland Police Bureau spokesperson Lt. Tina Jones said that anyone gathered near the intersection of SW Park Avenue and SW Morrison Street “must now leave the area immediately.” Jones added that the number of demonstrators was “dwindling” to about 400 people from a peak of around 1,200 people.
TRUMP THREATENS TO DESIGNATE ANTIFA A TERRORIST ORGANIZATION AHEAD OF EXPECTED PORTLAND CLASHES
Authorities said at least 13 people were arrested but did not immediately release further details. Earlier in the day, police tweeted images of weapons it had seized from multiple groups, including bear spray, shields and metal and wooden poles.
Police said one injured person was taken to a local hospital, but no further information about the victim was released. Four others had been evaluated by Portland fire medics. All the injuries were considered to be minor. Another individual was treated for a medical condition unrelated to the demonstrations, Jones said.
Portland Police✔@PortlandPolice
At approximately 1:40 pm, law enforcement officers came upon an injured individual at SW Harvey Milk and SW Naito. They, along with @PDXFire medics, rendered assistance. The individual was transported to an area hospital. No further information at this time. #ppbalert435:52 PM – Aug 17, 2019
Jones said that there had been “limited interactions” between individuals and called witnesses to submit information about potential criminal activity to the police.
Flag-waving members of the Proud Boys and Three Percenters militia group began gathering late in the morning, some wearing body armor and helmets. Meanwhile, black-clad, helmet and mask-wearing Antifa members were also among the several hundred people on the streets. The groups gathered on both sides of the Willamette River, which runs through the city.
Authorities used sound trucks and loudspeakers to remind demonstrators both sides to stay out of the streets or they would be arrested. They also set up concrete barriers and closed streets and bridges in an effort to contain and separate the rival groups.
Portland Police✔@PortlandPolice
#ppbalert Officers have seized weapons from multiple groups, including bear spray, shields, and metal and wooden poles.
More than two dozen local, state and federal law enforcement agencies, including the FBI, were in the city for the right-wing rally, which was expected to draw people from across the country. Portland Police said all of the city’s 1,000 officers would be on duty for the gathering that was hyped on social media and elsewhere for weeks.
Not all who gathered Saturday were with right-wing groups or Antifa. Also on hand were people dressed in colorful outfits and those who attended a nearby prayer service, holding signs that said slogans such as “No Trump, No NRA.”
Police formed a physical barricade beneath the Morrison Bridge in Tom McCall Waterfront Park to separate the rival groups from sparring. The Proud Boys and their supporters were on the south side of the divide while the counter-protesters remained on the north side, according to reports by The Oregonian.
TRUMP THREATENS TO DESIGNATE ANTIFA A TERRORIST ORGANIZATION AHEAD OF EXPECTED PORTLAND CLASHES
KPTV and The Oregonian reported that some of the demonstrators began to leave in the early afternoon, with authorities briefly re-opening the Hawthorne Bridge to allow them to pass. Police used officers on bikes and in riot gear to prevent members of Antifa from following them. The Oregonian reported that a group of left-wing demonstrators attacked a bus carrying a group of Proud Boys out of downtown Portland, breaking some windows.
“The Proud Boys contacted us or contacted the units on the ground saying that they wanted to leave and so we facilitated for them to leave the area,” Multnomah County Sheriff’s Office Sgt. Brandon White told the newspaper. “It wasn’t planned. It wasn’t orchestrated. We had a request that they would like to leave the area and so we facilitated.”
Later in the afternoon, The Oregonian also reported that a group of left-wing counter-demonstrators had surrounded two people wearing American flag-themed clothing and were “taunting, threatening, and chasing them.”
Among those attending the demonstration was Patriot Prayer’s Joey Gibson, who organized similar rallies in 2017 and 2018 that erupted in clashes. Gibson surrendered Friday on an arrest warrant for felony rioting but was released on bail hours later.
“I’m just here for the ride,” Gibson told The Oregonian.
The Oregonian✔@Oregonian · 5hReplying to @Oregonian
A large number of protesters are marching south through Waterfront Park, approaching the Hawthorne Bridge.
The Oregonian✔@Oregonian
Police have arrested one person who reportedly stayed in the street after being told to move.
Organizer Joe Biggs told the paper that the demonstrators “wanted national attention and we got it.”
“Go look at President Trump’s Twitter,” Biggs said. “He talked about Portland, said he’s watching Antifa. That’s all we wanted … Mission success.”
President Trump tweeted Saturday morning that he is considering designating Antifa a domestic terror group.
“Major consideration is being given to naming ANTIFA an ‘ORGANIZATION OF TERROR,’” Trump said. “Portland is being watched very closely. Hopefully the Mayor will be able to properly do his job!”
Donald J. Trump✔@realDonaldTrump
Major consideration is being given to naming ANTIFA an “ORGANIZATION OF TERROR.” Portland is being watched very closely. Hopefully the Mayor will be able to properly do his job!124K10:04 AM – Aug 17, 2019
Portland Mayor Ted Wheeler said the message to protestors on both sides is “We don’t want your hatred, we don’t want your violence, but if you come here, we’re going to be prepared,” he said in an interview on Fox News’ “Outnumbered Overtime” on Friday.
“Again, when it comes to enforcement of our community standards, we support people’s rights to demonstrate, but we don’t care about who you are or your politics are,” he said. “If you engage in violence in this city, you will be held accountable.”
The Associated Press contributed to this report. Vandana Rambaran is a reporter covering news and politics at foxnews.com.




![Final Batch of Pfizer Documents Released Shows FDA Knew Safety Monitoring System Was 'Not Sufficient' | USNN World News Recent documents disclosed as part of a Freedom of Information Act (FOIA) lawsuit against the U.S. Food and Drug Administration (FDA) show the agency knew its safety monitoring system was “not sufficient” for assessing the risk of heart conditions associated with Pfizer’s COVID-19 vaccine when it licensed the company's “Comirnaty” vaccine. Documents also reveal numerous manufacturing problems in Pfizer batches released to the public and show the FDA knew about a phenomenon known as vaccine-associated enhanced disease (VAED) in those vaccinated who experience breakthrough COVID-19. The FDA released the final batch of documents it relied upon in licensing Pfizer’s Comirnaty COVID-19 vaccine for ages 16 and up—more than 800 days after the agency approved the shot. The memo states: “The CBER Sentinel Program is NOT sufficient to assess the serious risks of myocarditis and pericarditis, and subclinical myocarditis associated with COMIRNATY (BNT162b2) in lieu of PMR safety studies under FDAAA [Food and Drug Administration Amendments Act]. “At the time of BLA [Biologics License Application] approval, the data sources in the CBER Sentinel Program are not sufficient to identify the outcomes due to lack of sufficient power to assess the magnitude of risk in patients 12-30 years of age. In addition, CBER Sentinel Program is not sufficient to follow up cases for recovery status and long-term sequelae, or for identification and characterization of subclinical myocarditis cases.” Cardiac Disorders Higher in Vaccine Trial Group According to an Aug. 23, 2021, BLA Clinical Review Memorandum, there were more cardiac disorders in trial participants who received Pfizer’s COVID-19 vaccine compared to the placebo group and more instances of tachycardia in the younger vaccinated age group. Cardiac conditions were reported as the cause of death in nine participants 25 to 128 days after having received at least one dose of Pfizer’s COVID-19 vaccine, including seven cases of cardiac arrest, one case of cardiovascular disease, and one case of congestive heart failure. Five cardiac-related deaths in the placebo group occurred 15 to 81 days after having received a placebo, including two cases of myocardial infarction, one aortic rupture, and two cardiac arrests. “Because COVID-19 mRNA and its Spike protein are found in the human heart at autopsy causing inflammation and heart damage, it is incontrovertible that the COVID-19 vaccines are cardiotoxic,” cardiologist Dr. Peter McCullough told The Epoch Times in an email. “Younger individuals with healthy hearts take up more of the damaging vaccine into the cardiac tissue resulting in symptoms of chest pain, palpitations, fluctuations in blood pressure, dizziness, and sadly, some, end up with cardiac arrest either during exercise or in the early morning waking hours. At both time periods, an internal surge of adrenalin appears to be the trigger for the fatal arrhythmia in those with COVID-19 vaccine myocarditis,” he added. Despite nearly double the number of reported cardiac events in vaccine recipients versus placebo recipients, the FDA concluded the deaths were “unlikely to be related to vaccination.” “As a cardiologist, these serious adverse events are unacceptable,” Dr. McCullough said. “I have called for all COVID-19 vaccines to be removed from the market with an urgent push for research strategies to prevent cardiac death after injection.” Vaccines Released Despite Manufacturing Issues According to the Pfizer Andover Response to Form FDA 483 included in the released documents, numerous manufacturing issues and inadequacies in quality oversight were also identified. Several batches of COVID-19 vaccines were flagged for deviating from product quality standards, yet the affected batches were released to the public in various lots, the numbers of which were redacted. In November 2021, whistleblower Brook Jackson, who worked as a regional director at testing sites by Pfizer contractor Ventavia, told the British Medical Journal that Pfizer's trial was riddled with issues. Ms. Jackson said the company “falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial.” Ms. Jackson, a trained clinical trial auditor with more than 15 years of experience in clinical research coordination and management, emailed a complaint to the FDA and was fired later that day. She subsequently filed a lawsuit against Ventavia and Pfizer, alleging Pfizer had defrauded the government while developing its COVID-19 vaccine. FDA Acknowledges Vaccine-Associated Enhanced Disease In its Pharmacovigilance Plan Review Memorandum, the FDA referenced a condition called “vaccine-associated enhanced disease.” According to the journal Vaccine, VAED is the modified presentation of a clinical infection affecting individuals exposed to the wild-type pathogen after having received a vaccine for the same pathogen. In its memo, the FDA stated there are reported deaths in the Vaccine Adverse Event Reporting System (VAERS) in patients reported to be fully vaccinated. Although the agency said that passive surveillance and spontaneous adverse event reporting generally cannot be used to conclude vaccine effectiveness because of the lack of a control group, reporter bias, and underreporting, “severe manifestations and death from COVID-19” increase the possibility of developing VAED, which has “overlapping clinical manifestations with natural SARS-CoV-2 infection, making it difficult to differentiate VAED from severe COVID-19 disease in individual VAERS reports.” The FDA said Pfizer was assessing the condition in its continuation of Phase 3 clinical studies and active surveillance studies. VAED has been observed in other vaccine trials involving the dengue virus, respiratory syncytial virus, and measles. FDA Took Over 800 Days to Release Data The Public Health and Medical Professionals for Transparency (PHMPT), a nonprofit consisting of public health and medical professionals, scientists, and journalists, filed a FOIA lawsuit against the FDA in September 2021 to force the release of hundreds of thousands of documents relied upon by the agency in licensing Pfizer’s COVID-19 vaccine for individuals age 16 and older. Even though the FDA said in a news release it was committed to “ensuring full transparency, dialogue and efficiency” regarding COVID-19 vaccines and reiterated its commitment to full transparency when it licensed Pfizer's Comirnaty vaccine, they wanted 75 years to produce an estimated 451,000 documents at a rate of 500 pages per month. It previously estimated it had 329,000 pages of responsive records and wanted 55 years to release them to the public. Attorney Aaron Siri, who filed the lawsuit on behalf of the group, said the federal government was shielding Pfizer from liability, gave it billions of dollars, and forced Americans to get vaccinated while preventing the safety and efficacy data supporting the licensure of Pfizer’s COVID-19 vaccine from being released until the year 2076. Yet it only took 108 days from when Pfizer started producing records to the agency for the FDA to license its vaccine.](https://www.usnn.news/wp-content/uploads/2023/12/Final-Batch-of-Pfizer-Documents-Released-Shows-FDA-Knew-Safety-Monitoring-System-Was-Not-Sufficient-150x150.jpg)
