Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Monday, June 23, 2025

Brecheen, Lankford ask EPA for answers on negative effects of abortion pill on water supply

A new report out this week finds abortions are increasing across the country, despite the Dobbs decision, primarily because of massive growth in "telehealth" prescriptions of abortion pills. Oklahoma Congressman Brecheen and Senator Lankford are asking the EPA about the impact of these pills on the American water supply.


Congressman Josh Brecheen Leads Letter to EPA Asking for Answers on Negative Effects of Mifepristone Abortion Pill

Washington, D.C. (June 18, 2025) –  Today, Congressman Josh Brecheen (R-OK), Senator James Lankford (R-OK), and over 20 lawmakers sent a letter to the Administrator of the U.S. Environmental Protection Agency (EPA) Lee Zeldin inquiring about the full negative effects of the chemical abortion drug mifepristone, specifically on its potential contaminant effects on America’s water supply.

Monday, March 03, 2025

Thompson's food safety bill advances to OK Senate floor


Senator Kristen Thompson’s Food Safety Bill Advances in Senate
SB 4 Prohibits Harmful Food Additives Linked to Health Risks

OKLAHOMA CITY(March 3rd) – The Oklahoma Senate Committee on Agriculture and Wildlife has passed Senate Bill 4, legislation by Senator Kristen Thompson, R-Edmond, aimed at protecting public health by banning certain harmful food additives.

Senate Bill 4 prohibits the manufacturing, sale and distribution of 21 substances commonly found in processed foods that have been linked to health risks, including hyperactivity in children, hormonal disruption, and potential carcinogenic effects.

Thursday, June 22, 2023

Congressman Brecheen introduces two bills to protect taxpayers, ag producers

I'm a bit behind on posting these, but Oklahoma's 2nd District Congressman Josh Brecheen recently filed two pieces of legislation, the Stop Government Overreach in Ranching Act and the Healthy SNAP Act.

The Stop Government Overreach in Ranching Act would reverse FDA guidance, “GFI 263,” which restricts the use of commonly used livestock antibiotics, such as penicillin. This has put added expense and hardship upon the those involved in agriculture and livestock. The Healthy SNAP Act would exclude soft drinks, candy, ice cream, and prepared desserts from being purchased with SNAP benefits (informally known as food stamps). 

Read below for more details on both:

Thursday, December 22, 2022

Hern introduces pro-life legislation aimed at blocking Biden's rabid abortion policies


Hern Introduces Pro-Life Legislation

Washington, D.C. – Representative Kevin Hern (OK-01) introduced the Protecting Life from Chemical Abortions Act, which will prevent the Executive Branch from declaring an abortion-related public health emergency. Second, this legislation reinstates safety regulations and in-person dispensing requirements for dangerous chemical abortions. It further bars the FDA from waiving these protections in the future.

Monday, May 23, 2022

Jett encourages Oklahomans to voice support of bill prohibiting vax mandates and passports


Jett encourages Oklahomans to voice support of bill prohibiting vaccine mandates and passports

OKLAHOMA CITY (May 20th) – With just days left in the legislative session, Sen. Shane Jett has amended House Bill 2335 to restrict state agencies from imposing vaccine mandates and requiring vaccine passports. The Shawnee Republican is encouraging Oklahomans to call their local senators and share their support of the legislation and ask that it be approved immediately. A list of state Senators is available at http://www.oklegislature.gov.   

Friday, May 13, 2022

Bice introduce legislation to address infant formula supply shortage


Bice, Feenstra Introduce Legislation to Strengthen and Stabilize Domestic Infant Formula Supply

WASHINGTON, D.C. (May 12th) – Yesterday, amid a crisis-level infant formula shortage in the United States, U.S. Reps. Stephanie Bice (R-OK) and Randy Feenstra (R-IA) introduced the Formula Act, which is legislation that would direct the Food and Drug Administration (FDA) to establish and communicate to Congress clear standards by which it domestically regulates infant formula. These standards would in turn be applied to foreign infant formula to allow formula imports and support domestic manufacturers.

Currently, the United States does not import foreign infant formula because the FDA does not have interchangeable standards in place to regulate foreign formula to ensure it complies with U.S. health code and regulations. By codifying standard regulations for infant formula, this legislation would allow America to safely import foreign infant formula to complement domestic production, particularly during times of severe shortage like American families are now facing.

“Over the last 6 months, we’ve seen shortages for infant formula skyrocket to nearly 40%,” said Rep. Bice. “This is why I introduced the Formula Act with my friend Rep. Feenstra. This legislation is critical in combating formula shortages that are negatively affecting millions of American families. This problem has quickly evolved into a crisis. The House of Representatives should immediately take up this legislation.”

“The infant formula shortage is dire in Iowa, threatening babies who rely on formula for their health and development,” said Rep. Feenstra. “That’s why I introduced the Formula Act with my friend Rep. Bice to ensure that the FDA has clear, consistent standards in place to regulate foreign infant formula so that we can import supplies when domestic production fails to meet demand. Iowa families deserve to be able to easily buy infant formula at fair prices without worrying if the shelves are fully stocked. This is a distressing problem, and I am committed to finding a solution.”

Click here to read more about the Formula Act in the DailyWire’s article.

Wednesday, February 16, 2022

Lankford opposes Biden's controversial, pro-abortion FDA nominee


Lankford Opposes Controversial, Pro-Abortion FDA Nominee

WASHINGTON, DC – Senator James Lankford (R-OK) today opposed the nomination of Dr. Robert Califf to serve as the Commissioner of the Food and Drug Administration (FDA). Califf previously held the position under President Obama.

“I am deeply concerned about President Biden’s decision to once again place someone in a health care-related role who openly pushes for more abortion, including mail-order chemical abortions,” said Lankford. “Since Biden is obsessed with abortion, he continues to recycle Obama-era nominees or employees that promote abortion rather than health care. Dr. Califf wants to make dangerous, chemical abortion easier to access, not save lives of moms and babies. He’s not who we need in charge of medication and health safety.”

When Dr. Califf served previously as FDA Commissioner, Lankford led a letter to him to express concern and request information about the agency’s decision at the time to change policies regarding the abortion drug mifepristone. Dr. Califf did not respond to the letter.

Lankford has been the leading voice in Congress for the protection of life. Lankford pushed back on the Biden Administration’s rule to allow taxpayer-funded abortions. He successfully secured language in the Democrats partisan $3.5 trillion Fiscal Year 2022 budget resolution to save the long-standing Hyde and Weldon Amendments, which prohibit the use of taxpayer dollars to fund abortions and abortion-related discrimination against health care workers, including insurers. He is also an original cosponsor of the SAVE Moms and Babies Act, which would stop the FDA from approving more chemical abortion drugs.

Thursday, February 10, 2022

AG: Physicians not prohibited from prescribing off-label meds to fight C-19

Attorney General O'Connor Assures Oklahoma Physicians Are Not Prohibited From Prescribing Off-Label Medicines to Fight COVID-19

OKLAHOMA CITY (Feb 8th) - Today, Attorney General John O’Connor responded to inquiries about whether an Oklahoma licensed physician is prohibited from prescribing a drug approved by the U.S. Food and Drug Administration (FDA) for the “off-label” purpose of treating or preventing COVID-19.

The Attorney General’s office finds no legal basis for a state medical licensure board to discipline a licensed physician for exercising sound judgement and safely prescribing an FDA-approved drug – like ivermectin or hydroxychloroquine – for the off-label purpose of treating a patient with COVID-19.

“I stand behind doctors who believe it is in their patients’ best interests to receive ivermectin and hydroxychloroquine,” said Attorney General O’Connor. “Our healthcare professionals should have every tool available to combat COVID-19. Public safety demands this. Physicians who prescribe medications and follow the law should not fear disciplinary action for prescribing such drugs.”

The Attorney General’s office neither condones nor condemns a specific course of treatment for COVID-19. Our office maintains that proper healthcare decisions are to be made between a patient and his or her physician, and the government should not interfere with their relationship.


State Reps. Sean Roberts (left) and Kevin West (right)

Roberts, West Respond to AG Statement Regarding Off-Label Treatment and Prevention of COVID-19

OKLAHOMA CITY (Feb. 9th) – Rep. Sean Roberts, R-Hominy, and Rep. Kevin West, R-Oklahoma City, today issued statements regarding Oklahoma Attorney General John O'Connor's response to the legality of disciplinary actions against doctors who use off-label therapeutics to treat or prevent COVID-19.

In his statement yesterday, O'Connor said that the Attorney General's office finds "no legal basis for a state medical licensure board to discipline a licensed physician for exercising sound judgment and safely prescribing an FDA-approved drug – like ivermectin or hydroxychloroquine – for the off-label purpose of treating a patient with COVID-19."

Tuesday, May 11, 2021

OK Attorney General announces deal to return state's Hydroxychloroquine stockpile

Well, let's take a look at what we've got:
  • In January, Attorney General Mike Hunter filed a petition in district court for over $1.8 million over a personal protective equipment order that a company never delivered to the Oklahoma Department of Health.
  • In April, AG Hunter filed a lawsuit against a company for failing to deliver an order of ventilators to the Oklahoma State Department of Health at the onset of the Coronavirus pandemic. In the lawsuit, the state claims the OSDH paid over $890,000 for 40 ventilators last April. The company had only delivered two ventilators by June 2020. Despite canceling the order in October, the company had 21 ventilators delivered in December. The Oklahoma State Department of Health returned the wrongfully delivered ventilators but has not received a refund.
And here we learn that the OSDH is getting a refund for returning $2.6 million worth of hydroxychloroquine that was purchased during the well-intentioned but seemingly misguided Trump-fueled craze for the drug last spring.


Attorney General Hunter Strikes Deal to Return Hydroxychloroquine Stockpile

OKLAHOMA CITY – Attorney General Mike Hunter today announced he has reached an agreement with FFF Enterprises to return the state’s stockpile of hydroxychloroquine for a refund.

Based on the unique circumstances encountered by the Oklahoma Department of Health, the company has agreed to return to the Department of Health the full purchase price paid for the medication last year.

The Oklahoma State Health Department purchased hydroxychloroquine at the onset of the Coronavirus pandemic ​after the federal Food and Drug Administration granted emergency use authorization for the drug as a treatment for the virus.

After ​the federal Food and Drug Administration revoked the emergency use authorization, the Oklahoma State Health Department asked the attorney general to get involved.

Tuesday, October 29, 2019

Eye doctors: non-prescription Halloween-themed contact lenses can be dangerous


Eye Doctors: Non-Prescription, Halloween-Themed Contact Lenses Can Be Dangerous

OKLAHOMA CITY – Oklahoma’s eye doctors are warning their communities against using illegal, non-prescription color contacts as accessories in Halloween costumes. Research shows these products are often contaminated and can damage vision health.

In 2017, the Food and Drug Administration published a study revealing that a majority of unapproved, counterfeit contact lenses tested positive for the kinds of microbial contamination frequently found in hospital wastewater or spoiled food. The lenses, which are federally banned for sale by the Fairness to Contact Lens Consumer Act, are frequently obtained illegally in novelty stores, tattoo parlors, flea markets and internet marketplaces.

“Decorative lenses might seem like a cool costume addition, but the reality is they can be dangerous,” said Dr. Selina McGee, an Edmond optometrist and the president of the Oklahoma Association of Optometric Physicians. “This isn’t like wearing makeup; you are putting something in direct contact with your cornea for several hours. The lens can be contaminated, or your eyes can react poorly for any number of reasons. It is really important that anyone who believes they need contacts see an optometrist and then purchase a legitimate product that they have a prescription for.”

Oklahomans can find an optometrist near them at OAOP.org.