There is a law in New York that says you can’t block the state from making masks. At Houston Methodist Hospital in 2021, nurses give a monoclonal antibody treatment to a Covid-19 patient who is 43 years old: the credit score, Brandon Thibodeaux works for the New York Times.

The Food and Drug Administration has officially stopped the use of antibody therapies that didn’t work as well when they came into contact with the Omicron variant. This means that a treatment that had been widely used, even by people who didn’t want to get vaccinated, has been put on hold.

Many health care providers stopped using antibody treatments weeks ago because Omicron became more common. This is why. And even tho doctors have welcomed the news that there are more treatments, like antiviral pills, they say that the trickle of pills and other treatments can’t keep up with the geyser of recent times.

In a statement on Monday, the Food and Drug Administration said it was limiting the emergency use authorizations for the Regeneron and Eli Lilly antibody therapies because the Omicron variant is the most common, which the Centers for Disease Control and Prevention has estimated to be 99.5 percent of all new cases in the United States. The infusions should not be used now, the FDA said.

During the first wave of the Delta variant, these drugs from Regeneron and Lilly were very good at keeping people from going to the hospital if they were given early enough. As Omicron came out, it became clear that the therapies wouldn’t be able to get rid of the virus, so a lot of big health systems, like some in New York City, stopped taking them in December.

Federal officials tried to stop using them right away, but Republican governors said they could still help some people who had the Delta variant. That has become more and more shaky because most doctors have a hard time figuring out which variant each person has.

Since then, a monoclonal antibody made by GlaxoSmithKline and Vir Biotechnology has been effective against Omicron, even tho doctors say it’s hard to get. Doctors on the front lines who stopped using the ineffective treatments in December started looking for new ones as the number of patients rose.

In January, federal officers started giving out the antiviral pills Paxlovid from Pfizer and molnupiravir from Merck. Due to Paxlovid’s interactions with many other medications, and molnupiravir’s risks to women of childbearing age, the drugs have been difficult to give out.

They’ve also been hard to find, with doctors saying they have to make a lot of calls to pharmacies to find pills that are in stock.

High-risk patients who can’t get antibody treatments are getting treatment that’s the same as what they got in 2020, including extra oxygen and steroids. As for the antiviral pills and the effective antibody treatments, they’re “very hard to find.”

For my part, these medicines aren’t actually available to us at all, Dr. Morocco said.

On the other hand, he said that the number of people at the emergency room is so high that some people spend the whole nite waiting in line or leave before they see a doctor. “That’s the worst thing that could happen to us all,” he said.

Federal records show that about 20,000 doses of the Regeneron and Eli Lilly products were given to patients last week alone, with the most in Florida, Louisiana, and Michigan.

The treatments, which are thought to be safe, can have side effects like shortness of breath, nausea, and vomiting.

COVID’s early treatment options are getting more and more options. On Friday, the Food and Drug Administration approved the use of remdesivir for outpatients because researchers found that it can cut down on hospitalizations when used early.

Brii Biosciences has said that its monoclonal antibody works well against Omicron and is being tested by the Food and Drug Administration.

In fact, new, effective treatments can’t come quickly enough, says Dr. Steve Pergam, a professor at the Fred Hutchinson Cancer Research Center who also sees patients.

He said there are so few parts that early treatments are going to people with leukemia who have the best chance of dying from COVID, and with the current delays in testing, it’s a big job to match the highest-risk cancer patients to the few treatments that work best for them.

He said you should do everything you can to avoid getting this. “Because it could still be very dangerous,” he added.