Because the flu vaccines are not mRNA-based and have decades of safety records.
Covid vaccines do not.
“On April 13, the Centers for Disease Control and Prevention, as well as the Food and Drug Administration, recommended providers pause on administering the Johnson & Johnson/Janssen COVID-19 vaccine after more than 6.8 million people in the United States received the one-dose vaccine. It comes after six women who received the vaccine experienced blood clots in the brain within two weeks after vaccination”
Many of these drugs weren’t recalled until many years on the market because the drug companies did not want to admit to the negative side effects.
Valdecoxib (Bextra)Pemoline (Cylert) …
Bromfenac (Duract)
Levamisole (Ergamisol)
Isotretinoin (Accutane)
Sibutramine (Meridia)
Terfenadine (Seldane)
Efalizumab (Raptiva)
thalidomide
Vioxx, 2004
"Vioxx, also known as Rofecoxib, was a painkiller often prescribed to treat arthritis pain. More than 20 million people used the drug at its peak, earning $2.5 billion in annual sales for Merck & Co.
Then researchers discovered Vioxx increased the chance of heart attack and stroke. One Vioxx report estimated that up to 140,000 people suffered from coronary heart disease after taking it. Merck voluntarily recalled Vioxx in 2004."
However, subsequent reports suggested that both Merck and the FDA had ignored evidence of dangerous side effects for years before Vioxx was recalled. In 2006, Merck sponsored a report on Vioxx, which many criticized for being self-serving. The company spent $21 million for legal help to publish the report, which determined that Merck acted in good faith.
Eventually, Merck settled all Vioxx-related litigation for $4.8 billion. The Vioxx recall is considered one of the largest drug recalls in United States history.
“How did thalidomide pass all the drug tests? During early testing, researchers at the company found that it was virtually impossible to give test animals a lethal dose of the drug (based on the LD50 test). Largely based on this, the drug was deemed to be harmless to humans.”
From our old friend Pfizer: (I am not saying that Pfizer has not produced some great drugs. I am saying they are not to be trusted. Much like Boeing, profit before safety)
Bextra, 2005
Pfizer manufactured and marketed Bextra as an anti-inflammatory drug. Physicians prescribed the drug to treat inflammatory disorders and arthritis. However, researchers found that the drug was to blame for heart and stomach problems and could cause severe skin conditions. But that was far from the whole story.
Researchers learned that one of the skin conditions caused by Bextra was Stevens-Johnson syndrome (SJS), a reaction that causes blistering on the skin and internal organs. SJS has a high fatality rate, with 1 in 10 cases resulting in death. Some SJS cases result in toxic epidermal necrolysis, which has a 50% fatality rate.
In response, the FDA blocked the sale of Bextra in 2005.