The Curious Epinephrine/EpiPen Recall
Before getting to the mysteries and inconsistencies, if you or someone you care for use Epinephrine, often referred to as an EpiPen, the Lot Numbers/Expiration Dates of the products being Recalled can be found HERE.
The irony of one of the deadliest government agencies in America feigning concern for the health of the citizenry, especially given its role in promoting, bribing, coercing, threatening, and otherwise pressuring people to inject themselves and their children with a genocidal bioweapon, should not be lost on anyone.
In the case of Epinephrine, the horsehockey spewing from the FDA takes that irony to a whole new height: Government/Depopulationists have long pushed "vaccines" to cull the herd, which as one of their intended ("side" my a**) effects is to maim the young people who survive with a multitude of "allergies". Such as "peanut allergies" caused by those "vaccines", which of course “require” another drug to save the person's life.
True, the human body could be said to be "allergic" to injected poisons. Likewise, the human body is “allergic” to bullets, hand grenades, and being hit straight-on by a semi going 60 miles per hour.
Let's turn to the article, Link below, and see what is going on.
“The U.S. Food and Drug Administration (FDA) announced the recall of three epinephrine lots, used to treat severe allergic reactions, after consumer complaints.
According to an announcement on Jan. 9, manufacturer Spectrum Laboratory Products said it voluntarily recalled the lots after the product was found to be discolored.”
So, “discolored” =, um, what?
“'The use of a finished dose product manufactured or compounded with this recalled product could result in less-effective product, and incomplete treatment of life-threatening conditions including, low blood pressure, heart failure, anaphylaxis, irregular heartbeat, and heart attack,' the recall bulletin also said. 'Treatment with a less-effective product, essentially underdosing epinephrine, could result in death.'”
Read that again: “could result in [a] less-effective product”. What does that mean? That all of the lots were somehow watered down? Maybe, but the quoted press release is rather ambiguous. And nowhere in the article is it explained how a lifesaving product left the factory, visibly different than the “full dose” product, without any random testing detecting a problem.
Or is there no random statistically meaningful testing taking place? If there was “testing”, why did it not catch any potential problem with a life-and-death drug?
According to the FDA's announcement, the Recall was due to “discoloration”. Nothing there about dilution or reduced effectiveness.
While consumers are urged to return any product covered by the Recall, there is no mention either in the article or in the FDA announcement whether the consumer will get a brand new supply at no cost, or whether they will be expected to fork over some money if, for example, they return only half of the purchased product.
Who makes this stuff? Consider the full name of the company: Spectrum Chemical Manufacturing Corporation, a division of Spectrum Laboratory Products, Inc.. Does that give you a warm fuzzy feeling about putting their products into your body? Me neither. The name invokes visions of Walter White hard at work...
Under the category of “Chemicals”, 11,056 of 'em? No, that's just the number of items you can wade through on Spectrum's website. According to the introduction for the “chemicals” section: “Our product offering includes over 45,000 fine chemicals”. Um, “fine”, if I need some hardcore cleaning products, this might be the place to go. Otherwise, I'll pass.
Doing some homework on how to detoxify so one doesn't end up taking one dangerous drug to hopefully counter death from another without doing too much new harm in the process, strikes me as a much better strategy. But hey, drugs are usually cheap, always easy, and if slow/painful—or sudden—death is a “side effect”, oh well.
FDA Announces Recall of Epinephrine
The irony of one of the deadliest government agencies in America feigning concern for the health of the citizenry, especially given its role in promoting, bribing, coercing, threatening, and otherwise pressuring people to inject themselves and their children with a genocidal bioweapon, should not be lost on anyone.
In the case of Epinephrine, the horsehockey spewing from the FDA takes that irony to a whole new height: Government/Depopulationists have long pushed "vaccines" to cull the herd, which as one of their intended ("side" my a**) effects is to maim the young people who survive with a multitude of "allergies". Such as "peanut allergies" caused by those "vaccines", which of course “require” another drug to save the person's life.
True, the human body could be said to be "allergic" to injected poisons. Likewise, the human body is “allergic” to bullets, hand grenades, and being hit straight-on by a semi going 60 miles per hour.
Let's turn to the article, Link below, and see what is going on.
“The U.S. Food and Drug Administration (FDA) announced the recall of three epinephrine lots, used to treat severe allergic reactions, after consumer complaints.
According to an announcement on Jan. 9, manufacturer Spectrum Laboratory Products said it voluntarily recalled the lots after the product was found to be discolored.”
So, “discolored” =, um, what?
“'The use of a finished dose product manufactured or compounded with this recalled product could result in less-effective product, and incomplete treatment of life-threatening conditions including, low blood pressure, heart failure, anaphylaxis, irregular heartbeat, and heart attack,' the recall bulletin also said. 'Treatment with a less-effective product, essentially underdosing epinephrine, could result in death.'”
Read that again: “could result in [a] less-effective product”. What does that mean? That all of the lots were somehow watered down? Maybe, but the quoted press release is rather ambiguous. And nowhere in the article is it explained how a lifesaving product left the factory, visibly different than the “full dose” product, without any random testing detecting a problem.
Or is there no random statistically meaningful testing taking place? If there was “testing”, why did it not catch any potential problem with a life-and-death drug?
According to the FDA's announcement, the Recall was due to “discoloration”. Nothing there about dilution or reduced effectiveness.
While consumers are urged to return any product covered by the Recall, there is no mention either in the article or in the FDA announcement whether the consumer will get a brand new supply at no cost, or whether they will be expected to fork over some money if, for example, they return only half of the purchased product.
Who makes this stuff? Consider the full name of the company: Spectrum Chemical Manufacturing Corporation, a division of Spectrum Laboratory Products, Inc.. Does that give you a warm fuzzy feeling about putting their products into your body? Me neither. The name invokes visions of Walter White hard at work...
Under the category of “Chemicals”, 11,056 of 'em? No, that's just the number of items you can wade through on Spectrum's website. According to the introduction for the “chemicals” section: “Our product offering includes over 45,000 fine chemicals”. Um, “fine”, if I need some hardcore cleaning products, this might be the place to go. Otherwise, I'll pass.
Doing some homework on how to detoxify so one doesn't end up taking one dangerous drug to hopefully counter death from another without doing too much new harm in the process, strikes me as a much better strategy. But hey, drugs are usually cheap, always easy, and if slow/painful—or sudden—death is a “side effect”, oh well.
FDA Announces Recall of Epinephrine
Substack Permalink:
posted by TLC's Place at 11:43 PM
0 Comments:
Post a Comment
<< Home