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» LymeNet Flash » Questions and Discussion » General Support » FDA Rx Approval Process disaster - Nuplazid

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Author Topic: FDA Rx Approval Process disaster - Nuplazid
Keebler
Honored Contributor (25K+ posts)
Member # 12673

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Not just about the disaster of Pimavanserin / Nuplazid -- also about the FDA Approval Process, Dampening of Concerns, the cause of so much more misery for some patients and their families . . .

and, of course from where we're sitting, knowing that at least some of these patients might have / had as the cause of Parkinson's a tick-borne infection that went / goes undiagnosed.

It has happened, for some, to have been diagnosed with Parkinson's (or ASL, or MS) when lyme / TBD were the root issues. Some have seen proper diagnosis and treatment for lyme / TBD cause the other neurological misdiagnoses to fade away.

Few reading this article will also know of that compounding error / damage / lost chance, though.

Yet this article is about how disregarding due diligence & squashing concerns has caused so much damage. And, if the FDA does this with one drug, what about the others?


https://www.cnn.com/2018/04/09/health/parkinsons-drug-nuplazid-invs/index.html

FDA worried drug was risky; now reports of deaths spark concern

By Blake Ellis and Melanie Hicken, CNN Investigates - April 9, 2018
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

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I don't have the energy or a proper command to write concisely. Yet if anyone here feels they can reach out and share lyme / TBD possible misdiagnoses with this team, please do so.

Following the CNN report in post above is this note:

Do you have information to share about Nuplazid or other drugs targeting the elderly?

Email us [email protected]
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

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