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  • Anonymous
    Participant
    Post count: 93172

    Warriors,
    This is just an idea about the report but as a group
    it may not be a bad idea to drsft a letter to the FDA under what is called the “Freedom of Information Act”.
    what this does is allows us access to all information the FDA has on record for the levothyroxine sodium and synthroid products on the market including recalls as a user of the products which would give us vital information between the dates of lets pick ten years 9/87-9/97.

    Under FOIA, the “need to know” is shifted to the “right to know” doctrine. The statute requires agencies to provide the fullest disclosure of information to the public.

    In the report there is an addrss for citizens actions or to write directly to the FDA. They have ten days to comply with the request. It may be good to mention
    the following, your name, a phone number to reach you
    and the records we want.

    Any comments, feedback or should we throw this idea out the window!

    Just let me know, DEE

    Anonymous
    Participant
    Post count: 93172

    Can we make iit for all thyroid replacement hormones, not just levothyroxine.
    There are many:
    Cytomel – T3 only
    Thyrolar and Armour thyroid – T3 & T4
    Synthroid – T4 only (levothyroxine)
    and maybe more?

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