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c/compounding·submitted 1 year ago by u/lukas_vermeulen

[Question] Ireland — has anyone got a straight answer on shortage list

Questionbranch of 7 comments

The title is the whole question — Ireland — has anyone got a straight answer on shortage list — but here is why I am asking. Paid noticeably more at one clinic than another for what turned out to be the same facility behind both. Switched between two compounded preparations and the concentration on the label was…

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7 comments, started 1 year ago
u/yannick_petrov25 points·1 year ago·edited

Disagree — a 503B being registered does not make its preparations equivalent to an approved product. Different regulatory category entirely.

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u/swirl_dont_shakereconstitution9 points·1 year ago

Asked for potency testing on the finished preparation. They had it. I had assumed they would not.

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u/lukas_vermeulenOP0 points·1 year ago

What concentration is on the label, and does it match what you were expecting?

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u/lukas_vermeulenOP1 point·1 year ago

What is the beyond-use date and what is it based on?

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[removed]16 points·1 year ago

[removed by moderator]

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u/tobias_vukovic8 points·1 year ago·edited

That figure is the starting material purity, not the finished preparation potency. Two different tests.

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u/runa_grimaldi4 points·1 year ago

That is not what patient-specific means. It refers to the prescription, not to a customisation of the formula.

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Compounded GLP-1s as a supply route: the 503A/503B distinction, the shortage-list mechanics that made compounding legal and then didn't, state board rules, telehealth prescriber models, and what a compounding pharmacy will and will not tell you about its API source.

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