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Here's the situation: I'm a pharmacy tech. My Pharmacist-in-charge (PIC) does everything 100% by the book.
The assistant pharmacist (AP) likes to cut corners.
When we print the rx labels, the drug information monographs print out and sometimes carry over to a 2nd page. Also, a 3rd page sometimes prints, like "Important things you need to know about" [drug name] along with warnings and information.
By the book, we're supposed to fold the 2nd and 3rd pages in a letter-style 3-way fold, which are then placed in the bag with the bottles before being stapled closed.
AP hates the extra pages. S/he wants me to throw them out and not include them, since "patients never read them anyway." That may be true, but PIC says that some of those things are federally mandated, and AP is possibly risking his/her license by discarding them.
AP also tells me not to bother with putting auxiliary labels on the bottles, since it slows down production.
As a tech, is AP putting my certification or state registration in danger by his/her actions?
The assistant pharmacist (AP) likes to cut corners.
When we print the rx labels, the drug information monographs print out and sometimes carry over to a 2nd page. Also, a 3rd page sometimes prints, like "Important things you need to know about" [drug name] along with warnings and information.
By the book, we're supposed to fold the 2nd and 3rd pages in a letter-style 3-way fold, which are then placed in the bag with the bottles before being stapled closed.
AP hates the extra pages. S/he wants me to throw them out and not include them, since "patients never read them anyway." That may be true, but PIC says that some of those things are federally mandated, and AP is possibly risking his/her license by discarding them.
AP also tells me not to bother with putting auxiliary labels on the bottles, since it slows down production.
As a tech, is AP putting my certification or state registration in danger by his/her actions?
