Someone please email or comment or something and reassure me that
I am not going to die from having an IVP. :-)
My mother once had to take these weird dye tablets to have an xray of her gall bladder, and after the first one she turned beet red for a few hours. She was supposed to take more of those pills, but they told her not to lest her throat close off from the reaction.
I know that dye is required for an IVP (Intravenous Pyelography) and that that dye is similar to the dye that mum had a scary reaction to.
Is reaction to IV dye familial? Will they give me a test dose first? I suppose I could just call them up :-)
The kidney stone is still present and accounted for, although it has been quiet today. Tuesday was an awful day – had a follow up MD appt and kidney stone wanted to be there, so it started in on me around 8am. I took Vicodin all day long, which was probably a mistake, because then after I awoke from the Vicodin-induced coma, I was extremely nauseated. Even though I did not exceed the prescribed amount.
(Btw, GruntDoc – it was not difficult to take Vicodin while having pain. In fact, it was the only thing keeping me away from the ER. I did also have Toradol with both visits, which sadly did nothing. I had very high hopes for it.)