Hello all
There have been some posts in this previously but following a recent update from the FDA I wanted to start a new thread and get some new opinions.
My daughter was prescribed ranitidine end of 2018. During Sep/Oct 2019 some NDMA was discovered in some batches and since then there have been voluntary recalls globally.
At the time I was distraught and anxious thinking my baby could have had a contaminated batch. The FDA released the results of their testing revealing it was no worse than having a grilled piece of meat.
This relieved my anxieties somewhat however last week the FDA is now saying that the NDMA increases over the time so essentially the longer you have the medicine the higher the NDMA.
I am beyond worried/anxious/scared. I feel sick to the Pitt of my stomach.
My daughter was only on this s for a short period of time and I know there are thousands of people who took this medication daily for years but I am so worried.
Is anyone else as anxious or am I being unreasonable with my thoughts and anxieties?
The European results are yet to be published, could these be different to the FDA?
Please, any advice would be appreciated xx
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Ranitidine recall - AIBU
5 replies
Star39 · 06/04/2020 12:29
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