My GP So far the UK has not followed the FDA which is carrying out special monitoring of those drugs in light of the experiences reported in their Yellow Card system and also anecdotally here in the Forum.
We have this note on this site for Forxiga
America’s Food and Drug Administration (FDA) still have doubts over granting approval…
www.diabetes.co.uk
Its not keto diet
There is no BNF contraindication for Low Carb
But it happens
Sodium-glucose cotransporter-2 (SGLT2) inhibitors are a relatively novel class of oral medications for the treatment of type 2 diabetes mellitus (T2DM…
www.sciencedirect.com
These are Low Carb
www.endocrine-abstracts.org
Low carbohydrate diet while taking dapagliflozin: A case report and review of literature
pubmed.ncbi.nlm.nih.gov
Sodium-glucose cotransporter-2 (SGLT2) inhibitors are a relatively novel class of oral medications for the treatment of type 2 diabetes mellitus (T2DM). Their use has increased recently due to their beneficial renal and cardiovascular outcomes, but ...
www.ncbi.nlm.nih.gov
At the moment the GLP-1 meds are not contraindicated for low carb diets, but there are reports that it may increase the risk of pancreatitis due to the higher fat intake. Gall bladder problems may also be exacerbated as has been reported in this forum but that may be the keto diet side effect. Increased constipation has also been reported and this can be severe but again that may be a possible diet side effect being made worse
Again these meds are known to cause pancreatitis, AKI, gall bladder issues ands a keto diet may axacerbate their effects. Higher risk of hypo. (see manufacturer website.) There is a slight risk of euDKA with this med. But Foxiga is only found in the UK market, and our Yellow Card system is not very well used so notification may take a while, NG 28 was last updated in 2022 and is not due for update until 2026.
It took over 10 years for the problems with Actos and Avandia to get to the NHS to take action. They banned Avandia in the UK but Actos is still available. I had two strokes while I was on Actos and my GP reluctantly stopped it because it was not contraindicated even after the scandal. But because I had the strokes I was taken off it. So yes, I am banging the drum. I actually got hold of the FDA licence test data for both meds, and they had several deaths during the trials in both meds. But because the participants in the study were all elderly diabetics on the stroke ward, they already had increased risks before they started, so the deaths were claimed as natural causes and unrelated to the medication.
That is why I critique study reports so deeply. They are generally hiding info and often in plain sight. I have seen studies where the conclusion and abstract bear no correlation to the data that the team recorded. Obviously the team said this is what we did and thiis what we saw, but the boss says this is what I think happened. The press will love me.
So, just because there is no contraindication showing in the BNF for a drug, does not mean that there are not some unpleasant surprises lurking. I find the FDA far more proactive and willing to issue warningss more readily. the UK is generally a couple of years behind. I always wondered why it was Farxiga in the USA, but Forxiga in the UK. same drug formulation apparently, but different prescribing and patient info it seems. Same with Gliclazide and Glipizide.
I see Thalidomide is on prescription in the UK still.