
I did feel a little dizzy one time and took the opportunity to eat some sugar. I still eat some sugar snacks even though I have cut way back. I usually eat a small meal and a snack for lunch, and a damp meal and a snack for dinner and sometimes two snacks. When I first started I cut way down on sugar so I was easily able to attribute how I felt to needing some sugar at least that is what I figured.Hichewgoddess said:I’ve just started Reta 1mg per week and currently on week 4. After about 24 hours I get a blood sugar drop. I get dizzy, nauseous, and feel feint. At least I’m assuming that’s what it is as it seems to be fixed by water and a small piece of candy/sugary food. I am eating carbs, drinking my water, and drinking my electrolytes (1 packet of liquid IV per day), and still feel like I have to really be careful. Is this hypoglycemia? Low blood pressure due to not enough water/electrolytes?


Are you using an intermittent pinprick BGL measurement or a CGM? I did notice it varies throughout the day.dondada109 said:I usually eat bigger portions of carb before and after my workouts, 3 weeks in and didn't had any drops as for now

I'm drinking 3-4 packets of electrolytes per dayHichewgoddess said:....drinking my water, and drinking my electrolytes (1 packet of liquid IV per day)...

Be careful. Liquid IV has 500mg of sodium per packet.kobeanbry24 said:I'm drinking 3-4 packets of electrolytes per day![]()

You are so rightBNLFL said:Be careful. Liquid IV has 500mg of sodium per packet.


I don’t see anyone in this thread concerned about asymptomatic hypoglycaemia. If I could be asymptomatically hypoglycaemic long term I’d be over the moon given we know there’s a direct correlation between elevated HbA1c and atherosclerotic burden.tubby said:Lots of FUD here:
"Asymptomatic hypoglycemia" isn't a legitimate concern. This is actually part of the reason why (although I think it would be a great thing) doctors are often opposed to prescribing CGMs for non-diabetics (or even many type 2 diabetics). They know their patients are going to read too deeply into the numbers and start role-playing as if they were type-1 diabetics (e.g. sugar snacks when things go lower and making other bizarre decisions to smooth out the number shown on their phone app). You're also conflating initial common GLP symptoms with hypoglycemia. I experienced those symptoms too initially. I have worn a CGM for years. My blood sugar went down on reta. It regularly hovered in the 50-60 mg/dL range during periods of dose escalation. It's not unusual. Normally I'd have to fast for 4-5 days to get it to hover in that range.
If you're injecting insulin and taking sulfonylureas then you should be tracking your blood sugar and doing things like a sugar snack if you start to see it dip. Otherwise, unless you have something highly unusual going on, you're not going to benefit from role-playing type-1 diabetic behavior.

I didn't use the word "can't." My point was that there's a reason why doctors will warn you about hypoglycemia when starting injectable insulin or a sulfonylurea, but they won't warn you about it when starting a GLP. It's because (symptomatic) hypoglycemia isn't a common risk factor associated with GLP use (unless that person is also taking injectable insulin or a sulfonylurea).Lear00 said:It is certainly brave to be so confident that someone can’t have hypoglycaemia related symptoms

tubby said:I didn't use the word "can't." My point was that there's a reason why doctors will warn you about hypoglycemia when starting injectable insulin or a sulfonylurea, but they won't warn you about it when starting a GLP. It's because (symptomatic) hypoglycemia isn't a common risk factor associated with GLP use (unless that person is also taking injectable insulin or a sulfonylurea).
Now every once in a blue moon someone will have something deranged going on with their metabolism where adding a GLP into the mix could lead to symptomatic hypoglycemia, just as every once in a blue moon someone will go blind after starting a GLP. Both are rare conditions and in the case of hypos that person is usually aware that it's a problem for them before starting the GLP because it's historically been a problem.
What you're doing it reading into values on your CGM and even in the absence of feeling light headed, clammy, or losing consciousness you're convincing yourself that you're at risk of something. This is causing you to misapply type-1 diabetic thumb rules in regards to hypoglycemia and think 50-60 mg/dL is a dangerously low blood sugar, despite being a very common level one will achieve on an extended fast and a significant number of normal healthy people will see as a reactive level after a meal without experiencing those symptoms.
Here's what's tripping you up: A type 1 diabetic will sweat a 50-60 mg/dL level, not because that level itself is harmful, but because of the trend that it represents. If their blood sugar is trending downwards AND their body lacks the ability to course correct then by the time they see 50-60 mg/dL on their CGM it's likely their actual blood sugar level is already lower than that. Also, since their body lacks the ability to course correct on its own hormonally, it's important that they initiate action now, since if they wait until it has fallen to a harmful level, it will be too late for them to do so.
So again, everyone is free to wear a CGM and role-play being a type 1 diabetic, but the vast majority of the time it will be unnecessary.

Lear00 said:I am a medical doctor, and I certainly don’t have 1/10th of the confidence you seem to have in making such sweeping and definitive statements about a relatively new research use only medication that we are still actively learning about. Internet armchair expertise is risky at the best of times, but particularly so when discussing medications like this.
All the best

Lear00 said:- There is likely a subset of the population like me which already have a ‘borderline’ BGL on no medication, who would be at risk of hypoglycaemia whilst on a GLP1 and not know about it. It’s important to remember the population selected in all the trial so far are pre-disposed to insulin resistance (I.e BMI >31). On the other hand anyone can use it on the grey market and that population isn’t reflected well in trials.
quoted said:External validity refers to the extent to which we can generalize the results of a trial to the population
quoted said:Look for the main characteristics of the study population. You should be asking how much this population matches the patients you see or how much do they differ. If they differ too much then no matter how good the results are they it will be difficult to justify applying the treatment to your patient from a given paper.

But I'm not treating patients. I'm offering commentary on pharma products.Lear00 said:This is a good website to learn how to critically appraise studies and evaluate them for applicability/generalisability.
https://www.cebm.ox.ac.uk/resources/ebm-tools/making-a-decision