When should i up dose of reta?

donzilla

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This is my first week on 1mg reta which ive tolerated and felt mild hunger suppression. Should I up my dose to 2mg? i wanna take it to the next level for fat loss
 
One week is a relatively short time to assess your response. But the trials started at 2 mg, so if you find the sides tolerable, or even non-existent at this point, I think you could move to 2 mg. Remember it takes 4 weeks to reach therapeutic levels, so if you move to 2 mg, you should stay there for a month. I did 1 mg twice a week for my first two weeks before moving to 2 mg once a week, but in hindsight, I could have started at 2 mg per dose, but that's me. It all depends on your individual response.
 
It takes ~4 weeks to reach steady state for a given dose. Steady state is not the same as therapeutic levels.

I switched from Tirz to Reta for the GCGR signaling. Therapeutic levels for that to be reliably signaled are thought to be ~6-8mg/week, which is 7.5-10mg average exposure at steady state with troughs from ~5mg to peaks of ~14.5mg at single weekly dosing.

Since I was already on Tirz, I moved up on Reta quickly with numerous small doses, watching out for side effects. I went to 7.5mg of accumulated level on day 16, and have stayed above 7.5mg since day 18. No nasty side effects, it was an easy and smooth transition for me, 36 days in now.
 
It takes ~4 weeks to reach steady state for a given dose. Steady state is not the same as therapeutic levels.

I switched from Tirz to Reta for the GCGR signaling. Therapeutic levels for that to be reliably signaled are thought to be ~6-8mg/week, which is 7.5-10mg average exposure at steady state with troughs from ~5mg to peaks of ~14.5mg at single weekly dosing.

Since I was already on Tirz, I moved up on Reta quickly with numerous small doses, watching out for side effects. I went to 7.5mg of accumulated level on day 16, and have stayed above 7.5mg since day 18. No nasty side effects, it was an easy and smooth transition for me, 36 days in now.
I think if someone brand new to GLPs and just starting with Reta, like it sounds the OP is, therapeutic levels and steady state are pretty close together. I felt my first 1 mg dose later the same day. Each week just reinforced the effects I felt that first day, so going by "feels" it felt therapeutic to me from the start. If someone is concerned about moving from 1 mg to 2 mg after a week, I don't think it's an issue but everyone is different.
 
This is my first week on 1mg reta which ive tolerated and felt mild hunger suppression. Should I up my dose to 2mg? i wanna take it to the next level for fat loss
Depends on personal tolerance. I started at 2 and upped .5 every 5 days. I am pinning 4 next, possibly 4.5 because my sides are mild and I am still eating a good bit just not snacking and gorging myself out...
 
This is my first week on 1mg reta which ive tolerated and felt mild hunger suppression. Should I up my dose to 2mg? i wanna take it to the next level for fat loss
I would have no problem titrating immediately to 2mg and stay there for a few weeks to see how you are handling it.
 
One week is a relatively short time to assess your response. But the trials started at 2 mg, so if you find the sides tolerable, or even non-existent at this point, I think you could move to 2 mg. Remember it takes 4 weeks to reach therapeutic levels, so if you move to 2 mg, you should stay there for a month. I did 1 mg twice a week for my first two weeks before moving to 2 mg once a week, but in hindsight, I could have started at 2 mg per dose, but that's me. It all depends on your individual response.
wdym by it takes 4 weeks to reach therapeutic levels?
 
wdym by it takes 4 weeks to reach therapeutic levels?
It takes a full 28 days for the GLP to reach full effect or the saturation level for that dose. It might have some effect before then, but doesn't reach full effect whether that's 2mg or 4 mg or whatever. I didn't mean zero effect.

The best way to visualize how your dosage reaches saturation, and what levels you're at and when, is with a plotter. You can plug in your dosage, or project your dosage, and see what it looks like. https://glp1plotter.com/
 
FWIW, I have zero sides on Reta on 4 mg every 84 hours.

If it's working at 1 mg / week for you, I'd stay there for the full four weeks before you consider titrating up.

It's likely perfectly fine for you to titrate next week since 2 mg is the Phase III starting dose and you've tolerated it well.

Nb. though that this is a marathon, not a sprint. GLPs take time to build in the body and reach full therapeutic levels. If nothing else, it'll save you some money since you can stretch your supply further on the lower dose.
 
I think it depends a bit on where you are and what you want from it . If you are severely overweight in some ways it makes more sense to go slowly, losing lots of weight fast carries extra risks of gallstones, fainting etc.
The fact is if you up doses faster than every 4 weeks you increase your chances of getting bad side effects, and as the drug has such a long half life they can take a week or more to subside. The standard common side effects are nausea vomiting diarrhoea and constipation. The problem is vomiting for a week is a real problem that could land you in hospital on a drip if you are unlucky. The other thing to know is peak side effects are normally at about month 2 to 4 after starting at mid range doses as they are increasing. But everyone is different in terms of side effects.
You absolutely need to understand the pharmacodynamics of the drug before upping doses faster, and use glp plotter to see what different doses do to blood levels, and understand that it takes 4 weeks at a given dose to get to maximum levels in your blood which is why the recommendation is to only increase doses every 4 weeks.
The only semi safe way to increase doses faster is to use frequent small doses, every second or 3rd day, so that when you overshoot your tolerance and get side effects that are unpleasant, it wont take a whole week for levels to drop to where they were before you had that dose. Even doing this and checking out glp plotter, you are much more likely to get unpleasant side effects if you try to increase doses any faster than the standard.
At only 1mg having another 1mg dose 3 to 4 days after the last dose is a lower risk way to do it than a 2mg dose a week later. And then you see what happens in terms of side effects vs hunger suppression. And you can always work out a weekly dose once you are at a dose that suits you and swap to that, which is simply the sum of the smaller doses over a week.
 
What if you’re using pre filled pens? I’ve heard the potency wears off as the solution is already mixed. So people tend to start higher? But if your mixing with bac water and reconstituting it yourself, you should start lower?
 
What if you’re using pre filled pens? I’ve heard the potency wears off as the solution is already mixed. So people tend to start higher? But if your mixing with bac water and reconstituting it yourself, you should start lower?
It sounds like you need to do some more reading before using GLP peptides. The dose is the dose, and how it is delivered is irrelevant, it matters a lot that you understand the correct dose to take , how to mix the peptide with bac water and how to make sure you end up using the dose you intended to use. Getting this wrong is super easy, the biggest risk of diy GLP's is dosing errors. There are no guard rails to stop you hurting yourself. Do lots of reading and watch tutorials.
Once mixed any peptide solution is going to degrade a bit, but generally if refrigerated this effect is insignificant , at most 1-2% or so over a few months ( for most of them ). Peptides prepared by pharmaceutical companies and sold in prefilled pens are very carefully formulated to degrade very slowly and be fine to use for years, though most also need to be kept in the fridge to minimise degradation. Self mixed peptides , in vials mixed with bac water are not as precisely formulated and should ideally be used in a month and kept in the fridge, though I am happy to use them for up to 3 months as a few percent degradation that might or might not happen is totally insignificant in terms of effect on dose.
 

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