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#dosing-titration 2025-12-19

Friday50 messages9 participantstimes are UTC
Highlights from this day
  • underfill_uma — my dose day has drifted 4 days later over 15 months, does it matter dose day drift is mostly harmless with a weekly compound, but pick a day and defend it 19:24
  • wren_weighs_in — coming down from 10 to 7.5, how bad is the appetite rebound 21:51
  • underfill_uma — i log dose, day, weight and one line about how the week felt. thats enough to make decisions on 22:01
BW

plateau versus set point is not answerable in under six months of data, we shall see

WW

if it "stopped working after four days" that is almost never pharmacokinetics, anyway

dose day drift is mostly harmless with a weekly compound, but pick a day and defend it

WW

sorry to jump in the argument for splitting is a flatter curve. the argument against is you have doubled your injections for a guess

is there a point where going up stops buying you anything

n of 1

UU

my dose day has drifted 4 days later over 15 months, does it matter
dose day drift is mostly harmless with a weekly compound, but pick a day and defend it

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MM

my rule: if a side effect is still there at day five, i hold. if it clears by day three, i step

JJ

small steps are better than big ones and the only reason people take big ones is impatience

JJ

came down from a treatment dose to maintenance over about three months and it was uneventful

🤝12

i escalate on symptoms. if the current dose is still doing something i stay on it, i have it written down somewhere

i would hold

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WW

i jumped a rung once to catch up after a supply gap and it was a bad week. would not repeat

whats the smallest step anyone has managed between doses

pick a day and stick to it

slightly off topic but i went to the top of the ladder, felt no better than two rungs down, and came back. that is data for me and nobody else

MM

whats your rule for when a side effect means hold rather than push

MM

the ladder in the trials is a starting point, not a schedule you owe anyone, we shall see

[edited]

came down, no regrets

two weeks is nothing

NW

the trials escalated on a fixed schedule because a trial has to. you are not a trial

my titration ladder took 1 months to climb and i would do it slower again

after a gap of more than about three weeks i restart one rung lower. thats my own rule, not advice

LN

genuine question split dosing has no trial behind it. people here do it and report on it, thats all

wk 1-4    2.5mg
wk 5-8    5.0mg
wk 9-20   7.5mg   <- stayed here
wk 21-24  10.0mg  (no extra benefit for me)
wk 25+    7.5mg   (came back down)
LN

i drifted from sunday to wednesday over a year and only noticed when i checked the log

while im here if you are asking whether to go up, the fact you are asking usually means not yet

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thats normal

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no trial for that

U-100 syringe: 1 unit = 0.01 ml
  10u = 0.10 ml
  25u = 0.25 ml
  50u = 0.50 ml
 100u = 1.00 ml
mg drawn = ml drawn x mg/ml
NT

with a roughly seven day half-life you are near steady state after about five weeks at a dose

JJ

sorry to jump in i went from 7.5 to 2.5 and honestly could not tell the difference in appetite, your mileage will differ

WW

coming down from 10 to 7.5, how bad is the appetite rebound

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WW

if you are going up because the scale stalled for two weeks, wait. two weeks is noise, your mileage will differ

NT

anyone tracked whether a smaller more frequent dose changed their side effects

*PeptideMeter not the other one

update from 6 months ago: held at the same dose the whole time and still losing slowly