Accepted answer
Take it from the STEP 3 adverse-event table by arm, and check the unit before you use it. An incidence can be the proportion of participants who reported the event at least once, or the count of events divided by exposure time, and the two differ by however many people had it repeatedly. Then subtract the placebo arm, because the untreated rate is not zero. And read the discontinuation column beside it: an event that made people leave the trial is under-counted at every later visit, so a low late-timepoint incidence can mean the event was severe rather than rare.
This is one of the most distressing reported effects and one of the most reliably temporary.
Nothing topical has strong evidence for accelerating recovery from telogen effluvium specifically, as distinct from androgenetic loss where the evidence is entirely different.
In telogen effluvium a stressor shifts a large fraction of follicles from anagen into telogen simultaneously. Because telogen lasts around two to three months, the shed appears two to four months after the trigger rather than during it.
Low ferritin is associated with increased shedding in observational studies at thresholds above those used to define anaemia.
The trigger is the rate of loss, not the compound. Slowing it helps future follicles.
3Thank you — this is the answer I was looking for. – ellis_thorne 2 months ago 2The red-flag list should be higher up the answer, not at the bottom. – e_dziedzic 23 days ago add a comment