50 karma · joined March 7, 2016
Edit: further, to your comment about "prescription strength" nomenclature, look at section 14 of the Cialis/tadalafil prescribing information, IIRC, table of clinical studies, where they have the second two outcomes of the clinical studies broken down by dose. Efficacy increases pretty directly with increasing dose, and these are where the observed side effects show up. It seems like patients may well self-escalate. Maybe the OTC countries have public data on this?
Can you name specific examples where the number of pills/capsules/tablets has been increased to improve drug safety? Increased pill counts historically reduces patient adherence, which worses disease management. This is just the first example I found which measured it: https://pubmed.ncbi.nlm.nih.gov/31298592/ This review explicitly states it in the abstract even: https://pubmed.ncbi.nlm.nih.gov/30561486/
If you want to get more reasonably unhappy with market exclusivity, look at Celgene's grip on thalidomide/lenalidomide/pomalidomide for the treatment of multiple myeloma.
Doesn't the measurement of current in the presence of light mean photo-voltaic?
However, they bring up a reasonable question, which is that of conflicts-of-interest. I do not now, nor have a I ever, received any compensation from a current or historical manufacturer of medications targeting ADHD. I do not anticipate receiving any such compensation in the future. However, I am married to a physician. (Side note: she also has ADHD. One of the smartest people I've ever met, but nearly failed her first USMLE because she couldn't execute on review/studying prior to the test. Went on meds and passed the rest of her exams with scores right in the middle of the distribution. The meds don't make us super-human, they just let us be normal.)
- Slept better. No more tossing and turning for an hour or two before I fell asleep.
- Ate more regularly. My stomach starts to hurt if I wait too long between meals.
- Remembered people's names when meeting them, at least to the point where I could say it again after they introduced themselves and started talking.
- More realistic outlook. Things aren't perfect and they aren't the worst, they just either kind of suck for now or this is a good moment.
- No longer have to make a giant mental effort to get something done on the weekend. If I want to read a book, I read it. If I want to play video games, I play them. If I want to clean the house, I clean the house.
- No longer a giant mental effort to get something done at work. Need to send an email? Send it. Need to annotate some data? Annotate it. Need to schedule a meeting? Schedule it.
Physicians can and do use drugs off-label at their discretion all the time; the FDA is not charged with regulating that. (They do, however, regulate the advertising of a drug with claims which are unsupported by clinical trials.)
https://www.computerworld.com/article/2527153/opinion-the-un...
I'm a little dismayed by the great number of comments I had to read before someone pointed this out...
Trash UX is really awful. In my office it's even worse - the custodial staff just dump the at-desks blue recycling bins into the same large trash can as the black waste bins. Why the heck do we even have recycling bins if it's just going to be commingled anyway?
I'm not saying the DMCA is a good thing or a bad thing; I'm just trying to get calibrated to what is being proposed in the directive. Thanks for the help!