-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._- ``.~. r-. (*) -=~ .___ __. , ___ _ __ ' ' / \ // `| R \\ / \\ /: ^ / / '. \\ \/ ====| - | | ! || < :|. _ //.| 0 | /|: |*| | | A | || ||: = \*/ + || / | =|\ |. 0 |. \ | : | | a || | V | >=== -= v \ || \==- | ^ |. \\ // \\/ \v/ \_ --, \'/ : ~-= |`. `" ~ `~ u ' V |__| V .====| <- Back to 2006.03.09. Via e-mail, several individuals provided responses paraphrased below. Certain measures were taken to protect the innocent, and to make me look good. >All opiods have the property of respiratory suppression (of >which one useful property is cough suppression). >Dextromethomorphan (as in Robitussin "DM") is an opiod No, it's a dissociative tranquilizer whose effects are primarily mediated through the NMDA receptor. >but retains its useful property of suppressing cough. Neither opioids nor DXM have any selectivity for cough. // I did some research on acetaminophen, and found no reason to believe my recommendations would be harmful. I also didn't find any support for my claim that Tylenol is better than Advil for fever. I still suspect I'm right, but I pulled that section of my post anyway. Two studies I saw found them to be equally effective at reducing fever in young children. In any case, it isn't the strength of the anti-fever effect that's the risk factor for Reye's syndrome. That's a special problem with Aspirin. Ibuprofen is now approved for children -- I didn't know that. >As to the analgesic effects of assorted OTC medication >including NSAIDs, they all have roughly the same analgesic >effects, probably because, unlike opiods, they exhibit a ceiling >effect -- after a certain dose additional drug will not provide >any additional analgesia. I agree. But I wouldn't want to take the amount of Aspirin required to give the relief 400mg ibuprofen does. // >I myself am one of the chicken noodle types. Getting good nutrition while sick is super-important. Chicken broth has very digestible protein and stuff in it, and hot fluids can help clear the head. >Sudafed is definitely a better first-line agent I don't know if patient outcomes have ever been studied with Sudafed, but they definitely don't improve and almost certainly worsen if it's taken long enough. Epinephrine is clearly immuno- suppressive -- since it's adrenergic, it shuts down sexual, immune, and (whaddya know) digestive function. I titled my post "Curing..." because I have something I think improves outcomes for rhinovirus infection. Of course this should be studied, but since there's "no established medical use" of cannabis (which isn't even true, since there are FDA-approved antiemetics based on cannabinoids), it's very hard to do studies to establish any. >given its [THC's] side-effect profile What side-effects are you referring to? The only thing I can think of is that in some cases it appears to suppress imumne response -- in one Canadian study, it seemed to stop macrophages from destroying lung tissue in response to smoke. Which, it was suggested, accounted for the less-than-expected lung damage observed in pot smokers. Overall it's not understood. All that's really known is that some immune cells express cannabinoid receptors. >When I was on the medicine service, I took every opportunity to >use Marinol for my patients who weren't eating very well for >whatever reason just to see if it worked. AIDS, cancer, etc >(This was only 5 patients or so). They invariably got zonked >out, confused, lethargic, with the notable exception of my one >AIDS patient who had a long drug history. Maybe her previous >marijuana use made her less susceptible to the drug's bad >effects. All of them ate like champions though, which was nice >to see. Obviously these people were in sorry shape to begin >with, and are not comparable to the healthy patients who ate the >brownies. I've never tried Marinol. I'm glad it worked. If people were getting zonked, the dose was probably too high. It's good to take THC with a little fat -- smooths out plasma peaks -- but otherwise on a near-empty stomach. A small (3 in^3) piece of brownie is the carrier I use, on an otherwise empty stomach with a dose that's low enough to be rendered inactive in some if taken after a full meal. Though I can believe that really ill patients might get zonked on any amount. The word on the street is that the plant source is preferred, supposedly because of its broad cannabinoid profile. I've read that other cannabinoids are so much less active than THC that they could have no importance. However, I don't think anybody really knows this, and it would be a way to explain the apparent subjective differences between varieties of pot. Another complaint is that oral delivery is problematic if the patient is vomiting. I believe I heard there is an inhaler in trials... A puff of smoke did save my life once after a vicious night of drinking, after fasting, water, salted pretzels, and Pepto Bismol failed. The effect was instantaneous. >Perhaps other medications with similar effects might be worth >trying out? I think so. It would also be nice to have a selective CB2 agonist, and to identify CB3 if it exists... http://en.wikipedia.org/wiki/Cannabinoid_receptor Wow, I hadn't seen this page. Excellent stuff here. Looks like such an agonist may be coming down the pike. The language in that section is a bit suspect, though, so I won't hold my breath. -`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._-`._- clumma@gmail.com