Bromo-Dragonfly Trials
I recently acquired 3 ampoules filled with 2ml of 40% ethanol solution and 1mg of Bromo-Dragonfly via mail. I consider myself an experienced user and abuser of psychedelics. I had tried 5-MeO-DMT, DPT HCl, DPT Freebase, LSD, psilocin mushrooms, mescaline cacti and Salvinorin A (as well as salvia divinorum), 2C-I and 2C-B prior to the experiments. I have also had my focus on psychedelic drugs although I have ingested a lot of other substances as well in my 6 years of drug use and abuse. These include a number of uppers and downers, several dissociatives, empathogens, inhalants, alcohol and a whole lot of cannabis.
I began my trials with a very low dose of 10µg orally. I did not expect anything to happen, but wanted to check for allergic reactions.
The next day I ingested 25µg which had no effect either. What I then did cannot be considered very smart…
The following trials were certainly not spaced far enough apart which might have resulted in a tolerance.
Within the next week, I upped the dose to 50µg which seemed to induce a mood lift, increased sociability, yawning, a tingling body feeling and the perception of colors being brighter than usual, but was later disregarded as a placebo effect when the next trial of 100µg on the following day did not succeed to produce these same feeling again. I therefore upped the dose with another 120µg at T+06:00 which seemed to result in no effects either. At T+09:00 I smoked 20mg of DPT Freebase which resulted in effects that were appropriate for such a dose, judging by my experience with DPT. Continuing to smoke DPT Freebase in the course of the evening a pleasant trip evolved which might have had a phenethylamine twist to it. I was able to fall asleep at around T+13:00 and now think it is rather unlikely that the BDFL had any noticeable effect on me that day.
1 day after this 220µg trial I administered 50µg rectally dissolved in 1ml of 4% ethanol solution which did not produce any change in mood or perception.
I then waited 7 days until my next trial. On the 7th day I got up at 8:00am, ingested 400µg of the substance and went back to sleep which took me about 30 minutes. I then had about an hour of sleep which was accompanied by very vivid dreams. The dreams were interconnected and memory was excellent. One of them happened to be the longest lucid dream I have ever experienced since I usually awake when gaining lucidity. This time I did not even have to use a technique to stay asleep, I kept dreaming and stayed lucid. I woke up at 9:30am and wrote down 5 DIN A4 pages summarizing the dreams.
At this point I did notice some effects, but it seemed clear that the experience was not going to satisfy my expectations so I ingested another 250µg.
The trip slowly started building up and reached it’s first peak at T+05:00 as expected. Dosis wise this was comparable to about 10mg of 2C-B. Quiet smooth. Symptoms included stickiness of the saliva, increased muscle tension (especially in the jaw), acidic feeling throughout the gastrointestinal and urinary tract, yawning, increased appreciation of taste (especially fruit which was the only thing that was eaten until T+15:00) and music , perception of brighter colors, sharper edges which shifted around slightly, especially when focused. Things seemed alive, like they were going to jump at me any second. Neither were there any complex visuals present like patterning, fractal visions or COV’s nor was there a lot of movement involved.
These effects kept increasing until T+07:30 which I consider the second peak. Even at this very peak was I still socially and mentally fully functional. I was able to post on a forum, ride my bike, make sense of time, chat in the IRC, make and receive phone calls, ride my bike, seal packages with electric devices the proper way and even speak coherently with my friend’s mum when I was faced with this situation unexpectedly while visiting said friend at T+11:00. I did not feel comfortable with walking into the supermarket in order to buy whippets (N2O containers). That’s why I sent a friend to do it for me. 15 whippets were consumed between T+11:00 and T+13:00 along with 50mg of cocaine HCl (sublingually) which resulted in a headache and difficulty keeping my balance which faded within an hour. The N2O did not effect the trip significantly which was a little disappointing for me.
The negative effects included the mentioned acidic feeling of the whole urinary and gastrointestinal tract starting in the throat and an increased sensibility for pain. I suffer of chronic back pain and chronic pain of the tendon sheaths of my hands which was severely increased to the point that I had to ingest 200mg of Kratom alkaloids at T+17:00 to get rid of the pain. I have never before used pain medication as a treatment to give you an idea of how bad the pain was perceived. I was able to get rid of the pain almost completely. To my surprise the acidic feeling disappeared as well and the Kratom diminished most of the trip. I was very mellow and tired from that point on.
By T+21:00 I was asleep which lasted until T+30:00. At that point I had no more visuals at all and there was no detectable afterglow either.
crOOk
I recently acquired 3 ampoules filled with 2ml of 40% ethanol solution and 1mg of Bromo-Dragonfly via mail. I consider myself an experienced user and abuser of psychedelics. I had tried 5-MeO-DMT, DPT HCl, DPT Freebase, LSD, psilocin mushrooms, mescaline cacti and Salvinorin A (as well as salvia divinorum), 2C-I and 2C-B prior to the experiments. I have also had my focus on psychedelic drugs although I have ingested a lot of other substances as well in my 6 years of drug use and abuse. These include a number of uppers and downers, several dissociatives, empathogens, inhalants, alcohol and a whole lot of cannabis.
I began my trials with a very low dose of 10µg orally. I did not expect anything to happen, but wanted to check for allergic reactions.
The next day I ingested 25µg which had no effect either. What I then did cannot be considered very smart…
The following trials were certainly not spaced far enough apart which might have resulted in a tolerance.
Within the next week, I upped the dose to 50µg which seemed to induce a mood lift, increased sociability, yawning, a tingling body feeling and the perception of colors being brighter than usual, but was later disregarded as a placebo effect when the next trial of 100µg on the following day did not succeed to produce these same feeling again. I therefore upped the dose with another 120µg at T+06:00 which seemed to result in no effects either. At T+09:00 I smoked 20mg of DPT Freebase which resulted in effects that were appropriate for such a dose, judging by my experience with DPT. Continuing to smoke DPT Freebase in the course of the evening a pleasant trip evolved which might have had a phenethylamine twist to it. I was able to fall asleep at around T+13:00 and now think it is rather unlikely that the BDFL had any noticeable effect on me that day.
1 day after this 220µg trial I administered 50µg rectally dissolved in 1ml of 4% ethanol solution which did not produce any change in mood or perception.
I then waited 7 days until my next trial. On the 7th day I got up at 8:00am, ingested 400µg of the substance and went back to sleep which took me about 30 minutes. I then had about an hour of sleep which was accompanied by very vivid dreams. The dreams were interconnected and memory was excellent. One of them happened to be the longest lucid dream I have ever experienced since I usually awake when gaining lucidity. This time I did not even have to use a technique to stay asleep, I kept dreaming and stayed lucid. I woke up at 9:30am and wrote down 5 DIN A4 pages summarizing the dreams.
At this point I did notice some effects, but it seemed clear that the experience was not going to satisfy my expectations so I ingested another 250µg.
The trip slowly started building up and reached it’s first peak at T+05:00 as expected. Dosis wise this was comparable to about 10mg of 2C-B. Quiet smooth. Symptoms included stickiness of the saliva, increased muscle tension (especially in the jaw), acidic feeling throughout the gastrointestinal and urinary tract, yawning, increased appreciation of taste (especially fruit which was the only thing that was eaten until T+15:00) and music , perception of brighter colors, sharper edges which shifted around slightly, especially when focused. Things seemed alive, like they were going to jump at me any second. Neither were there any complex visuals present like patterning, fractal visions or COV’s nor was there a lot of movement involved.
These effects kept increasing until T+07:30 which I consider the second peak. Even at this very peak was I still socially and mentally fully functional. I was able to post on a forum, ride my bike, make sense of time, chat in the IRC, make and receive phone calls, ride my bike, seal packages with electric devices the proper way and even speak coherently with my friend’s mum when I was faced with this situation unexpectedly while visiting said friend at T+11:00. I did not feel comfortable with walking into the supermarket in order to buy whippets (N2O containers). That’s why I sent a friend to do it for me. 15 whippets were consumed between T+11:00 and T+13:00 along with 50mg of cocaine HCl (sublingually) which resulted in a headache and difficulty keeping my balance which faded within an hour. The N2O did not effect the trip significantly which was a little disappointing for me.
The negative effects included the mentioned acidic feeling of the whole urinary and gastrointestinal tract starting in the throat and an increased sensibility for pain. I suffer of chronic back pain and chronic pain of the tendon sheaths of my hands which was severely increased to the point that I had to ingest 200mg of Kratom alkaloids at T+17:00 to get rid of the pain. I have never before used pain medication as a treatment to give you an idea of how bad the pain was perceived. I was able to get rid of the pain almost completely. To my surprise the acidic feeling disappeared as well and the Kratom diminished most of the trip. I was very mellow and tired from that point on.
By T+21:00 I was asleep which lasted until T+30:00. At that point I had no more visuals at all and there was no detectable afterglow either.
EDIT
Recommendations
Since it is still not certain whether I had built up a significant tolerance or not, I would probably start off low with this one, at 500ug.
Judging by this report only I would say a full blown trip would equal about 1000ug, but then again it might be way too much if there really was a tolerance. So I recommend to start at 500ug after checking that no extraordinary sensitivity to this substance exists in the test subject with a low dose like 50ug.
crOOk
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