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1 nistered Delta(9)-tetrahydrocannabinol (THC; dronabinol).
2 availability and clearer dose-linearity than dronabinol.
3  given 1 dose of placebo or 2.5 mg or 5.0 mg dronabinol.
4  marijuana and -0.04 (CI, -0.20 to 0.14) for dronabinol.
5 s of marijuana (0.00, 1.98, or 3.56% THC) to dronabinol (0, 10, or 20 mg).
6 g/d liquid suspension plus placebo, (2) oral dronabinol 2.5 mg twice a day plus placebo, or (3) both
7                  Marijuana (1.98, 3.56%) and dronabinol (20 mg) also increased abuse-related subjecti
8                   We compared the effects of dronabinol, a nonselective agonist of the cannabinoid re
9                                              Dronabinol affected fasting distal MI in patients, regar
10                                              Dronabinol affected fasting proximal MI in patients with
11 among advanced cancer patients compared with dronabinol alone.
12 lerance did not differ between marijuana and dronabinol, although dronabinol produced analgesia that
13 ent group, 329 received at least one dose of dronabinol and 164 received at least one dose of placebo
14 d Drug Administration-approved cannabinoids (dronabinol and nabilone), which include nausea and vomit
15                             In all patients, dronabinol decreased fasting proximal left colonic MI co
16         Compared with placebo, marijuana and dronabinol decreased pain sensitivity (3.56%; 20 mg), in
17 t under controlled conditions, marijuana and dronabinol decreased pain, with dronabinol producing lon
18 agonist, Delta(9)-tetrahydrocannabinol (THC; dronabinol), decreases marijuana withdrawal symptoms, ye
19                 We investigated whether oral dronabinol (Delta(9)-tetrahydrocannabinol) might slow th
20 ydrocannabinol marijuana cigarette, a 2.5-mg dronabinol (delta-9-tetrahydrocannabinol) capsule, or a
21                                              Dronabinol did not alter sensation or tone.
22 s safety concerns (114 [35%] patients in the dronabinol group had at least one serious adverse event,
23                          145 patients in the dronabinol group had EDSS score progression (0.24 first
24 -PHYS score was 0.62 points (SD 3.29) in the dronabinol group versus 1.03 points (3.74) in the placeb
25 ary end point (marijuana group, 20 patients; dronabinol group, 22 patients; and placebo group, 20 pat
26                        Our results show that dronabinol has no overall effect on the progression of m
27                                              Dronabinol has poor bioavailability, which may contribut
28 ents were randomly assigned (2:1) to receive dronabinol or placebo for 36 months; randomisation was b
29 ared with placebo (overall P = .05; for 5 mg dronabinol, P = .046), decreased fasting distal left col
30  gave an estimated between-group difference (dronabinol-placebo) of -0.9 points (95% CI -2.0 to 0.2).
31 r between marijuana and dronabinol, although dronabinol produced analgesia that was of a longer durat
32 arijuana and dronabinol decreased pain, with dronabinol producing longer-lasting decreases in pain se
33 ients with IBS with diarrhea or alternating, dronabinol reduces fasting colonic motility; FAAH and CN
34 erage changes in viral load in marijuana and dronabinol relative to placebo were -15% (CI, -50% to 34
35 harmaceuticals, Somerset, NJ, USA), Marinol (dronabinol; THC; AbbVie, Inc., North Chicago, IL, USA),
36 te improvement and weight gain compared with dronabinol-treated patients: 75% versus 49% (P =.0001) f
37 of analgesic effects of smoked marijuana and dronabinol under well-controlled conditions using a vali
38                               The effects of dronabinol were greatest in patients with IBS with diarr

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