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1 nt therapy during hospitalization (nine with amitriptyline).
2  of neuropathic pain, such as gabapentin and amitriptyline.
3 compared with use of headache education plus amitriptyline.
4 d the cannabinoid WIN 55,212-2, but not with amitriptyline.
5 as modulated by treatment with reserpine and amitriptyline.
6 amine cyproheptadine, and the antidepressant amitriptyline.
7 mpared with aged controls) after 6 months of amitriptyline.
8  (p < 0.05) decreased in the aged rats after amitriptyline.
9 d, double-blind, placebo-controlled trial of amitriptyline (1 mg per kilogram of body weight per day)
10 95% confidence interval, [CI] 0.61-1.13) for amitriptyline, 1.16 (95% CI, 0.90-1.50) for fluoxetine,
11 sia were randomized to 4 weeks of placebo or amitriptyline (10 mg/d, weight <35 kg; 20 mg/d, weight >
12  used for the treatment of neuropathic pain, amitriptyline (10 mg/kg) and fluoxetine (5 mg/kg), to ra
13  most commonly prescribed antidepressant was amitriptyline (45.2% of treated patients), administered
14 by 39 subjects given placebo (40%), 51 given amitriptyline (53%), and 37 given escitalopram (38%) (P
15 dized acupuncture regimen vs control points, amitriptyline (75 mg/d) vs placebo, or both for 14 weeks
16 and murine pRBCs were stored with or without amitriptyline, a functional inhibitor of acid sphingomye
17 and murine pRBCs were stored with or without amitriptyline, a functional inhibitor of acid sphingomye
18  serotonin-norepinephrine reuptake inhibitor Amitriptyline (AMI) for treatment of mental health probl
19 Drug Administration-approved antidepressant, amitriptyline (AMI) has shown efficacy in treating neuro
20                 In lesioned animals, chronic amitriptyline (AMI; 5 mg/kg) treatment resulted in a sig
21                              Patients taking amitriptyline (AMT) have an increased risk of sudden car
22             Each group received 1 mg/kg/d of amitriptyline and a 20-week end point visit.
23              Under voltage-clamp conditions, amitriptyline and bupivacaine remained as potent blocker
24 inergic and serotonergic antagonists such as amitriptyline and citalopram recapitulate this effect.
25 as previously reported for desipramine, both amitriptyline and fluoxetine increase the pain threshold
26 iked to the same concentration with the drug amitriptyline and imaged in the same experiment using is
27 d modified electrode was highly selective to Amitriptyline and it was shown a wide linear range from
28              This pattern of aODNs effect on amitriptyline and mianserin modulation of GABA-stimulate
29 The inhibitory effect of the antidepressants amitriptyline and mianserin on GABA-stimulated 36Cl(-) i
30  the GABA(A) receptor regulate the effect of amitriptyline and mianserin on the GABA(A) receptor chlo
31 failed response showed no difference between amitriptyline and placebo (P = .83).
32  There was no significant difference between amitriptyline and placebo after 4 weeks of treatment.
33                                         Both amitriptyline and placebo were associated with excellent
34          Topiramate, valproate, propranolol, amitriptyline, and methysergide have been widely prescri
35 , including testosterone, 17 beta-estradiol, amitriptyline, and most notably aflatoxin (AF) B1.
36 d feeling better and 5% feeling worse in the amitriptyline arm compared with 57.5% feeling better and
37 in the same experiment using isotope labeled amitriptyline as internal standard.
38 nth follow-up; again, half were treated with amitriptyline at doses of 10-30 mg/day.
39        Chronic antidepressant treatment with amitriptyline attenuated the maladaptive neurogenic, epi
40 ropion (beta [SE]: -0.063 [0.027]; P = .02), amitriptyline (beta [SE]: -0.081 [0.025]; P = .001), and
41                                              Amitriptyline, but not escitalopram, appears to benefit
42 lly efficacious as gabapentin (Neurontin) or amitriptyline, but respectively >350- and >75-fold more
43 t on heat hypersensitivity was observed with amitriptyline, carbamazepine, diazepam and gabapentin.
44 n tactile hypersensitivity was observed with amitriptyline, carbamazepine, rofecoxib, and diazepam.
45                        We included trials of amitriptyline, citalopram, clomipramine, desipramine, du
46 -0.08 (95% CI, -0.21 to 0.06; P=.26) and for amitriptyline compared with placebo was 0.00 (95% CI, -0
47 points option), and 136 patients were in the amitriptyline comparison (125 in the factorial option an
48                 For both the acupuncture and amitriptyline comparisons, changes in pain score were no
49 e data suggest that long-term treatment with amitriptyline decreases the prevalence of cognitive impa
50 from rats chronically (14 days) administered amitriptyline demonstrates that TNF inhibition of NE rel
51 oniazid, nefazodone, phenelzine, imipramine, amitriptyline, duloxetine, bupropion, trazodone, tianept
52                                         This amitriptyline effect is opposite to the inhibition of GA
53 es that the mixed action antidepressant drug amitriptyline enhances norepinephrine (NE) release by tr
54 pressant treatment is similar among users of amitriptyline, fluoxetine, and paroxetine compared with
55    Administration of the antidepressant drug amitriptyline for 1 day or 14 days to rats significantly
56 group vs 6.8 for the headache education plus amitriptyline group (difference, 4.7 [95% CI, 1.7-7.7] d
57 than 20 points were assigned to the CBT plus amitriptyline group (n = 64) or the headache education p
58 roup (n = 64) or the headache education plus amitriptyline group (n = 71).
59  vs. 14%) and dry mouth (25% vs. 12%) in the amitriptyline group and paresthesia (31% vs. 8%) and wei
60                        Three patients in the amitriptyline group had serious adverse events of altere
61 adache were reduced by 11.5 for the CBT plus amitriptyline group vs 6.8 for the headache education pl
62 0.11 to 0.12; P=.88) and for patients in the amitriptyline group vs those in the placebo group was -0
63 in the primary efficacy analysis (132 in the amitriptyline group, 130 in the topiramate group, and 66
64 which occurred in 52% of the patients in the amitriptyline group, 55% of those in the topiramate grou
65  compounded topical gel containing baclofen, amitriptyline HCL, and ketamine, these agents may be off
66  index antidepressant prescription including amitriptyline hydrochloride, bupropion hydrochloride, ci
67 ssigned to receive tricyclic antidepressant (amitriptyline hydrochloride, up to 100 mg/d, or nortript
68  difenoxin) and the tricyclic antidepressant amitriptyline improve continence in patients with diarrh
69 f this study was to evaluate the efficacy of amitriptyline in children with pain-predominant function
70 ve immunoassay for the detection of the drug amitriptyline in human serum.
71 he model was fitted to the concentrations of amitriptyline in plasma and the heart.
72 om protonated nordoxepin, nortriptyline, and amitriptyline increase almost 1 order of magnitude acros
73       Furthermore, chronic administration of amitriptyline increases stimulation-evoked NE release an
74                                Of relevance, amitriptyline-induced ASMase inhibition in human hepatoc
75                      Treatment of pRBCs with amitriptyline inhibited acid sphingomyelinase activity,
76                      Treatment of pRBCs with amitriptyline inhibited acid sphingomyelinase activity,
77                                              Amitriptyline is a common antidepressant; however, it ha
78 t for the analysis of verapamil, citalopram, amitriptyline, lidocaine, and sunitinib in dried blood s
79                                      Neither amitriptyline nor escitalopram appeared to affect GE or
80                                              Amitriptyline, nortriptyline, desipramine, clomipramine,
81 tion for the following nine antidepressants: amitriptyline, nortriptyline, desipramine, clomipramine,
82 rison (125 in the factorial option and 11 in amitriptyline option vs placebo option).
83                            Co-application of amitriptyline or bupivacaine, which targeted the LA rece
84 ated after transfusion of pRBCs treated with amitriptyline or from acid sphingomyelinase-deficient mi
85 ated after transfusion of pRBCs treated with amitriptyline or from acid sphingomyelinase-deficient mi
86 l, 2.1 to 2.8) for doses of 50 mg or more of amitriptyline or its equivalent, and for the serotonin-r
87                        Patients who received amitriptyline or topiramate had higher rates of several
88 omly assigned to groups given placebo, 50 mg amitriptyline, or 10 mg escitalopram for 10 weeks.
89  double-blind 2 x 2 factorial design of SAR, amitriptyline, or the combination compared with placebo,
90 15% and good in 35% of children treated with amitriptyline (P = .85).
91 were investigated for three different drugs: amitriptyline, promethazine, and methadone.
92  treatment of wt mice with the Asm inhibitor amitriptyline recapitulated the phenotype of Asm-deficie
93                                              Amitriptyline reduced anxiety scores (P < .0001).
94                               Treatment with amitriptyline reduces MP generation in vitro and in vivo
95 y after 2002, while rates for fluoxetine and amitriptyline remained stable.
96 s with chronic migraine, the use of CBT plus amitriptyline resulted in greater reductions in days wit
97  and successfully developed and validated as Amitriptyline sensor using cyclic voltammetry (CV), chro
98 tine (SMD, -1.33 [CrI, -1.82 to -0.86]), and amitriptyline (SMD, -0.72 [CrI, -1.35 to -0.08]) were mo
99 amate (SMD, 0.20; 95% CI, -0.36 to 0.76), or amitriptyline (SMD, 0.29; 95% CI, -0.17 to 0.76).
100 ed 36Cl- response to GABA in the presence of amitriptyline that is increased by flumazenil, unlike au
101 ty in childhood and adolescent migraine with amitriptyline, topiramate, or placebo over a period of 2
102 ) but is similar to that seen in tissue from amitriptyline-treated rats or dominant rats.
103                                              Amitriptyline treatment from midlife preserved water maz
104 ged male Lister hooded rats (16 months) with amitriptyline until they were 24 months of age, and thei
105 trol points, or (3) a double-blind design of amitriptyline vs placebo.
106 roup, and 61% of those in the placebo group (amitriptyline vs. placebo, P=0.26; topiramate vs. placeb
107 ebo, P=0.26; topiramate vs. placebo, P=0.48; amitriptyline vs. topiramate, P=0.49).
108               The total cardiac clearance of amitriptyline was calculated as 0.316 L/h.
109       In this study, neither acupuncture nor amitriptyline was more effective than placebo in relievi
110            The combination of fluoxetine and amitriptyline was reported to be more beneficial than ei
111            Subjects with ulcer-like FD given amitriptyline were >3-fold more likely to report adequat

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