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1 occasions, in the presence and absence of a nicotine patch.
2 curred in 1993 after the introduction of the nicotine patch.
3 rse event rates between e-cigarettes and the nicotine patch.
4 be as effective for smoking cessation as the nicotine patch.
5 utcomes for smoking cessation treatment with nicotine patch.
6 Single-dose (21- or 35-mg) nicotine patch.
7 eutical company could market its transdermal nicotine patch.
8 human smokers or in users of the transdermal nicotine patch.
9 human smokers or in users of the transdermal nicotine patch.
10 nd in smokers or in users of the transdermal nicotine patch.
11 g (12.6 +/- 10.1%) and 21-mg (11.8 +/- 9.9%) nicotine patches.
12 king and during treatment with 14- and 21-mg nicotine patches.
13 ine and during treatment with at least 14-mg nicotine patches.
14 ents with ADNFLE who use tobacco products or nicotine patches.
15 (odds ratio [OR] 3.61, 95% CI 3.07 to 4.24), nicotine patch (1.68, 1.46 to 1.93), and bupropion (1.75
16 245 of 2006 participants]), abnormal dreams (nicotine patch, 12% [251 of 2022 participants]), and hea
18 assigned to 8 weeks of treatment with active nicotine patches (15 mg per 16 hours) or matched placebo
19 l-free quitline were sent a 6-week course of nicotine patches (2 weeks each of 21 mg, 14 mg, and 7 mg
20 and C-NRT, 26.8% [113/421]) or at 52 weeks (nicotine patch, 20.8% [50/241]; varenicline, 19.1% [81/4
21 t fast event-related fMRI twice: once with a nicotine patch (21 mg) and once with a placebo patch.
22 y, placebo-controlled and active-controlled (nicotine patch; 21 mg per day with taper) trial of varen
23 ing point-prevalence abstinence at 26 weeks (nicotine patch, 22.8% [55/241]; varenicline, 23.6% [100/
24 ustained-release bupropion (244 subjects), a nicotine patch (244 subjects), bupropion and a nicotine
25 cotine patch (244 subjects), bupropion and a nicotine patch (245 subjects), and placebo (160 subjects
27 e patch+denicotinized cigarette smoking, (2) nicotine patch+abstinence from smoking, (3) placebo patc
29 f placebo (placebo pill plus placebo patch), nicotine patch (active patch plus placebo pill), or vare
30 ers and control subjects, implies that acute nicotine patch administration is insufficient to modify
32 ned to one of three double-blind treatments: nicotine patch alone (control condition); "rescue" treat
33 ence rates at end of treatment were 16% with nicotine patch alone and 28% with bupropion augmentation
34 have failed to achieve abstinence if left on nicotine patch alone by identifying these smokers before
35 blocked randomization to receive either the nicotine patch alone for a standard 10-week, tapering co
38 d efficacy of varenicline and bupropion with nicotine patch and placebo in smokers with and without p
39 omised, placebo-controlled efficacy trial of nicotine patches and a survey of associated resource use
41 on physician time and the retail cost of the nicotine patch, and benefits were based on quality-adjus
42 Varenicline was more effective than placebo, nicotine patch, and bupropion in helping smokers achieve
43 easons and cessation treatments, such as the nicotine patch, are preferentially beneficial to men.
45 involving more intensive counseling and the nicotine patch as adjuvant therapy are particularly meri
46 vide support both for the routine use of the nicotine patch as an adjunct to physicians' smoking cess
48 o did not respond adequately to precessation nicotine patch benefited from bupropion augmentation; ab
49 The incremental cost-effectiveness of the nicotine patch by age group ranged from $4390 to $10 943
51 with varenicline and slow metabolisers with nicotine patch could optimise quit rates while minimisin
52 29 adult smokers across four conditions: (1) nicotine patch+denicotinized cigarette smoking, (2) nico
54 idence interval (CI) excluded an effect from nicotine patches equal to that from cigarette smoking it
55 l subjects received 8 weeks of a transdermal nicotine patch, five group counseling sessions, and acti
56 ed more frequent adverse events than did the nicotine patch for vivid dreams, insomnia, nausea, const
58 he bupropion group, 25 (2.5%) of 1006 in the nicotine patch group, and 24 (2.4%) of 999 in the placeb
59 he bupropion group, 53 (5.2%) of 1016 in the nicotine patch group, and 50 (4.9%) of 1015 in the place
60 n the placebo group (3.8 percent), 16 in the nicotine-patch group (6.6 percent), 29 in the bupropion
61 group, as compared with 16.4 percent in the nicotine-patch group, 30.3 percent in the bupropion grou
62 kg, as compared with a gain of 1.6 kg in the nicotine-patch group, a gain of 1.7 kg in the bupropion
64 tment, varenicline was more efficacious than nicotine patch in normal metabolisers (OR 2.17, 95% CI 1
67 sation clinical trials and were treated with nicotine patch (n=623), nicotine nasal spray (n=189), bu
69 pering course (n = 64) or the combination of nicotine patch, nicotine oral inhaler, and bupropion ad
71 If GPs were allowed to prescribe transdermal nicotine patches on the NHS, for up to 12 weeks, the inc
72 moking cessation pharmacotherapy groups: (1) nicotine patch only (n = 241); (2) varenicline only (inc
74 roxycotinine:cotinine), predicts response to nicotine patch or varenicline for smoking cessation.
77 ith those reported in previous research, the nicotine patch plus lozenge produced the greatest benefi
79 nicotine patch, sustained-release bupropion, nicotine patch plus nicotine lozenge, bupropion plus nic
81 ase bupropion alone or in combination with a nicotine patch resulted in significantly higher long-ter
84 he effect of smoking cessation (3 weeks) and nicotine patch supplementation, (4) the effect of aspiri
85 of 6 treatment conditions: nicotine lozenge, nicotine patch, sustained-release bupropion, nicotine pa
86 dult smokers from the general population for nicotine patch therapy and based the patch dosage on smo
87 hs was more effective than standard-duration nicotine patch therapy for outpatient smokers with medic
89 Of those subjects not smoking at the end of nicotine patch therapy who entered the relapse preventio
97 daily) or placebo, as well as eight weeks of nicotine-patch therapy (21 mg per day during weeks 2 thr
99 of 606 cigarette smokers started open-label nicotine patch treatment 2 weeks before the quit date.
100 moking cessation treatment strategy in which nicotine patch treatment was initiated before a quit dat
101 how a sufficient initial response to prequit nicotine patch treatment, combination treatment with var
105 t per life year saved by GP counselling with nicotine-patch treatment over GP counselling alone.
107 oking, 12 weeks of open-label treatment with nicotine patch, varenicline, or C-NRT produced no signif
108 on initial therapeutic response, either the nicotine patch was continued or alternative pharmacother
109 ho abstained from smoking, the OR for use of nicotine patches was 0.25 (95% CI: 0.01, 1.67); among th
110 , respectively; the RDs for comparisons with nicotine patch were -1.07 (-2.21 to 0.08) and 0.13 (-1.1
111 -0.24 to 3.81), respectively; the RDs versus nicotine patch were 1.22 (-0.81 to 3.25) and 1.42 (-0.63
115 way to use NRT is to combine the long-acting nicotine patch with a shorter-acting product (lozenge, g
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