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1 the effect of treatment with prednisolone or pentoxifylline.
2 a group that received both prednisolone and pentoxifylline.
3 eceiving prednisolone; 546 were treated with pentoxifylline.
4 ich was less frequent in the group receiving pentoxifylline.
5 chloride] but not by the TNF-alpha inhibitor pentoxifylline.
6 (1501-S) and the oxidized side chain analog, pentoxifylline.
7 penicillin; 4 patients were not treated with pentoxifylline.
8 -controlled study of adjunctive therapy with pentoxifylline (1800 mg/day) as a timed-release formulat
9 mg of prednisolone once a day and 400 mg of pentoxifylline 3 times a day (n=133) for 28 days, or 40
11 nty-nine patients were randomized to receive pentoxifylline 400 mg p.o. t.i.d. or matching placebo fo
12 treatment with prednisolone (40 mg daily) or pentoxifylline (400 mg 3 times each day) in patients wit
15 2 and were receiving continuous therapy with pentoxifylline 800 mg 3 times a day and ciprofloxacin 50
16 apsing fever were infused intravenously with pentoxifylline 90 min before intramuscular injection of
17 estigated on pulmonary arterial responses to pentoxifylline, acetylcholine, and isoproterenol during
20 o determine whether or not administration of pentoxifylline after trauma-hemorrhagic shock has any sa
21 mortality; low quality evidence showed that pentoxifylline also decreased short-term mortality (RR,
23 lline-matched placebo, a group that received pentoxifylline and a prednisolone-matched placebo, or a
26 Based on direct and network meta-analysis, pentoxifylline and obeticholic acid improve fibrosis, an
28 h alcoholic hepatitis, 4-week treatment with pentoxifylline and prednisolone, compared with prednisol
31 icantly reduced the vasodilator responses to pentoxifylline and to acetylcholine, whereas NG-L-nitro-
32 Inhibitors of TNF-alpha production (GM6001, pentoxifylline) and TNF-alpha Ab's reduced serum and kid
34 the perfusion-modifying drugs nicotinamide, pentoxifylline, and hydralazine were used to manipulate
35 harmacologic interventions (corticosteroids, pentoxifylline, and N-acetylcysteine [NAC], alone or in
36 oderate-quality evidence supports that TZDs, pentoxifylline, and obeticholic acid decrease lobular in
37 h as progestational agents, cyproheptadines, pentoxifylline, and thalidomide may work by down-regulat
47 present data also suggest that responses to pentoxifylline during increased tone conditions may, in
48 injection of a TNFalpha synthesis inhibitor, pentoxifylline, during skin tumor promotion completely p
49 ately incubated in the sampling syringe with pentoxifylline, erythro-9-(2-hydroxy-3-nonyl) adenine, a
52 odestly between baseline and 6 months in the pentoxifylline group, but not in the placebo group, and
56 odulators, and more recently thalidomide and pentoxifylline have been used to treat BD with varying d
57 s fed the high-protein liquid diet and given pentoxifylline in a dose of 5 mg/kg/day demonstrated imp
59 early reports of renal protective effects of pentoxifylline in bone marrow transplant recipients prom
63 rsus-host disease prophylaxis with steroids, pentoxifylline, intravenous immunoglobulin, and total bo
65 one of four groups: a group that received a pentoxifylline-matched placebo and a prednisolone-matche
66 bo, a group that received prednisolone and a pentoxifylline-matched placebo, a group that received pe
68 ilable in patients with type 1 HRS, although pentoxifylline may be effective to treat HRS in patients
70 of malignant cells with the c-Rel inhibitor pentoxifylline not only reduced c-Rel nuclear translocat
71 tions (prednisone plus creatine inhibited by pentoxifylline) of combinatorial therapies taken by some
74 a was attenuated by administration of either pentoxifylline or anti-TNF-alpha serum, and liver injury
75 rticosteroids (alone and in combination with pentoxifylline or NAC) can reduce short-term mortality.
77 paring vitamin E, thiazolidinediones (TZDs), pentoxifylline, or obeticholic acid to one another or pl
80 nical use of the methyl xanthine derivative, pentoxifylline (PF), for the treatment of T cell-depende
81 acebo group, 19% (50 of 258 patients) in the pentoxifylline-placebo group, and 13% (35 of 260 patient
83 s, 6-month survival was not different in the pentoxifylline-prednisolone and placebo-prednisolone gro
84 onths was not significantly different in the pentoxifylline-prednisolone and the placebo-prednisolone
90 ctive, randomized trial to determine whether pentoxifylline (PTF), which reduces albuminuria, in addi
91 ategy using two PKC (NF-kappa B) inhibitors, pentoxifylline (PTX) and Go-6976, and a stably expressed
95 of this study was to compare the effects of pentoxifylline (PTX) versus placebo on the histological
97 ntiangiogenic potential of an existing drug, pentoxifylline (PTX), which inhibits PKC-dependent activ
99 oderate-quality evidence supports the use of pentoxifylline (RR, 0.26; 95% CrI: 0.05-1.00) and obetic
100 val [CrI], 0.39-0.73) or in combination with pentoxifylline (RR, 0.53; 95% CrI, 0.36-0.78) or NAC (RR
103 of this study was to evaluate the ability of pentoxifylline to alter gut cytokine production in a rat
108 was also inhibited by both dexamethasone and pentoxifylline, two pharmacological agents with potentia
109 The odds ratio for 28-day mortality with pentoxifylline was 1.07 (95% confidence interval [CI], 0
110 medications such as S-adenosylmethionine and pentoxifylline will need further confirmation by additio
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