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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
10                 Relative to enprofylline 2b, pentoxifylline 35 was equipotent and 1-propylxanthine 3
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
13                                    Saline or pentoxifylline (5 or 20 mg/kg im) was administered daily
14                                              Pentoxifylline (50 mg/kg body weight) or an equivalent v
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
18                 Low-dose (but not high-dose) pentoxifylline administration reduced production of some
19                                              Pentoxifylline administration, however, significantly in
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,
22  failure; in animal models its blockade with pentoxifylline ameliorates AP.
23 lline-matched placebo, a group that received pentoxifylline and a prednisolone-matched placebo, or a
24                     Vasodilator responses to pentoxifylline and acetylcholine were not significantly
25                  In patients with severe AH, pentoxifylline and corticosteroids (alone and in combina
26   Based on direct and network meta-analysis, pentoxifylline and obeticholic acid improve fibrosis, an
27 ltration rate or creatinine was seen between pentoxifylline and placebo groups at any interval.
28 h alcoholic hepatitis, 4-week treatment with pentoxifylline and prednisolone, compared with prednisol
29                             The abilities of pentoxifylline and recombinant interleukin-10 (rIL-10) t
30                              Combinations of pentoxifylline and rIL-10 led to additive or synergistic
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
33             Clinical trials with cladibrine, pentoxifylline, and budesonide have failed to demonstrat
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
38                             Prednisolone and pentoxifylline are both recommended for the treatment of
39                            Administration of pentoxifylline at 5 mg/kg/day also down regulated the pr
40            Intraperitoneal administration of pentoxifylline before LPS inhibited TNF-alpha synthesis
41                                              Pentoxifylline consistently inhibited the accumulation o
42                           Patients receiving pentoxifylline demonstrated improved AROM, PROM, and mus
43 induced G2 arrest by treatment with the drug pentoxifylline did not abrogate apoptosis.
44                                              Pentoxifylline did not attenuate this process and had no
45                                              Pentoxifylline did not improve survival in patients with
46                                              Pentoxifylline did not prevent clearance of the B. recur
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
50                               Treatment with pentoxifylline failed to prevent fever, increase in puls
51                                          The pentoxifylline group had fewer intensive care unit admis
52 odestly between baseline and 6 months in the pentoxifylline group, but not in the placebo group, and
53 13% (35 of 260 patients) in the prednisolone-pentoxifylline group.
54                           Patients receiving pentoxifylline had no adverse effects.
55                         These data show that pentoxifylline has significant vasodilator activity in t
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
58  72 hours of pSAP is safe; a larger study of pentoxifylline in AP is needed to confirm efficacy.
59 early reports of renal protective effects of pentoxifylline in bone marrow transplant recipients prom
60                              The efficacy of pentoxifylline in predicted severe AP (pSAP) was tested
61                                              Pentoxifylline inhibits expression of TNF-alpha and HIV.
62                             After 8 weeks of pentoxifylline intervention, 20 of 23 patients with impa
63 rsus-host disease prophylaxis with steroids, pentoxifylline, intravenous immunoglobulin, and total bo
64                              Prednisolone or pentoxifylline is recommended for severe alcoholic hepat
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
67                   Emerging data suggest that pentoxifylline may also be beneficial in improving serum
68 ilable in patients with type 1 HRS, although pentoxifylline may be effective to treat HRS in patients
69                     A series of analogues of pentoxifylline metabolites were prepared in the purine,
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
72 , and a study showing the effect of systemic pentoxifylline on ocular blood flow and diabetes.
73 ected alveolar macrophages were treated with pentoxifylline or anti-TNF-alpha antibody.
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.
76 e randomized within 72 hours of diagnosis to pentoxifylline or placebo.
77 paring vitamin E, thiazolidinediones (TZDs), pentoxifylline, or obeticholic acid to one another or pl
78 nimals given the high dose (20 mg/kg/day) of pentoxifylline (p< .05).
79                                              Pentoxifylline (PF) has been used in a wide variety of c
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
82  postoperative days (POD) 1, 3, 5, and 7; or pentoxifylline pre-reperfusion and at POD 1 to 5.
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
85  block of JHR was attempted by administering pentoxifylline prior to antibiotic treatment.
86 rats with anticytokine agents, etanercept or pentoxifylline, produced very similar results.
87                                     Although pentoxifylline produces various beneficial effects follo
88                                              Pentoxifylline promotes gut ketogenesis following trauma
89                                              Pentoxifylline (PTF) inhibits synthesis of some cytokine
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
92                                              Pentoxifylline (PTX) directly decreases lung endothelial
93                                              Pentoxifylline (PTX) improved the histological features
94             Previous studies have shown that pentoxifylline (PTX) in combination with alpha-tocophero
95  of this study was to compare the effects of pentoxifylline (PTX) versus placebo on the histological
96       We hypothesized that administration of pentoxifylline (PTX), a phosphodiesterase inhibitor know
97 ntiangiogenic potential of an existing drug, pentoxifylline (PTX), which inhibits PKC-dependent activ
98                                              Pentoxifylline resulted in decreased plasma HIV RNA and
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
101                        New agents, including pentoxifylline, thalidomide, and infliximab have proved
102             There was no association between pentoxifylline therapy and the risk of serious infection
103 of this study was to evaluate the ability of pentoxifylline to alter gut cytokine production in a rat
104 10 appeared to interfere with the ability of pentoxifylline to block iNOS accumulation.
105                 The addition of NAC, but not pentoxifylline, to corticosteroids may be superior to co
106                                        Thus, pentoxifylline treatment of patients with relapsing feve
107 leukin 6, or interleukin-8 was observed with pentoxifylline treatment.
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
111                                              Pentoxifylline within 72 hours of pSAP is safe; a larger

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