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1 f patients with chemical gastritis caused by nonsteroidal antiinflammatory drugs.
2 ostaglandin synthesis and are the targets of nonsteroidal antiinflammatory drugs.
3  dipyrone, and is potently inhibited by some nonsteroidal antiinflammatory drugs.
4 ions in AERD patients following ingestion of nonsteroidal antiinflammatory drugs.
5  may receive both low-dose aspirin and other nonsteroidal antiinflammatory drugs.
6  effects of COX-1 inhibition associated with nonsteroidal antiinflammatory drugs.
7 l side effects of the indomethacin family of nonsteroidal antiinflammatory drugs.
8 de rate ratio of death was 0.68 for users of nonsteroidal antiinflammatory drugs.
9 al volunteers, even in the absence of recent nonsteroidal antiinflammatory drugs.
10 d arthritis (RA) and its response to chronic nonsteroidal antiinflammatory drugs.
11 enases (COXs) are the therapeutic targets of nonsteroidal antiinflammatory drugs.
12 rgery, 55% of patients received prescription nonsteroidal antiinflammatory drugs, 58% received opioid
13 ling to the macrophage inhibitory cytokine-1/nonsteroidal antiinflammatory drug-activated gene-1 prom
14 ted RNA for macrophage inhibitory cytokine-1/nonsteroidal antiinflammatory drug-activated gene-1, a T
15 oints or to conservative treatment (CT) with nonsteroidal antiinflammatory drugs alone.
16 ng antirheumatic drugs, corticosteroids, and nonsteroidal antiinflammatory drugs, alone or in combina
17        Twelve analogues of diclofenac (1), a nonsteroidal antiinflammatory drug and known inhibitor o
18 These enzymes are pharmacological targets of nonsteroidal antiinflammatory drugs and cyclooxygenase (
19 Recommendations for the perioperative use of nonsteroidal antiinflammatory drugs and glucocorticoids
20 n of >/=6 months and inadequate responses to nonsteroidal antiinflammatory drugs and glucocorticoids)
21 nd analgesic properties yet differs from the nonsteroidal antiinflammatory drugs and inhibitors of pr
22                            Stable dosages of nonsteroidal antiinflammatory drugs and low-dose prednis
23 ic drugs were discontinued; stable dosage of nonsteroidal antiinflammatory drugs and oral corticoster
24 hite blood cell count, and use of nonaspirin nonsteroidal antiinflammatory drugs and other medication
25 e in the induction of 15-LOX-1 expression by nonsteroidal antiinflammatory drugs and related agents.
26  AF-2 activity in cells were detected: three nonsteroidal antiinflammatory drugs and the thyroid horm
27                                 Therapy with nonsteroidal antiinflammatory drugs and traditionally us
28 ting for cardiovascular risk factors, use of nonsteroidal antiinflammatory drugs, and a history of ga
29 be induced by some medications, particularly nonsteroidal antiinflammatory drugs, and has been associ
30 nt angiotensin-converting enzyme inhibitors, nonsteroidal antiinflammatory drugs, and immunosuppressi
31 esophageal adenocarcinoma but did agree that nonsteroidal antiinflammatory drugs are associated with
32                                              Nonsteroidal antiinflammatory drugs are used in rheumato
33 indings are potentially game-changing in the nonsteroidal antiinflammatory drug arena.
34 ndin biosynthesis and are the targets of the nonsteroidal antiinflammatory drugs aspirin and ibuprofe
35 on of cyclooxygenases, the central action of nonsteroidal antiinflammatory drugs (but not a prominent
36 xplain the cancer chemoprotective effects of nonsteroidal antiinflammatory drugs by defining a mechan
37                                              Nonsteroidal antiinflammatory drugs can cause regression
38 of dosing with prednisolone, methotrexate, 3 nonsteroidal antiinflammatory drugs (celecoxib, diclofen
39 rrays of bioactive lipid mediators via COX-2-nonsteroidal antiinflammatory drug-dependent oxygenation
40                                    Important nonsteroidal antiinflammatory drug derivatives such as (
41                                              Nonsteroidal antiinflammatory drug enteropathy is a step
42 r hypoalbuminaemia are useful indications of nonsteroidal antiinflammatory drug enteropathy.
43                                              Nonsteroidal antiinflammatory drugs, especially Voltaren
44   Here, we show that the R-enantiomer of the nonsteroidal antiinflammatory drug etodolac inhibited tu
45 plexes of beta- and gamma-cyclodextrins with nonsteroidal antiinflammatory drugs ibuprofen, naproxen,
46  repair and create concerns about the use of nonsteroidal antiinflammatory drugs in patients with ske
47  inhibitors are as effective as nonselective nonsteroidal antiinflammatory drugs in relieving pain an
48      Aspirin is unique among clinically used nonsteroidal antiinflammatory drugs in that it irreversi
49                                              Nonsteroidal antiinflammatory drugs, including ibuprofen
50           It is unclear whether nonselective nonsteroidal antiinflammatory drugs increase or decrease
51 e reaction of three solid-state forms of the nonsteroidal antiinflammatory drug indomethacin with amm
52 f 2B5 was indistinguishable from that of the nonsteroidal antiinflammatory drug indomethacin, which b
53 tions, including inflammatory bowel disease, nonsteroidal antiinflammatory drug-induced gut injury, a
54 uch as capsule endoscopy studies demonstrate nonsteroidal antiinflammatory drug-induced small bowel e
55                                              Nonsteroidal antiinflammatory drugs inhibit the developm
56 tosis in human colon cancer cells by certain nonsteroidal antiinflammatory drugs involves increased e
57 3 effects to blockade by two analgesics (the nonsteroidal antiinflammatory drug ketoprofen and the mu
58                        Surprisingly, certain nonsteroidal antiinflammatory drugs known to shift the s
59 this disease, the chemopreventive effects of nonsteroidal antiinflammatory drugs may be related to th
60                                     Existing nonsteroidal antiinflammatory drugs may be safer than or
61 research suggests that rectally administered nonsteroidal antiinflammatory drugs may reduce the incid
62 of drugs that inhibit PG production, such as nonsteroidal antiinflammatory drugs, may be deleterious
63 gs that are widely used to treat OA, such as nonsteroidal antiinflammatory drugs, may have limited ef
64 rtitioning and nature of interactions of two nonsteroidal antiinflammatory drugs, namely aspirin and
65  epidemiological studies have shown that the nonsteroidal antiinflammatory drug naproxen may be usefu
66 tioxidant ester and amide derivatives of the nonsteroidal antiinflammatory drug naproxen was designed
67 management for Helicobacter pylori-negative, nonsteroidal antiinflammatory drug-negative ulcer patien
68 -116 colon cancer cells with and without the nonsteroidal antiinflammatory drug NS-398 or the histone
69 chronic arthritis: 1) a generic nonselective nonsteroidal antiinflammatory drug (NSAID(NS)) alone; 2)
70 ee OA underwent a washout of their analgesic/nonsteroidal antiinflammatory drug (NSAID) agents (durat
71 The present study compared the effect of the nonsteroidal antiinflammatory drug (NSAID) diclofenac, w
72 he small intestine is a more common site for nonsteroidal antiinflammatory drug (NSAID) toxicity than
73 abolite profiles but only modestly decreased nonsteroidal antiinflammatory drug (NSAID) turnover whil
74      The authors conducted a cohort study of nonsteroidal antiinflammatory drug (NSAID) use and risk
75                                              Nonsteroidal antiinflammatory drug (NSAID) use is a know
76            In the present study, sulindac, a nonsteroidal antiinflammatory drug (NSAID), was tested f
77     Analogues of diflunisal, an FDA-approved nonsteroidal antiinflammatory drug (NSAID), were synthes
78                                              Nonsteroidal antiinflammatory drug (NSAID)-associated ga
79                                     Aspirin, nonsteroidal antiinflammatory drugs (NSAID), and acetami
80 ces the effectiveness of both currently used nonsteroidal antiinflammatory drugs (NSAIDs) (diclofenac
81                            Among nonusers of nonsteroidal antiinflammatory drugs (NSAIDs) (Pinteracti
82 e cancer and whether use of aspirin or other nonsteroidal antiinflammatory drugs (NSAIDs) affects ris
83 hors used PSC to assess the relation between nonsteroidal antiinflammatory drugs (NSAIDs) and 1-year
84 ardiovascular risk, studies of nonselective, nonsteroidal antiinflammatory drugs (NSAIDs) and acetami
85                          Previous studies on nonsteroidal antiinflammatory drugs (NSAIDs) and breast
86 rs have reported an inverse relation between nonsteroidal antiinflammatory drugs (NSAIDs) and colon c
87 tive on patient preferences for nonselective nonsteroidal antiinflammatory drugs (NSAIDs) and cycloox
88     The association between long-term use of nonsteroidal antiinflammatory drugs (NSAIDs) and non-Hod
89 pidemiologic data on the association between nonsteroidal antiinflammatory drugs (NSAIDs) and ovarian
90  investigations have identified a variety of nonsteroidal antiinflammatory drugs (NSAIDs) and structu
91  prevented by a concurrent administration of nonsteroidal antiinflammatory drugs (NSAIDS) and/or low-
92 umatic diseases and because apparently safer nonsteroidal antiinflammatory drugs (NSAIDs) are being p
93                                              Nonsteroidal antiinflammatory drugs (NSAIDs) are commonl
94                                     Although nonsteroidal antiinflammatory drugs (NSAIDs) are ineffec
95                                              Nonsteroidal antiinflammatory drugs (NSAIDs) block prost
96 nal CCEs, whereas treatment with 2 different nonsteroidal antiinflammatory drugs (NSAIDs) blocked neu
97                                              Nonsteroidal antiinflammatory drugs (NSAIDs) can inhibit
98  It is well established that taking multiple nonsteroidal antiinflammatory drugs (NSAIDs) can lead to
99                                          The nonsteroidal antiinflammatory drugs (NSAIDs) continue to
100 ntrol studies have shown that regular use of nonsteroidal antiinflammatory drugs (NSAIDs) decreases b
101                                              Nonsteroidal antiinflammatory drugs (NSAIDs) form a para
102                                              Nonsteroidal antiinflammatory drugs (NSAIDs) have been r
103                       Here, we show that the nonsteroidal antiinflammatory drugs (NSAIDs) ibuprofen a
104                                     Although nonsteroidal antiinflammatory drugs (NSAIDs) in general
105                                          All nonsteroidal antiinflammatory drugs (NSAIDs) inhibit the
106    Epidemiologic studies suggest that use of nonsteroidal antiinflammatory drugs (NSAIDs) is associat
107 f cyclooxygenase-inhibiting (COX-inhibiting) nonsteroidal antiinflammatory drugs (NSAIDs) is often co
108                 The cardiovascular safety of nonsteroidal antiinflammatory drugs (NSAIDs) may be infl
109            Renal prostaglandin inhibition by nonsteroidal antiinflammatory drugs (NSAIDs) may decreas
110  (LUTS), raising the possibility that use of nonsteroidal antiinflammatory drugs (NSAIDs) may inhibit
111   Several studies have suggested that use of nonsteroidal antiinflammatory drugs (NSAIDs) may reduce
112         The potentially protective effect of nonsteroidal antiinflammatory drugs (NSAIDs) on prostate
113 ategies for knee monarthritis were compared: nonsteroidal antiinflammatory drugs (NSAIDs) only, NSAID
114 of nine measures of high-risk prescribing of nonsteroidal antiinflammatory drugs (NSAIDs) or selected
115 nd experimental studies suggests that use of nonsteroidal antiinflammatory drugs (NSAIDs) reduces ris
116 cal studies have shown that long-term use of nonsteroidal antiinflammatory drugs (NSAIDs) reduces the
117                                     Although nonsteroidal antiinflammatory drugs (NSAIDs) show great
118                             Both traditional nonsteroidal antiinflammatory drugs (NSAIDs) that inhibi
119 c has gastrointestinal liabilities common to nonsteroidal antiinflammatory drugs (NSAIDs) that might
120                                              Nonsteroidal antiinflammatory drugs (NSAIDs) transcripti
121 nnesota, to determine whether daily users of nonsteroidal antiinflammatory drugs (NSAIDs) were at low
122                                    Different nonsteroidal antiinflammatory drugs (NSAIDs) were used t
123 X inhibitors, including coxibs, nonselective nonsteroidal antiinflammatory drugs (NSAIDs), and meloxi
124 ibitors of prostaglandin production, such as nonsteroidal antiinflammatory drugs (NSAIDs), and pharma
125                            Acid suppression, nonsteroidal antiinflammatory drugs (NSAIDs), and statin
126 inuation for any reason did not differ among nonsteroidal antiinflammatory drugs (NSAIDs), but discon
127 s of other drugs, including D-penicillamine, nonsteroidal antiinflammatory drugs (NSAIDs), calcium ch
128  use of ODC inhibitors and aspirin, or other nonsteroidal antiinflammatory drugs (NSAIDs), in combina
129  of celecoxib, as compared with nonselective nonsteroidal antiinflammatory drugs (NSAIDs), remains un
130 tments for osteoarthritis (OA) pain, such as nonsteroidal antiinflammatory drugs (NSAIDs), simple ana
131                                              Nonsteroidal antiinflammatory drugs (NSAIDs), such as as
132 h as 5,8,11,14-eicosatetraynoic acid, and in nonsteroidal antiinflammatory drugs (NSAIDs), such as in
133 astrointestinal hemorrhage than nonselective nonsteroidal antiinflammatory drugs (NSAIDs), there has
134 ure on steroids is more limited than that on nonsteroidal antiinflammatory drugs (NSAIDs).
135 hromboxane and are the molecular targets for nonsteroidal antiinflammatory drugs (NSAIDs).
136 h fewer side effects than currently marketed nonsteroidal antiinflammatory drugs (NSAIDs).
137  body induction was inhibited by aspirin and nonsteroidal antiinflammatory drugs (NSAIDs).
138 hase isoform 1 (PGHS-1) is the target of the nonsteroidal antiinflammatory drugs (NSAIDs).
139                 Both isoforms are targets of nonsteroidal antiinflammatory drugs (NSAIDs).
140 ethotrexate (MTX), oral glucocorticoids, and nonsteroidal antiinflammatory drugs (NSAIDs).
141 iewed regarding the use of aspirin and other nonsteroidal antiinflammatory drugs (NSAIDs).
142 examined rectal cancer in relation to use of nonsteroidal antiinflammatory drugs (NSAIDs).
143 nd is the therapeutic target for widely used nonsteroidal antiinflammatory drugs (NSAIDs).
144 enase 2 inhibitors (coxibs) and nonselective nonsteroidal antiinflammatory drugs (NSAIDs).
145 e the most common undesirable effects of the nonsteroidal antiinflammatory drugs (NSAIDs).
146 atechins (naturally occurring flavonols) and nonsteroidal antiinflammatory drugs (NSAIDs).
147 or a growing proportion of prescriptions for nonsteroidal antiinflammatory drugs (NSAIDs).
148  coxibs and common active internal controls (nonsteroidal antiinflammatory drugs [NSAIDs], naproxen)
149 1 and COX-2 are both targets of nonselective nonsteroidal antiinflammatory drugs (nsNSAIDs) including
150 ity was apparent only among those not taking nonsteroidal antiinflammatory drugs (odds ratio = 0.49,
151 om colorectal cancer in individuals who take nonsteroidal antiinflammatory drugs on a regular basis c
152 al cancer in persons taking aspirin or other nonsteroidal antiinflammatory drugs on a regular basis.
153 nsistently indicated that sulindac and other nonsteroidal antiinflammatory drugs or cyclooxygenase in
154 wer or discontinue their background doses of nonsteroidal antiinflammatory drugs or disease-modifying
155                                       Use of nonsteroidal antiinflammatory drugs (OR = 1.7, 95% CI 1.
156 ct were long-term users of aspirin, ethanol, nonsteroidal antiinflammatory drugs, or a combination of
157  was found between the use of aspirin, other nonsteroidal antiinflammatory drugs, or acetaminophen an
158 ls are needed to determine whether steroids, nonsteroidal antiinflammatory drugs, or both can prevent
159     Patients were allowed to continue taking nonsteroidal antiinflammatory drugs, oral corticosteriod
160 s and adenocarcinomas, and its inhibition by nonsteroidal antiinflammatory drugs protects against col
161 n signaling was diminished by an analog of a nonsteroidal antiinflammatory drug (R-etodolac), at conc
162 ological and laboratory studies suggest that nonsteroidal antiinflammatory drugs reduce the risk of c
163                                              Nonsteroidal antiinflammatory drugs reduce the risk of c
164 ion was stronger among participants who used nonsteroidal antiinflammatory drugs regularly (highest v
165 ere noted at the start of therapy: age, sex, nonsteroidal antiinflammatory drug-related risk factors
166         Inhibition of the COX-2 component by nonsteroidal antiinflammatory drugs restored the apoptot
167 s technique to study the interactions of two nonsteroidal antiinflammatory drugs, salicylate and ibup
168 been applied to the analysis of a mixture of nonsteroidal antiinflammatory drugs separated by reverse
169                                              Nonsteroidal antiinflammatory drugs still remain mainsta
170  are pharmacologically important targets for nonsteroidal antiinflammatory drugs, such as aspirin and
171         Conversion of carboxylate-containing nonsteroidal antiinflammatory drugs, such as indomethaci
172 nt for the use or nonuse of aspirin or other nonsteroidal antiinflammatory drugs; the presence or abs
173     Indomethacin (INDO) was one of the first nonsteroidal antiinflammatory drugs to be characterized
174 mall intestine may be a more common site for nonsteroidal antiinflammatory drug toxicity than the gas
175                                              Nonsteroidal antiinflammatory drug toxicity to the small
176 s who had previously received treatment with nonsteroidal antiinflammatory drugs underwent stratifica
177 d beneficiaries in New Jersey, the effect of nonsteroidal antiinflammatory drug use on 1-year all-cau
178                      We investigated whether nonsteroidal antiinflammatory drug use was associated wi
179 dex, smoking, physical activity, aspirin and nonsteroidal antiinflammatory drug use, alcohol consumpt
180                        Two-thirds of regular nonsteroidal antiinflammatory drug users develop subclin
181 of antibiotics (primarily fluoroquinolones), nonsteroidal antiinflammatory drugs (Voltaren and ketoro
182 erence to study medications and avoidance of nonsteroidal antiinflammatory drugs were excellent.
183 , composition of fluids ingested, and use of nonsteroidal antiinflammatory drugs were not.
184  PsA and a history of inadequate response to nonsteroidal antiinflammatory drugs were randomized to r
185                                              Nonsteroidal antiinflammatory drugs, which inhibit COX-2

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