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1 es the gastrointestinal safety advantages of etodolac.
2 t upper gastrointestinal (CSUGI) events with etodolac.
3 creased event rates with naproxen 2-fold and etodolac 9-fold.
4  associated with a pretreatment regimen with etodolac, a nonsteroidal anti-inflammatory drug (NSAID),
5                                            R-etodolac also induces apoptosis against primary cells is
6                                            R-etodolac also inhibits viability of MM cells adherent to
7 mary outcome was the CSUGI event rate of the etodolac and naproxen groups without concomitant low-dos
8 ence in gastrointestinal event rates between etodolac and naproxen when low-dose aspirin was taken co
9 g of a nonsteroidal antiinflammatory drug (R-etodolac), at concentrations that increased apoptosis of
10         Our data, therefore, indicate that R-etodolac circumvents drug resistance in MM cells at clin
11                    The apoptotic effect of R-etodolac could be controlled by manipulating cellular RX
12                              Patients in the etodolac group received two 300 mg capsules 30 minutes p
13 y, neither IL-6 nor IGF-1 protects against R-etodolac-induced cytotoxicity in MM cells.
14      Immunoblot analysis demonstrates that R-etodolac induces apoptosis characterized by caspase-8, -
15 er of the nonsteroidal antiinflammatory drug etodolac inhibited tumor development and metastasis in t
16                                              Etodolac is a generic COX-2 selective inhibitor that red
17                                              Etodolac is a generic nonsteroidal anti-inflammatory dru
18    Previous in vitro studies have shown that etodolac is a selective inhibitor of cyclooxygenase (COX
19 g of the nonsteroidal anti-inflammatory drug etodolac, known as SDX-308, and its effects on osteoclas
20 teran patients (5596 patient-years) received etodolac or naproxen during a 3-year period without conc
21 GI events was .78% and .24% for naproxen and etodolac, respectively.
22 GI events was .99% and .24% for naproxen and etodolac, respectively.
23               In this study we report that R-etodolac (SDX-101), at clinically relevant concentration
24                                            R-etodolac specifically bound recombinant RXRalpha, inhibi
25  the first postsurgical dose was greater for etodolac than for the combination drug.
26      SDX-101 is another structural analog of etodolac that is already used in clinical trials for the
27                      Subcytotoxic doses of R-etodolac up-regulate myeloid cell leukemia-1 proapoptoti
28                      Compared with naproxen, etodolac was associated with a reduction in upper gastro
29                         The combination of R-etodolac with Dex results in a highly synergistic cytoto

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