ライフサイエンスコーパス: hydromorphone

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1 em as well as on the material leading to ent-hydromorphone.

2 -day test sessions evaluated the response to hydromorphone (0, 6, and 18 mg intramuscular in random o

3 4526 to 3190), fentanyl (59%; 59 to 24), and hydromorphone (15%; 718 to 609), and increased for morph

4 , oxycodone (23%; 1.6 to 2.0 million g), and hydromorphone (19%; 118,455 to 141,325 g), and a decreas

5 derivatives of naltrexone, oxymorphone, and hydromorphone (4-9).

6 nans derived from naloxone, oxymorphone, and hydromorphone (7a-k) were synthesized and evaluated for

7 ncrease in cyanide generation was seen after hydromorphone administration and this increase was block

8 The finding that the hydromorphone analogues (8, 9) were full mu agonists and

9 202 participants; 100 randomized to receive hydromorphone and 102 to diacetylmorphine.

10 to receive intrathecal fentanyl or systemic hydromorphone at the first request for analgesia.

11 cond-generation approach to the synthesis of hydromorphone by oxidative dearomatization/Diels-Alder c

12 whom it is contraindicated or unsuccessful, hydromorphone could be offered as an alternative.

13 Among the ligands studied, the hydromorphone-derived 4-chlorophenylpyridomorphinan 7h w

14 response to NMDA similar to cyanide and the hydromorphone effect was blocked by cyanide scavengers.

15 produced immediate and sustained blockade of hydromorphone effects (liking maximum effect, CAM2038, 2

16 Hydromorphone enhanced the response to NMDA similar to c

17 n opioid analgesics: oxycodone, hydrocodone, hydromorphone, fentanyl, morphine, and tramadol.

18 ean differences between diacetylmorphine and hydromorphone for the ITT and PP analyses were reported.

19 idomorphinans possessing the oxymorphone and hydromorphone framework displayed nearly equal binding a

20 ship with the injection medication, 5 in the hydromorphone group and 24 in the diacetylmorphine group

21 To determine whether cyanide release by hydromorphone has functional significance in a neuronal

22 gnificantly increased by mu-opiate agonists (hydromorphone, morphine) and blocked by naloxone.

23 d opioids, including hydrocodone, oxycodone, hydromorphone, oxymorphone, and codeine.

24 ence to suggest noninferiority of injectable hydromorphone relative to diacetylmorphine for long-term

25 Systemic administration of hydromorphone to rats increased brain cyanide levels by

26 ed to receive injectable diacetylmorphine or hydromorphone (up to 3 times daily) for 6 months under s

27 The second-generation synthesis of hydromorphone was completed in both enantiomeric series.

28 ormal synthesis of the natural enantiomer of hydromorphone was completed.

29 Noninferiority of hydromorphone was confirmed in the PP analysis (-1.44; 9

30 s infusion narcotics (fentanyl, morphine, or hydromorphone) were used more frequently among patients

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