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1 ve lumbar nerve blocks with triamcinolone or betamethasone.
2 ng volumes for two, three, and four doses of betamethasone.
3 volume after fetal exposure to four doses of betamethasone.
4 ncreased risk of neonatal hypoglycemia after betamethasone.
5 ive dose was equivalent to 15 (IQR 10-19) mg betamethasone.
9 rse were randomly assigned to receive either betamethasone, 12 mg intramuscularly repeated once in 24
10 course of antenatal corticosteroids (either betamethasone, 12 mg intramuscularly repeated once in 24
12 Of 2831 children, 1026 enrolled and 949 (479 betamethasone, 470 placebo) completed the DAS-II at a me
13 e patients received a mixture of 1 mL of the betamethasone, 6 mg/mL, and 1 mL of 0.5% bupivacaine hyd
14 ture of betamethasone-phosphate (Beta-P) and betamethasone-acetate (Beta-Ac) - the clinical drug.
19 ys) were included in the cohort: 475 with no betamethasone and 1331 with exposure to a single dose of
20 drift-times for the protonated diastereomers betamethasone and dexamethasone are reproducibly differe
22 cific differences, if any, in the actions of betamethasone and dexamethasone of measured fetal respon
27 ts of fetal treatment with clinical doses of betamethasone and dexamethasone; (2) define specific dif
28 ric changes in the lungs of lambs exposed to betamethasone and T4 48 h before preterm delivery at 121
31 d 76% at 2 weeks with vehicle, pimecrolimus, betamethasone, and clobetasol, respectively, with parall
33 isrupted serotonin signalling and identified betamethasone as a drug which normalises the excessive d
34 the United States by finding that antenatal betamethasone at 34 to 36 weeks decreased short-term neo
35 domized to receive saline (controls) or 6 mg betamethasone (beta) 48 and 24 h before delivery at 125
37 flexion spasms based on prenatal exposure to betamethasone combined with postnatal administration of
39 were randomly assigned to weekly courses of betamethasone, consisting of 12 mg given intramuscularly
40 xpectedly high percentage of those receiving betamethasone-containing dermatologic preparations had d
44 igator site daily for 14 days: pimecrolimus, betamethasone dipropionate, clobetasol propionate, and a
46 12/group) that were chronically treated with betamethasone (glucocorticoid receptor agonist) or vehic
47 s farinae were divided into six groups: 1) a betamethasone group (betamethasone ointment, six times a
48 curred in 165 of 1427 infants (11.6%) in the betamethasone group and 202 of 1400 (14.4%) in the place
49 Neonatal hypoglycemia was more common in the betamethasone group than in the placebo group (24.0% vs.
50 ) in the placebo group (relative risk in the betamethasone group, 0.80; 95% confidence interval [CI],
54 lubricating gel and drops, chloramphenicol, betamethasone, homatropine, oral vitamin C, and doxycycl
55 emonstrated that antenatal administration of betamethasone in the late preterm period (between 34 to
57 fants exposed to multiple doses of antenatal betamethasone, infants who did not receive intensive car
58 Following baseline, either saline (n = 9), betamethasone (n = 9), or dexamethasone (n = 6) was infu
60 ally, three times a week), 3) an FTY720 plus betamethasone ointment group, 4) an ointment base group
62 suggest that the combination of FTY720 plus betamethasone ointment is a promising candidate for trea
63 d into six groups: 1) a betamethasone group (betamethasone ointment, six times a week), 2) an FTY720
67 domized to receive 1 to 4 doses of 0.5 mg/kg betamethasone or saline placebo at 7 d intervals from 10
68 two intramuscular doses of a 1:1 mixture of betamethasone-phosphate (Beta-P) and betamethasone-aceta
69 , 42% of triamcinolone recipients and 58% of betamethasone recipients demonstrated improvement in low
70 , 42% of triamcinolone recipients and 53% of betamethasone recipients had improvement in low back pai
71 , 45% of triamcinolone recipients and 58% of betamethasone recipients had improvement in low back pai
72 s 49% of triamcinolone recipients and 55% of betamethasone recipients had improvement in lower extrem
73 s 52% of triamcinolone recipients and 57% of betamethasone recipients had improvement in lower extrem
74 s 55% of triamcinolone recipients and 57% of betamethasone recipients had lower extremity pain improv
75 the timing from administration of antenatal betamethasone to birth may reduce mortality and morbidit
80 tion and the effectiveness of prenatal MgSO4/betamethasone treatments between males and females in a
84 (Fingolimod), alone and in combination with betamethasone valerate ointment, in the NC/Nga mouse mod
86 than 85, which occurred in 82 (17.1%) of the betamethasone vs 87 (18.5%) of the placebo group (adjust
88 even short duration of exposure to antenatal betamethasone was associated with improved neonatal surv