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1 ff-label use of sedative antihistamines (eg, promethazine).
2 ; N-(4-aminobutyl)-1-naphthalenesulfonamide; promethazine; 2-[N-(4-methoxybenzenesulfonyl)]amino-N-(4
3 und no difference between metoclopramide and promethazine after 24 hours (episodes of vomiting, 1 [IQ
4 The analytical approach was then applied to promethazine, an FDA-approved drug previously shown to i
7 uate nutrition; ondansetron, metoclopramide, promethazine, and intravenous glucocorticoids may be req
9 or moderate symptoms, pyridoxine-doxylamine, promethazine, and metoclopramide were associated with gr
10 ophotometric method could be developed using promethazine as a chromogenic reagent to accurately quan
11 phenothiazine neuroleptics (chlorpromazine & promethazine) as additive neuroprotectants, with the aim
12 lline, CGP35348 (GABAB receptor antagonist), promethazine, atropine, d-tubocurarine and suramin had n
13 These results support the hypothesis that promethazine can be effectively used in a sustainable sp
15 aneous quantitative analysis of three drugs (promethazine, enalapril, and verapamil) using deuterated
16 er MB derivatives, 2-chlorophenothiazine and promethazine, exert no effect on cellular bioenergetics
17 emetics with lesser QT-prolonging potential (promethazine, metoclopramide, or prochlorperazine) and t
18 e-claims database (n = 364 733), exposure to promethazine, one of the candidate drugs, was associated
19 CTs compared corticosteroids with placebo or promethazine or metoclopramide in women with severe symp
20 0-5] for metoclopramide vs 2 [IQR, 0-3] for promethazine [P = .81], VAS [0-10 scale] for nausea, 2 [
22 ns (pH 7) in the presence of chlorpromazine, promethazine, procaine, and dextromethorphan, frequently
23 dium, potassium bromate was found to oxidize promethazine, producing a red-colored compound with maxi
25 oxidized forms, while for chlorpromazine and promethazine the suppression of the cocaine signal is re
26 loratadine and simvastatin and tegaserod and promethazine were predicted to have a strong DDI through
27 (N-(6-aminohexyl)-1-naphthalenesulfonamide; promethazine), were also found to block activation of th
28 general structural class that inhibits mPT, promethazine, were protective in both in vitro and mouse