Zobrazeno 1 - 10
of 19
pro vyhledávání: '"William J. Rusho"'
Autor:
Jianxing Zhang, Xiaoyu Xu, Narayanam V Rao, Brian Argyle, Lindsi McCoard, William J Rusho, Thomas P Kennedy, Glenn D Prestwich, Gerald Krueger
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e16658 (2011)
Rosacea is a common disfiguring skin disease of primarily Caucasians characterized by central erythema of the face, with telangiectatic blood vessels, papules and pustules, and can produce skin thickening, especially on the nose of men, creating rhin
Externí odkaz:
https://doaj.org/article/66cb7a2b996f4befaeaaf8e2803a99e3
Publikováno v:
American Journal of Health-System Pharmacy. 62:1969-1976
Vasopressin is a peptide hormone that is released by the hypothalamus in response to decreases in blood pressure and blood volume.[1][1] Previously, the most common therapeutic use for vasopressin was the treatment of variceal hemorrhage.[2][2] This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a3ecbf3bd2123d597764f07929ae1a5
https://doi.org/10.2146/ajhp040267
https://doi.org/10.2146/ajhp040267
Autor:
William J. Rusho
Publikováno v:
Journal Of Pain & Palliative Care Pharmacotherapy. 18:69-76
The United States Pharmacopeia (USP) is the United States' congressionally authorized book of standards for pharmaceutical manufacturing in the United States. The most current edition of the USP includes a new chapter entitled Pharmaceutical Compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b09380fdf638302f02cff8faff45412
https://doi.org/10.1300/j354v18n04_08
https://doi.org/10.1300/j354v18n04_08
Publikováno v:
The Journal of Pediatric Pharmacology and Therapeutics. 10:36-42
OBJECTIVES Commercially available lorazepam solution contains both polyethylene glycol (PEG) and propylene glycol. When large doses are administered for deep sedation in the pediatric intensive care unit (PICU), PEG may cause diarrhea, and the accumu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d04f65ad330b7b760203cd351b4b0613
https://doi.org/10.5863/1551-6776-10.1.36
https://doi.org/10.5863/1551-6776-10.1.36
Autor:
William J. Rusho, Zohre Najari
Publikováno v:
American Journal of Health-System Pharmacy. 54:181-184
The Y-site compatibility of medications routinely used in bone marrow transplant patients was studied. Two methods were used to evaluate the compatibility of pairs of various i.v. drugs and nutrient fluids. In the first, the drugs were combined in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4968b927c34679c51efb41bd37063100
https://doi.org/10.1093/ajhp/54.2.181
https://doi.org/10.1093/ajhp/54.2.181
Publikováno v:
American Journal of Health-System Pharmacy. 53:2185-2188
The compatibility of cefmetazole sodium and selected other drugs during Y-site delivery was evaluated. Cefmetazole 100 mg/mL (as the sodium salt) in sterile water for injection and each of 34 drugs or solutions commonly used with it were mixed togeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5611935483224c0365d5d712ed868fa
https://doi.org/10.1093/ajhp/53.18.2185
https://doi.org/10.1093/ajhp/53.18.2185
Autor:
William J. Rusho
Publikováno v:
Journal of Pharmaceutical Care in Pain & Symptom Control. 4:5-20
Extemporaneous compounding of medication dosage forms has increased dramatically in the past two decades. The rapid growth of hospice care and other specialized patient care services has increased the demand for patient-specific dosage forms that are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3d6706344a61da412787f4a73583ead
https://doi.org/10.1300/j088v04n04_02
https://doi.org/10.1300/j088v04n04_02
Publikováno v:
American Journal of Health-System Pharmacy. 59:853-855
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::952343f6c2f6c8590fa1cb815653b79c
https://doi.org/10.1093/ajhp/59.9.853
https://doi.org/10.1093/ajhp/59.9.853
The objective of this study was to determine the chemical stability of extemporaneously prepared lorazepam suspension (1 mg/mL) stored at two temperatures (4°C and 22°C) for 3 months. Lorazepam tablets marketed by two manufacturers (Mylan Pharmaceu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::562858fefed3f41484905ba28bd1c5b1
https://europepmc.org/articles/PMC3469120/
https://europepmc.org/articles/PMC3469120/
Publikováno v:
American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists. 57(15)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebe5a23ed913dde8e4cad38d5b27a090
https://pubmed.ncbi.nlm.nih.gov/10938984
https://pubmed.ncbi.nlm.nih.gov/10938984