INT158083
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
AAS are found in both cities and smaller communities [3]. | |||||||||||||||
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The development of late combined drug use starting with AAS | |||||||||||||||
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One important finding was that most AAS users generally expressed a positive view about the effects of AAS. | |||||||||||||||
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The development of oscillating drugs of abuse and AAS use | |||||||||||||||
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By the age of 25, after five years of AAS abuse, he was tested for AAS use at the gym at which he trained. | |||||||||||||||
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Altogether, John was taking fourteen human and veterinary AAS products during a period of five years (oral: oxymetholone, stanozolol, methandrostenolone and methenolone acetate; injected: trenbolone acetate, testosterone blends, boldenone, nandrolone esters, methenolone and stanozolol). | |||||||||||||||
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An important finding in this study is that most of the patients describe their early experiences of AAS as definitely positive, perhaps even as the best time of their lives. | |||||||||||||||
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Early on in her AAS use, she also used ephedrine and other preparations to reduce subcutaneous fat and fluid in the muscles (e.g. bronchodilators and a drug which contained a combination of ephedrine, caffeine and aspirin). | |||||||||||||||
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In the six years during which she used hormones, she used four different types of AAS (oral: methandrostenolone and stanozolol; injected: methenolone enanthate and stanozolol). | |||||||||||||||
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The first AAS he bought was a testosterone product that was to be injected into the buttock. | |||||||||||||||
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One important finding was that most AAS users generally expressed a positive view about the effects of AAS. | |||||||||||||||
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The presence of AAS, which may indicate an early phase of allodynia, did not influence the efficacy of almotriptan therapy.
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"We usually do not pay for palpation, measuring blood pressure and weight, but do pay 200 shillings for laboratory test for urine, malaria, amount of blood, and ANC cards and this applies to government and private health facilities" (FGD participants, Kitomondo village, Mkuranga) | |||||||||||||||
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INTERVENTION: PCS or AAS using PR. | |||||||||||||||
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Each FGD comprised eight participants (only one FGD had seven people) and lasted for almost two hours. | |||||||||||||||
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Each FGD comprised eight participants (only one FGD had seven people) and lasted for almost two hours. | |||||||||||||||
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In addition to affording AAS induced renal impairment investigations, animal models will facilitate controlled comparative pharmacokinetic studies of short and long term AAS exposure in mice. | |||||||||||||||
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UGTs not only contribute to AAS glucuronidation but they also act as conjugating enzymes for various other pharmaceutical drugs [35,43]. | |||||||||||||||
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More research on AAS metabolism in the presence of UGT2B17 gene deletion is required. | |||||||||||||||
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The occurrence of renal disorders among AAS users | |||||||||||||||
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General Comments
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