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1 nulocytosis side effects associated with its long term use.
2 developed which would be more applicable for long-term use.
3 t hospital discharge, but few have evaluated long-term use.
4 determine whether this effect persists with long-term use.
5 the significant risks associated with their long-term use.
6 tential harms of HRT, particularly regarding long-term use.
7 reast or endometrium) precludes recommending long-term use.
8 d hormones are effective, side-effects limit long-term use.
9 e, which prevents loss in sensitivity during long-term use.
10 mposite material also make it preferable for long-term use.
11 re especially troubling in children and with long-term use.
12 d as a means to improve biocompatibility for long-term use.
13 adverse events or the risks associated with long-term use.
14 i-inflammatory drugs are not recommended for long-term use.
15 cal effects and biokinetic distribution with long-term use.
16 well short-duration usage measures predicted long-term use.
17 , most present significant side effects over long-term use.
18 es h(-1)), and relatively good stability for long-term use.
19 th limited potential side effects, even with long-term use.
20 are potential complications associated with long-term use.
21 positive airway pressure (CPAP) may predict long-term use.
22 there was no consistent association between long-term use and NHL for all NSAIDs combined, aspirin,
23 tion; however, emerging problems limit their long-term use, and an increasing number of patients inte
24 n skin model, indicated that MB was safe for long-term use, and did not cause irritation even at high
26 ramine was approved in the United States for long-term use as an appetite suppressant until it was re
27 rs are promising anticancer agents but their long-term use at high doses is associated with adverse c
28 y the most apoptosis-resistant cells survive long-term using autophagy-derived nutrients when growth
29 irculatory support systems for short-term or long-term use: bridging to transplant as well as for rec
31 g the rate of benzodiazepine use, especially long-term use by older adults, little information is ava
32 here was a significantly increased risk with long-term use compared with never use (for >5 years, HR
33 .99]), whereas the overall OR for cumulative long-term use (continuous or noncontinuous) was close to
37 results from the Valsartan Antihypertensive Long-Term Use Evaluation (VALUE) trial, in which the use
38 bridge to cardiac transplantation, but their long-term use for the purpose of enhancing survival and
40 uss the most recent literature regarding the long-term use (>/=52 weeks of follow-up) of antivascular
42 t use at least 16 years before diagnosis and long-term use in age-adjusted analyses but not in multiv
43 ods in xenogeneic hosts and are suitable for long-term use in an immunoexclusion device in a discorda
45 ., postoperative) and cancer pain, but their long-term use in chronic pain has met increasing scrutin
50 ilotinib is effective and well-tolerated for long-term use in patients with imatinib intolerance.
54 ropic actions in human myocardium, but their long-term use increases mortality in patients with heart
55 opamine release and neuron activity, whereas long-term use is associated with blunting of the dopamin
56 calcium available for contraction, but their long-term use is associated with increased mortality due
57 immune diseases are limited in efficacy, and long-term use is associated with severe adverse events.
58 s may be used to attenuate chronic pain, but long-term use is complicated by the possible increase in
64 Despite the popularity of GCs in the clinic, long-term use leads to numerous side effects, driving th
65 in the treatment of chronic pain, but their long-term use leads to the development of physiological
68 develops as a complication of pacemaker use, long-term use of a central venous catheter (CVC), or can
69 In male physicians aged 65 years or older, long-term use of a daily multivitamin did not provide co
75 that may have clinical implications for the long-term use of an L1-virus-like particle-based prophyl
78 cardiovascular morbidity and mortality with long-term use of angiotensin-converting enzyme inhibitor
81 bition accelerates disease, cautions against long-term use of anti-TNF-alpha therapeutics for AD, and
84 Until research fully substantiates that the long-term use of antioxidants is safe and effective, the
87 le clinical data do not support the routine, long-term use of aspirin dosages greater than 75 to 81 m
88 o assist clinicians with decisions regarding long-term use of asthma therapies, including omalizumab.
89 mune effector cells has implications for the long-term use of azathioprine in the management of infla
92 r the current clinical guidelines advocating long-term use of beta-blockers to treat most forms of co
93 Recently published studies confirm that the long-term use of biological agents targeting TNF-alpha i
94 Recently published studies confirm that the long-term use of biologicals targeting tumor necrosis fa
95 t, we did not observe an association between long-term use of bisphosphonates and risk of colorectal
96 to be time-dependent with higher risk after long-term use of bisphosphonates in older MM patients of
97 tatus, smoking, cardiovascular risk factors, long-term use of bronchodilators or steroids for lung di
98 sts about breast cancer risk associated with long-term use of calcium channel blockers (CCBs) or angi
104 E-/- mice has important implications for the long-term use of cholinesterase inhibitors and other cho
109 Due to concerns regarding the safety of long-term use of COX-2 inhibitors as well as a desire to
110 S and biopsy-proven IgM nephropathy, and (2) long-term use of CsA in moderate doses with closely moni
114 onstrate any health concerns associated with long-term use of EC in relatively young users who did no
120 e healing in our mouse model is dependent on long-term use of high-dose bisphosphonates, immunosuppre
121 to the growing body of evidence that recent long-term use of HRT is associated with an increased ris
122 and outer retinal involvement in short- and long-term use of hydroxychloroquine before the developme
133 ad already developed side effects from their long-term use of L-dopa revealed, in some cases, the pre
134 of antiviral resistance have been found with long-term use of lamivudine, in up to 76% of patients tr
139 idemiologic study of the association between long-term use of lithium and risk of upper urinary tract
142 a potential mechanistic explanation for why long-term use of low doses of NSAIDs, including aspirin,
143 (VTE) in high-risk patients, but whether the long-term use of low-dose aspirin reduces risk in health
145 arding disease prognosis and decisions about long-term use of medical, endoscopic, and diet therapies
147 tes of antidepressant use and a reduction in long-term use of minor tranquilizers for up to 2 years,
148 tanding the molecular changes in response to long-term use of morphine is likely to aid in the develo
153 studies and clinical trials demonstrate that long-term use of non-steroidal anti-inflammatory drugs (
154 s of epidemiological studies have shown that long-term use of non-steroidal anti-inflammatory drugs,
155 term, continuous use of low-dose aspirin and long-term use of nonaspirin NSAIDs were associated with
157 Epidemiological studies have shown that long-term use of nonsteroidal anti-inflammatory drugs (N
158 dies suggest reduced AD risk associates with long-term use of nonsteroidal anti-inflammatory drugs (N
159 Epidemiological studies have shown that long-term use of nonsteroidal antiinflammatory drugs (NS
163 t pattern in this research is that continued long-term use of NSAIDs is required for an anticancer ef
165 a nationwide analysis of patients in Sweden, long-term use of OCs, particularly the combination type,
168 SCD is mostly reliant upon opioids; however, long-term use of opioids is associated with multiple sid
171 Little is known of the risks associated with long-term use of oral bisphosphonates despite their use
172 acquisition decreased with age, income, and long-term use of oral contraceptives and increased with
173 onsistent with the observation in women that long-term use of oral contraceptives or multiple pregnan
174 ncy department, the use of rescue therapy or long-term use of oral corticosteroids, or the dispensing
176 egrity in most osteoporotic patients and the long-term use of osteoporosis drugs is controversial.
177 exacerbates pathogenesis and argues against long-term use of pan-anti-TNF-alpha inhibitors for the t
178 ), high levels of physical activity, and the long-term use of pharmacotherapy combined with lifestyle
179 Relative to nondiabetics, the cumulative long-term use of pioglitazone reduced the dementia risk
182 f proton pump inhibitors (PPIs), focusing on long-term use of PPIs for three common indications: gast
185 onal studies of outcomes associated with the long-term use of preventive therapies are subject to the
186 atter finding is potentially relevant to the long-term use of protein farnesyltransferase inhibitors,
187 observational studies, between high-dose or long-term use of proton pump inhibitor drugs and certain
188 iew is to evaluate the risks associated with long-term use of proton pump inhibitors (PPIs), focusing
190 No new safety events were identified with long-term use of ranibizumab; rates of SAEs potentially
208 rm trials, the current evidence supports the long-term use of these drugs for the treatment of patien
209 onsteroidal analgesics and opiates; however, long-term use of these drugs is commonly associated with
210 y reduces inflammation, pain, and fever, and long-term use of these drugs reduces fatal thrombotic ev
213 Studies over the past decade suggest that long-term use of these heparins in both primary and seco
214 ing fetal exposure to drugs and xenobiotics, long-term use of these medications may affect fetal drug
218 and clinical studies have reported that the long-term use of topical medications in chronic ophthalm
219 ment of resistance is the main threat to the long-term use of toxins from Bacillus thuringiensis (Bt)
221 ator levels in patients with RA, despite the long-term use of various anti-inflammatory drugs, sugges
223 and prostaglandin E2 (PGE2) expression, but long-term use produced significantly higher levels of th
224 however, the apparent benefit decreased with long-term use (relative risk, 0.80; 0.67 to 0.96, after
226 ubtedly cause irreversible brain damage with long-term use, the jury is still out on the party drug e
229 cannabinoids has been widely observed after long-term use, with concomitant receptor desensitization
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