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1 rious adverse events (primarily bleeding and severe pain).
2 0 to 10, with higher scores indicating more severe pain).
3 e seen in 6 patients; 8 patients experienced severe pain.
4 10-point scale, with 10 indicating the most severe pain.
5 the choice for the treatment of moderate to severe pain.
6 ugs (NSAIDs) in the treatment of moderate to severe pain.
7 resent a new therapeutic approach to control severe pain.
8 e patients reported experiencing moderate to severe pain.
9 terminally ill patients reported moderate or severe pain.
10 ts had no body pain; 38% had moderate and 4% severe pain.
11 re were 2554 visits; 60% of the patients had severe pain.
12 algesics are widely used in the treatment of severe pain.
13 t supplies of opioids to treat patients with severe pain.
14 algesics; 41% of patients reporting pain had severe pain.
15 mplained of shortness of breath, chills, and severe pain.
16 t and most potent drugs for the treatment of severe pain.
17 mainstay analgesics for treating moderate to severe pain.
18 trical shocks can damage the heart and cause severe pain.
19 s is an attractive alternative treatment for severe pain.
20 tients with Parkinson's disease and chronic, severe pain.
21 pain, 10.3% had moderate pain, and 13.2% had severe pain.
22 ids for moderate pain and strong opioids for severe pain.
23 n clinical trials for the treatment of acute severe pain.
24 analgesics for the treatment of moderate to severe pain.
25 , causes debilitating joint inflammation and severe pain.
26 reported intermediate pain, and 12% reported severe pain.
27 se with moderate pain, and 67% of those with severe pain.
28 and presented with similar symptoms, such as severe pain.
29 associated with receiving OPs for those with severe pain.
30 mong the most used clinical drugs to relieve severe pain.
31 : 1.01-14.9) were associated with persistent severe pain.
32 arter were aggressive, mainly verbally, with severe pain.
33 Sickle cell disease causes severe pain.
34 Opioids are the gold-standard treatment for severe pain.
35 rized in most kindreds by early-age onset of severe pain.
36 More than 60% of Latinos reported severe pain.
37 potent analgesic drugs for the treatment of severe pain.
38 natives for the pharmacological treatment of severe pain.
39 A score of >or=7 was defined as severe pain.
40 erized by loss of feeling in extremities and severe pain.
41 d after onset of a migraine with moderate to severe pain.
42 verbal rating scale, from "no pain" to "very severe pain."
44 .4%, P < .001), self-reported pain (moderate/severe pain, 41.1% vs 24.2%, P = .003), burning/stinging
49 a well-recognized problem, with moderate to severe pain affecting 15% to 20% of women at 1 year from
51 roblem in lactating women that may result in severe pain and abrupt termination of breastfeeding, the
57 als such as ammonia (smelling salts) elicits severe pain and inflammation through unknown mechanisms.
60 ave reported a high incidence of moderate to severe pain and poor analgesia in intensive care units a
61 n the relationship between moderate and more severe pain and prescription opioid use disorders in the
63 performed among adults with moderate or more severe pain and with nonmedical opioid use at wave 1.
64 is characterized by a more acute onset, more severe pain, and a rapid response to systemic corticoste
65 IV Parkinson's disease, at least one type of severe pain, and an average 24-h pain score of at least
69 es that were sufficient to treat patients in severe pain, as compared with 72 percent of pharmacies i
70 rapid initiation of opioids for treatment of severe pain associated with a vasoocclusive crisis, and
74 ients with prodromal symptoms or moderate or severe pain at presentation were also more likely to exp
76 al rating scale (score 0-5; 0 = no pain, 5 = severe pain) before surgery and 6 weeks postoperatively.
80 inctive rare condition characterized by less severe pain but marked autonomic activation during attac
81 Opioids remain the mainstay of treatment for severe pain, but the associated hyperalgesia and toleran
82 and dependence among adults with moderate to severe pain, careful monitoring and consideration of non
83 st widely prescribed therapy for moderate to severe pain clinically, they have been noted to alter mi
84 MOR agonist prescribed for the treatment of severe pain conditions that has addictive properties.
86 a highly variable phenotype characterized by severe pain crises, acute clinical events, and early mor
90 ssociated with fewer days of severe and very severe pain (difference of -0.22 days; 95% CI, -0.41 to
91 ded voltage-gated Na(+) channel NaV1.9 cause severe pain disorders ranging from neuropathic pain to c
92 ing stable opioid therapy and experiencing a severe pain episode were randomly assigned to either 100
93 apy to become the standard for management of severe pain events in children and adults with SCD requi
94 elf-limited toxicities of 3F8 treatment were severe pain, fever, urticaria, and reversible decreases
96 and intervention for a middle-aged man with severe pain from spinal metastases to discuss 4 key ques
97 rol was more likely among patients with more severe pain, greater anxiety, depression, and alteration
99 trial, patients with one CAF and moderate-to-severe pain (>/=50 mm on a 100 mm visual analog scale [V
103 However, these drugs can cause unexplained severe pain in patients, often referred to as calcineuri
105 tance): pain in the back or lower extremity, severe pain in the operated hip, poor mental health, mor
106 ed in diabetic patients with sudden onset of severe pain in the thigh or calf muscles who have MR ima
107 closely matches the incidence of moderate to severe pain in trauma patients, indicating appropriate p
109 ts millions of women and is characterized by severe pain, increased frequency of micturition, and chr
115 ndards were developed for minor pain (<30%), severe pain (<3%), vasovagal hypotension (<3%), signific
119 strong opioids in survivors with moderate to severe pain, most pain problems in cancer survivors will
120 all Ultraflex; n=6), food obstruction (n=3), severe pain (n=2), esophageal rupture (n=2), hemorrhage
122 reported extremely severe pain or moderately severe pain occurring at least half of the time, and nea
123 tis (odds ratio, 5.6 [95% CI, 1.9 to 16.8]), severe pain (odds ratio, 2.5 [CI, 1.4 to 4.8]), and a co
124 intestinal tract or abdominal viscera causes severe pain often with vomiting due to oedematous bowel
125 minally ill patients experienced moderate to severe pain, only 30% of them wanted additional pain tre
130 or scale (VDS) ("none", "mild", "moderate", "severe" pain) or a 100-mm visual analog scale (VAS) anch
132 or a child with sciatic nerve zoster who had severe pain over the lower back 6 days before appearance
134 rer general function (HAQ; P < 0.0001), more severe pain (P = 0.002), greater fatigue (P = 0.0005), g
135 ks, fewer NCPB patients reported moderate or severe pain (pain intensity rating of > or =5/10) vs opi
136 or chemotherapy had failed and who reported severe pain (pain score > or = 4 [scale of 0-10]) over a
138 nduced neuropathy is characterized by acute, severe pain, peripheral nerve degeneration, and autonomi
139 ar efficacy in reducing early, moderate, and severe pain-related responses, suggesting that TRPV1 may
140 ent of analgesic agents for the treatment of severe pain requires the identification of compounds tha
142 ue scale, with higher scores indicating more severe pain), return emergency department visits, hospit
144 pain and less likely to receive opioids for severe pain, suggesting a different threshold for treatm
145 ache," "hurt," and "discomfort," may reflect severe pain symptoms, disability, and more serious joint
150 iring joint replacement and with moderate-to-severe pain that had been inadequately controlled by wea
151 fects to analgesic treatment for moderate to severe pain that interfered with functional activity; ho
153 arge proportion of patients have moderate to severe pain that needs treatment with opioid analgesics.
157 patients with OA of the knee and moderate-to-severe pain were enrolled in a randomized, double-blind,
160 atients who required therapy for moderate to severe pain were randomized to CR oxycodone every 12 hou
161 0 to 100, with higher scores indicating more severe pain) were similar in the placebo, lavage, and de
162 DRG neuron hyperexcitability associated with severe pain, whereas loss of the Na(v)1.7 channel in pat
164 arly in patients with moderate to moderately severe pain who do not respond to or who cannot tolerate
166 ing severe unrelenting pain alone (group 1), severe pain with intermittent acute exacerbations (group
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