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1 ch a diagnosis and may predict the risk of a systemic reaction.
2 of the 21 subjects who received stings had a systemic reaction.
3 anut-allergic subjects suffering from severe systemic reactions.
4 There were no serious local or systemic reactions.
5 reported a higher incidence of food-induced systemic reactions.
6 ated with mostly mild and transient local or systemic reactions.
7 rointestinal AEs, and AR predicted increased systemic reactions.
8 Ultrarush initiation increases the risk of systemic reactions.
9 dministration intervals, but it caused fewer systemic reactions.
10 es include nuisance biting and cutaneous and systemic reactions.
11 een reported, including cutaneous and rarely systemic reactions.
12 that are associated with a high incidence of systemic reactions.
13 stration is associated with a risk of severe systemic reactions.
16 form of meat allergy characterized by severe systemic reactions 3-7 h after consumption of red meat.
17 ll tolerated, with occasional, usually mild, systemic reactions (abdominal pain, arthralgia, and diar
22 ll-tolerated with only grade 1 to 2 local or systemic reactions and no treatment-limiting adverse eve
23 Approximately 42% of subjects experienced systemic reactions, and 49% experienced gastrointestinal
24 se showed promising efficacy, small risk for systemic reactions, and immunomodulatory changes in this
26 Vaccine administration induced no local or systemic reactions, and no laboratory abnormalities were
29 se 4 was associated with increased local and systemic reactions, but the overall safety profile of a
30 all patients suggesting a radiation-induced systemic reaction; (c) changes in DTPA t 1/2 values were
31 (pain, erythema, induration, and warmth) and systemic reactions (chills, arthralgias, and myalgias) i
32 me was the occurrence of 1 or more objective systemic reactions during venom immunotherapy initiation
34 p large local swelling or strictly cutaneous systemic reactions generally do not require immunotherap
35 frequently reported adverse events included systemic reactions (Group 1: 21% of patients, Group 2: 3
36 ed and who had a history of mild (cutaneous) systemic reaction (i.e., one with only cutaneous manifes
37 We sought to investigate the occurrence of systemic reactions in children with isolated sensitizati
38 er incidence of mild, self-limited local and systemic reactions in the vaccine group, but only during
39 well tolerated, with no significant local or systemic reactions in the women and no adverse outcomes
40 om immunotherapy may reduce the incidence of systemic reactions in those with a history of venom-trig
42 nd in untreated patients with a history of a systemic reaction involving at least two different organ
45 s (aP) vaccines has considerably reduced the systemic reactions observed with diphtheria-tetanus toxo
49 The acute-phase response (APR) represents a systemic reaction of the organism to multiple nonspecifi
50 eater number of moderate or severe local and systemic reactions (of 16 participants, 4 had local reac
51 There was no pattern of vaccine-associated systemic reactions or clinically significant laboratory
54 ensitization and region on the occurrence of systemic reactions (P = 0.0185 and P = 0.0436, respectiv
57 ntrast administration can be associated with systemic reactions, renal disease, and thyroid dysfuncti
60 fact stimulate more robust inflammatory and systemic reactions than RF at liver ablation, the author
61 rticipants, 4 had local reactions and 13 had systemic reactions) than did vaccine formulated with MF5
62 errulatus-envenomed victims exhibit local or systemic reaction that culminates in pulmonary oedema, p
65 against GVHD, vaccination elicited local and systemic reactions that were qualitatively similar to th
66 There is evidence that the severity of the systemic reaction to infection (severe sepsis) is strong
67 d food challenge, 1 boy with a previous mild systemic reaction to peanut experienced lip swelling, st
68 ldren leads to a significantly lower risk of systemic reaction to stings even 10 to 20 years after tr
70 sp venom, and 32 controls without history of systemic reactions to Hymenoptera stings and no sIgE to
73 tosis and/or elevated sBT tryptase level and systemic reactions to hymenoptera venoms were analyzed f
76 If the child had a documented history of systemic reactions up to grade I anaphylaxis, double-bli
77 plasma tryptase and EDN, and the severity of systemic reactions was correlated with levels of tryptas
83 hough the overall reaction rate was similar, systemic reactions were more common during OIT than duri
91 frequency and severity of injection-site and systemic reactions within 28 days of each vaccination.
92 The primary safety endpoints were local and systemic reactions within 7 days after each injection, a
94 , at 4-7 days for postimmunization local and systemic reactions, within 28 days for adverse events, a
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