குறியிடப்பட்டது
  • அகாடமிக் ஜர்னல்ஸ் டேட்டாபேஸ்
  • ஜெ கேட் திறக்கவும்
  • ஜெனமிக்ஸ் ஜர்னல்சீக்
  • கல்வி விசைகள்
  • JournalTOCகள்
  • சீனாவின் தேசிய அறிவு உள்கட்டமைப்பு (CNKI)
  • Ulrich's Periodicals Directory
  • எலக்ட்ரானிக் ஜர்னல்ஸ் லைப்ரரி
  • RefSeek
  • ஹம்டார்ட் பல்கலைக்கழகம்
  • EBSCO AZ
  • OCLC- WorldCat
  • SWB ஆன்லைன் பட்டியல்
  • உயிரியல் மெய்நிகர் நூலகம் (vifabio)
  • பப்ளான்கள்
  • மருத்துவக் கல்வி மற்றும் ஆராய்ச்சிக்கான ஜெனீவா அறக்கட்டளை
  • யூரோ பப்
  • கூகுள் ஸ்காலர்
இந்தப் பக்கத்தைப் பகிரவும்
ஜர்னல் ஃப்ளையர்
Flyer image

சுருக்கம்

Treatment with the SQ-Standardised Grass Allergy Immunotherapy Tablet is well Tolerated in Children, Adolescents and Adults in Real Life Application-A Non-Interventional Observational Study

Christine Gronke, Hendrik Wolf, Jörg Schnitker and Eike Wüstenberg

Background: Efficacy and safety of the SQ-standardised grass allergy immunotherapy tablet (GRAZAX®) has been reported in a large number of randomised, controlled clinical trials in children and adults performed in Europe and the US. GRAZAX® became available for routine treatment in children from 5 years of age in Germany and Austria in 2008.To examine the safety and tolerability of GRAZAX® in patients that were less highly selected as in the controlled trials we performed an open label, uncontrolled, non-interventional study in children and adults who were routinely treated in allergists´ offices.

Materials and methods: Patients with allergic rhinoconjunctivitis with or without asthma were treated with GRAZAX® and observed for 3-4 visits every 3 months with the last visit after the first grass pollen season. Adverse seasons before and during therapy.

Results: Treatment was documented in 1,761 patients (797 <18 years; 964 ≥18 years) treated by 373 allergists in Germany and Austria between November 2008 and January 2010. Adverse drug reactions were reported in 31.8% of patients (27.3% ≥18 years, 37.3% <18 years). The higher number of patients <18 years with reactions was due to a higher frequency of local oral reactions. The overall tolerability profile was similar in children and adults. Nasal symptoms improved in 82.7% of patients and no or less symptomatic medication was used by 89.7%.The compliance was rated >75% in 89.8% of patients, >95% of patients and physicians were satisfied with treatment.

Conclusion: The results of our study confirm the safety and tolerability profile observed in controlled clinical trials with GRAZAX®. Treatment satisfaction during routine application was rated high and was combined with a high compliance.