Cetirizin (Slovenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cetirizin" in Slovenian language version.

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  • Portnoy JM, Dinakar C (2004). »Review of cetirizine hydrochloride for the treatment of allergic disorders«. Expert Opin Pharmacother. 5 (1): 125–135. doi:10.1517/14656566.5.1.125. PMID 14680442.
  • Simons FE, Simons KJ (1999). »Clinical pharmacology of new histamine H1 receptor antagonists«. Clin Pharmacokinet. 36 (5): 329–352. doi:10.2165/00003088-199936050-00003. PMID 10384858.
  • Chen C (2008). »Physicochemical, pharmacological and pharmacokinetic properties of the zwitterionic antihistamines cetirizine and levocetirizine«. Curr. Med. Chem. 15 (21): 2173–2191. doi:10.2174/092986708785747625. PMID 18781943.
  • Simons FE (2002). »Comparative pharmacology of H1 antihistamines: clinical relevance«. Am. J. Med. 113 Suppl 9A (9): 38S–46S. doi:10.1016/s0002-9343(02)01436-5. PMID 12517581.
  • Gupta, A; Chatelain P; Massingham R; Jonsson EN; Hammarlund-Udenaes M (Februar 2006). »Brain distribution of cetirizine enantiomers: comparison of three different tissue-to-plasma partition coefficients: K(p), K(p,u), and K(p,uu)«. Drug Metab. Dispos. 34 (2): 318–23. doi:10.1124/dmd.105.007211. PMID 16303872.
  • Ekhart, C.; Van Der Horst, P.; Van Hunsel, F. (2016). »Unbearable Pruritus After Withdrawal of (Levo)cetirizine«. Drug Safety - Case Reports. 3 (1): 16. doi:10.1007/s40800-016-0041-9. PMC 5124431. PMID 27889900.
  • Zhang L, Cheng L, Hong J (2013). »The clinical use of cetirizine in the treatment of allergic rhinitis«. Pharmacology. 92 (1–2): 14–25. doi:10.1159/000351843. PMID 23867423.
  • Orzechowski RF, Currie DS, Valancius CA (2005). »Comparative anticholinergic activities of 10 histamine H1 receptor antagonists in two functional models«. Eur. J. Pharmacol. 506 (3): 257–64. doi:10.1016/j.ejphar.2004.11.006. PMID 15627436.
  • Taglialatela M, Pannaccione A, Castaldo P, Giorgio G, Zhou Z, January CT, Genovese A, Marone G, Annunziato L (1998). »Molecular basis for the lack of HERG K+ channel block-related cardiotoxicity by the H1 receptor blocker cetirizine compared with other second-generation antihistamines«. Mol. Pharmacol. 54 (1): 113–21. doi:10.1124/mol.54.1.113. PMID 9658196.
  • Hulhoven R, Rosillon D, Letiexhe M, Meeus MA, Daoust A, Stockis A (2007). »Levocetirizine does not prolong the QT/QTc interval in healthy subjects: results from a thorough QT study«. Eur. J. Clin. Pharmacol. 63 (11): 1011–7. doi:10.1007/s00228-007-0366-5. PMID 17891537. The equivalent dose of 60 mg cetirizine is also the highest dose ever administered in healthy subjects [13].
  • Paśko P, Rodacki T, Domagała-Rodacka R, Palimonka K, Marcinkowska M, Owczarek D (2017). »Second generation H1 – antihistamines interaction with food and alcohol-A systematic review«. Biomed. Pharmacother. 93: 27–39. doi:10.1016/j.biopha.2017.06.008. PMID 28622592.

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  • Portnoy JM, Dinakar C (2004). »Review of cetirizine hydrochloride for the treatment of allergic disorders«. Expert Opin Pharmacother. 5 (1): 125–135. doi:10.1517/14656566.5.1.125. PMID 14680442.
  • Simons FE, Simons KJ (1999). »Clinical pharmacology of new histamine H1 receptor antagonists«. Clin Pharmacokinet. 36 (5): 329–352. doi:10.2165/00003088-199936050-00003. PMID 10384858.
  • Chen C (2008). »Physicochemical, pharmacological and pharmacokinetic properties of the zwitterionic antihistamines cetirizine and levocetirizine«. Curr. Med. Chem. 15 (21): 2173–2191. doi:10.2174/092986708785747625. PMID 18781943.
  • Simons FE (2002). »Comparative pharmacology of H1 antihistamines: clinical relevance«. Am. J. Med. 113 Suppl 9A (9): 38S–46S. doi:10.1016/s0002-9343(02)01436-5. PMID 12517581.
  • Gupta, A; Chatelain P; Massingham R; Jonsson EN; Hammarlund-Udenaes M (Februar 2006). »Brain distribution of cetirizine enantiomers: comparison of three different tissue-to-plasma partition coefficients: K(p), K(p,u), and K(p,uu)«. Drug Metab. Dispos. 34 (2): 318–23. doi:10.1124/dmd.105.007211. PMID 16303872.
  • Ekhart, C.; Van Der Horst, P.; Van Hunsel, F. (2016). »Unbearable Pruritus After Withdrawal of (Levo)cetirizine«. Drug Safety - Case Reports. 3 (1): 16. doi:10.1007/s40800-016-0041-9. PMC 5124431. PMID 27889900.
  • Zhang L, Cheng L, Hong J (2013). »The clinical use of cetirizine in the treatment of allergic rhinitis«. Pharmacology. 92 (1–2): 14–25. doi:10.1159/000351843. PMID 23867423.
  • Orzechowski RF, Currie DS, Valancius CA (2005). »Comparative anticholinergic activities of 10 histamine H1 receptor antagonists in two functional models«. Eur. J. Pharmacol. 506 (3): 257–64. doi:10.1016/j.ejphar.2004.11.006. PMID 15627436.
  • Taglialatela M, Pannaccione A, Castaldo P, Giorgio G, Zhou Z, January CT, Genovese A, Marone G, Annunziato L (1998). »Molecular basis for the lack of HERG K+ channel block-related cardiotoxicity by the H1 receptor blocker cetirizine compared with other second-generation antihistamines«. Mol. Pharmacol. 54 (1): 113–21. doi:10.1124/mol.54.1.113. PMID 9658196.
  • Hulhoven R, Rosillon D, Letiexhe M, Meeus MA, Daoust A, Stockis A (2007). »Levocetirizine does not prolong the QT/QTc interval in healthy subjects: results from a thorough QT study«. Eur. J. Clin. Pharmacol. 63 (11): 1011–7. doi:10.1007/s00228-007-0366-5. PMID 17891537. The equivalent dose of 60 mg cetirizine is also the highest dose ever administered in healthy subjects [13].
  • Paśko P, Rodacki T, Domagała-Rodacka R, Palimonka K, Marcinkowska M, Owczarek D (2017). »Second generation H1 – antihistamines interaction with food and alcohol-A systematic review«. Biomed. Pharmacother. 93: 27–39. doi:10.1016/j.biopha.2017.06.008. PMID 28622592.

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