Læknablaðið : fylgirit - 01.05.1978, Qupperneq 49

Læknablaðið : fylgirit - 01.05.1978, Qupperneq 49
“AM4'£Í.AM>. bCHVJM rjNCt.NTklIl.TN > MtAN : iC T :i>'h JÍTOl!'■ ►.<?*» ,4 ce 10 12 U '6 16 20 THE F1RST OAV OF AOMiNISTRATION TlME (haur*) I *------------------* 08 iC 12 K 16 !6 20 íHE 10 Ih OAY Oí' AhMlNISTRATION TlME(hours) SIDE LFFECTS DURING BEXORYLATi: TREATMFNT 22 patientr. Sic!( eiiects Number of paticnts lncreased values of seriun aspartate aminotransferase ö Frolongation of bleeding time 5 Patiioi. P+ P prothrombin test 4 Microscopic haematuria 5 Microscopic leukocj’turia 5 Stool blood loss 2 Diarrhoea 2 Fig. 6 Paracetamol serum levels on the first and lOth day of the test period. The steady state in paracetamol serum levels was reached aiready or. the second day of the test. In morning samples during the steady state, the mean paracetamol serum level was about 5 ug/ml, which is at the lowest limit of the thera- peutic level. (Figure 5) The maximum paracetamol serum concentration was reached at two hours after intake of the drug. After 6 hours, the serum levels had again fallen to the lower limit of the therapeutic level. According to this, the dosage intervals may be too long, if benorylate is administered twice daily. (Figure (>) The ciinical results of tliese tests were not veiy impressivc. Four children showet! a reductior. oí morning stiffness, the mean number of aetive joints showed only a slight reduction during the test. The clinical effect was considered to be good in two cases only. The side effects in this series are seen in Table 1 Conclusion: In childrcn, the dosage of benorylatc c-f 200 r.'.y/ kg/day, divided in two doses, seems to l.>c unsatisfactory for the management of rheumatoi;! arthritis. Increased daily doses could be onc solution as far as the higher dosage do not causc mort side effects. I would also suggest, that bcnorvlate should be administcred four times daily. In this respcct, however, further investigations are needed. The content of sorbitol in the benoryiate mixture is rather high, and may explair. a more rapid passage tiirough tlie gut. This probably is the most important reason to diarrhoea, which mav impair the resorption of the drug, and, whic.h in some cases may iead to discountinuation oí the medication. REFERENCES Powell, R.K. and Ansell, B.M.: Eenorylate in management of Still's disease. liritish Med J 20 : i-iö 1974 47
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