תבנית:תרופה/האמט-פ 500 IU - Haemate-p 500 i.u.

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××× ×× ×× × ××¡×¤××	×××× ×¤× 1000IU FVIII / 2400IU VWF - haemate p 1000 iu fviii / 2400 iu vwf ×××× ×¤× 250IU FVIII / 600IU VWF - Haemate p 250 iu fviii / 600 iu vwf ×××× ×¤× 500IU FVIII / 1200IU VWF - Haemate p 500 iu fviii / 1200 iu vwf ××××-×¤ 1000 IU - Haemate-p 1000 i.u ××××- ×¤ 250 IU - Haemate-p 250 i.u.
×§×××¦× ×¤×¨××§××××××ª (ATC4)	B02BD Blood coagulation factors
××¨××× ×¤×¢×× (ATC5)	Â Factor viii (human) 500 IU / 10 ML âB02BD07 Von willebrand factor 1200 IU / 10 ML âB02BD07
×¦××¨×ª ××ª×	×ª××-××¨××× - I.V
×¦××¨×ª ××× ××	×××§× ××××¡ ×××× ×ª ×ª×××¡× ××××¨×§×\××× ×¤××××, POWDER AND SOLVENT FOR SOLUTION FOR INJECTION/INFUSION ××× ××¢×ª ××× ×× ××ª×¨ ×× ××¨×¢×× ××© ××××× ××ª ××ª×¨××¤× ×××ª×× ×××× ×× ××××××¥ ××¤× ×©×××¤××¢ ××¢××× ××¦×¨××
××ª××××	Congenital and acquired deficiency of blood clotting factor VIII: severe or moderate haemophilia, prophylaxis during operation, Von Willebrands disease.
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