The MAH was asked to provide data on safety and efficacy for these subgroups of patients (Losartan, Atenolol, Losartan + HCTZ, Atenolol + HCTZ) in order to gain more insight into the contribution of HCTZ to the overall benefit risk ratio.
Od imetnika dovoljenja za promet z zdravilom so zahtevali podatke o varnosti in učinkovitosti pri omenjenih podskupinah bolnikov (losartan, atenolol, losartan + HCTZ, atenolol + HCTZ), da bi z njimi dobili boljši vpogled v prispevek, ki ga ima HCTZ na skupno razmerje med koristnimi učinki in tveganjem.