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Adcetris · 4.8 · In the pivotal phase 2 population (SG035-0003 and SG035-0004), the median duration of Grade 3 or Grade 4 neutr
Eintrag öffnenAlecensa · 4.8 · 8 phase II clinical trials (NP28761, NP28673; N = 253), the median duration of exposure to Alecensa was 11.2 m
Eintrag öffnenAlecensa · 4.8 · In BO40336 (ALINA; N = 128), the median duration of exposure to Alecensa was 23.9 months. In BO28984 (ALEX; N
Eintrag öffnenAloxi · 4.8 · 6 * Includes the following: burning, induration, discomfort and pain
Eintrag öffnenAvamys · 4.8 · Epistaxis *In paediatric clinical studies of up to 12 weeks duration the incidence of epistaxis was similar be
Eintrag öffnenAwiqli · 4.8 · ONWARDS 6 trial was followed by an extension part of 26 weeks treatment duration in order to investigate long-
Eintrag öffnenAwiqli · 4.8 · The main phase of ONWARDS 1 trial was followed by an extension part of 26 weeks treatment duration in order to
Eintrag öffnenBaraclude · 4.8 · Treatment beyond 48 weeks: continued treatment with entecavir for a median duration of 96 weeks did not reveal
Eintrag öffnenBaraclude · 4.8 · Treatment beyond 48 weeks: continued treatment with entecavir for a median duration of 96 weeks did not reveal
Eintrag öffnenBimervax · 4.8 · Injection site induration, malaise, axillary pain and arthralgia occurred at higher frequencies in adolescents
Eintrag öffnenBimervax · 4.8 · Injection site induration, malaise, axillary pain and arthralgia occurred at higher frequencies in adolescents
Eintrag öffnenBimervax · 4.8 · Injection site induration, malaise, axillary pain and arthralgia occurred at higher frequencies in adolescents
Eintrag öffnenBimervax · 4.8 · Injection site induration, malaise, axillary pain and arthralgia occurred at higher frequencies in adolescents
Eintrag öffnenBlincyto · 4.8 · The duration of hepatic adverse reactions has generally been brief and with rapid resolution, often when conti
Eintrag öffnenBrukinsa · 4.5 · 32 the BRUKINSA dose to 160 mg (one tablet) for the duration of the inhibitor use. Patients should be closely
Eintrag öffnenCablivi · 4.8 · In clinical studies, bleeding events occurred in different body systems, independent of treatment duration. In
Eintrag öffnenCasgevy · 4.8 · The median (min, max) duration of follow-up after being administered Casgevy was 22.8 (2.1, 51.1) months for p
Eintrag öffnenCholib · 4.5 · If treatment with fusidic acid is necessary, Cholib treatment should be discontinued throughout the duration o
Eintrag öffnenCholib · 4.8 · 11 Tabulated list of adverse reactions During four double blind clinical trials of 24-week duration 1,237 pati
Eintrag öffnenCholib · 4.8 · Tabulated list of adverse reactions During four double blind clinical trials of 24-week duration 1,237 patient
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