Примери за използване на To treatment discontinuation на Английски и техните преводи на Български
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Computer
None of these adverse reactions led to treatment discontinuation.
ADRs that led to treatment discontinuation occurred in 9.2% of patients.
None of cases was of severe intensity and led to treatment discontinuation.
Adverse events led to treatment discontinuation in 13% of patients.
All events were mild or moderate in severity anddid not lead to treatment discontinuation.
The events led to treatment discontinuation in 3.9% and 5% of patients.
Facial paresis was generally reversible and led to treatment discontinuation in 0.9%(2/217).
Adverse events led to treatment discontinuation in 24% of patients receiving ADCETRIS.
The events were reversible, andno event led to treatment discontinuation.
Peripheral neuropathy led to treatment discontinuation in 7%, dose reductions in 21%, and dose delays in 1% of patients.
Blood creatine phosphokinase elevations were transient and asymptomatic, anddid not lead to treatment discontinuation.
Thrombocytopenia rarely leads to treatment discontinuation(1.6% of patients).
Of the 130 SPRYCEL-treated paediatric subjects with CML-CP, 2(1.5%)experienced adverse reactions leading to treatment discontinuation.
Painful injections leading to treatment discontinuation is mainly seen with anakinra.
In general, headache, diarrhoea, nausea and alopecia, were mild to moderate, transient andinfrequently led to treatment discontinuation.
Both rash and nail disorders led to treatment discontinuation in 0.6% of Nerlynx-treated patients.
In the overall population of 2,712 SPRYCEL-treated adult subjects, 520(19%)experienced adverse reactions leading to treatment discontinuation.
The most common side effects leading to treatment discontinuation were local injection site reactions.
All events reported in clinical studies in patients with LD have been mild or moderate in severity andnone have led to treatment discontinuation.
Frequency of patients with TEAE leading to treatment discontinuation was similar in both arms(4.3% vs 4.4%).
In patients treated with Combo 450, dermatitis acneiform occurred in 4.4%(12/274) of patients, was Grade 1 and 2 andno event led to treatment discontinuation.
The most common adverse reactions which led to treatment discontinuation in the lixisenatide group were nausea(3.1%) and vomiting(1.2%).
A haemorrhage event led to dose interruption or reduction in 3.2% and0.8% patients respectively and to treatment discontinuation in 1.7% of patients.
The most common adverse events(AEs)leading to treatment discontinuation were diarrhoea(4.5%), asthenia and fatigue(2.9% each) and pneumonia(1.3%).
Thrombocytopenia, or decreased platelet counts, was commonly reported with trastuzumab emtansine andwas the most common adverse reaction leading to treatment discontinuation(see section 4.8).
Most common adverse reactions leading to treatment discontinuation in patients treated with Praluent were local injection site reactions.
One patient on belatacept MI regimen developed Guillian-Barré syndrome which led to treatment discontinuation and subsequently resolved.
Marked increases in liver enzymes leading to treatment discontinuation or dose modification occurred in controlled clinical studies(see section 4.8).
Among the group of subjects treated with naltrexone/ bupropion,both cases of seizures were considered as serious and led to treatment discontinuation(see section 4.4).
Adverse reactions led to treatment discontinuation in 23% and 32% of patients receiving brentuximab vedotin in the phase 2 and the phase 3 population, respectively.