Examples of using Laboratory abnormalities in English and their translations into Hungarian
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Grade 3 liver laboratory abnormalities should be managed with vemurafenib treatment interruption
Treatment-emergent laboratory abnormalities that were observed at a higher incidence in simeprevir-treated patients than in patients treated with placebo,
If severe adverse reactions or laboratory abnormalities develop during treatment with ViraferonPeg monotherapy or combination therapy, modify the dosages of ViraferonPeg and/or ribavirin as appropriate, until the adverse reactions abate.
Most laboratory abnormalities noted during the clinical trial returned to baseline levels shortly after discontinuation of treatment.
When clinical or laboratory abnormalities can not be identified,
no infants experienced any adverse events or laboratory abnormalities.
paraesthesia) and laboratory abnormalities(elevated liver enzymes) have been observed when efavirenz is co-administered with ritonavir dosed as an antiretroviral agent.
All symptoms and laboratory abnormalities resolved without treatment after discontinuation of the study medicinal product.
No Grade 3-4 laboratory abnormalities for AST/ALT or Grade 3-4 adverse reactions of transaminase increased were reported(see section 5.1).
Clinically significant laboratory abnormalities frequently(≥ 5%) occurred including increases in alkaline phosphatase;
2 liver laboratory abnormalities, Cotellic and vemurafenib should be continued at the prescribed dose.
Frequency categories are derived from adverse reactions and/or potentially clinically significant laboratory abnormalities, and are defined according to the following conventions.
The list also includes marked laboratory abnormalities that have been observed with the saquinavir soft capsule in combination with ritonavir(at 48 weeks).
Laboratory abnormalities included increased amylase
Laboratory abnormalities should be managed with dose reduction,
Laboratory abnormalities were reported as adverse events less frequently by investigators than as indicated by laboratory value tables.
Haematologic laboratory abnormalities observed during the first 20 weeks of the trial included anaemia(26% of patients experienced a haemoglobin level of<
Table 2: Incidence of adverse reactions and marked laboratory abnormalities reported in the literature in adults
Laboratory abnormalities included increased amylase
The list also includes marked laboratory abnormalities that have been observed with nelfinavir(at 48 weeks).