Examples of using Function abnormalities in English and their translations into Slovenian
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Medicine
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Colloquial
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Ecclesiastic
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Financial
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Computer
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Official/political
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Programming
Liver function abnormalities have been associated with PAH.
Hepato-biliary disorders: liver function abnormalities.
Evere liver function abnormalities(determined by laboratory tests).
Hepatobiliary disorders: rare: hepatitis not known: liver function abnormalities.
Any patient developing significant liver function abnormalities during treatment must be monitored closely.
The Sitaxentan population also included patients(N= 53)who had discontinued another endothelin receptor antagonist due to liver function abnormalities.
Any patient developing significant liver function abnormalities during treatment must be monitored closely.
Toremifene treatment has been associated with changes in liver enzyme levels(increases of transaminases)and in very rare occasions with more severe liver function abnormalities(jaundice).
Hepatic enzymes and function abnormalities, cholestasis and jaundice, hepatocellular damage and hepatitis, cholangitis.
The most commonly reportedtreatment-related events(investigator assessment) are: liver function abnormalities, diarrhoea, headache, rash, hypertension.
Frequency of liver function abnormalities during combination antiretrovir l ther py(CART) and should be monitored according to standard practice.
The most commonly reported ADRs(investigator assessment)are liver function abnormalities(3.5%), diarrhoea(2.7%), headache(1.8%), nausea(1.7%), rash(1.5%).
Endocrine system Thyroid function abnormalities or worsening of pre-existing thyroid disorders have been reported with the use of alpha interferons, including Pegasys.
Patients with pre-existing liver dysfunction including chronic activehepatitis have an increased frequency of liver function abnormalities during combination antiretroviral therapy and should be.
Any patient developing liver function abnormalities during treatment with IntronA must be monitored closely and treatment discontinued if signs and symptoms progress.
Patients with pre-existing liver dysfunction, including chronic active hepatitis B or C,have an increased risk for liver function abnormalities including severe and potentially fatal hepatic adverse reactions.
Not known:• reduced number of red blood cells(anaemia),• reducednumber of thrombocytes,• migraine,• cough,• liver function abnormalities,• muscle and joint pain,• changes in kidney function(may be reversible upon discontinuation of treatment) including kidney failure,• flu-like symptoms,• increase in blood urea,• serum creatinine and serum potassium in patients with heart failure,• back pain and urinary track infection.
Readministration to patients who previously had ASAT or ALATgt; 5 ULN during nevirapine therapy andhad recurrence of liver function abnormalities upon readministration of nevirapine(see section 4.4).
Patients with pre-existing liver dysfunction including chronichepatitis have an increased frequency of liver function abnormalities during combination antiretroviral therapy and should be monitored according to standard practice.
The most commonly reported adverse reactions in clinical trials(4,072 subjects treated at least with a dose from 10 mg to 300 mg)and post-marketing experience are gout flares, liver function abnormalities, diarrhoea, nausea, headache, rash and oedema.
Patients with pre-existing liver dysfunction including chronic activehepatitis have an increased frequency of liver function abnormalities during combination therapy and should be monitored according to standard practice.
Summary of the safety profile The most commonly reported adverse reactions in clinical trials(4,072 subjects treated at least with a dose from 10 mg to 300mg) and post-marketing experience are gout flares, liver function abnormalities, diarrhoea, nausea, headache, rash and oedema.
Patients with pre-existing liver dysfunction including chronichepatitis have an increased frequency of liver function abnormalities during CART and should be monitored according to standard practice.
Patients with pre-existing liver dysfunction including chronic activehepatitis have an increased frequency of liver function abnormalities during combination antiretroviral therapy and should be monitored according to standard practice.
Patients with pre-existing liver dysfunction including chronic activehepatitis have an increased frequency of liver function abnormalities during combination antiretroviral therapy and should be monitored according to standard practice.
Patients with pre-existing liver dysfunction including chronic activehepatitis have an increased frequency of liver function abnormalities during combination antiretroviral therapy and should be monitored according to standard practice.
Patients with pre-existing liver dysfunction, including chronic active hepatitis,have an increased frequency of liver function abnormalities during combination antiretroviral therapy and should be monitored according to standard practice.