Examples of using Hyperkalaemia in English and their translations into German
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Medicine
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Political
Hyperkalaemia* Anxiety* Nervousness* Nightmare.
The main causes of hyperkalaemia are oliguria and M. Addison.
Medicinal products that may increase potassium levels or induce hyperkalaemia e. g.
In addition, hyperkalaemia was occasionally observed.
Conversely, due to the aliskiren component of Rasilez HCT, hyperkalaemia might occur.
Hyperkalaemia should be corrected prior to Provenge administration see section 4.2.
The main risk factors for hyperkalaemia to be considered are.
The risk of hyperkalaemia appears to be greater during longer treatment, but hyperkalaemia is usually reversible.
However, in patients receivingaliskiren there was a significantly higher rate of hyperkalaemia, hypotension and kidney dysfunction when compared to the placebo group.
Hyperkalaemia has been reported in the literature in few patients with large ulcerated haemangioma see section 4.4.
Caution should be exercised in patients taking drospirenone-containing medicines with conditions that predispose them to hyperkalaemia or patients taking potassium-sparing diuretics.
Hyperkalaemia, cachexia, hypercalcaemia, hypocalcaemia, hypernatraemia, hyponatraemia, hypoglycaemia, hyperuricaemia, vitamin B12 deficiency, appetite increased, hypomagnesaemia, hypophosphataemia.
The most commonly reported adverse reactions for tacrolimus(occurring in> 10% of patients) are tremor, renal impairment, hyperglycaemic conditions,diabetes mellitus, hyperkalaemia, infections, hypertension and insomnia.
Hypotension, syncope, stroke, hyperkalaemia, and decreased renal function(including acute renal failure) have been reported in susceptible individuals, especially if combining medicinal products that affect this system see section 5.1.
Blood urea nitrogen increased, creatine phosphokinase increased, haematocrit decreased,haemoglobin decreased, hyperkalaemia, leukocytes decreased, platelets decreased, serum creatinine increased, uric acid increased.
Hyperkalaemia may be fatal in the elderly, in patients with renal insufficiency, in diabetic patients, in patients concomitantly treated with other medicinal products that may increase potassium levels, and/or in patients with intercurrent events.
Increased AST, increased ALT, increased alkaline phosphatase, increased lipase, increased amylase, hypocalcaemia, increased creatinine, lymphopaenia, leucopoenia, thrombocytopaenia, anaemia,hypercalcaemia, hyperkalaemia, hypokalaemia, hypomagnesaemia, hyponatraemia.
Heparin can suppress adrenal secretion of aldosterone leading to hyperkalaemia, particularly in patients with diabetes mellitus, chronic renal failure, pre-existing metabolic acidosis, a raised plasma potassium or taking potassium-sparing diuretics.
In addition, an increased incidence of serious adverse outcomes was observed with aliskirencompared to placebo for renal complications(4.7% versus 3.3%), hyperkalaemia(36.9% versus 27.1%), hypotension(18.4% versus 14.6%) and stroke 2.7% versus 2.0.
In July 2016, Galenica announced the acquisition of US-listed Relypsa, a transaction that gave its division Vifor Pharma a dedicated US commercial organization as well as global rights to the drug Veltassa®,a potassium binder used for the treatment of hyperkalaemia.
In a clinical study conducted in type 2 diabetic patients with nephropathy,9.9% of patients treated with Losartan tablets developed hyperkalaemia> 5.5 mEq/ l and 3.4% of patients treated with placebo see section 4.4,‘ Electrolyte imbalances.
Cellulitis, erysipelas hyperkalaemia myalgia paraneoplastic cerebellar degeneration membranous glomerulonephritis, glomerulonephropathy, renal failure bronchospasm, respiratory distress, acute pulmonary oedema, respiratory insufficiency, dyspnoea, hypoxia, laryngeal oedema, acute respiratory distress, acute respiratory distress syndrome, Cheyne-Stokes breathing, pulmonary infiltrates, pneumonia, pneumonitis, pulmonary fibrosis.
Increased AST, bincreased ALT, b increased alkaline phosphatase, b increased creatinine, b decreased lymphocytes, b decreased platelet count, b decreased haemoglobin, b hypercalcaemia, b hypocalcaemia,b hyperkalaemia, b hypokalaemia, b hypomagnesaemia, b hyponatraemiab.
In addition, more than 1 patient in 100 with type 2 diabetes andkidney disease has the following side effects: hyperkalaemia(high blood potassium levels), orthostatic dizziness(dizziness when standing up), orthostatic hypotension(low blood pressure when standing up) and musculoskeletal(joint) pain.
Hyperkalaemia(high blood potassium levels), syncope(fainting), insomnia(difficulty sleeping), vertigo(a spinning sensation), hypotension(low blood pressure), dyspnoea(difficulty breathing), abdominal(tummy) pain, diarrhoea, dry mouth, dyspepsia(heartburn), flatulence(gas), hyperhidrosis(excessive sweating), pruritus(itching), myalgia(muscle pain), renal impairment(kidney problems) including renal failure(kidney failure), and chest pain.
The most commonly reported side effects with Envarsus(seen in more than 1 patient in 10) are tremor(shaking), headache, nausea(feeling sick), diarrhoea, kidney problems, hyperglycaemia(raised blood glucose levels),diabetes, hyperkalaemia(raised blood potassium levels), hypertension(high blood pressure) and insomnia difficulty sleeping.
In CA209017 and CA209063, the proportion of patients who experienced a shift from baseline to a Grade 3 or 4 laboratory abnormality was as follows: 13.2% for decreased lymphocytes, 9% for hyponatraemia,2.9% for hypercalcaemia and hyperkalaemia, 2.5% for decreased haemoglobin(all Grade 3), 2.0% for hypokalaemia, 1.6% for decreased neutrophil count, 1.3% for hypomagnesaemia, 1.2% for hypocalcaemia, 0.8% for increased total bilirubin, and 0.4% for increased AST, decreased platelet, hypermagnesaemia, and hypernatraemia.
Adult patients The most commonly reported(> 20%) events following dual or triple therapy in both treatment groups(basiliximab vs. placebo) were constipation, urinary tract infection, pain, nausea, peripheral oedema, hypertension, anaemia,headache, hyperkalaemia, hypercholesterolaemia, postoperative wound complication, weight increase, increase in blood creatinine, hypophosphataemia, diarrhoea and upper respiratory tract infection.
Clinical trial data has shown that dual blockade of the RAAS through the combined use of ACEIs, ARBs or aliskiren is associated with a higher frequency of adverse events such as hypotension,stroke, hyperkalaemia and decreased renal function(including acute renal failure) compared to the use of a single RAAS-acting agent see sections 4.3, 4.4 and 5.1.
In adults, the most common side effects(seen in more than 20% of patients) were constipation, urinary tract infections(infection of the structures that carry urine), pain, nausea(feeling sick), peripheral oedema(swelling), hypertension(high blood pressure), anaemia(low red blood cell counts),headache, hyperkalaemia(high blood potassium levels), hypercholesterolaemia(high blood cholesterol levels), surgical wound complication, weight increase, increased serum creatinine(a marker of kidney problems), hypophosphataemia(low blood phosphate levels), diarrhoea and upper respiratory tract infection colds.