Examples of using Hyperkinesia in English and their translations into Slovak
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Medicine
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Colloquial
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Ecclesiastic
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Official/political
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Computer
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Programming
Hyperkinesia, confusional state.
Choreoathetosis, dyskinesia, hyperkinesia.
Amnesia, hyperkinesia, sudden onset of sleep, syncope.
Choreoathetosis, d yskinesia, hyperkinesia.
Hyperkinesia, tremor, dysphonia, paresthaesia, hypoaesthesia, hyperaesthesia, concentration impaired, somnolence.
Dizziness, psychomotor hyperactivity Hyperkinesia, confusional state.
Dizziness, headache, somnolence sudden onset of sleep, syncope amnesia,dyskinesia, hyperkinesia.
Ataxia, Convulsion, Headache, High-pitched crying, Hyperkinesia, Hypersomnia, Lethargy, Tremor.
Hyperkinesia, tremor, dysphonia, paresthaesia, hypoaesthesia, hyperaesthesia, concentration impaired, somnolence.
Dizziness, headache, somnolence sudden onset of sleep dyskinesia, hyperkinesia.
Dizziness, dyskinesia, somnolence amnesia, headache hyperkinesia, sudden onset of sleep, syncope.
Headache, dizziness Hyperkinesia, tremor, dysphonia, paresthaesia, hypoaesthesia, hyperaesthesia, concentration impaired, somnolence.
Rare: ataxia, convulsion, headache, high pitched crying, hyperkinesia, hypersomnia, lethargy, tremor.
Headache, dizziness Hyperkinesia, tremor, dysphonia, paresthaesia, hypoaesthesia, hyperaesthesia, concentration impaired, somnolence.
Disorders of motor development: spasticity, coordination problems, hyperkinesia, impaired motor control.
Hyperkinesia, tremor, dysphonia, paresthaesia, hypoaesthesia, hyperaesthesia, concentration impaired, somnolence, disturbance in attention, poor quality of sleep.
EPS included a pooled analysis of the following terms: dyskinesia,dystonia, hyperkinesia, Parkinsonism, and tremor.
Seizure, delirium, hallucinations, agitation, dyskinesia, hyperkinesia, poriomania, dizziness, headache, restlessness, stupor.
Therapists who work with these children implementing the INPP therapy face some additional difficulties such as: the enormous possibility of causing side effects at the beginning of the treatment: challenging, irritable and sometimes even aggressive personalities,as well as symptoms such as hyperkinesia or impulsivity that do not seem to evolve positively with treatment.
Common: amnesia, ataxia, convulsion, dizziness, headache, hyperkinesia, tremor, balance disorder, disturbance in attention, memory impairment.
The expected adverse events would be those related to the pharmacodynamic profile of a dopamine agonist, including nausea, vomiting, hyperkinesia, hallucinations, agitation and hypotension.
The following adverse reactions are expected under the use of Pramipexole Teva: abnormal dreams, confusion, constipation, delusion, dizziness, dyskinesia, fatigue, hallucinations,headache, hyperkinesia, hypotension, increased eating(binge eating, hyperphagia), insomnia, libido disorders, nausea, peripheral oedema, paranoia; pathological gambling, hypersexuality and other abnormal behaviour, somnolence, weight increase, sudden onset of sleep, pruritus and rash and other hypersensitivity.
The expected adverse events would be those related to the pharmacodynamic profile of a dopamine agonist, including nausea,vomiting, hyperkinesia, hallucinations, agitation and hypotension.
Very common: somnolence Common: amnesia, ataxia, convulsion, dizziness,headache, hyperkinesia, tremor, balance disorder, disturbance in attention, memory impairment.
The expected adverse reactions would be those related to the pharmacodynamic profile of a dopamine agonist, including nausea,vomiting, hyperkinesia, hallucinations, agitation and hypotension.
Expected adverse events The following adverse reactions are expected under the use of MIRAPEXIN: abnormal dreams, amnesia, behavioural symptoms of impulse control disorders and compulsions such as binge eating, compulsive shopping, hypersexuality and pathological gambling; confusion, constipation, delusion, dizziness, dyskinesia, fatigue, hallucinations,headache, hyperkinesia, hyperphagia, hypotension, insomnia, libido disorders, nausea, paranoia, peripheral oedema; pruritus, rash and other hypersensitivity; restlessness, somnolence, sudden onset of sleep, syncope, visual disturbance including vision blurred and visual acuity reduced, vomiting, weight decrease, weight increase.
The expected adverse events would be those related to the pharmacodynamic profile of a dopamine agonist, including nausea,vomiting, hyperkinesia, hallucinations, agitation and hypotension.
Additional events that were more often seen in the paroxetine compared to placebo group were: decreased appetite, tremor,sweating, hyperkinesia, agitation, emotional lability(including crying and mood fluctuations).