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ž
patients with a creatinine clearance above 50 ml/ min require no reduction in daily dose.
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Ž
9.
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(ž
coadministration of antipsychotic medicinal products with pramipexole should be avoided (see section 4.4), e. g. if antagonistic effects can be expected.
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dĖ utĖ Ž
blister/ (al/ al)
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kas Ž 2.
2.
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jimas (ž
batch:
Last Update: 2012-04-11
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narbutaitės ž.)
narbutaitė)
Last Update: 2017-03-31
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Ž (žemas)
age of ship
Last Update: 2014-11-21
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galimą alą ž.
in human volunteers, a dose-dependent decrease in prolactin was observed.
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, nuo a ii k ž
26mars2008.indd 26-27
Last Update: 2014-02-06
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mg/ kg per parą ž
development or exacerbation of diabetes occasionally associated with ketoacidosis or coma, including some fatal cases (see section 4.4) hypothermia
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ž mis, kurioms iurkė
90% of absorbed active substance is excreted through the kidneys.
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ž sudė yra aspartamo (iš
contains aspartame.
Last Update: 2012-04-11
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todėpacientai ir slaugytojai turi ž
63% of patients on pramipexole and 52% of patients on placebo reported at least one adverse drug reaction.
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aukštas lygis v — — — Ž
white
Last Update: 2014-11-21
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poveikis (ž 5. 3 skyrių
18 however, it should be noted that the incidence of somnolence is increased at doses higher than 1.5 mg/ day (see section 4.8).
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pacientams. (ž 4. 4 skyrių
date of first authorisation:
Last Update: 2012-04-11
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000 vaisto vartojusių monių 1 ž
like all medicines, oprymea can cause side effects, although not everybody gets them.
Last Update: 2011-10-23
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kadangi tyrimų žsu monė neatlikta, ž
dosing in children and adolescents oprymea is not recommended for use in children and adolescents below 18 years due to a lack of data on safety and efficacy.
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jimas (ž 4. 4 skyrių r.
investigations very common:
Last Update: 2012-04-11
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