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ž
patients with a creatinine clearance above 50 ml/ min require no reduction in daily dose.

Ž
9.

(ž
coadministration of antipsychotic medicinal products with pramipexole should be avoided (see section 4.4), e. g. if antagonistic effects can be expected.

dĖ utĖ Ž
blister/ (al/ al)

kas Ž 2.
2.

jimas (ž
batch:

narbutaitės ž.)
narbutaitė)

Ž (žemas)
age of ship

galimą alą ž.
in human volunteers, a dose-dependent decrease in prolactin was observed.

, nuo a ii k ž
26mars2008.indd 26-27

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

ž mis, kurioms iurkė
90% of absorbed active substance is excreted through the kidneys.

ž sudė yra aspartamo (iš
contains aspartame.

todėpacientai ir slaugytojai turi ž
63% of patients on pramipexole and 52% of patients on placebo reported at least one adverse drug reaction.

aukštas lygis v — — — Ž
white

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).

pacientams. (ž 4. 4 skyrių
date of first authorisation:

000 vaisto vartojusių monių 1 ž
like all medicines, oprymea can cause side effects, although not everybody gets them.

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.

jimas (ž 4. 4 skyrių r.
investigations very common: