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lyfjaupplýsingar

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IJslands

kynnið ykkur lyfjaupplýsingar deferoxamíns.

Engels

the product information of deferoxamine should be consulted.

Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
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IJslands

sjá lyfjaupplýsingar erlótíníbs varðandi skömmtun og gjöf erlótiníbs.

Engels

for the posology and method of administration of erlotinib, please refer to the full erlotinib prescribing information.

Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
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IJslands

byggt á aukningu lípasa og hækkun á meðalgildum lípasa sem gefið var til kynna í klínískum rannsóknum og eftir markaðssetningu, álítur prac að uppfæra skuli lyfjaupplýsingar og bæta

Engels

based on the signal on lipase increased and the events of increase in mean lipase values received from clinical trials and from post­marketing sources, the prac considered that the product information should be updated to add the adverse reactions ‘increased lipase’ and ‘increased amylase’ in section

Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
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IJslands

by ggt á ofangreindu, er talið réttlætanlegt að skrá í lyfjaupplýsingar fyrir öll lyf sem innihalda levetiracetam að „heilakvilli“ komi mjög sjaldan fyrir.

Engels

based on the above, it is considered justified to document that cases of “encephalopathy” have been observed rarely in the product information of all levetiracetam-containing products.

Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
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IJslands

prac taldi að uppfæra ætti lyfjaupplýsingar aripíprazóls með upplýsingum um aukaverkunina „hiksti“ í kafla 4.8 í samantektinni á eiginleikum lyfsins þar sem ekki var hægt að útiloka áhrif aripíprazóls hjá tilkynntum tilvikum.

Engels

the prac considered that the product information of aripiprazole should be updated to include the adverse event ‘hiccups” in section 4.8 of the smpc, since a contributory role of aripiprazole in the reported cases could not be ruled out.

Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
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IJslands

Þar af leiðandi ættu markaðsleyfishafar að bæta aukaverkuninni „rákvöðvalýsa“ undir líffæraflokkinn stoðkerfi og stoðvefur (tíðni „mjög sjaldgæf“) í lyfjaupplýsingar fyrir öll lyf sem innihalda levetiracetam.

Engels

therefore, the mahs should add the undesirable effect “rhabdomyolysis” under the soc musculoskeletal and connective tissue disorders (frequency ‘rare’) in the product information of all levetiracetam-containing products.

Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
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