Adverse Effects

Pharmacovigilance

The agency received 71 adverse reaction reports for human MP in 2006. Twenty-four of those were rated serious, involv­ing twenty medicinal products. One adverse reaction report was received for a veterinary medicinal product. It has been decided to use Eudravigilance databases (human and vet) for all adverse reaction report in Iceland.


Drugs that possibly have caused serious adverse reaction in 2006.

ATC-group Active substance Brand name Number of reports
J02AA01 Amphotericin B Ambisome

1

R03CC03 Terbutalinum Bricanyl

1

C10AA07 Rosuvastatinum Crestor

1

D10BA01 Isotretinoinum Decutan

1

D11AX15 Pimecrolimus Elidel

1

C01CA24 Epinephrinum EpiPen

1

B05DA Ísótónísk lausn Extraneal

1

L01BC02 Fluorouracilum Flurablastin

1

J04AC51 Isoniazidum Isoniazid

1

B01AB05 Enoxaparinum Klexane

1

B01AA03 Warfarinum Kóvar

1

C01AA05 Digoxinum Lanoxin

1

B02BD08 Faktor VII Novoseven

1

A06AD17 Natríumfosföt Phosphoral

2

B05DB Hýpertónísk lausn Physioneal

1

L04AA21 Efalizumab Raptiva

1

L04AA12 Infliximabum Remicade

3

N05AB04 Prochlorperazinum Stemetil

1

N06BA09 Atomoxetine Strattera

1

L01BC06 Capecitabinum Xeloda

2

 


þetta vefsvæði byggir á eplica. eplica heimasíðurheimasíður - nánari upplýsingar á heimasíðu eplica.