Pharmacovigilance

 

If you suspect  an adverse reaction, inform your doctor or pharmacist. You should proceed in the same way in case of any  adverse reactions that are not listed in the Patient Information Leaflet of the medicinal product. You can also report  adverse reactions directly through the national  adverse reaction reporting system. Further information about the report can be found at: http://www.olecich.cz/hlaseni-pro-sukl/nahlasit-nezadouci-ucinek

Correspondence address:

Státní ústav pro kontrolu léčiv (State Institute for Drug Control)
oddělení farmakovigilance (Pharmacovigilance Department)
Šrobárova 48
100 41 Praha 10
e-mail: farmakovigilance(at)sukl.cz.

By reporting  adverse reactions, you can contribute to obtaining more information about the safety of the medicinal product.

System of services for ensuring the safety of human medicinal products and medical  devices. Non-stop service for receiving reports of  adverse reactions of medicinal products and  adverse reactions of medical  devices:

PharmDr. Jana Tomovič Čačaná

Tel. 24/7: +421 911 056 862
E-mail: pv-biomedica(at)emmes.com
Adresa: EMMES BIOPHARMA GLOBAL s.r.o., V Jámě 1, 110 00 Prague 1, Czech Republic