Publicly accessible professional information service
(Veřejně přístupná odborná informační služba – VPOIS)
You have entered the publicly accessible area that contains information about all Biomedica medicinal products registered in the Czech Republic. The obligation to establish this “Publicly accessible professional information service – VPOIS“ results from Act No. 378/2007 Sb., as amended (§ 33 odst. 3 písm. g) bod 1).
If your inquiry is urgent, please contact your doctor, or the 24/7 medical service.
If you suspect and 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
Státní ústav pro kontrolu léčiv (State Institute for Drug Control)
oddělení farmakovigilance (Pharmacovigilance Department)
100 41 Praha 10
By reporting of adverse reactions, you can contribute to obtaining more information about the safety of the medicinal product.
You can also report the suspicion of adverse reactions and other information about the safety of medicinal products of Biomedica, spol. s r.o. by e-mail: email@example.com or by phone: +420 257 084 204.
Current information about the preparations of Biomedica, spol. s r.o. can be found on the website of the State Institute for Drug Control.
Information from the Summary of Product Characteristic (SPC) is intended for healthcare professionals, whilst information from the Patient Information Leaflet (PIL) is for the general public.
In case of any questions about a specific product of Biomedica, spol. s r.o. contact us at firstname.lastname@example.org or +420 257 084 204.