Report an adverse reaction
For Top Pharma products
DRUG MANUFACTURING COMPANIES:
BIAL – Portela & Cª, Portugalia
Deerland Probiotics Enzymes, Danemarca
Krewel Meuselbach, Germania
Fidia Farmaceutici S.p.A., Italia
Qualiphar N.V., Belgia
Pharma Line S.r.l., Italia
ICB PHARMA, Polonia
PLEURAN, s.r.o., Slovacia
Iuppa Industriale S.r.l., Italia
Gifrer Barbezat, Franța
Laboratorio Farmaceutico C.T. S.r.l., Italia
Alkaloid AD Skopje, Macedonia de Nord
ADM Denmark A/S, Danemarca
OMIKRON ITALIA S.r.l., Italia
STE PHARMACEUTICALS S.L.U, Spania
Lallemand, Canada
SAS Lallemand, Franța
PharmaS, Croația
RAD Neurim Pharmaceuticals EEC SARL, Franța
Biomedica Foscama Industria Chimico-Farmaceutica S.p.A., Italia
REPORT TO MANUFACTURER
1. Send the information to the email address: pharmacovigilance@toppharm.md if you have had an adverse reaction.
2. Contact the person in charge of the pharmacovigilance system at Top-Pharm at numbers:
Mobile phone available 24/7: +373 78 897 141
Phone during office hours: +373 22 241 126
REPORT TO MMDA
1. Download Patient record from the Medicines and Medical Devices Agency (MMDA) website (https://amdm.gov.md/ro/page/alte-mod-derap ).
The form should be printed, filled in with the most accurate information and sent to MMDA at the email address:pharmacovigilenta@amdm.gov.md.
2. Contact the Pharmacovigilance and Clinical Trials Department of MMDA at:+373 22 88 43 38.