PHARMACOVIGILANCE

Pharmacovigilance is the scientific field of monitoring the safety of drugs and procedures in order to minimize risks and improve the therapeutic effects of their use. To achieve this, the collection and management of data related to drug safety, detection of signs of danger, and evaluation of data is required.

 

Pharmacovigilance is the scientific field of monitoring the safety of drugs and procedures in order to minimize risks and improve the therapeutic effects of their use. To achieve this, the collection and management of data related to drug safety, detection of signs of danger, and evaluation of data is required.

 

Information on the occurrence of adverse events comes either directly from Healthcare Professionals (Pharmacists, Physicians, Nurses) or/and through the Marketing Authorization Holders (MAHs), or from the patients themselves, through the Healthcare Professionals.

 

Adverse events can be reported in any way.

 

• To Healthcare Professionals (Pharmacists, Physicians, Nurses)

 

To the Marketing Authorization Holder:

• By phone at: (+30) 2310909656
• By phone at: (+30) 2310909656
• By e-mail at: info@crosspharma.gr

 

To the Pharmacovigilance Department:

• By phone at: (+30) 210-2838200
• By e-mail at: pv@globaldevelopment.gr

 

To the National Agency for Medicines (NAM), Department of Adverse Events, by submitting a Yellow Card in the following ways:

• To the National Agency for Medicines (NAM), Department of Adverse Events, by submitting a Yellow Card in the following ways: http://www.eof.gr/web/guest/yellowgeneral
• Sending the Yellow Card in print by post, free of charge, to the Department of Adverse Events of the NAM (284, Mesogeion Av., Cholargos, 15562). Contact phone no.: (+30) 20.40.380 or (+30) 213.20.40.337
• Submit the yellow card by fax at: (+30) 6549.585

 

When submitting a report, please provide as much information as possible, including information on medical history, any co-administration of other medicines, as well as the dates when the medicines were taken and the adverse events occurred.