ViiV Healthcare would like to inform you of a potential safety issue which has been brought to our attention by the Principal Investigator of the above study conducted in Botswana. The potential safety issue is related to Neural Tube Defect (NTD) cases in infants born...
In collaboration with the South African Health Products Regulatory Authority (SAHPRA), the below listed companies would like to inform you of a risk of acute kidney injury (AKI) in patients treated concomitantly with ACE inhibitors / Angiotensin Receptor Blockers (ARBs) and fluoroquinolones....
In collaboration with the South African Health Products Regulatory Authority (SAHPRA), the below listed companies would like to inform you of a risk of acute kidney injury (AKI) in patients treated concomitantly with ACEIs / Angiotensin Receptor blockers (ARBs) and fluoroquinolones....
In collaboration with the South African Health Products Regulatory Authority (SAHPRA), the below listed companies would like to inform you of a risk of acute kidney injury (AKI) in patients treated concomitantly with Angiotensin Converting Enzyme Inhibitors (ACEIs) Angiotensin receptor blockers (ARBs) and fluoroquinolones....
In collaboration with the South African Health Products Regulatory Authority (SAHPRA), the below listed companies would like to inform you of a risk of acute kidney injury (AKI) in patients treated concomitantly with ACEls / Angiotensin receptor blockers (ARBs) and fluoroquinolones. ...
In collaboration with the South African Health Products Regulatory Authority (SAHPRA), the below listed companies would like to inform you of a risk of acute kidney injury (AKI) in patients treated concomitantly with Angiotensin-converting enzyme inhibitors (ACEls) / Angiotensin receptor blockers (ARBs) and fluoroquinolones.
Notification of an important new warning with treatment of patients with anti phospholipid syndrome (APS) and the use Pradaxa: Increased risk of thrombo-embolic events ...
Important safety information on the treatment of patients with antiphospholipid syndrome (APS) and the use of rivaroxaban (Xarelto®) Possible increased risk for recurrent thrombotic events ...
Pfizer Laboratories (Pty) Ltd, in agreement with South African Health Products Regulatory Authority (SAHPRA), would like to inform you of the following changes to the Professional Information of Eliquis (apixaban). ...
In collaboration with the South African Health Products Regulatory Authority (SAHPRA), Novartis SA (Pty) Ltd would like to inform you of a risk of acute kidney injury (AKI) in patients treated concomitantly with Angiotensin Converting Enzyme Inhibitors (ACEIs) /Angiotensin receptor blockers (ARBs) and fluoroquinolones. ...
