Warnings

Serious Safety concerns with the use of Edetate Disodium

January 16, 2008 – The U.S Food and Drug Administration (FDA), the equivalent of the Saudi Food and Drug Authority (SFDA...

2008-01-20

SEVERE BONE, JOINT AND/OR MUSCLE PAIN WITH THE POPULAR BISPHOSPHONATE DRUGS USED TO TREAT OSTEOPOROSIS

January 7, 2008 – The U.S. FDA, the equivalent of the Saudi Food and Drug Authority issued an alert on the possibility...

2008-01-09

US FDA: Dangerous Or Fatal Skin Reactions In Patients With A Particular Human Leukocyte Antigen following Carbamazepine therapy

12th December 2007, FDA informed healthcare professionals that dangerous or even fatal skin reactions (Stevens Johnson...

2008-01-05

Use of intravenous magnesium to treat acute onset atrial fibrillation

The objective was To assess the effects of intravenous magnesium on converting acute onset atrial fibrillation to sinus...

2007-11-28

EMEA adds warnings in the prescribing information of Strontium Ranelate (Protelos)

On November 16, 2007, the European Medicine Agency (EMEA), the European's equivalent to the Saudi Food and Drug...

2007-11-20

Use of CellCept (mycophenolate mofetil) associated with increased pregnancy loss and congenital malformations

October, 29th , 2007, US FDA, the American's equivalent to the Saudi Food and Drug Authority (SFDA), Published...

2007-10-31

Information for Healthcare professionals about Exenatide (marketed as Byetta)

October 16, 2007 , The U.S Food and Drug Administration (FDA), equivalents of the Saudi Food and Drug Authority (SFDA)...

2007-10-22

Prexige to be withdrawn in Canada

October 4, 2007, Health Canada the equivalent of the Saudi Food and Drug Authority (SFDA), announced that it has stopped...

2007-10-22

FDA Takes Action to Stop Marketing of Unapproved Hydrocodone Products

September 28, 2007 – The U.S Food and Drug Administration (FDA), equivalents to the Saudi Food and Drug Authority (SFDA)...

2007-09-30