Warnings

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Prexige to be withdrawn in Canada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

Recall of a Batch of Baby's Bliss Gripe Water, Apple flavor from US markets

September 22, 2007, the US Food and drug Administration, the American's equivalent to the Saudi Food and Drug Authority...

2007-09-22