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Warning Date
    2007-08-13

FDA Warns Consumers in USA to Avoid Red Yeast Rice Products Promoted on Internet as Treatments for High Cholesterol

2007-08-13

The U.S. Food and Drug Administration is warning consumers in USA not to buy or eat three red yeast rice products promoted and sold on Web sites. The products may contain an unauthorized drug that could be harmful to health. The products are promoted as dietary supplements for treating high cholesterol.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-08-18

Risk of Serious Adverse Drug Events Associated with the Use of Botulinum Toxin Products (Botox)

2007-08-18

The Medicines and Healthcare products Regulatory Agency (MHRA), the British equivalent of the Saudi Food and Drug Authority (SFDA), announced that reports have been received of serious adverse drug reactions, including deaths, associated with the use of botulinum toxin products. Botox is the only brand name product registered by the Ministry of Health in Saudi Arabia.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-08-19

Stronger Heart Failure Risk Warnings for the Diabetes Drugs Rosiglitazone (Avandia) and Pioglitazone (Actos)

2007-08-19

The American Food and Drug Administration (FDA), the U.S. equivalent to the Saudi Food & Drug Authority(SFDA), that the manufacturers of the drugs rosiglitazone (Avandia) and pioglitazone (Actos) will revise the prescribing information for these drugs to include stronger warnings about the risk of congestive heart failure when these drug are used to treat type-2 diabetes.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-08-20

Possible Life-Threatening Adverse Effects in Babies of Nursing Mothers Prescribed the Painkiller Codeine

2007-08-20

The U.S. equivalent of the Saudi Food and Drug Authority (SFDA) announced important new information about serious, potentially life-threatening adverse drug effects in nursing infants whose mothers are taking the common painkiller and cough suppressant codeine. A list of some codeine containing products available in The Kingdom accompanies this alert.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-08-29

Prexige 200mg and 400mg tablets to be withdrawn in New Zealand

2007-08-29

Consents allowing the supply of 200mg and 400mg tablets of the COX-2 anti-inflammatory medicine Prexige have been revoked in New Zealand by the Medicines and Medical Devices Safety Authority, Medsafe.

Novartis, the pharmaceutical company sponsoring the medicine, is issuing a recall notice to suppliers of the tablets today.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-08-29

Confidence Inc. Issues A Voluntary Recall Of One Lot Of METABOSLIM Apple Cider Vinegar Brand Dietary Supplement Because It Contains The Undeclared Drug Ingredient Sibutramine

2007-08-29

Confidence Inc. informed consumers and healthcare professionals that the company is recalling one lot of METABOSLIM Apple Cider Vinegar Brand Dietary Supplement Capsules (Lot: 3001006, Exp. 10/2009) because the product contains the undeclared drug ingredient sibutramine, an FDA approved drug used as an appetite suppressant for weight loss. The FDA has not approved METABOSLIM Apple Cider Vinegar Brand Dietary Supplement Capsules as a drug, therefore the safety and effectiveness of this product is unknown.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-08-29

Health Canada reminds consumers about the risks of buying drugs online

2007-08-29

Health Canada is reminding Canadians about the potential dangers of buying prescription drugs online, following the July 4th release of the British Columbia Coroner’s report on the death of a woman which was attributed to prescription drugs purchased online.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-09-17

Normal Saline Flush Syringes Manufactured By B. Braun Medical Inc. Recalled Due To Presence Of Medical Grade Silicone

2007-09-17

September 15, 2007, the US Food and drug Administration, the American's equivalent to the Saudi Food and Drug Authority (SFDA), announced important safety information regarding Normal Saline Flush Syringes

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-09-22

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

2007-09-22

September 22, 2007, the US Food and drug Administration, the American's equivalent to the Saudi Food and Drug Authority (SFDA), announced a recall of Baby's Bliss Gripe Water, apple flavor, with a code of 26952V and expiration date of October 2008 (10/08) is being recalled from the US market due to the presence of Cryptosporidium infection.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

Warning Date
    2007-09-30

FDA Takes Action to Stop Marketing of Unapproved Hydrocodone Products

2007-09-30

September 28, 2007 – The U.S Food and Drug Administration (FDA), equivalents to the Saudi Food and Drug Authority (SFDA), informed healthcare professionals and consumers in USA of its intent to take action against companies that market unapproved prescription products containing hydrocodone.

  • To report sector-related issues

  • Call Centre 19999


Other Warnings

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