AZN AstraZeneca PLC

AstraZeneca Initiates Voluntary Nationwide Recall of One Lot of BRILINTA 90mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle from That Lot

AstraZeneca today announced that the Company is notifying physicians and consumers that it is voluntarily recalling one lot of professional (physician) sample bottles containing eight tablets of BRILINTA® (ticagrelor) 90mg tablets as a precautionary measure. This voluntary recall follows a report that a professional sample bottle containing eight tablets of BRILINTA 90mg also contained another medicine called ZURAMPIC® (lesinurad) 200mg tablets which is also manufactured by AstraZeneca.

This Smart News Release features multimedia. View the full release here: http://www.businesswire.com/news/home/20170525006119/en/

 BRILINTA 90mg (Photo: Business Wire)

BRILINTA 90mg (Photo: Business Wire)

This precautionary measure is limited to one lot (BRILINTA lot #JB5047) of professional sample bottles containing eight tablets of BRILINTA 90mg distributed to physicians in the US between March and April of 2017. Other forms and dosage strengths of BRILINTA, including medicine obtained via US retail or mail order pharmacies, are not affected by this voluntary recall. This recall does not affect ZURAMPIC.

Unintentional dosing with ZURAMPIC has the potential to lead to adverse renal effects including acute renal failure which is more common when ZURAMPIC is given alone as it should be used in combination with a xanthine oxidase inhibitor. BRILINTA has a warning in its prescribing information regarding discontinuation of the medicine. Missed doses of BRILINTA increases the risk of heart attack and stroke. People who are treated with a stent and miss doses of BRILINTA have a higher risk of getting a blood clot in the stent, having a heart attack, or death. Patients should not stop taking BRILINTA without talking to their prescribing doctor. To date, AstraZeneca has not received any reports of adverse events related to this recall.

BRILINTA is indicated to reduce the rate of CV death, heart attack and stroke in patients with acute coronary syndrome (ACS) or a history of heart attack. BRILINTA also reduces the rate of stent thrombosis in patients who have been stented for treatment of ACS. ZURAMPIC is a prescription medicine used together with a xanthine oxidase inhibitor such as allopurinol or Uloric in adults with gout who still have a high uric acid level.

BRILINTA 90mg tablets are supplied as a round, biconvex, yellow, film-coated tablet, and imprinted with 90 above a T on one side of the pill. ZURAMPIC tablets 200mg are blue in color and elliptical/oval in shape. They are imprinted with LES200 on one side of the pill.

AstraZeneca is notifying physicians by recall letter and is arranging for return of all recalled products. Consumers that have medicine which is being recalled should contact their physician.

Consumers with questions regarding this recall can contact the AstraZeneca Information Center at 1-800-236-9933 between the hours of 8 a.m. and 6 p.m. (Eastern Time) Monday to Friday, excluding holidays. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this medicine.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Patient safety is a top priority for AstraZeneca and we are working closely on this recall with the knowledge of the U.S. Food and Drug Administration in taking the appropriate course of action.

About AstraZeneca

AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines, primarily for the treatment of diseases in three main therapy areas - Oncology, Cardiovascular & Metabolic Diseases and Respiratory. The Company also is selectively active in the areas of autoimmunity, neuroscience and infection. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information, please visit www.astrazeneca-us.com and follow us on Twitter @AstraZenecaUS.

EN
25/05/2017

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on AstraZeneca PLC

AstraZeneca PLC - September 2025 (LTM): Peer Snapshot

Compares key performance metrics against industry peers.

Dominic Rose ... (+2)
  • Dominic Rose
  • Naresh Chouhan

Thematic - 2026 Outlook - "5 More Years" (55pgs)

For access to the full note, please contact Naresh Chouhan ( ) With EU Pharma (ex-Novo) now having reached decade high valuations vs EuroStoxx600, we believe the sector has broken out & the sustainability of the growth profile will now generate continued strong performance. Consensus 5yr sales & EPS CAGR’s stand at 4% & 7% for 15x 2026 PE. We show there is upside to this from underestimated pipelines where cons. rarely fully models “monster” drugs & from M&A which we expect to be strong at JPM ...

AstraZeneca: 1 director

A director at AstraZeneca sold 7,500 shares at 177.269USD and the significance rating of the trade was 69/100. Is that information sufficient for you to make an investment decision? This report gives details of those trades and adds context and analysis to them such that you can judge whether these trading decisions are ones worth following. Included in the report is a detailed share price chart which plots discretionary trades by all the company's directors over the last two years clearly sho...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch