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Drug Safety and Recall Information
Gateway Health Plan® is committed to providing our members with the highest quality of care. In order to do so, we find it necessary to provide you with drug safety information. Drug safety information can come in the form of drug safety alerts or Medication Guides.
The Food and Drug Administration (FDA) approves Medication Guides, which are handouts that come with specific drugs you get at the pharmacy. The FDA requires Medication Guides be given with these drugs to provide patients with information about the drug to prevent serious side effects. All medication guides provided by the FDA can be found at this link: http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm085729.htm
Drug Recalls and Withdrawals
Gateway Health Plan® has been notified by the Food and Drug Administration (FDA) that the medications will no longer be available due to safety reasons.
If you are currently taking any of these medications, Gateway Health Plan® will contact you and your physician to make you aware of this drug withdrawal. In the meantime, it is suggested you do the following:
- Call your doctor right away. You and your doctor should talk about if you should stop taking the drug immediately. Your doctor may suggest another drug that is safe and effective for treating your condition.
- If you have questions about the right way to dispose of the drug, call the pharmacy that filled the drug for help.
Your doctor will be able to answer your questions about how this may or may not have an effect on your health. There are covered alternatives that may be available to replace the drug that has been withdrawn from the market. If your doctor has questions about coverage of an alternative drug that has been or will be prescribed for you, your doctor can call our pharmacy services department.
If you have any questions or concerns about this matter, please call our member services department at 1-800-685-5209, 8:00am-8:00pm, 7 days a week. TTY users should call 1-800-654-5988.
| Drug |
Date Withdrawn from the Market |
| Two lots of GammaGard Liquid made by Baxter BioScience (lot LE12J370AB, expiration date November 21, 2012 and lot LE12J379AB, expiration date November 29, 2012 |
Date released: 6/4/2010 |
All lots of certain liquid over-the-counter (OTC) products including Tylenol, Motrin, Benadryl, and Zyrtec products.
To view the full list of products being recalled, click on the following link:
www.mcneilproductrecall.com
|
Date released: 5/3/2010 |
Seven Asthma and COPD Inhalers that contain Ozone-depleting chlorofluorocarbons (CFCs)
Full product list and their phase out schedule can be viewed by clicking on the following link:
http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm208302.htm |
Date Released: 4/14/2010 |
Eight lots of One Touch® Sure Step® Test Strips made by LifeScan (lots 2969251, 2969798, 2982369, 2983467, 2969795, 2982566, 2969481, 2998193) |
Date Released: 2/26/2010 |
Moban tablets all strengths (5mg, 10mg, 25mg, and 50mg) Discontinuation by Endo Pharmaceuticals |
Supply expected to be depleted by June 30, 2010 |
Certain OTC products made by McNeil Consumer Healthcare Full product list can be viewed by clicking on the following link: FULL RECALLED PRODUCT LIST (PDF - 179.38 KB) |
Date Released: 1/15/2010 |
| TYLENOL® Arthritis Pain Caplet 100 count bottles, with the red EZ-OPEN CAP, (all lots made by McNeil Consumer Healthcare) |
Date Released: 12/28/09 |
| Azmacort Inhaler Discontinuation by Abbott Laboratories |
12/31/09 |
| Accusure Insulin Syringes made by Qualitest Pharmaceuticals |
Date Release: 10/28/09 |
| Generic Adderall 20mg made by Barr Laboratories, Inc. (Lot number 311756) |
Date Release: 8/13/09 |
| Novolin Innolet and PenFills (N, R, and 70/30) by NovoNordisk, Inc. |
Date Release: 8/10/09
*Will be available until supplies are exhausted |
| Intal Inhaler Discontinuation by King Pharmaceuticals, Inc. |
Date Release: 7/31/2009
*Will be available until supplies are exhausted |
| Concentrated Acetaminophen Drops (80mg/0.8mL) made by Brookstone Pharmaceuticals |
7/14/2009 |
| Digoxin 0.25mg repackaged by AS Medication Solutions |
5/11/2009 |
| Raptiva (efalizumab) made by Genentech, Inc. |
Date Released: 4/8/2009
Date Withdrawn from market: 6/8/2009 |
| Digoxin (Caraco Brand) 0.125mg and 0.25mg tablets |
3/31/2009 |
| Propafenone HCl 225mg tablets (lot 112680A) made by Watson Pharmaceuticals, Inc. |
3/25/2009 |
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