Digitek recall fda

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digitek

390388 tn?1279636213 00 -0500 Actavis Totowa LLC, a United States manufacturing division of the international generic pharmaceutical company Actavis Group, is initiating a Class I nationwide recall of Digitek (digoxin tablets, USP, all strengths) for oral use. The products are distributed by Mylan Pharmaceuticals Inc., under a "Bertek" label and by UDL Laboratories, Inc. under a "UDL" label.
162069 tn?1224677411 I was talking to my husband just the other day about her. We were speaking about the old digoxin recall (back in April) that was posted and I was wondering how she was doing. I'm so glad to hear the good news. Now hopefully the pac's will ease up too. :-) Take care.
Avatar n tn I did have a chest infection about one-month before my last heart episode. Did you also hear about the Digitek recall and that problem? I stopped taking it the week my breathing problem stopped?
1916673 tn?1420233270 On April 22, 2015, the FDA announced that Nylabone Products of Neptune, New Jersey, is recalling one lot of its Puppy Starter Kit dog chews due to possible contamination with Salmonella bacteria. For more information, please follow this link: http://clicks.aweber.com/y/ct/?l=AeZ.
Avatar n tn I did have a chest infection about one-month before my last heart episode. Did you also hear about the Digitek recall and that problem? I stopped taking it the week my breathing problem stopped?
675347 tn?1365460645 The FDA has announced that Midwestern Pet Food is expanding its recent recall to include more brands and over 1000 lots of its dog and cat foods because they contain potentially deadly levels of aflatoxin. FDA is aware of at least 70 deaths and 80 illnesses in dogs who ate the affected products. For full details, please visit the following link: https://www.dogfoodadvisor.
Avatar f tn Lanoxin has not been recalled.... digitek was recalled..
Avatar f tn As Toprol also reduces blood pressure and I have low blood pressure as it is, I started having dizziness and nausea. He then put me on Digitek, which has since been recalled and I havebeen on 0.25 mg of digoxin for about 2 months. I recently started to have cramps, abnormal bowel movements and I feel very exhausted. The doctor reduced the dosage to .125 mg and on the first day I felt better until about 6PM and then the cramps started again.
566175 tn?1278430472 And even if you have peanut butter products that arent included in the recall, it still may be a good idea to throw out any thing that you're not sure about. Taking care of our September mommies and babies!!
Avatar f tn t know if they still are but earlier the website was having technical issues and it was saying that ANY lot number you put in was not part of the recall. I followed the link on the main recall page that gives you a pdf of ALL lot numbers that are part of it just to be safe because we use Similac too. The can I've been using isn't listed but I'm still scared to use it.
Avatar f tn By Parija Kavilanz, senior writerMay 14, 2010: 8:28 PM ET NEW YORK (CNNMoney.com) -- The quality and safety violations that led to the shutdown of a Tylenol plant were extremely serious, and could lead to tough action by regulators on drugmaker Johnson & Johnson.
82861 tn?1333453911 Me967 just sent me this information from the FDA. Thanks!
356518 tn?1322263642 http://www.iguard.org/r/058JiD8999Cs * * * * WHAT DOES THIS MEAN? This recall for Ultram ER Extended-Release Tablets, 100 mg was issued at a warehouse and pharmacy level only. The FDA and the manufacturer have determined that any recalled product that may have been dispensed to patients does not pose a significant health risk. If you take Ultram ER Extended-Release Tablets, 100 mg, you should follow up with your physician if you are concerned or are experiencing side effects..
874521 tn?1424116797 //efoodalert.blogspot.com/2010/08/fda-focus-on-pet-products-stimulates.
Avatar f tn I was a participant in the thread on this forum in 2008, and there was a recall on digitek ( a generic) and it was an overdose issue and caused serious injury. If my memory serves. I find it interesting, and it may be true, if telling a patient of the possible side effect may have a placebo effect.
94902 tn?1330479667 There has been a recall of certain Infants and Childrens Tylenol. You can get more info at the following link: www . tylenol.com/page.jhtml?id=tylenol/news/subpchildinfantnews. inc (take out the spaces). Also there is even more info at McNeil Consumer Healthcare that states that the Tylenol may have been exposed Burkholderia cepacia (B. cepacia) bacteria.
Avatar f tn t improved at all in the 6 months he has been seeing me, HOWEVER I am able to control my diplopia about 95% of the time. Currently I will be seen every 3 months to determine if muscle surgery will be performed. In the meantime, I will live with the double vision. My question for you Dr. Hagan, is that if in the future, you do more research on cataract surgery anesthesia and diplopia if I could be involved in your study.
179856 tn?1333547362 The contaminated product has the potential to cause serious problems, including dangerous blood clots, Amgen said in a press release announcing the recall. However, Amgen said there had been no complaints that can be directly attributed to the presence of glass. It said certain lots were being voluntarily recalled as a precaution.
1118724 tn?1357010591 Genentech Informs Customers of Important Information about Triad Group's Alcohol Prep Pads Consumers Alerted to Discontinue Use of Alcohol Prep Pads Packaged with Boniva Injection, Fuzeon, Nutropin A.Q. Pen, Pegasys, TNKase Medicines South San Francisco, Calif. -- January 13, 2011 -- Genentech, Inc.
29837 tn?1414534648 Today I got not one but two calls from the FDA, so apparently my persistence is paying off. They are going to do whatever the pharmaceutical companies suggest, especially since there are no other alternative drugs except Interferon and Ribavirin. My contact at Vertex, who I just spoke to, is going to look once more into the IND application (Compassionate Use), and see if there's been any changes in their (Vertex) policy for allowing it.
675347 tn?1365460645 December 30, 2020 — The FDA is alerting consumers that Midwestern Pet Foods, Inc. is recalling nine lots of Sportmix pet food products because they contain potentially fatal levels of aflatoxin. FDA is aware of at least 28 deaths and 8 illnesses in dogs that ate the recalled products. For more information please go to the website Dog Food Advisor: https://www.dogfoodadvisor.