... After the judgement, the defendant actually filed bankruptcy even though they had revenues of $22m in 2020 alone. Inappropriate content . On 6 June 2020, mayor of Kaohsiung, Han Kuo-yu, became the first mayor to be recalled. When Your Drug is Recalled. There have been only a few vaccine recalls or withdrawals due to concerns about either how well the vaccine was working or about its safety. if you have ever had an allergic reaction to this product or any of its ingredients, trouble urinating due to an enlarged prostate gland, persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema, a cough which is accompanied by excessive phlegm (mucus), taking prescription drugs for asthma, obesity, weight control, depression, or psychiatric or emotional conditions, taking any drug that contains phenylephrine, pseudoephedrine, ephedrine, or caffeine (such as for allergy, cough-cold, or pain), avoid foods or beverages that contain caffeine, avoid dietary supplements containing ingredients reported or claimed to have stimulant effect, your asthma is getting worse (see Asthma Alert), you have tremors, nervousness, or seizure. On Sept. 17, 2020, Acella Pharmaceuticals further announced that one lot of 15 mg and one lot of 120 mg NP Thyroid (thyroid tablets, USP) are being recalled because testing has found these lots to be subpotent. have more than 2 asthma attacks in a week. Continued What to Do if a Drug You're Taking Is Recalled. It seems just as the seasons begin … Ask a doctor or pharmacist before use if you are. Luckily it's also half the guafinesin. It helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus, drain bronchial tubes and … 13 September 2017 . Bronkaid contains 63.24% of pure ephedrine and 36.76% sulfate ions. Although neither amlodipine nor hydrochlorothiazide are currently under recall on their own, they are when combined with some other medications. If the pressure is too high, there’s a risk that the heart will work too hard. Teva Pharmaceuticals USA has issued a voluntary nationwide recall of "all lots of Amlodipine / Valsartan combination tablets and Amlodipine / Valsartan / Hydrochlorothiazide combination tablets. your risk of heart attack or stroke increases if you: have a history of high blood pressure or heart disease, take this product more frequently or take more than the recommended dose, Taxotere side effects include permanent hair loss, Diabetes drug Invokana lawsuit information, Problems from Essure birth control procedure, use more than 4 caplets in 24 hours for more than 3 days a week. Hey everybody, If you don't feel like reading this post, all the information is at the top in quotes. My wife has severe asthma, and Primatene is the only thing that keeps us from having to drive to the emergency room once or twice a month. The investigation is ongoing and the FDA continues to update the list of medications being recalled here. Follow Following. When a drug or device manages to get past the testing of a drug company, or that company intentionally lets it get through, and it is found to cause an unacceptable level of harm, it may be recalled. Do not take more than 6 caplets in 24 hours or as directed by a doctor. When medications are recalled the FDA issues an announcement, as do the drug companies responsible for the drug being recalled. Tulsie N. Patel, MD is a chief resident in psychiatry from Dallas, TX, working with the ABC News Medical Unit. THe study found that the vehicle most often recalled during the period in question was the Mercedes-Benz C-Class. FSIS Issues Public Health Alert for Meat and Poultry Taquitos and Chimichangas Containing FDA-Regulated Diced Green Chilies That Have Been Recalled Due to Possible Foreign Matter Contamination (Aug 1, 2020) December 9, 2020 Spirit Halloween Recalls Children’s Flashlights Due to Fire and Burn Hazards Sold at: Walmart.com. High blood pressure can develop for several reasons, including having a family history, obesity, smoking, high-salt diets, diabetes, lack of exercise and underlying kidney disease. A product recall is a request from a manufacturer to return a product after the discovery of safety issues or product defects that might endanger the consumer or put the maker/seller at risk of legal action.. Other lots of losartan as well as other drugs from several manufacturers have been recalled voluntarily in recent months as well due to contamination from other chemicals. The rep urged that anyone who is taking these medications should call Torrent Pharmaceuticals Limited at 1-888-280-2040. The engine ground cable is too short and may fail. Following is a list of possible medication recalls, market withdrawals, alerts and warnings. If you hear that a medication you are using has been recalled, you should take a few steps: Learn more about the recall. Why would a vaccine, or certain batches of a vaccine, be withdrawn or recalled? Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Bayer Consumer Care has begun a voluntary recall of 56 lots of Bronkaid (ephedrine sulfate and guaifenesin) Caplets Dual Action Formula. The FDA Alert(s) below may be specifically about Bronkaid Mist or relate to a group or class of drugs which include Bronkaid Mist (epinephrine). 939,090 votes within 969,259 agreed the recall. Some of the recalled lots contain a combination of medications. There was something else they replaced it with, but it was an inhaler and not a tablet. Generic drugs are recalled more often, overall. The Recalls, Market Withdrawals & Safety Alerts are available on FDA’s website for three years before being archived. Torrent Pharmaceuticals Limited said it suspects that contamination is related to manufacturing at a specific site and is therefore working on "manufacturing and distributing new pills without the contaminant.". NDMA is a chemical that forms in both industrial and natural processes. I notice the generic is E HCL where Bronkaid is Sulfate. Studies now show a link between the drugs and chronic kidney disease, in which the kidneys lose their ability to filter blood effectively. Blood pressure measurements are actually two measurements: systolic, which is when the heart squeezes blood through the body, and diastolic, which is the pressure of blood when the heart is at rest. Over the past year, the FDA has recalled multiple blood pressure medications from several manufacturers after discovering potential carcinogens in some batches. If you’re taking a blood pressure medication that was recently recalled, do not stop taking it. Primatene contains 81.92% of pure ephedrine and 18.08% hydrogen chloride ions. While your target blood pressure is often determined by your age and medical conditions, most doctors recommend keeping it around 120/80. So I purchased primatene tablets and it’s hcl, just curious to know the difference. The product may have as low as 87% of the labeled amount of levothyroxine (T4). Poorly written . Several vaccine lots have been recalled in recent years because of a possible safety concern before anyone reported any injury. They are asked to consult their physicians or pharmacists before making any changes to their medication regimen. MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. A voluntary recall of 56 lots of Bronkaid Caplets Dual Action Formula was initiated by Bayer HealthCare’s Consumer Care division after discovering that certain information was inadvertently omitted from the product carton label. Drug shortages statistics, and best practices, guidelines and publications related to drug shortages For example, a combination of valsartan, amlodipine and hydrochlorothiazide is one product that has been recalled. Those voluntary recalls came after the discovery of the chemicals NDMA and NDEA -- both probable human carcinogens -- at levels far above what the FDA considers an acceptable daily intake. Talk to your doctor to find out if you can switch to a different medication safely. This could increase your risk of heart attack or stroke, which may cause death. It’s believed they became contaminated during the manufacturing process. Stopping any medication cold turkey is a bad idea. The engine ground cable is too short and may fail Autocar is recalling 116 model year 2020-2021 Xpeditors equipped with X12N engines. It’s believed they became contaminated during the manufacturing process. If the recall involves an over-the-counter drug, stop taking it at once. Losartan, a blood pressure medication in the angiotensin II receptor blocker (ARB) class, helps reduce blood pressure by preventing blood vessels from narrowing or constricting. I bought the Walgreens Primatine generic. A year after the 2015 Ukrainian local elections, voters can achieve a recall election of an elected deputy or mayor if as … Over the past year, the FDA has recalled multiple blood pressure medications from several manufacturers after discovering potential carcinogens in some batches. Found out there is a Bronkaid recall. If your doctor says your blood pressure is 130/80, the 130 would be systolic and the 80 would be diastolic. Although the FDA may identify concerns regarding the safety of a drug, it is the responsibility of the manufacturer to initiate and execute a recall. The recalled products have U.S. Food and Drug Administration (FDA) approval and in many cases, are widely ingested, injected or implanted before being recalled. 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