These risks depend on several factors that a health care professional must assess. Suddenly stopping corticosteroids after long-term use or high doses can result in a serious withdrawal syndrome that includes fatigue, nausea, low blood pressure, low blood glucose levels, fever, dizziness, muscle and joint pain, and shortness of breath. These drug ingredients, which are not listed on the product label, can also interact with other drugs a consumer is taking.įDA has received adverse event reports, including of liver toxicity and death, associated with the use of Artri King products, since the agency issued its first warning about an Artri Ajo King product on January 5, 2022. Methocarbamol (a muscle relaxant) that can cause sedation, dizziness, and low blood pressure.Diclofenac sodium (an anti-inflammatory drug) that can lead to adverse cardiovascular events, such as heart attack and stroke, or serious gastrointestinal damage, including bleeding, ulceration, and fatal tears of the stomach and intestines, or liver toxicity including liver failure that can cause the need for a liver transplant or death.Dexamethasone (a corticosteroid) that can cause serious adverse events, including infections, increased blood glucose (sugar) levels, changes in blood pressure, damage to bones, psychiatric problems, and adrenal dysfunction.These products are promoted for treating arthritis, muscle pain, osteoporosis, bone cancer, and other conditions and are sold on various websites and in some retail stores.įDA laboratory analyses revealed certain Artri and Ortiga products contain the undeclared drug ingredients: FDA urges consumers taking these products to immediately talk to their health care professional (e.g., doctor) to safely discontinue use of the product because suddenly stopping these drugs may be dangerous. FDA is warning consumers not to purchase or use products marketed with variations of the names “Artri” or “Ortiga” due to potentially dangerous hidden active drug ingredients not listed on the product label. FDA has received over 60 reports of adverse event reports from use of Artri King and similarly named products since the initial publication of the alert.
FDA continues to warn consumers that use of Artri and Ortiga products carries the risk of symptoms such as sedation, dizziness, low blood pressure, liver toxicity, bleeding in the gastrointestinal track, perforation of the intestines and stomach, or death. Walmart and Latin Foods Market already issued voluntary recalls for these products. In support of public safety, and because some of these products may still be available on the market, FDA issued warning letters to Amazon, Walmart, and Latin Foods Market for distributing various “Artri” and/or “Ortiga” unapproved and misbranded drug products.
In addition, the agency issued a warning letter and an import alert for certain products. FDA continues to warn consumers to avoid use of these products that contain potentially harmful hidden ingredients. Some of these problems can be life threatening or fatal. Reported harmful effects include sudden weight gain, serious gastrointestinal damage including bleeding and ulceration, increased blood glucose (sugar) levels, adrenal dysfunction, liver toxicity, and other serious conditions. Since April 20, 2022, FDA learned that more than 30 additional consumers have experienced a serious health effect after using unapproved over-the-counter products with “Artri” or “Ortiga” in the product name.
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