![]() improvement of lymphatic drainage, the non-specific immune defense, and conditions such as benign hypertrophy of lymph nodes, chronic tonsillitis, tonsillar hypertrophy and lymphatic edema.” treatment of nerve pain, soft tissue rheumatism and symptoms of disc protrusion.” support of the immune system to reduce severity and duration of symptoms in viral infections, particularly in the early stages of colds and influenza-like illnesses.” treatment of injuries, inflammatory and degenerative conditions of the musculoskeletal system and for the relief of associated symptoms such as pain.” ![]() ![]() treatment of arthrosis/osteoarthritis, and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.” In addition, the FDA warned that the products are concerning because they are labeled to contain ingredients such as “mercurius solubilis” (mercury) and “embryo totalis suis,” which could be toxic or otherwise harmful.Īccording to the FDA, claims made by MediNatura on its website include: In its letter, dated June 11, the FDA referenced several MediNatura products, including “Zeel Injection Solution,” “Traumeel Injection Solution,” “Engystol Injection Solution,” “Neuralgo Rheum Injection Solution,” “Lymphomyosot X Injection Solution” and “Spascupreel Injection Solution.” According to the FDA, these products are unapproved new and misbranded drugs under the Federal Food, Drug, and Cosmetic Act. These warning letters reflect our continued commitment to patient safety.” The FDA warned that some injectable homeopathic products are concerning because they are labeled to contain “potentially toxic or otherwise harmful ingredients, such as ‘mercurius solubilis’ (mercury) and ‘embryo totalis suis.’”Īshley added that “these products are further concerning given that they are labeled to contain potentially toxic ingredients intended for injection directly into the body. “These unapproved injectable drugs are particularly concerning because they inherently present greater risks to patients because of how they are administered.” Ashley, JD, director of the Office of Compliance in the FDA’s Center for Drug Evaluation and Research, said in a press release. “The FDA’s drug approval requirements are designed to protect patients by ensuring, among other things, that drugs are safe and effective for their intended uses,” Donald D. The FDA has issued a warning letter to MediNatura Inc., ordering the company to cease illegal marketing of unapproved injectable homeopathic products that claim to treat “inflammatory and degenerative conditions of the musculoskeletal system” and relieve pain, swelling and joint stiffness. If you continue to have this issue please contact to Healio
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