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The U.S. Food & Drug Administration (FDA) is warning the public that some vials of Tyenne have been recalled.
The affected vials are being recalled over concerns they may contain glass particles.
Here’s how to tell if your medication is included in the recall.
If you have rheumatoid arthritis and take an injection medication to treat your symptoms, you may want to take another look at your medicine cabinet. Injection vials of the prescription arthritis medication Tyenne are being recalled nationwide, according to the U.S. Food & Drug Administration (FDA).
Tyenne is a common medication used for adults who have moderate to…
Read the full article at PREVENTION.COM
