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Posted January 30, 2018

Limbrel for Osteoarthritis Recalled Due to Risk of Adverse Effects

On January 26, 2018, Primus Pharmaceuticals, Inc. of Scottsdale, Arizona issued a recall of all unexpired lots of Limbrel products. FDA  requested the recall due to rare but serious side effects (which are reversible), including drug-induced liver injury and/or hypersensitivity pneumonitis, associated with the use of Limbrel

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