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Recent Alerts & Recalls

Alert: Recall of gabapentin capsules
Aurobindo Pharma USA is voluntarily recalling a single lot of gabapentin capsules 300 mg in 100-count bottles. The affected lot number is GESB14011-A with an expiration date of 12/2015 and has NDC ...

Alert: Report of PML with Tecfidera
The US Food and Drug Administration (FDA) is warning that a patient with multiple sclerosis (MS) who was being treated with Tecfidera (dimethyl fumarate) developed a rare and serious brain infectio...

Alert: Possible skin reactions with medicine for mental health
The US Food and Drug Administration (FDA) is warning that the medicine ziprasidone (marketed under the brand name, Geodon) is associated with a rare but serious skin reaction known as DRESS (which ...

Alert: Use of male hormone replacement treatment
The Food and Drug Administration (FDA) has issued a Drug Safety Communication to caution that prescription testosterone products are approved only for men who have low testosterone levels caused by...

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