How Side Effects of the Medication Actos Can Change Your Life

Actos (pioglitazone hydrochloride) is a prescription drug used in the treatment of ‘Type 2’ Diabetes and was approved for use some thirteen years ago.
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Where the Actos Lawsuits Stand

Actos is a prescription drug manufactured by Takeda, a Japanese pharmaceutical corporation, over thirteen years ago and is used in the treatment of Type 2 diabetes. While there were many adverse health issues reported among users of Actos
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The Stryker Orthopedics PER Letter: Why All Rejuvenate and ABGII Hip Implant Recipients Should be Cautious

If you are the recipient of a Stryker Rejuvenate or ABGII hip implant then perhaps you have experienced problems related to the implant. Like other metal-on-metal hip implants, the Rejuvenate and ABGII have the potential of causing metallosis even though the design calls for a ceramic head rather than a metal one.
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Stryker Rejuvenate and ABGII Hip Implant Recipients Beware: The Stryker PER Letter and What it could mean for You

It appears that some recipients of the Stryker Rejuvenate or Stryker ABGII hip implant may have received a Product Experience Report or “PER” Letter from Stryker Orthopedics in response to either the patient, or the patient’s doctor, or even the patient’s treatment facility notifying Stryker of any issues with a specific implant.
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The Stryker Product Experience Report Letter: What every Rejuvenate and ABGII Hip Implant Recipients Should Know

Perhaps you are one of the many recipients of a Stryker Rejuvenate or ABGII hip implant who have experienced problems with the implant and are unsure what to do. The Stryker Rejuvenate and Stryker ABGII were both recalled this past July, 2012.
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