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FDA Issues Public Health Advisory on Bextra as its Manufacturer Voluntarily Withdraws the Product “[The] FDA has asked Pfizer, Inc. to withdraw Bextra (valdecoxib) from the market because the overall risk versus benefit profile for the drug is unfavorable…Pfizer has agreed to suspend sales and marketing of Bextra in the U.S., pending further discussions with the agency…”

Click here to see the complete FDA recall on Bextra

If you or a loved one are taking the prescription medication Bextra, contact your physician at once.

If you have been taking Bextra and have had a heart attack or stroke symptoms, or any serious skin reactions (such as Stevens Johnson Syndrome), you have legal rights and may be entitled to compensation.

Harrell & Harrell is currently representing clients who have suffered serious injuries while taking Bextra and are preparing to file claims against Pfizer for the side effects of Bextra.

We continue to investigate claims involving serious injury or death concerning Bextra and would welcome the opportunity to talk to you about your individual situation. Please contact us.

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