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Mississippi, Arkansas and Tennessee Reglan Attorney Releases Allegations Against Wyeth

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Lawsuits have been filed on behalf of those injured after taking the drug Reglan. While the lawsuits contain many pages and are crafted to deal with the particulars of each particular plaintiff, the following still show the pathetic conduct of the pharmaceutical giant, if the allegations are found to be true:

  • Wyeth knowingly, intentionally and negligently disseminated misleading information
    to physicians’ across the country, through a publication known as the Physicians’
    Desk Reference, labeling information for Reglan, metoclopramide and metoclopramide
    HCl which mislead the medical community, physicians and Plaintiff’s physician
    about the risks of long term ingestion of the drug.
  • Wyeth knowingly, intentionally and negligently disseminated misleading information
    to physicians’ across the country, through a publication known as the Physicians’
    Desk Reference, labeling information for Reglan, metoclopramide and metoclopramide
    HCl which mislead the medical community, physicians and Plaintiff’s physician
    about the increased risk of extrapyramidial side effects, including tardive
    dystonia, diabetics were exposed to.
  • Wyeth, Schwarz and Pliva had access to and knew that severe side effects would
    result from the use of Reglan/ metoclopramide in the manner in which physicians
    were prescribing Reglan, metoclopramide HCl and/or metoclopramide and the fact
    that physicians did not fully understand the risks associated with Reglan,
    metoclopramide HCl and/or metoclopramide through the defendants participation,
    individually and jointly, in or its ability to review data from clinical studies
    that were not publicly available, through its review of domestic and international
    medical literature concerning Reglan/ metoclopramide and through ongoing
    litigation.
  • Wyeth failed to adequately warn physicians about the risks associated with Reglan,
    metoclopramide HCl and/or metoclopramide despite the fact that Wyeth knew that
    physicians, the medical community, the generic pharmaceutical industry, Plaintiff
    and other similarly situated relied on Wyeth to disclose what it knew and what it
    should have known from a prudent review of the information that it possessed or to
    which it had access.
  • Defendant Wyeth knew, or should have known through the exercise of reasonable
    care, that the package insert for Reglan, metoclopramide HCl and/or metoclopramide
    substantially understated the prevalence of acute and long term side effects of
    Reglan, metoclopramide HCl and/or metoclopramide. Wyeth failed to use reasonable
    care to modify the package insert to adequately warn physicians about the true
    risks of both short term use and long term use, even after several injured
    patients filed lawsuits alleging inadequate warnings and produced competent expert
    testimony supporting their allegations.

Do not stop taking Reglan without talking with a physician, but contact us today for a free case evaluation if you have tremmors, shakes or been disagnosed with tardive dyskinesia. We may be able to help.

Metoclopramide is available in a several forms and the names include some version of Reglan or the actual word, metoclopramide. More than 2 million people in this country are taking some form of the drug, according to FDA estimates. Reglan manufacturers including Wyeth, a successor-in-interest to A.H. Robins, Inc., and American Home Products Corporation, and Schwarz Pharma, Inc. Generic manufacturers of metoclopramide including Teva Pharmaceuticals and Actavis Elizabeth.

If you have been injured…

DO NOT DELAY. YOUR ABILITY TO RECOVER MONETARY COMPENSATION MAY BE LIMITED BY STATE LAW. CALL ED WALLIS OR FILL OUT THE FORM BELOW FOR A FREE CASE EVALUATION:

CALL: (901) 527-2125

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Other Materials to Read:

Tennessee Reglan Lawyers To Provide Free Case Evaluations

Food and Drug Administration (FDA) video on Reglan Warning, potential lawsuit help and free case evaluation

Reglan Attorneys in Tennessee

Tennessee: Help for Reglan Injuries

Reglan litigation page

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ADVANCED BIONICS COCHLEAR IMPLANT RECALL

If you were the recipient of an Advanced Bionics Model HiRes90k cochlear implant and have sustained physical or emotional injuries as a result of the recall of this medical device, please call Tim Edwards or Ed Wallis at (901) 527-2125 or send us an E-MAIL today. You can also visit the COCHLEAR IMPLANT LITIGATION PAGE for more information on the HiRes90k recall.



WELLBUTRIN MAY CAUSE BIRTH DEFECTS

A recent study published in the American Journal of Obstetrics and Gynecology suggests that women who take Wellbutrin during early pregnancy may run a greater risk for having a child born with a heart birth defect, including left outflow heart defects. If you took Bupropion hydrochloride, Wellbutrin®, Wellbutrin XL®, and Wellbutrin XR® and your child was born with a birth defect, please call Tim Edwards or Ed Wallis at (901) 527-2125 or send us an E-MAIL today. You can also visit the WELLBUTRIN HEART DEFECT INFORMATION PAGE for more information.