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Rituxan® Attorneys Jacksonville

FDA Recall, Warning or Action: The Federal Drug Administration requires that a “black box” warning be placed on the labeling of the prescription drug. This is the strongest warning issued by the agency.

Medical providers and patients both depend upon pharmaceutical companies to design, develop and market new products in the best interest of the general public. When we learn that a pharmaceutical producer or products provider has been singled out as putting profits over patients, our lawyers begin a deliberate search to determine potential liability. In some cases, the FDA will have already issued directives as to how the product is used and which contraindicated situations should be avoided.

Side Effects of Rituxan® Use

Rituxan® (rituximab) works to prevent the growth and spread of cancerous cells. The injectable solution marks the cells which alerts the immune system to destroy them. Possible side effects or negative patient outcomes include:

  • Severe Mucocutaneous Reactions
  • Fatal Infusion Reaction
  • Tumor Lysis Syndrome
  • Progressive Multifocal Leukoencephalopathy
  • Death

NOTE: Rituxan® has been approved for the treatment of non-Hodgkin’s lymphoma and adult rheumatoid arthritis when used in conjunction with other medications.

Our personal injury or wrongful death attorneys will investigate and quantify your injuries to seek compensation for damages to include emergency expenses, hospital bills, lost income, pain and suffering, future costs for health care and permanent disabilities. If you or a loved one was injured or died due to a dangerous drug or failed medical device, contact us at 904-251-1111 or 1-800-251-1111 for a FREE initial consultation.

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