Medication Litigation and Recall Information

You’ve probably seen a cliché television commercial referencing
“dangerous” or “potentially harmful” drugs –
but what you may not know is that these types of situations are fairly
common. Illness, injury, and other life-altering outcomes are frequently
attributed to a medical device or medication meant to better an ailment.
Unfortunately, the medication outcomes are not always as expected.

In recent months, there have been numerous instances of litigation with
the topic of medication dangers. Three of those medications attributed
to physical dangers include:

  1. Fluoroquinolone Antibiotics: while antibiotics are known to have significant
    side effects, fluoroquinolones have been attributed to specific harm to
    consumers. Levaquin, Avelox, and Cipro are common fluoroquinolone medications
    prescribed in years past. In fact, Levaquin was the highest selling U.S.
    antibiotic in 2010. These medications have been linked with over 3,400
    lawsuits and possibly 5,000 deaths from 1996 until 2010. Unfortunately,
    the FDA only recently began warning consumers and doctors of the possible
    dangers associated with these medications, so many people were likely
    exposed unnecessarily.
  2. Zofran: approximately 250 lawsuits have already been filed in the Zofran
    multidistrict litigation that was formed in the fall of 2015. The original
    intent of Zofran was to decrease nausea as a side effect of surgery and
    chemotherapy. Although it was never tested for use in pregnant women,
    GlaxoSmithKline improperly promoted the use of Zofran to help battle morning
    sickness and vomiting while pregnant. Further investigation revealed that
    the medication has the potential to cause birth defects, such as a cleft
    palate or heart defect, if used by a pregnant mother.
  3. Risperdal: Janssen Pharmaceuticals, a subsidiary of Johnson & Johnson,
    manufactured Risperdal originally to be used for adults with schizophrenia,
    autism, or bipolar disorder. It is an anti-psychotic that can make symptoms
    of these diseases more bearable. The medication began being sold in the
    U.S. in 1994, but Janssen soon requested approval from the FDA for a pediatric
    indication. The FDA did not approve this 1997 request, but Janssen marketed
    and promoted Risperdal for use in adolescents and children regardless.
    Adverse effects of the medication in children included the development
    of breasts in male, as well as gynecomastia. In 2013, charges were settled
    for $2.2 billion – but about 1,750 additional claims have been filed
    against the company.

Jones & Swanson is currently investigating Mass Tort medication legal
claims such as these, so if you believe you or a loved one was negatively
affected by one of these drugs please contact our office today. We aim
to bring justice for those adversely affected by companies looking to
make a profit without properly determining the dangers associate with
medications prior to launching them on the market.

Medication Litigation and Recall Information syndicated from


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