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Home » Areas Of Practice » Medical Pharmaceutical Injury Cases » Celexa Lawsuits


Birth Defect Attorney

Celexa is in the selective serotonin reuptake inhibitor (SSRI) class of antidepressants. Celexa is manufactured and marketed in the United States by Forest Laboratories. Celexa is a sister compound to Lexapro, which is also an antidepressant manufactured and marketed by Forest Laboratories.

These antidepressants are similar to other SSRIs and SNRIs such as Paxil, Prozac, Zoloft, Effexor, Pristiq and Wellbutrin, which have been linked to an increased risk of birth defects in children who are exposed in utero.


Based on the medical literature and experts in the field, Celexa and Lexapro can be linked to the following types of birth defects:

  • Anal Atresia (complete or partial closure of the anus)
  • Autism or Autism Spectrum Disorder
  • Cardiac defects or heart defects
  • Cleft lip or cleft palate
  • Club foot or bilateral club foot (one or both feet turn downward and inward)
  • Craniosynostosis (skull defects)
  • Limb defects or limb reductions
  • Neural-tube defects (spina bifida, anencephaly, and other brain and spinal cord birth defects)
  • Omphalocele (stomach defect where organs develop outside the stomach wall)
  • PPHN (Persistent Pulmonary Hypertension of the Newborn)

Celexa Birth Defect Warning

As discussed, Celexa is an SSRI, and in the same class of drugs as Paxil. Evidence of Paxil’s link to an increased risk of cardiac defects and birth defects was revealed in September of 2005. ( read details here )

In a separate study in early 2006, the New England Journal of Medicine published an abstract, which found that babies exposed to SSRIs in utero, including Celexa and Lexepro, had more than six-fold increased risk of beign born with Persistent Pulmonary Hypertension (PPHN). ( read details here )

On July 19, 2006, the FDA released Public Heath Advisory: Treatment Challenges of Depression in Pregnancy and the Possibility of Persistent Pulmonary Hypertension in Newborns. ( read details here )


Surprising to most Americans, the FDA does not do independent testing on pharmaceutical drugs. Instead, it is the pharmaceutical company’s responsibility to research and test the safety of their drug. Unfortunately, the warnings in 2005 and 2006 from the FDA and antidepressant manufactures came more than ten years after most SSRIs and SNRIs were first released on the market. As a result, many doctors prescribed these medications to mothers not knowing the risks to the unborn children.

Contact a Celexa Birth Defect Lawyer

A birth defect injury attorney can help you decide what the best course of action is for you and your injured child. If your child was born with one of the above-mentioned birth defects and you took Celexa or Lexapro, contact The Dwyer Law Firm today to determine whether you qualify for financial compensation.