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Celexa Heart Problems & Birth Defects Lawsuit

The antidepressant citalopram is sold under the brand name Celexa, but also less commonly under various generic names. Researchers are currently trying to determine whether Celexa has caused birth defects in children born to mothers who were taking the drug while pregnant.

You shouldn’t have to go through more trouble to be compensated for the harm you’ve already suffered. The Rottenstein Law Group, a Celexa law firm, knows this, and we want you to believe it. You need a sympathetic advocate who will represent only your interests—and who will make the process as painless as possible.

If you’ve taken Celexa and have been harmed, contact RLG for a free consultation immediately.

What Is Celexa and What Is It Prescribed For?

Celexa is the brand name for the drug citalopram. Made and sold by Danish pharmaceutical company Lundbeck AG while working with the American-based Forest Laboratories, this prescription medication is used to treat major depression and general anxiety disorder. Lundbeck developed the drug in the 1980s, but its patent expired in 2003. It is sold in 10mg, 20mg, and 40mg oral doses.

Working with Forest, Lundbeck “evergreened” citalopram by using the same research to create escitalopram, another antidepressant it patented in 2001. By 2003, the manufacturers phased out Celexa and began aggressively marketing Lexapro as its brand-name replacement even though consumers could buy generic citalopram from other companies. Ultimately, Forest Laboratories paid out $313 million in damages under the False Claims Act for illegally marketing Celexa and Lexapro to minors and for paying doctors kickbacks to prescribe the drug. Forest Laboratories also settled dozens of Celexa lawsuits by people claiming it didn’t warn them that Celexa could cause suicidal ideations and violent behaviors. These lawsuits all predate the FDA’s October 2004 black box Celexa warning. Aside from these cases, the Rottenstein Law Group does not know of any Celexa class action lawsuits.

Celexa is a potent member of the Selective Serotonin Reuptake Inhibitor (SSRI) class of antidepressants. SSRIs prevent receptors in the human brain from absorbing serotonin that has already been released. Serotonin helps maintain feelings of well-being in people, so preventing its re-absorption alleviates negative feelings. Unlike other drugs, such as buproprion (Wellbutrin), SSRIs minimally affect noradrenaline and dopamine, which regulate stress levels. SSRIs take several weeks to affect users, and they can cause many side-effects in the process, particularly nausea, somnolence, and sexual side-effects.

As the adverse effects of Celexa become better known, the FDA has required more stringent product warnings and prescription requirements. Meanwhile, concerns that antidepressants, including Celexa, are less effective than advertised are growing. For example, the New York Times reported that negative studies on their efficacy are often suppressed.

Celexa Causes Birth Defects

The Rottenstein Law Group’s birth defect lawyers have discovered that Celexa causes numerous birth defects, injuries, and other complications usually when used during the first trimester. The FDA issued a Celexa birth defect warning in 2006. If you used Celexa while pregnant and your baby was born with the following defects, you may be eligible for compensation via a birth defect lawsuit.

  • Premature birth.
  • Miscarriage. An article in the Canadian Medical Association Journal reported a study on antidepressants showing that 5.5% of the pregnant women on them suffered spontaneous abortions as opposed to a non-antidepressant-using control group’s 2.7%.
  • Withdrawal symptoms, such as: breathing difficulties, turning blue, low blood sugar, jaundice, changing body temperatures, feeding problems, convulsions, vomiting, floppiness, stiffness, irritability, jitteriness, abnormal crying, and tremors.
  • Clubbed foot. Called “Congenital Talipes Equinovarus” by medical professionals, one or both feet of children born with this condition are turned inward at the ankle. Most cases are easily treated non-surgically.
  • Cleft lip or palate. A cleft lip occurs when the tissue forming a child’s upper lip fails to fuse properly. A cleft palate means the bones comprising the roof of a child’s mouth did not properly join, connecting the mouth to the nasal cavity. Both can be resolved surgically, though a cleft palate can sometimes be fixed by placing a prosthetic device in the palate.
  • Delayed development. A February 2010 study published in Pediatrics determined that on average, children born to women who used antidepressants began sitting upright sixteen days later than average, and began walking one month later as well.
  • Persistent Pulmonary Hypertension (PPHN). An article in the February 2006 issue of the New England Journal of Medicine demonstrated that babies born to women using antidepressants past their 20th week of pregnancy were six times more likely to develop PPHN than women who were not using an antidepressant. PPHN is a life-threatening condition in which high pressure in blood vessels in children’s lungs results in insufficiently oxygenated blood.
  • Gastroschisis. Usually a genetic hernia, gastroschisisis a defect on one side of the umbilical cord that allows a portion of the infant’s intestines to protrude out of the body. It is often undetectable before birth, but surgeons can repair the damage by either pushing the intestines back into the body or by stitching a mesh around the protrusion.
  • Enlarged heart is condition in which the heart is both too large and weak to efficiently pump blood through the body.
  • Septal heart defects. The most common heart defect associated with antidepressants, the wall (septum) separating the left side of the heart from its right is malformed. Sometimes surgery is necessary to correct the damage. The September 2009 edition of the British Medical Journal contained an article showing that women on antidepressants during their first trimesters were twice as likely to give birth to children with septal defects as normal. Taking more than one antidepressant during the first trimester quadrupled the probability of a septal heart defect versus women who did not take the drugs.
  • Left outflow tract heart defects. This defect refers to a child born with a narrow aorta, the body’s primary artery, and it requires surgical correction.
  • Macroephaly is a condition in which the child’s head is abnormally large, measured at two standard deviations above the average in head circumference. Macroephaly correlates to infections, internal bleeding in the skull, cysts on the brain, and other defects.
  • Craniosynostosis is a condition in which portions of the child’s skull fuse prematurely, which causes the skull plates to grow in different directions to accommodate the expanding brain. If the skull fails to grow sufficiently, the intracranial pressure on the child’s brain can lead to visual and cognitive impairments.
  • Neural tube defects. A neural tube defect consists of an opening in a child’s spinal cord or brain caused by a failure of specialized nerve cells to fuse properly. The several types of defects are horrific and in some instances the child is born without significant portions of the skull and brain. In many circumstances the child does not survive more than a few hours after birth.
  • Spina bifida. A more common, specific kind of neural tube defect. Spina bifida is not as fatal as the ones mentioned above because it affects the lower spinal column. In some instances, the spinal cord protrudes through the gap between the unfused bones, and in others a fluid-filled sac surrounds the spinal cord. Sometimes surgeons can close the opening in patients’ backs.

The Rottenstein Law Group is a birth defect law firm, and we accept cases by those whose children have suffered Celexa birth defects.

Other Celexa Side Effects

Celexa has been found to cause two other significant side effects: increased thoughts of suicide, and complications for those with pre-existing heart conditions.

As early as 1990, people reported that antidepressants caused increased suicidal thoughts and behaviors. The FDA considered the issue, but it did nothing more. It became clear that antidepressants could adversely affect children and teenagers, making them hostile, irrational, violent, or suicidal. In 2006, the FDA analyzed the results of 372 studies of antidepressants, finding that even young adults (ages 18-25) were also afflicted with behavioral changes. As a result, the FDA ordered antidepressant manufacturers, including Lundbeck and Forest for Celexa, to include added warnings to consumers. However, a study published in the February 6, 2012 edition of the medical journal, Archives of General Psychology, contradicted earlier findings that connected SSRI use to increased suicidal activity in youths. Although, the researchers did not detect a decrease in suicidal thoughts and behaviors compared to adults and geriatric patients.

Recently, a study conducted at Duke University concluded that those with coronary artery disease faced greater risk of death due to Celexa use. The researchers could not determine the reasons for the connection, but they found the connection statistically significant. For those with heart disease, in an average three years of follow-up, 21.4 percent of the participants still on antidepressants died as opposed to 12.5 percent who were not on antidepressants.

On August 24, 2011, the FDA issued a Celexa warning in the form of a drug safety communication. The communication advised physicians and users that Celexa use above 40mg per day can cause abnormal changes in the heart’s electrical activity. The FDA also determined that doses above 40mg were ineffective at combating depression. According to the data the agency gathered, Celexa prolongs the QT interval of the heartbeat. QT interval prolongation can indicate a type of irregular heartbeat called torsades de pointes, and it is a risk factor for sudden death.

RLG’s Celexa Lawyers Will Make Things Easier

The process of demanding compensation for the harm you’ve suffered (caused by a defective product manufactured by a blameworthy company) can be complicated, even if it doesn’t seem fair that you should have to go through even more trouble to be made whole again. The Celexa lawyers at the Rottenstein Law Group believe that getting satisfaction from the company that harmed you shouldn’t be just more hardship. That’s why we do everything we can to streamline the process, and we will file a Celexa lawsuit on your behalf if necessary.

If you have taken Celexa and experienced adverse side effects, contact RLG today.

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rlg Previous Comments

  1. Guest
    on September 3, 2012 at 7:35 pm

    I took celexa for about 1.5 years and had to take nausea meds and I contracted gastritis along with a change to blood pressure meds.

  2. Guest
    on May 3, 2012 at 3:40 am

    My daughter was born in 2004 and I was taking celexa the whole time. I had gestational diabetes and she had to come out 1 week early. She was blue in color, no crying and even when they poked her with a needle still wouldn't cry. They looked concerned. She could not leave the hospital until her blood sugar levels came up. And now that shes older, it's strange her lips and nails turn blue and her heart starts pumping fast and really high temp. Every time I would take her in, it would be a UTI. I'm confused because this happens even without the UTI she will get sick if she don't eat every 2 hours. I pleaded with doctors to refer me and they say she's fine.

  3. Guest
    on November 23, 2011 at 12:11 pm

    I am upset because Celexa is made by different manufactures. I have had it from different ones. There is one that works effectively for me. Others make me tired and severely depressed. I want to know what seems to be the same drug that can affect me so differently. I have suffered for a long time with a defective drug. Thank you.

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