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Cymbalta Birth Defects and Withdrawal Symptoms
Cymbalta (duloxetine) is in a class of drugs known as SNRIs (Selective Serotonin/Norepinephrine Reuptake Inhibitors), similar to SSRIs. It is an antidepressant used to treat depression and anxiety. It is also used to manage osteoarthritis, fibromyalgia, and other painful conditions. Cymbalta side effects include severe psychiatric problems such as suicidal thoughts and birth defects in the newborn when taken by the mother during pregnancy (Although the drug has a black box warning about suicidal thoughts, Cymbalta Suicide Lawsuits have been filed). A number of people experiencing severe Cymbalta Withdrawal symptoms have filed Cymbalta Withdrawal lawsuits.
En Español [CYMBALTA DEFECTOS DE NACIMIENTO]
Dozens of people nationwide have filed Cymbalta Withdrawal lawsuits against Eli Lilly & Co., claiming withdrawal symptoms were so severe that they were unable to discontinue the drug. The lawsuits allege the drug manufacturer failed to warn about the risk of severe withdrawal symptoms, including "brain zaps". One lawsuit claims that the prescribing information on Cymbalta is deficient because it warned that the amount of patients experiencing withdrawal are "greater than or equal to 1 percent". However, studies have found that 50 percent of patients experience withdrawal and 10 percent of those patients experience severe Cymbalta withdrawal symptoms.
Cymbalta Side Effects
The Institute for Safe Medication Practices (ISMP) in October 2012 investigated results of clinical studies. The non-profit healthcare consumer safety watchdog found that "withdrawal symptoms were reported in 44-50% of patients abruptly discontinuing duloxetine [Cymbalta] at the end of clinical studies for depression, and more than half of this total did not resolve within a week or two."The clinical trial was required by the FDA to investigate withdrawal from Cymbalta but the participant/patients only took the drug for 8-9 weeks before they were switched to a placebo and then monitored for just 1-2 weeks. Although the clinical trial lasted two months, many people take Cymbalta for years.
The French Medical Journal ( Prescrire) in 2009 published findings of a study that concluded Cymbalta risks outweighed its benefits. Another report by QuarterWatch in 2012 reviewed 48 FDA event reports of serious withdrawal symptoms, from appetite changes and blackouts to suicidal thoughts. It found that many of those 48 cases required hospitalization.
A common Cymbalta (generic name Duloxetine hydrochloride) withdrawal complaint is "brain zap", which patients describe as a sudden electric-like shock through the brain which result in debilitating headaches and bouts of nausea and dizziness. Health professionals believe it may be a form of paresthesia— an abnormal sensation of the body, such as numbness, tingling, or burning. Other severe Cymbalta side effects after discontinuing use include neurological problems and mood swings, which can lead to suicidal thoughts.
Cymbalta Withdrawal Symptoms
Eli Lilly & Co. in January, 2013 asked a federal judge in California to throw out a Cymbalta class action, according to Law360 (Case 2:12-cv-09366-SVW-MAN). Plaintiffs Jennifer L. Saavedra, Dr. Melissa Strafford, Carol Jacquez, and David Matthews allege that "Lilly has failed to disclose material facts to consumers and healthcare professionals about the frequency, severity, and/or duration of symptoms associated with stopping Cymbalta, a condition known as Cymbalta withdrawal."
Cymbalta Withdrawal Class Action Lawsuit
In November, 2014 Eli Lilly & Co was awarded summary judgment in a Cymbalta lawsuit. Plaintiff Jesse McDowell argued that the Prescribing Information on Cymbalta was deficient because it only warned that "greater than or equal to 1%"of patients experience withdrawal. U.S. District Judge Robert W. Sweet, however, decided that Eli Lilly adequately warned about the risk of severe withdrawal symptoms. According to Law360.com, thedecision could diminish the chances of federal judges consolidating dozens of similar lawsuits in a federal Multi-District Litigation (MDL).
In 2013, seven Cymbalta withdrawal personal injury cases were filed across the country (Arizona, California, New York and Pennsylvania). In August of 2014, more Cymbalta withdrawal cases were filed in California, Florida, Georgia, Louisiana, Maryland, Minnesota, Ohio, Oregon, North Carolina, Pennsylvania, and Wisconsin. Cymbalta consumers claim that the drug maker misled them regarding Cymbalta' propensity to induce withdrawal side effects and forced them to keep taking the drug.
Cymbalta Withdrawal Lawsuit
SSRIs have been linked to serious side effects including heart defects and persistant pulmonary hypertension in the newborn (PPHN) when taken by the mothers during pregnancy.
Cymbalta Birth Defects
In July of 2006, the FDA issued a Health Advisory advising people of serious side effects if taking SNRI/SSRIs while pregnant. The New England Journal of Medicine published a study that showed mothers who took SNRIs such as Cymbalta during the second half of their pregnancy were six times more likely to have a baby with PPHN or heart defects.
An infant with PPHN suffers from constricted blood vessels in the lungs, preventing blood from being enriched with oxygen. During pregnancy, the baby's circulation is controlled by the placenta and the lungs are not used. After birth, however, circulation switches to the lungs and the ductus arteriosus then closes. In babies with PPHN the ductus arteriosus remains open, causing blood flow to continue bypassing the lungs.
The blood therefore does not enter the lungs, and is pumped back to the other organs of the body very low in oxygen. Without oxygen, the organs go into stress and put the infant's life at risk.
Persistant Pulmonary Hypertension in the Newborn is usually diagnosed within 12 hours of birth. Even if they are treated, babies may experience heart failure, brain hemorrhage, seizures, and organ damage. Ten to 20 percent of newborns who develop PPHN do not survive.
Babies with PPHN experience difficulty in breathing and bluish skin and may suffer long-term side effects including difficulty breathing, hearing loss, seizures, and developmental disorders.
PPHN occurs naturally in about one or two infants per 1,000 births, but if the baby is exposed to SSRIs during the second half of pregnancy the rate jumps to six to twelve infants per 1,000 births that developed PPHN.
Babies exposed to Cymbalta during gestation also suffer withdrawal symptoms such as incessant crying, agitation and sleeplessness. Cymbalta can also be transmitted to an infant being breast-fed.
Eli Lilly, makers of Cymbalta, have allegedly failed to adequately warn users that birth defects are a possible side effect of taking Cymbalta during pregnancy. Please contact a lawyer who may be able to help you gain restitution if your child was born with birth defects after being exposed to Cymbalta during pregnancy.
Cymbalta Legal HelpIf you or a loved one has suffered from Cymbalta side effects, please click the link below and your complaint will be sent to a Drug & Medical Device lawyer who may evaluate your claim at no cost or obligation.
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I took cymbalta while I was pregnant. I had my son prematurely and he was only 5 lbs.He was in the nicu for 11 days and going through withdrawal symptoms from the cymbalta as well. He also had jaundice and had to be treated under the bilirubin lights for several days as well. Then he also had torticollis and he also has gastrointestinal defects that caused him to projectile vomit that at 21 months old now he still projectile vomits. We are going to have him evaluated by a specialist at children's hospital of Pittsburgh medical center on the 24th of January. He also had torticollis which he had to get physical therapy for the treatment in our home for over a year. He also had several developmental defects that caused him to have motor skills delays. He still has delays from the cymbalta withdrawal. At 21 months old now he wants to be carried around and it's hard for me bcuz I have scoliosis disease and it's hard for me to carry him around with my disease. His intestinal defects will be evaluated and then hopefully we can have the defects corrected by the specialist at children's hospital of Pittsburgh medical center.
My son was in the neonatal intensive care unit for five weeks. He had open heart surgury at six days old. My husband and I were out of work for in excess of five months. We have a 6 year old daughter who has been greatly effected by this situation as well. The impact has been so great to my family and the damages are so far reaching that it is difficult to expess. My son will definatively need additional surgeries in the future as well as ongoing therapies to meet his special needs. The hospital where he was born was also greatly neglegent in their care of both myself and my baby. I gave birth without a doctor present...he was not transferred to an appropriate medical hospital until he was three days old. He was diagnosed after transfer within an hour having congestive heart failure due to cynonotic heart disease. I was also breast feeding while on the cymbalta with the hospitals awareness of the medication...the neonatalogist did not read my chart and was therefore unaware of my medication. I requested my records from the hospital two weeks ago and have not yet received them
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