Defective Drug and Medical Device Blog

The risk of anti-depressants during pregnancy

28November
2012

A new study released by the Oxford Journal Human Reproduction suggests that women who take a popular class of anti-depressants may be risking the health of their unborn fetus.

According to the article the use of selective serotonin re-uptake inhibiters (SSRIs) such as Paxil, Celexa, Prozac, and Zoloft during pregnancy can increase the possibility of miscarriage, pre-term birth and pregnancy complications such as neuro-behavioral conditions like autism. “”There is clear and concerning evidence of risk when pregnant women use these medications,” said Dr. Adam Urato, who spearheaded the study.

Additionally, Urato said that there is no definitive evidence that SSRI anti-depressants are effective for a mother in terms of alleviating mild-to-moderate depression.

According to the study, anti-depressants are the most prescribed medication among adults 18-44 with 13 percent of pregnant mothers taking some form of anti-depressant. The research indicates that SSRIs might actually impair women’s effort to get pregnant as well as increase the likelihood of miscarriage in the women who do get pregnant. The strongest correlation was for the use of Paxil during pregnancy and congenital heart conditions.

There are alternatives for pregnant mothers who are battling depression. According to Alice Domar therapeutic interventions such as acupuncture, psychology, nutrition and restorative yoga are just as effective for mothers suffering from mild-to-moderate depression.

Urato added, “We’re not saying women should not take SSRIs. The goal is to give them information so they can make the right decision for them.”

Original Article

 

Posted in Anti-depressants |

Lawsuits Amount as Tylenol Increasingly Linked to Liver Failure

12November
2012

The fallout regarding acetaminophen-based products, such as popular brand Tylenol, continues on. In recent years, the universally self-prescribed pain killer has been increasingly linked to reports of liver damage or failure. Tylenol, one of the most popular and readily available brands in the United States, has done little to warn users of the fatal consequences involved.

Health Q&A: When is Tylenol not safe?

The health consequences surrounding Tylenol has spurred a multitude of lawsuits, many of which are still currently pending. Manufacturer McNeil has taken great lengths to avoid having to post ‘severe liver damage’ as a possible side effect of taking the drug on the label. Many of those affected with failing liver health understandably feel they never received advance warning regarding the dangers produced.

With the sheer amount of lawsuits already on the table, the amount of testing and screening of the drug has been placed under significant scrutiny. Many early lawsuits have the effect of seeming completely disregarded by the manufacturer, a move clearly based on maintaining positive public perception and shielding profits.

The basis of the argument seeks to prove the manufacturer failed to provide advance warning of serious liver damage to consumers despite being aware of the unique consequences beforehand. It took several years for the Food and Drug Administration to acknowledge Tylenol as a possible damaging agent to the liver but more recently progress has been made.

Consumers should be aware that Tylenol is linked to liver damage despite following recommended dosages.

Posted in Lawsuits |