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Archive for the ‘Dangerous Drugs’ Category

10 Epilepsy Drugs Appear To Cause Birth Defects

Wednesday, October 12th, 2011

There is an ever-increasing list of prescription drugs found to increase the risk of birth defects, and new evidence shows that FDA should add some of the most common epilepsy drugs to the list.

AdverseEvents, Inc. a company that analyzes the FDA’s adverse drug event database says that 10 of the most popular epilepsy drugs in the United States have been found to have a large numbers of birth defect-related adverse events.

Carbatrol/Tegretol, Depacon/Kene/Kote, Dilantin, Keppra (and IR, Klonopin, Lamictal, Neurontin, Topomax, Trileptal, and Zonegran were found to have more than 25 individual birth defect case reports.

AdverseEvents is recommending that the drugs be re-classified to D class from C class, associating them with “positive evidence of human fetal risk”. Class D drugs are generally not prescribed to pregnant women unless there is no less risky alternative.

It is especially significant that the FDA re-classify these drugs because most epileptic women do not have the option of not taking their medication while pregnant. Are you on epilepsy and considering getting pregnant? What do you think of these findings? Please let us know by commenting below.

If you think your child’s birth injury was due to medical negligence and would like to speak to an experienced birth trauma attorney, please fill out our form on the contact page or just give us a call at the number provided.

 

Yaz and Yasmin Birth Control Deaths May Exceed 190 in United States

Monday, May 16th, 2011

According to About Lawsuits, Yaz and Yasmin birth control pill related deaths may exceed 190 in United States alone, says a recent report. The German-based Coalition against Bayer Dangers reports that a search of the FDA’s adverse events database revealed that there have been 140 Yasmin deaths reported in connection to women taking the birth control pill and another 50 Yaz-related deaths reported in connection to newer version of the drug.

The numbers in the database only present women in the United States who may have died as a result of taking Yaz or Yasmin birth control pill. Many of the victims are young women with no reported medical or health problems, who suddenly developed dangerous blood cloths, pulmonary embolisms, suffered strokes or gallbladder diseases after taking the pill.

Bayer faces about 7,000 Yaz and Yasmin wrongful death lawsuits, which have been consolidated as a part of a multidistrict litigation in the U.S. District Court of the Southern District of Illinois. Several cases are pending against Bayer at the state level in New Jersey and Pennsylvania.

The Bayer birth control lawsuits were brought on by women injured by the drug, or the families of women who died as a result of taking Yaz or Yasmin, alleging that the company failed to adequately research the medications or warn about the possible side effects.

Joan Cummins of New Jersey filed a wrongful death lawsuit against Bayer Corporation alleging that its birth control Yaz caused the sudden death of her eighteen-year old daughter, Michelle Pfleger. Pfleger suddenly collapsed on her way to a college class. The autopsy report showed that the victim died from cardiac arrest triggered by a pulmonary emboli, a blood clot in the lungs that can lead to low blood pressure and sudden death. Cummins alleges that Yaz caused her daughter’s blood clot which lead to her death.

Acetaminophen in Pregnancy May Increase Asthma Risk in Children

Friday, April 8th, 2011

According to WebMD, acetaminophen during pregnancy may increase the risk of asthma in children. A new study by Richard Beasley, MD, professor of medicine at the Medical Research Institute of New Zealand, found that the results should not be a cause for alarm and the doctors should still consider the drug safe to take. It is unknown if the popular painkiller has a true cause and effect when taken during pregnancy.

In a pooled result, the study found that any prenatal exposure to acetaminophen was associated with increased chances of asthma and wheezing in the children ages 1 ½ to 7. These findings are consistent with a 2009 meta-analysis that found an association between use of acetaminophen during pregnancy and both asthma and wheeze, as reported in the issue of Clinical and Experimental Allergy. Overall, the study found that using the painkiller during pregnancy was associated with a 21% increased risk of asthma in young children. No information was available on dosage or frequency of use.

The researchers felt that the message of the study should be that more urgent analysis is needed and to reinforce the general principle to avoid unnecessary medication during pregnancy. The scientists urge pregnant women to abstain from unnecessary use of acetaminophen but should consider it as a preferred analgesic to bring down fever.
Another Spanish study found a link between the use of acetaminophen by mothers at least once a month during the gestational period and the chance a child had wheezing by preschool age.

FDA Warns Johnson and Johnson of Topamax Side Effects

Friday, March 18th, 2011

According to the Food and Drug Administration, Topamax should be closely monitored for increases in depression and potential mood changes that may result in an increase of suicidal thoughts. Topamax is a migraine and anticonvulsant medication linked to an increased risk of birth defects, specifically oral. Oral birth defects include cleft lip and cleft palate and occur in the first trimester of pregnancy when the lip or palate fails to fuse properly during development.

A pregnant woman taking Topamax during the first trimester is 20 times likely to risk their child developing an oral birth defect than a woman not taking the medication, says Reuters. The FDA warns pregnant women that they are at risk of having a baby develop the facial anomalies when exposed to dangerous drugs such as Topamax.

While Topamax has an FDA-approved seal to treat seizures and migraine headaches, it is being used off-label by doctors and health care providers for treatment of psychiatric conditions. Topamax made Johnson and Johnson $2 billion last year, thanks in part to its successful drug sales rep marketing campaign.

The FDA fined Johnson and Johnson for illegally marketing Topamax for psychiatric conditions. Despite the action, it has become a catch-all drug for a variety of pain conditions and other unapproved uses. It is used in the military and is known to cause brain-fogging, says Army Times.

In 2004, the FDA issued another warning to the drug maker, alleging its sales material downplayed the serious side effects associated with Topamax. The FDA raised concern over dangerous side effects such as acute myopia, secondary angle closure glaucoma, hyperthermia, metabolic acidosis and serious public health concerns in pediatric patients.