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d’Oliveira & Associates Seeks Clients That Have Been Affected by the Prescription Drug Topamax
Date:3/23/2013

medications developed the birth defects, whereas 1.4% of the infants exposed specifically to Topamax developed them*. It is important to note that in this study, the percentage of these birth defects in infants whose mothers were exposed to no anticonvulsant medications at all was a mere .07% and that the rate of cleft lip and cleft palate conditions found in infants who mothers took Tapomax was 11 times higher than the national average of children born with those conditions*.

In response to the increased risk of birth defects in pregnant Topamax users, the FDA has called for stronger warnings on the drug's labels and has also changed the drug's pregnancy warning to a Category D, meaning there is positive evidence that the drug poses risks to infants. Director of the FDA's Division of Neurology Products has urged doctors to "carefully consider the benefits and risks of [Topamax] when prescribing it to women of child-bearing age," and to consider "alternative medications" as a preferable option to Topamax.

If you or anyone you know has taken Topamax during a pregnancy, the attorneys at d'Oliveira & Associates urge you to contact them immediately. Working with some of the leading dangerous drug lawyers handling these cases, they want you to know that pregnant users of Topamax are entitled to representation and compensation for any related birth defects.

For a free legal consultation, call 1-800-992-6878 or visit their website at dmlaw.com.

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