Prescription Drug Injury

[...] expenses, future loss of income, pain and suffering, and depakote lawyer fees related to birth defects. At least one depakote attorney filed a lawsuit in Illinois on behalf of over a dozen [...]

[...] .   This is because Accutane could cause life-threatening or debilitating birth defects. Patients taking Accutane need to have regular blood and liver function tests to make sure the [...]

[...] Some consumers are currently involved in litigation, alleging that birth defects have been caused by Zoloft and other SSRIs.  Hundreds of these cases have been grouped [...]

[...] of Effexor allege that patients were not adequately warned about risks to infants, birth defects, including an increased risk of congenital heart defects, persistent pulmonary [...]

[...] Products Coming in at number 8 on the countdown is a joint venture between drug makers Abbott Laboratories and Takeda Chemical Industries. Tap Pharmaceutical Products agreed to pay 875 million [...]

[...] , lawsuits increased in many states. In Illinois, five separate cases were filed against Abbott Laboratories and AbbVie, Inc., the makers of AndroGel. Multiple lawsuits have also been filed in the [...]

[...] Capsules, which is a delivery system used for seizures. Depakote is manufactured by Abbott Laboratories, an American pharmaceutical company based near Chicago, Illinois. What are the reported [...]

[...] has been reported, as well as insomnia, feeling restless and a cough or throat. The more serious side effects can indicate an allergy to risperdone.  Patients should watch for fever or stiff [...]

[...] Embolism Death The warnings in the drugs’ information sheet also list the following serious side effects that require emergency medical help: sudden numbness or weakness, especially on one side [...]

[...] increased risk for diabetes. According to court documents, there are over 60 lawsuits in multidistrict litigation in South Carolina District court.  At least 170 other claims may be added, [...]

[...] Common allegations regarding Effexor have led the US Judicial Panel on multidistrict litigation to transfer Effexor lawsuits to the Eastern District of Pennsylvania. Effexor is an SNRI [...]

[...] antidepressants prescribed in the United States.  The U.S. Judicial Panel on Multidistrict Litigation said there are 475 Zoloft lawsuits under Judge Rufe in the U.S. District Court for the [...]

[...] fronts.  It’s the only hormonal IUD that has been approved by the Food and Drug Administration, and it’s good for up to five years. The Positive Side Effects This IUD has been a [...]

[...] must be made as fully-informed consumers. In addition, drug makers must keep the Food and Drug Administration informed about all known and reported side effects, even after the drug has won approval [...]

[...] the drug to treat rheumatoid arthritis before it was approved by the Food and Drug Administration for use in treating that condition. This settlement also resolved allegations in [...]