Actos Heart Attack Attorney | Prescription Drug injury Lawsuits
Actos (also marketed as Actoplus Met XR, and Duetact) has been linked to an increase rate of heart attacks and other forms of heart disease amongst persons taking the prescription drug medication used to treat type 2 diabetes. According to an FDA study in a 24 week patients hospitalized with a heart attack were more that 50% more likely to have taken Actos during the past month. Numerous other studies conducted by the drug manufacturer and independent studied have shown a definitive link to heart failure. In responses the FDA and the Manufacturers of Actos (Takeda Pharmaceutical Co) issued a new “black box warning” stating the known dangers of heart attack as well as congestive heart failure from the taking of Actos. If you or a loved one has suffered heart disease as a result of taking Actos you may be entitled to full and just compensation for your injuries.
How Can I tell I am having a heart attack: Heart attack sing and symptoms:
A heart attack (myocardial infarction) is a serious medical condition requiring immediate medical attention. If you or a loved one are experiencing any symptoms associated with a heart attack contact an emergency response team as soon as possible. Symptoms of a heart attack are numerous and may differ greatly based on the severity of the myocardial infarction and the general health of the victim. Some common sign and symptoms of heart attack are as follows:
- Chest pain felt like a tight band around the waist
- feeling of a bad ingestion
- heavy pressure on the chest
- Excessive sweating without physical exercise
- Light headedness
- General feeling of nausea including vomiting
- Pharmaceutical Drug Design Defect: Generally proven by showing of a failure to conduct proper testing of a drug before its distribution to the general public. Or by showing that frug manufactures knew or should have known of the dangerous side effects of the drug before its distribution to the general public.
- Pharmaceutical Drug Manufacturing Defect: Generally proven by showing that the final manufactures drug is markedly different and as a result more dangerous the intended design of the drug.
- Labeling Defect: Also referred to as failure to warn defect. Usually this claim can be established in the court of law by showing drug manufacturers refusal to adequately warn users of the drug of the known dangers posed by the taking of the defective drug.
- All medical expenses arising from Actos
- Future medical and rehabilitation costs
- Loss of current income due to inability to work
- Loss of earning capacity Future loss or reduction on income
- Pain and Suffering including mental trauma and post traumatic stress
- Loss of consortium
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