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« Washington Actos Bladder Cancer Lawsuits | Main  | Illinois Actos Bladder Cancer Lawsuits »
  Oregon Actos Bladder Cancer Lawsuits
An Oregon Actos bladder cancer lawsuit is a legal remedy for a person who has developed bladder cancer after using Actos. Bladder cancer is a side effect of Actos, and if it can be shown that you developed bladder cancer as a result of using Actos, Oregon law allows you to sue its manufacturer, Takeda Pharmaceuticals.

                           More HERE on Actos and Bladder Cancer

Deadlines for Oregon Actos Bladder Cancer Lawsuits

Oregon, like other states, sets deadlines for when lawsuits must be filed. These deadlines are called statutes of limitations. An Oregon Actos lawsuit is considered a product liability claim, and as such, must be filed no later than two years from the date the injury or damage is first discovered or should have been discovered, whichever comes first.

Please note: exactly when a cause of action accrues under Oregon law, and therefore also the deadline for bringing a claim for having developed bladder cancer as an Actos side effect, varies based on the specific facts of each person's case.

Actos Attorneys

If you or a loved one developed bladder cancer after using Actos, or another drug containing the same active ingredient such as Duetact, ActoPlus Met, or ActoPlus Met RX, contact the Actos attorneys at DeCarli Law for a free, no-obligation telephone consultation. Our main office is in San Francisco, but we assist clients throughout the United States and always offer free consultations to prospective clients.

Use the "Contact Us" form on the lower left side of the page to reach us, or use the toll free number to call us. We represent our clients on a contingency fee basis, which means you pay nothing unless and until we recover money for you. If we recover nothing for you, you will not be charged anything.


Relevant Oregon Statute, Or. Rev. Stat. § 30.905:
30.905 Time limitation for commencement of action. (1) Subject to the limitation imposed by subsection (2) of this section, a product liability civil action for personal injury or property damage must be commenced not later than two years after the plaintiff discovers, or reasonably should have discovered, the personal injury or property damage and the causal relationship between the injury or damage and the product, or the causal relationship between the injury or damage and the conduct of the defendant.

(2) A product liability civil action for personal injury or property damage must be commenced before the later of:

(a) Ten years after the date on which the product was first purchased for use or consumption; or

(b) The expiration of any statute of repose for an equivalent civil action in the state in which the product was manufactured, or, if the product was manufactured in a foreign country, the expiration of any statute of repose for an equivalent civil action in the state into which the product was imported.

(3) Subject to the limitation imposed by subsection (4) of this section, a product liability civil action for death must be commenced not later than three years after the decedent, the personal representative for the decedent or a person for whose benefit an action could be brought under ORS 30.020 discovers, or reasonably should have discovered, the causal relationship between the death and the product, or the causal relationship between the death and the conduct of the defendant.

(4) A product liability civil action for death must be commenced before the earlier of:

(a) Three years after the death of the decedent;

(b) Ten years after the date on which the product was first purchased for use or consumption; or

(c) The expiration of any statute of repose for an equivalent civil action in the state in which the product was manufactured, or, if the product was manufactured in a foreign country, the expiration of any statute of repose for an equivalent civil action in the state into which the product was imported.

(5) This section does not apply to a civil action brought against a manufacturer, distributor, seller or lessor of a manufactured dwelling, as defined in ORS 446.003, or of a prefabricated structure, as defined in ORS 455.010. Actions described in this subsection are subject to the statute of limitations provided by ORS 12.135.

Posted By DeCarli Law on August 24, 2011 11:45 am | Permalink 

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Address: 50 California Street, Suite 1500 San Francisco CA 94111 Toll Free: 1-800-401-4720 Phone: 1-415-738-6144
Debra DeCarli and Bob DeCarli are licensed by the State Bar of Texas and the State Bar of California.

DeCarli Law represents drug side effects and defective medical devices personal injury clients for claims, lawsuits and settlements in Alabama AL, Alaska AK, Arizona AZ, Arkansas AR, California CA, Colorado CO, Connecticut CT, Delaware DE, Georgia GA, Hawaii HI, Idaho ID, Illinois IL, Kansas KS, Maine ME, Maryland MD, Massachusetts MS, Minnesota MN, Mississippi MS, Montana MT, Nebraska NE, New Hampshire NH, New Jersey NJ, New Mexico NM, New York NY, North Carolina NC, North Dakota ND, Oklahoma OK, Oregon OR, Rhode Island RI, South Carolina SC, South Dakota SD, Tennessee TN, Utah UT, Vermont VT, Virginia VA, Washington WA, Washington D.C, West Virginia WV, Wisconsin WI and Wyoming WY. The attorneys of DeCarli Law are licensed in California and Texas. DeCarli Law's practice includes lawsuits for Propecia side effects, Finasteride lawsuits, Topamax lawsuits, Fosamax lawsuits, Gadolinium lawsuits, NSF lawsuits, Nephrogenic Systemic Fibrosis Lawsuits, YAZ lawsuits, Yasmin lawsuits, Ocella lawsuits, and Zarah lawsuits.