Defective Drugs:

Actonel Linked to Dead Jaw, Fractures

Actonel ClassAction.org Alert

This Alert Affects:
Patients who have taken Actonel and have a definitive diagnosis of dead jaw or suffered a thigh or femur fracture while taking the drug.
Damages: Actonel reportedly causes osteonecrosis of the jaw, also known as dead jaw, as well as femur fractures in users.
Company(ies): Proctor and Gamble
Additional Details: Actonel treats osteoporosis in postmenopausal women.
Date: The FDA issued an Actonel warning on Sept. 24, 2004.

Actonel Help :

If you believe you or someone you know has been affected by Actonel submit your details for a free evaluation. There is no cost or obligation.

Actonel

Actonel

Manufactured by Proctor and Gamble, actonel treats osteoporosis in men and postmenopausal women.  Actonel was once supplied in daily 5 milligram doses, but now can be taken as a monthly 150 milligram dose. The drug prevents bone loss by blocking cells that make bones weaker. It also increases bone mass and reverses bone loss. However, Actonel has been linked to a serious medical condition.

Women taking Actonel may be at risk for developing osteonecrosis of the jaw (ONJ). Osteonecrosis of the jaw occurs when bone tissue in the jaw does not heal after a small trauma, such as tooth removal. This serious medical condition leaves the jaw exposed, which can lead to infection. Victims of osteonecrosis may have to undergo lengthy antibiotic treatments and possibly even surgery to treat the infection. Symptoms of osteonecrosis, which is also known as dead jaw, include swelling and infections of the gums, loose teeth, heaviness or numbness in the jaw and exposed bone.

Women using this drug may also be at risk for femur fractures. Reportedly, Actonel and other bisphosphonates may carry an increased risk for femur fractures. If you or a loved one took Actonel and developed a femur fracture, complete our free case review form today. 

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