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Lisinopril (Prinivil & Zestril) Linked to Various Severe Adverse Effects

Propecia use has been linked to Erectile Dysfunction, General Sexual Dysfunction, Impotence, and Prostate Cancer

The FDA released a report in preparation for an Advisory Panel Meeting scheduled for September 9, 2011 to review and discuss the available data regarding the long-term (greater than 3 – 5 years) use of Fosamax for the treatment and/or prevention of osteoporosis.

A new report reveals that federal health regulators are considering tough new regulations for surgical mesh used to treat pelvic organ prolapse (POP), which has been linked to thousands of serious injuries and complications.

Asbestos is a naturally occurring mineral composed of microscopic clusters that can become airborne if disturbed. Because asbestos is a carcinogen, airborne asbestos fibers pose a serious health hazard. People who are subjected to prolonged asbestos exposure face a significant risk of developing a variety of conditions, including fibrosis, asbestosis, asbestos lung cancer and malignant mesothelioma.

Mesothelioma is a relatively rare form of cancer that develops in the tissue that surrounds certain internal organs of the body, including the chest, heart and abdomen. In fact, mesothelioma is named for that protective membrane, the mesothelium. The mesothelium protects the body’s vital internal organs, mainly by producing a lubricating fluid which provides a slick surface for these internal organs to slide past each other during movement.

European Medicines Agency Recommends New Contra-indications and Warnings for Pioglitazone to Reduce Small Increased Risk of Bladder Cancer

Public Citizen Urges FDA to issue a Recall for Transvaginal Mesh Due to High Risks of Permanent Injury While Providing No Significant Benefits

Boston Scientific sent an “Urgent Medical Device Recall” letter to customers who used the Pinnacle® Pelvic Floor Repair Kit for tissue reinforcement for pelvic organ prolapse (POP). In May, Boston Scientific issued a Field Safety Notice to healthcare professionals recalling 2 specific lots, citing the reason for recall as “low tensile strength between the needle and the suture, which could potentially lead to needle detachment during mesh leg placement.” According to the manufacturer, if needle detachment occurred, the user had the option of leaving the needle or having it removed. However, if retrieval is attempted, further complications (i.e. tissue trauma/perforation) may occur.

The FDA is investigating thousands of reports that link the Yaz, Yasmin, and Ocella to blood clots, breathing issues, heart attacks, strokes, and other serious health issues.