FiDA         Failed Implant Device Alliance

Showing posts with label adverse event. Show all posts
Showing posts with label adverse event. Show all posts
Wednesday, June 7, 2017

Bayer Essure: Banned in Finland, the Netherlands, England, Wales, Scotland, Northern Ireland and Brazil

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MORE PRESSURE ON BAYER AND FDA AS ESSURE DISCONTINUED IN UNITED KINGDOM Holly Kelly Ennis June 7, 2017   FiDA highlight Victims o...
Wednesday, May 10, 2017

Levaquin, Cipro for bacterial infections may cause irreversible severe harm.

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FDA Drug Safety Communication: FDA updates warnings for oral and injectable fluoroquinolone antibiotics due to disabling side effec...
Thursday, March 16, 2017

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Medical expert quits mesh implant review group By Lucy Adams FiDA highlight Political correspondent, BBC Scotland March 15, 2017 ...
4 comments:
Wednesday, March 15, 2017

Pelvic Surgical Mesh Scandal: FDA Wrongly Cleared Predicate Device

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Dr Peter Petros said he warned women about the 'very frightening' symptoms of his procedure   Joanne McCarthy   FiDA highligh...
Tuesday, March 14, 2017

Australian Pelvic Surgical Mesh Scandal Widens

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Difficulty issues remain about mesh surgery for women. JOANNE McCARTHY   FiDA Highlight 13 Mar 2016, 4 p.m. THE woman on the ...
2 comments:
Friday, March 10, 2017

4/27/2017 ACTION: Johnson & Johnson Annual Shareholders Meeting

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Who : Device and Drug Harmed Patients/Advocates:   Pelvic Surgical Mesh, Breast Implants, Hernia Mesh, Power Morcel...
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Joleen Chambers
Goals: implant product warranty, unique device identifier UDI, independent patient outcome registry, legal patient protections for continued care
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