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2. FDA classifies recall of Hologic's implant as 'most serious'

   www.aol.com/news/fda-classifies-recall-hologics...

   The agency also urged patients to report any side effects they experience following the placement of the device, which is implanted before future medical procedures, such as radiation for breast ...

3. FDA warns of potential risk from Hologic's devices implanted ...

   www.aol.com/news/fda-warns-potential-risk-ho...

   The company's devices, BioZorb Marker and BioZorb LP Marker, are implanted in soft tissue, including breast tissue, where the site needs to be marked for future procedures, such as radiation for ...

4. Danielle Fishel Says It ‘Hurts to Be Awake’ After 20 Rounds ...

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   Danielle Fishel has officially completed her treatment for breast cancer — but not without some painful side effects.. Fishel, 43, shared she was “officially” done with treatment during the ...

5. List of withdrawn drugs - Wikipedia

   en.wikipedia.org/wiki/List_of_withdrawn_drugs

   Anaphylaxis, possibly due to carrier oil (Cremophor EL). [3] Amineptine (Survector) 1999 France, US Hepatotoxicity, dermatological side effects, and abuse potential. [7] Aminopyrine: 1999 France, Thailand Risk of agranulocytosis and severe acne. [3] Amobarbital: 1980 Norway Risk of barbiturate toxicity. [3] Amoproxan: 1970 France

6. Radiation proctitis - Wikipedia

   en.wikipedia.org/wiki/Radiation_proctitis

   [2] [1] Radiation proctitis most commonly occurs after pelvic radiation treatment for cancers such as cervical cancer, prostate cancer, bladder cancer, and rectal cancer. RAVE and chronic radiation proctopathy involves the lower intestine , primarily the sigmoid colon and the rectum, and was previously called chronic radiation proctitis, pelvic ...

7. Drug recall - Wikipedia

   en.wikipedia.org/wiki/Drug_recall

   It was intended to be used to prevent prenatal problems during pregnancy. Women who took DES were shown to have a greater chance of having breast cancer. [4] It is estimated that 5 to 10 million persons were exposed to DES until its recall in 1971. Both mothers and second generation daughters are confirmed to have adverse side effects from DES. [5]