From Deseret News archives:
Family sues over Rx drug
Did pharmaceutical patch lead to death of the Utah woman?
Duragesic distributor, ALZA Corp., is being sued by the family of Marilyn Titus, who died Dec. 14, 2003, at age 72, two months after she began having serious side-effects from the pain medication fentanyl she was receiving through a skin patch, the lawsuit states.
She had sought help managing her chronic pain from two doctors, one of whom prescribed 50 micrograms of fentanyl dispensed timed-release through the patch, according to the suit.
Titus' first prescription 10 patches was filled at a local pharmacy in October 2003. On Nov. 22, she began to have difficulty breathing and lost consciousness while talking to a 911 dispatcher. She was taken to Pioneer Valley Hospital and airlifted to University Hospital, the lawsuit contends.
The Food and Drug Administration said earlier this year that it is investigating the patch, which it said is linked to deaths and poses risks that users might not understand.
Titus was diagnosed with Paget's disease, which caused her to experience episodes of extreme back pain, the complaint states.
The complaint against the two companies states they negligently and carelessly researched, tested and distributed the patches and failed to warn users of the patch's risks.
The FDA on its Web site issued a public health advisory in July stating the patches may cause death from overdose. "Patients who are using the fentanyl skin patch and their caregivers should be told about the directions for safe use of the patch and should follow the directions exactly," the advisory states.
Symptoms of fentanyl overdose are troubled or shallow breathing, tiredness, extreme sleepiness or sedation, inability to think, talk or walk normally and feeling faint, dizzy or confused.
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