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Index of reports
> Life Threatening Events (2)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Activella (Estradiol) life threatening events. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Activella side effects in 55 year old female
Reported by a consumer/non-health professional from United States on 2012-06-12
Patient: 55 year old female, weighing 68.5 kg (150.7 pounds)
Reactions: Product Formulation Issue
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Estradiol and Norethindrone Acetate
Dosage: see above nightly po
Administration route: Oral
Start date: 2010-11-30
End date: 2012-03-31
Activella
Dosage: see above' nightly po
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 2008-08-01
End date: 2010-11-01
Possible Activella side effects in 60 year old female
Reported by a consumer/non-health professional from United States on 2012-01-10
Patient: 60 year old female, weighing 70.3 kg (154.7 pounds)
Reactions: Breast Cancer Stage II
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Activella
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