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Activella (Estradiol) - Product Formulation Issue - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Product Formulation Issue (1)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Activella (Estradiol) where reactions include product formulation issue. 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

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