|
Index of reports
> Cases resulting in hospitalization (10)
> Cases with Breast Cancer (7)
Below is the selection of adverse event reports related to Activella (Estradiol) that includes cases resulting in hospitalization where reactions include breast cancer.
Adverse event in 54 year old female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-07-11
Patient: 54 year old female, weighing 49.4 kg (108.7 pounds)
Adverse reactions / side effects: Breast Cancer
Adverse event resulted in: hospitalization
Suspect drug(s):
Activella (Estradiol)
Other drugs received by patient: Fosamax; Effexor; Clorazepate Dipotassium; Augmentin '125'; Valium; Lamisil; Xanax; Metabolife (Ginseng Nos, Herbal Exteract Nos, Paullinia Cupana, Smilax; Aspirin
Adverse event in 55 year old female receiving Activella (Estradiol)
Reported by a physician from United States on 2007-07-11
Patient: 55 year old female, weighing 62.1 kg (136.6 pounds)
Adverse reactions / side effects: Breast Cancer
Adverse event resulted in: hospitalization
Suspect drug(s):
Activella
Indication: Hormone Replacement Therapy
Start date: 2001-06-01
End date: 2002-06-01
Prempro
Dosage: 0.625 mg / 2.5 mg
Indication: Hormone Replacement Therapy
Start date: 1996-01-01
End date: 2001-06-01
Estratest
Indication: Hormone Replacement Therapy
Start date: 1999-11-01
End date: 2002-06-01
Other drugs received by patient: Medroxyprogesterone Acetate; Provera; Estrace; Estring; Serzone; Effexor XR; Xanax
Adverse event in female receiving Activella (Estradiol)
Reported by a physician from United States on 2007-06-14
Patient: female, weighing 72.1 kg (158.6 pounds)
Adverse reactions / side effects: Breast Cancer
Adverse event resulted in: hospitalization
Suspect drug(s):
Activella
Dosage: unknown
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 1999-08-01
End date: 2002-10-01
Premarin
Dosage: .625 mg, unk
Indication: Menopausal Symptoms
Start date: 1987-01-01
End date: 1998-01-01
Provera
Dosage: 10 mg, unk
Indication: Menopausal Symptoms
Start date: 1994-04-01
End date: 1998-08-01
Provera
Dosage: 2.5 mg, unk
Start date: 1998-08-01
End date: 1998-11-01
Prempro
Dosage: .625 mg / 2.5mg, unk
Indication: Menopausal Symptoms
Start date: 1998-04-01
End date: 1998-11-01
Prempro
Dosage: .625 mg /2.5 mg
Start date: 1999-07-01
End date: 1999-11-01
Prempro
Dosage: .625 mg/ 0.5mg
Start date: 1998-11-01
End date: 1999-07-01
Prempro
Dosage: .625 mg/.05 mg
Start date: 1999-11-01
End date: 2001-04-01
MPA
Dosage: unknown
Indication: Menopausal Symptoms
Start date: 1987-01-01
End date: 2001-01-01
Other drugs received by patient: Naprosyn; Celebrex; Iron; Glucosamine; Vitamin E / 00110501 /; Elavil / 00002202 /; Fosamax
Adverse event in female receiving Activella (Estradiol)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-01
Patient: female, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Breast Cancer, Metastases TO Liver
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Activella
Administration route: Oral
Indication: Hormone Replacement Therapy
Start date: 2002-09-28
End date: 2003-06-13
Prempro
Administration route: Oral
Indication: Hormone Replacement Therapy
Start date: 1996-01-01
End date: 2003-01-01
Other drugs received by patient: Maxzide; Zocor; Pravachol; Norvasc; Timoptic
Adverse event in female receiving Activella (Estradiol)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-23
Patient: female, weighing 83.9 kg (184.6 pounds)
Adverse reactions / side effects: Breast Cancer
Adverse event resulted in: hospitalization
Suspect drug(s):
Activella
Dosage: unknown
Indication: Hormone Replacement Therapy
Start date: 2002-09-01
End date: 2003-11-24
Prempro
Dosage: 0.625 mg/2.5 mg
Administration route: Oral
Indication: Hormone Replacement Therapy
Start date: 1997-04-25
End date: 2002-11-01
Other drugs received by patient: Xanax; Elavil / 00002202 /; Paxil; Altace; Wellbutrin; Klonopin; Darvocet-N 100; Insulin; Effexor XR
Adverse event in female receiving Activella (Estradiol)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-27
Patient: female, weighing 79.4 kg (174.6 pounds)
Adverse reactions / side effects: Breast Cancer
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Activella
Dosage: unknown
Indication: Menopausal Symptoms
Start date: 2002-02-20
End date: 2002-12-01
Premarin
Dosage: .625 mg, unk
Indication: Menopausal Symptoms
Start date: 1994-08-01
End date: 1995-12-01
Prempro
Dosage: unknown
Indication: Menopausal Symptoms
Start date: 1995-12-01
End date: 1996-01-01
Prempro
Dosage: unknown
Start date: 1998-02-01
End date: 2001-03-01
Premphase 14 / 14
Dosage: unknown
Indication: Menopausal Symptoms
Start date: 1997-01-01
End date: 1998-01-01
Provera
Dosage: 10 mg, unk
Indication: Menopausal Symptoms
Start date: 1994-08-01
End date: 1995-12-01
Medroxyprogesterone
Dosage: unknown
Indication: Menopausal Symptoms
Other drugs received by patient: Evista; Vitamins NOS
Adverse event in female receiving Activella (Estradiol)
Reported by a individual with unspecified qualification from United States on 2007-02-16
Patient: female, weighing 75.3 kg (165.6 pounds)
Adverse reactions / side effects: Breast Cancer, Arthralgia, Oestrogen Receptor Assay Positive, Progesterone Receptor Assay Positive
Adverse event resulted in: hospitalization
Suspect drug(s):
Activella
Dosage: unk, unk
Indication: Menopausal Symptoms
Start date: 2002-09-25
End date: 2004-01-01
Provera
Dosage: 10 mg, unk
Indication: Menorrhagia
Start date: 1987-07-01
Provera
Dosage: 2.5 mg, unk
Start date: 1994-01-01
End date: 2002-01-01
Premarin
Dosage: .625 mg, unk
Indication: Menorrhagia
Start date: 1980-01-01
End date: 2002-01-01
Prempro
Indication: Menopausal Symptoms
Medroxyprogesterone Acetate
Dosage: 2.5 mg, unk
Indication: Menopausal Symptoms
Start date: 1980-01-01
End date: 2002-01-01
Other drugs received by patient: Lipitor; Fosamax; Zetia; Mobic; Celebrex; Claritin; Zoloft
|
