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This is an index of adverse event reports related to Activella (Estradiol). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (35)
Cases resulting in a serious event (34)
Cases resulting in death (3)
Cases resulting in hospitalization (10)
Cases resulting in other serious reactions (32)
Below is a sample of adverse event reports reports related to Activella (Estradiol). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 75 year old female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-07-13
Patient: 75 year old female, weighing 65.3 kg (143.7 pounds)
Adverse reactions / side effects: Breast Cancer Metastatic
Adverse event resulted in: hospitalization
Suspect drug(s):
Activella
Dosage: 1 mg/0.5 mg, oral
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 2000-11-22
End date: 2001-12-10
Activella
Dosage: 1 mg/0.5 mg, oral
Administration route: Oral
Indication: Osteoporosis
Start date: 2000-11-22
End date: 2001-12-10
Premarin
Dosage: 0.625 mg, oral
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 1989-09-25
End date: 2000-11-01
Provera
Dosage: 10 mg, oral
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 1989-09-25
End date: 2000-11-01
Femhrt
Dosage: oral
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 2001-12-27
End date: 2002-11-07
Hormone Replacements Drugs (Nos)
Indication: Menopausal Symptoms
Start date: 1991-10-31
Cycrin
Indication: Menopausal Symptoms
Start date: 1998-12-17
End date: 1999-07-14
Medroxyprogesterone Acetate
Indication: Menopausal Symptoms
Start date: 1999-09-27
End date: 2000-08-07
Other drugs received by patient: Lipitor; Fosamax; Synthroid; Enalapril (Enalapril); Vioxx; Elavil
Adverse event in 49 year old female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-07-11
Patient: 49 year old female, weighing 117.9 kg (259.4 pounds)
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Dosage: 1 mg/0.5 tab
Indication: Hormone Therapy
Start date: 2001-12-01
End date: 2002-09-09
Premarin
Dosage: 0.625 mg,; 1.25; 0.9
Indication: Hormone Therapy
Start date: 1994-09-20
End date: 2002-09-01
Premarin
Dosage: 0.625 mg,; 1.25; 0.9
Indication: Hormone Therapy
Start date: 1995-01-01
Premarin
Dosage: 0.625 mg,; 1.25; 0.9
Indication: Hormone Therapy
Start date: 1995-01-01
Provera
Dosage: 10 mg; 5 mg; 2.5 mg
Indication: Hormone Therapy
Start date: 1995-01-01
End date: 1999-01-01
Provera
Dosage: 10 mg; 5 mg; 2.5 mg
Indication: Hormone Therapy
End date: 2001-08-01
Provera
Dosage: 10 mg; 5 mg; 2.5 mg
Indication: Hormone Therapy
Start date: 1994-09-20
End date: 2001-12-01
Medroxyprogesterone
Dosage: 5 mg
Start date: 1994-09-20
End date: 2001-12-01
Estradiol
Dosage: 2 mg
Indication: Hormone Therapy
Start date: 1998-01-29
End date: 2002-09-27
Provera
Dosage: 10 mg
Indication: Hormone Therapy
Start date: 1994-09-20
End date: 2001-12-01
Other drugs received by patient: Marijuana (Cannabis Sativa); Hydrochlorothiazide; Ibuprofen; Paxil; Prozac; Triamcinolon / 00031901
Adverse event in female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-07-11
Patient: female
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Indication: Hormone Replacement Therapy
Prempro
Indication: Hormone Replacement Therapy
Adverse event in 55 year old female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-07-11
Patient: 55 year old female, weighing 77.6 kg (170.7 pounds)
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Indication: Menopausal Symptoms
Start date: 1990-01-01
End date: 1998-01-01
Activella
Indication: Menopausal Symptoms
Start date: 2002-01-02
End date: 2002-02-20
Prempro
Indication: Menopausal Symptoms
Start date: 1998-10-01
End date: 2002-01-01
Prempro
Indication: Menopausal Symptoms
Start date: 2002-02-20
End date: 2002-08-01
Provera
Dosage: 10 mg
Indication: Menopausal Symptoms
Start date: 1989-01-01
End date: 1990-01-01
Provera
Dosage: 10 mg
Indication: Menopausal Symptoms
Start date: 1997-01-01
End date: 1998-01-01
Premarin
Dosage: 0.625 mg
Indication: Menopausal Symptoms
Start date: 1989-01-01
End date: 1990-01-01
Premarin
Dosage: 0.625 mg
Indication: Menopausal Symptoms
Start date: 1997-01-01
End date: 1998-01-01
Estradiol
Indication: Menopausal Symptoms
Start date: 1990-01-01
End date: 1998-01-01
Estradiol
Indication: Menopausal Symptoms
Start date: 2002-01-01
End date: 2003-03-21
Other drugs received by patient: Prometrium; Claritin-D; Cozaar; Nasacort
Adverse event in female receiving Activella (Estradiol)
Reported by a individual with unspecified qualification from United States on 2007-07-11
Patient: female
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Indication: Hormone Replacement Therapy
Premarin
Indication: Hormone Replacement Therapy
Prempro
Indication: Hormone Replacement Therapy
Provera
Indication: Hormone Replacement Therapy
Medroxyprogesterone / 00115202 / (Medroxyprogesterone Acetate)
Indication: Hormone Replacement Therapy
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 female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-07-11
Patient: female
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Dosage: oral
Administration route: Oral
Indication: Hormone Replacement Therapy
Provera
Dosage: oral
Administration route: Oral
Indication: Hormone Replacement Therapy
Estrace
Dosage: oral
Administration route: Oral
Indication: Hormone Replacement Therapy
Adverse event in 55 year old female receiving Activella (Estradiol)
Reported by a individual with unspecified qualification from United States on 2007-07-11
Patient: 55 year old female, weighing 52.2 kg (114.8 pounds)
Adverse reactions / side effects: Breast Cancer in Situ
Suspect drug(s):
Activella
Dosage: oral
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 2001-10-03
End date: 2002-10-01
Prempro
Dosage: 0.625/205 mg, oral
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 1998-06-12
End date: 2001-09-04
Other drugs received by patient: Aspirin; Multivitamins Plus Iron (Ferrous Sulfate, Vitamins Nos); Calcium (Calcium)
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 consumer/non-health professional from United States on 2007-07-11
Patient: female
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Dosage: oral
Administration route: Oral
Indication: Menopausal Symptoms
Prempro
Dosage: oral
Administration route: Oral
Indication: Menopausal Symptoms
Adverse event in 56 year old female receiving Activella (Estradiol)
Reported by a individual with unspecified qualification from United States on 2007-07-11
Patient: 56 year old female, weighing 107.5 kg (236.5 pounds)
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Dosage: 1 tab, oral
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 2002-09-24
End date: 2004-10-01
Provera
Dosage: 10 mg
Indication: Postmenopausal Haemorrhage
Start date: 2000-07-28
End date: 2000-08-05
Medroxyprogesterone
Dosage: 10 mg
Indication: Postmenopausal Haemorrhage
Start date: 2000-03-17
End date: 2001-08-01
Premphase (Premarin;cycrin 14 / 14)
Dosage: 0.625 mg / 5 mg
Indication: Menopausal Symptoms
Start date: 2001-08-07
End date: 2002-09-01
Other drugs received by patient: Alesse (Ethinyestradiol, Levonorgestrel); Estrogens SOL / INJ; Furosemide; Lanoxin; Actos; Celebrex; Hyzaar; Glucophage; Zoloft; Aspirin; Lexapro; Enalapril (Enalapril); Potassium Chloride; Calcium (Calcium)
Adverse event in 60 year old female receiving Activella (Estradiol)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-09
Patient: 60 year old female
Adverse reactions / side effects: Endometrial Cancer
Adverse event resulted in: hospitalization
Suspect drug(s):
Activella (Estradiol)
Other drugs received by patient: Mobic; Soma; Ultracet
Adverse event in female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-07-02
Patient: female, weighing 76.7 kg (168.8 pounds)
Adverse reactions / side effects: Breast Cancer Metastatic
Adverse event resulted in: death
Suspect drug(s):
Prempro
Activella
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 lawyer from United States on 2007-06-12
Patient: female
Adverse reactions / side effects: Breast Cancer Metastatic
Suspect drug(s):
Premphase 14 / 14
Activella
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 2007-04-19
Patient: female
Adverse reactions / side effects: Venous Thrombosis
Suspect drug(s):
Activella
Dosage: 1.0 mg/0.5 mg
Administration route: Oral
Indication: Hormone Replacement Therapy
Start date: 2001-08-27
End date: 2002-08-19
Activella
Dosage: 1.0 mg/0.5 mg
Start date: 2004-08-05
Vagifem
Dosage: 25 ug, unk
Indication: Hormone Replacement Therapy
Start date: 2002-08-19
End date: 2006-08-01
Femhrt
Dosage: unknown
Indication: Hormone Replacement Therapy
Start date: 2000-08-29
End date: 2001-03-01
Prempro
Indication: Hormone Replacement Therapy
Start date: 2000-01-25
End date: 2000-08-01
Cenestin
Dosage: 1.25 mg, unk
Indication: Hormone Replacement Therapy
Start date: 2001-05-03
Prometrium
Dosage: 100 mg, unk
Indication: Hormone Replacement Therapy
Start date: 2001-05-03
Other drugs received by patient: Synthroid; Acyclovir / 00587301 /; Effexor XR; Chromagen / 00555001 /; Pamine
Adverse event in 50 year old female receiving Activella (Estradiol)
Reported by a individual with unspecified qualification from France on 2007-04-09
Patient: 50 year old female
Adverse reactions / side effects: Jaundice, Pruritus, Diarrhoea, Nausea, Cytolytic Hepatitis, Pyrexia, Abdominal Pain Upper
Adverse event resulted in: hospitalization
Suspect drug(s):
Escitalopram
Start date: 2007-01-06
End date: 2007-01-22
Mopral (Omeprazole)
Start date: 2007-01-03
End date: 2007-01-22
Zyprexa
Start date: 2007-01-04
End date: 2007-01-22
Cefpodoxime Proxetil
Start date: 2007-01-12
End date: 2007-01-22
Activella
Start date: 2007-01-12
End date: 2007-01-22
Claradol Caffeine
Start date: 2007-01-12
End date: 2007-01-22
Adverse event in 59 year old female receiving Activella (Estradiol)
Reported by a lawyer from United States on 2007-04-06
Patient: 59 year old female, weighing 78.5 kg (172.6 pounds)
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Dosage: unk, unk
Indication: Menopausal Symptoms
Premarin
Dosage: .0625 mg.
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 1995-03-01
End date: 2003-01-01
Estratest H.s.
Dosage: unknown
Administration route: Oral
Indication: Menopausal Symptoms
Start date: 1998-03-01
End date: 2003-01-01
Medroxyprogesterone Acetate
Dosage: 2.5 mg, unk
Indication: Menopausal Symptoms
Start date: 1997-12-01
Other drugs received by patient: Provera; Synthroid; Effexor XR; Coumadin
Adverse event in female receiving Activella (Estradiol)
Reported by a individual with unspecified qualification from United States on 2007-04-06
Patient: female, weighing 63.5 kg (139.7 pounds)
Adverse reactions / side effects: Breast Cancer Metastatic
Suspect drug(s):
Activella
Dosage: unknown
Indication: Menopause
Start date: 2002-05-15
Premarin
Dosage: unknown
Indication: Menopause
Start date: 2004-04-01
End date: 2004-09-01
Prempro
Dosage: unknown
Indication: Menopause
Start date: 1997-01-01
End date: 2004-01-01
Premphase 14 / 14
Dosage: unknown
Indication: Menopause
Start date: 2003-05-04
End date: 2003-06-02
Other drugs received by patient: Zestril; Aspirin
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 lawyer from United States on 2007-03-16
Patient: female
Adverse reactions / side effects: Breast Cancer Female
Suspect drug(s):
Provera
Administration route: Oral
Indication: Hormone Replacement Therapy
Start date: 1998-01-01
End date: 2003-01-01
Activella
Indication: Hormone Replacement Therapy
Start date: 1998-01-01
End date: 2003-01-01
Estrace
Indication: Hormone Replacement Therapy
Start date: 1998-01-01
End date: 2003-01-01
Adverse event in female receiving Activella (Estradiol)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-09
Patient: female, weighing 95.2 kg (209.5 pounds)
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Dosage: 1 mg/0.5 mg qd
Indication: Menopausal Symptoms
Start date: 2001-08-27
End date: 2003-06-14
Activella
Medroxyprogesterone
Dosage: 10 mg, qd
Indication: Menopausal Symptoms
Start date: 2001-01-01
Other drugs received by patient: Effexor XR; Effexor XR; Levothyroxine / 00068002 /; Flexeril; Naproxen
Adverse event in female receiving Activella (Estradiol)
Reported by a consumer/non-health professional from United States on 2007-03-06
Patient: female, weighing 88.4 kg (194.6 pounds)
Adverse reactions / side effects: Breast Cancer
Suspect drug(s):
Activella
Dosage: .5 mg, unk
Indication: Menopausal Symptoms
Start date: 2002-09-05
Premarin
Dosage: 1.25 mg, unk
Indication: Menopausal Symptoms
Start date: 1998-04-28
Premarin
Dosage: .625 mg, unk
Start date: 2001-09-26
Provera
Dosage: 10 mg, unk
Indication: Menopausal Symptoms
Start date: 1998-04-28
Provera
Dosage: 2.5 mg, unk
Start date: 2001-12-20
Medroxyprogesterone Acetate
Dosage: unknown
Indication: Menopausal Symptoms
Start date: 1999-01-01
End date: 2001-01-01
Other drugs received by patient: Synthroid; Zetia; Redux / 00061602 /; Mobic; Mobic
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
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