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Index of reports
> Cases with Oestrogen Receptor Assay Positive ()
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Provera (Medroxyprogesterone) where reactions include oestrogen receptor assay positive. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Provera side effects in female
Reported by a individual with unspecified qualification from United States on 2011-12-01
Patient: female, weighing 61.2 kg (134.7 pounds)
Reactions: Abdominal Pain, Muscle Atrophy, Breast Cancer in Situ, Loss of Consciousness, Breast Cancer Recurrent, Metastasis, Dyspepsia, Vulvovaginal Dryness, Mammogram, Breast Hyperplasia, Back Pain, Dyspareunia, Intervertebral Disc Protrusion, Dysphagia, Oestrogen Receptor Assay Negative, Breast Cancer Stage I, Ovarian Cyst, Breast Cancer Stage III, Breast Mass, Renal Cyst, Osteopenia, Colitis, Breast Necrosis, Excessive Granulation Tissue, Confusional State, Application Site Reaction, Head Injury, Osteoporosis, Pain, Fall, Weight Increased, Fibrocystic Breast Disease, Chest Pain, Intervertebral Disc Degeneration, Injury, Oestrogen Receptor Assay Positive, Depression, Hallucination, Gastrooesophageal Reflux Disease, Progesterone Receptor Assay Negative, Scoliosis, Bone Giant Cell Tumour, Radius Fracture, Anxiety, Atrophic Vulvovaginitis, Spinal Osteoarthritis, Arthritis, Physical Disability, Breast Fibrosis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Premarin
Dosage: 0.625 mg, unk
Administration route: Oral
Start date: 1992-10-01
End date: 1997-07-01
Provera
Dosage: 5/2.5 mg day 1-14
Administration route: Oral
Start date: 1992-10-01
End date: 1997-07-01
Ogen
Start date: 1992-06-01
End date: 1993-04-01
Estraderm
Dosage: 0.05 mg, 2x/wk
Start date: 1995-09-01
End date: 1995-11-01
Prempro
Dosage: 625/2.5 mg
Indication: Menopausal Symptoms
Start date: 1996-06-01
End date: 1996-06-01
Premarin
Other drugs received by patient: Multivitamins, Combinations; Xanax; Prozac; Evista
Possible Provera side effects in female
Reported by a lawyer from United States on 2011-11-28
Patient: female, weighing 59.0 kg (129.7 pounds)
Reactions: Abdominal Pain, Pulmonary Hypertension, Lymphocyte Count Increased, FAT Embolism, Myocardial Ischaemia, Endoscopy Upper Gastrointestinal Tract, Chronic Obstructive Pulmonary Disease, Lumbar Spinal Stenosis, Metastatic Lymphoma, Hypoxia, Back Pain, Pain in Extremity, Breast Cancer Stage I, Breast Mass, Renal Cyst, Osteopenia, Hepatic Steatosis, Breast Cancer Stage II, Bone Densitometry, Breast Necrosis, Ultrasound Abdomen Abnormal, Pleural Fibrosis, Dyslipidaemia, Osteoporosis, Aortic Aneurysm, Gastritis, Dyspnoea Exertional, Interstitial Lung Disease, Basal Cell Carcinoma, Blood Cholesterol Increased, Malignant Melanoma, Oestrogen Receptor Assay Positive, Myocardial Infarction, Emphysema, Scoliosis, Dyspnoea, Nausea, Squamous Cell Carcinoma, Spondylolisthesis, Peripheral Vascular Disorder, Progesterone Receptor Assay Positive, Pulmonary Fibrosis, Osteoarthritis, Cardiac Failure, Nuclear Magnetic Resonance Imaging Abnormal, Spinal Osteoarthritis, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Medroxyprogesterone
Indication: Hormone Replacement Therapy
Start date: 1997-01-01
End date: 2002-01-01
Prempro
Dosage: .625/2.5 mg
Administration route: Oral
Indication: Osteoporosis Prophylaxis
Start date: 1998-12-01
End date: 2002-10-01
Estraderm
Dosage: 0.05 mg, unk
Indication: Osteoporosis Prophylaxis
Start date: 1992-01-01
End date: 1998-12-01
Provera
Dosage: 2.5 mg, unk
Administration route: Oral
Indication: Osteoporosis Prophylaxis
Start date: 1992-01-01
End date: 1998-12-01
Other drugs received by patient: Letairis; Calcium; Coumadin; Zocor; Advair Diskus 100 / 50; Boniva; Hydrochlorothiazide; Cozaar; Vitamin D; Spiriva; Celebrex; Viagra; Fosamax
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