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BIOPSY BREAST ABNORMAL side effect

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Vivelle Side Effects Report #5597495-7
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Jan 16, 2008. Female patient, 53 years of age, weighting 156.0 lb, was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast cosmetic surgery, breast pain, breast reconstruction, cataract operation, chest pain, chronic obstructive pulmonary disease, . VIVELLE dosage: unknown. During the same period patient was treated with PREMARIN. Patient was hospitalized. Patient recovered.

Vivelle Side Effects Report #5506080-4
VIVELLE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 29, 2007. Female patient, 61 years of age, weighting 190.0 lb, was diagnosed with night sweats, amnesia, affective disorder and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast mass, depression, haemangioma of liver, knee arthroplasty, limb discomfort, lung infiltration, lymphadenectomy, . VIVELLE dosage: unknown. During the same period patient was treated with ESTRACE, ESTRATAB, ESTROPIPATE, PREMPRO, PREMARIN, PROVERA, FISH OIL. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5528620-1
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Mar 12, 2007. Female patient, 72 years of age, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, mammogram abnormal, . ESTRADERM dosage: 1 MG/DAY, TRANSDERMAL. During the same period patient was treated with PREMARIN, PREMPRO, PROVERA. Patient recovered.

Estraderm Side Effects Report #5528627-4
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 23, 2007. Female patient, 55 years of age, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer female, breast cyst, breast mass, depressed mood, depression, endometrial hyperplasia, fatigue, mammogram abnormal, . ESTRADERM dosage: 0.05 MG, TRANSDERMAL. During the same period patient was treated with PREMPRO, PREMARIN, CLIMARA, PROVERA, ESTRACE, CYCRIN. Patient recovered.


Vivelle Side Effects Report #5494190-X
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Oct 15, 2007. Female patient, 58 years of age, was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast cosmetic surgery, breast reconstruction, cataract operation, chronic obstructive pulmonary disease, colonic polyp, colonoscopy, . VIVELLE dosage: unknown. During the same period patient was treated with PREMARIN. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5461111-5
SANDOSTATIN LAR problem was reported by a Physician from UNITED STATES on Sept 14, 2007. Female patient, 67 years of age, was diagnosed with carcinoid syndrome and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, diarrhoea, malignant breast lump removal, metastases to heart, metastases to pancreas, . SANDOSTATIN LAR dosage: 40 MG Q3WEEKS. During the same period patient was treated with VITAMIN D, VITAMIN D, VITAMIN A, VITAMIN B CAP, ASCORBIC ACID, VITAMIN E, LOMOTIL. Patient recovered.

Estraderm Side Effects Report #5418206-1
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Aug 10, 2007. Female patient, 57 years of age, weighting 272.0 lb, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast cancer metastatic, breast cyst excision, cervical dysplasia, emotional distress, hypertension, inflammation, lobar pneumonia, . ESTRADERM dosage: 0.05 MG, UNK. During the same period patient was treated with PREMARIN, CENESTIN, NORTRIPTYLINE, FUROSEMIDE, CLONIDINE, GLYBURIDE, AVANDIA, METOPROLOL SUCCINATE. Patient was hospitalized. Patient recovered.

Vivelle Side Effects Report #5751581-7
VIVELLE problem was reported by a Consumer or non-health professional from UNITED STATES on May 19, 2008. Female patient, weighting 156.0 lb, was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast cancer metastatic, breast cosmetic surgery, breast pain, breast reconstruction, cataract operation, chest pain, . VIVELLE dosage: unknown. During the same period patient was treated with PREMARIN. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5699680-2
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Apr 04, 2008. Female patient, 57 years of age, weighting 272.0 lb, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast cancer metastatic, breast cyst excision, cervical dysplasia, emotional distress, hypertension, inflammation, lobar pneumonia, . ESTRADERM dosage: 0.05 MG, UNK. During the same period patient was treated with PREMARIN, CENESTIN, NORTRIPTYLINE, FUROSEMIDE, CLONIDINE, GLYBURIDE, AVANDIA, METOPROLOL TARTRATE. Patient was hospitalized. Patient recovered.


Elidel Side Effects Report #5317532-4
ELIDEL problem was reported by a Consumer or non-health professional from AUSTRALIA on May 03, 2007. Female patient, 37 years of age, was treated with ELIDEL. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast mass, breast microcalcification, fibroadenoma of breast, mammogram abnormal, mastectomy, ultrasound breast abnormal, . ELIDEL dosage: unknown. Patient recovered.

Estraderm Side Effects Report #5214943-2
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Jan 11, 2006. Female patient, 67 years of age, was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, oestrogen receptor assay positive, progesterone receptor assay positive, . ESTRADERM dosage: unknown. During the same period patient was treated with PROVERA. Patient recovered.

Sandostatin Side Effects Report #5254102-0
SANDOSTATIN LAR problem was reported by a Physician from UNITED STATES on Feb 20, 2007. Female patient, 67 years of age, was diagnosed with carcinoid syndrome and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, diarrhoea, malignant breast lump removal, . SANDOSTATIN LAR dosage: 40 MG Q3WEEKS. Patient recovered.

Sandostatin Side Effects Report #5265994-3
Physician from UNITED STATES reported SANDOSTATIN LAR problem on Mar 02, 2007. Female patient, 67 years of age, was diagnosed with carcinoid syndrome and was treated with SANDOSTATIN LAR. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, diarrhoea, malignant breast lump removal, . SANDOSTATIN LAR dosage: 40 MG Q3WEEKS. During the same period patient was treated with VITAMIN D, VITAMIN D, VITAMIN A, VITAMIN B CAP, ASCORBIC ACID, VITAMIN E. Patient recovered.

Rebif Side Effects Report #5276621-3
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 13, 2006. Female patient, 42 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast mass, . REBIF dosage: unknown. Patient recovered.


Vivelle Side Effects Report #5278793-3
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Mar 19, 2007. Female patient, 61 years of age, weighting 198.0 lb, was diagnosed with night sweats, amnesia, affective disorder and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: biopsy breast abnormal, breast cancer, breast mass, depression, haemangioma of liver, knee arthroplasty, limb discomfort, lung infiltration, lymphadenectomy, . VIVELLE dosage: unknown. During the same period patient was treated with ESTRACE, ESTRATAB, ESTROPIPATE, PREMPRO, PREMARIN, PROVERA, FISH OIL. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5682293-6
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 24, 2008. Female patient, 53 years of age, weighting 105.0 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy breast abnormal, breast calcifications, breast cancer, chondropathy, depression, hot flush, joint manipulation, lung disorder, . ESTRADERM dosage: 0.05 MG, UNK. During the same period patient was treated with PROVERA, ORTHO, ESTRACE, PREMPRO, CLIMARA, EVISTA, CALCIUM. Patient recovered.

Zometa Side Effects Report #5605851-3
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Jan 22, 2008. Female patient, 49 years of age, weighting 128.0 lb, was diagnosed with metastases to bone, breast cancer, pain in jaw and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy breast abnormal, bone disorder, breast cancer metastatic, decreased interest, deformity, dental caries, emotional distress, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA, VICODIN, FEMARA, CELEXA, COUMADIN, SIMVASTATIN, TAXOTERE. Patient recovered.

Estraderm Side Effects Report #5532756-9
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Female patient, 53 years of age, weighting 105.0 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy breast abnormal, breast cancer, breast microcalcification, chondropathy, depression, joint manipulation, lung disorder, lung neoplasm, . ESTRADERM dosage: unknown. During the same period patient was treated with PROVERA, ORTHO, ESTRACE, PREMPRO, CLIMARA. Patient recovered.

Zometa Side Effects Report #5553647-3
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Dec 05, 2007. Female patient, 49 years of age, weighting 128.0 lb, was diagnosed with metastases to bone, breast cancer, pain in jaw and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy breast abnormal, breast cancer metastatic, decreased interest, deformity, dental caries, emotional distress, mastectomy, . ZOMETA dosage: unknown. During the same period patient was treated with AREDIA, VICODIN, FEMARA, CELEXA, COUMADIN, SIMVASTATIN. Patient recovered.


Estraderm Side Effects Report #5528267-7
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2007. Female patient, 59 years of age, weighting 164.9 lb, was diagnosed with menorrhagia and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy breast abnormal, breast cancer in situ, breast cosmetic surgery, breast reconstruction, depression, dizziness, dysmenorrhoea, hot flush, . ESTRADERM dosage: 0.05 MG/DAY, Q4, TRANSDERMAL. During the same period patient was treated with VIVELLE, PREMPRO, PROVERA, MEDROXYPROGESTERONE, PREMARIN, PROMETRIUM, ACTIVELLA, AYGESTIN. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5528964-3
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Feb 26, 2007. Female patient, 60 years of age, weighting 188.9 lb, was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: anxiety, biopsy breast abnormal, breast cancer, breast microcalcification, emotional distress, headache, hot flush, hysteroscopy, injury, . ESTRADERM dosage: unknown. During the same period patient was treated with PREMPRO, ORTHO, PROVERA, PREMARIN, DIOVAN. Patient was hospitalized and became disabled. Patient recovered.

Estraderm Side Effects Report #5530102-8
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 26, 2007. Female patient, 67 years of age, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: aspiration pleural cavity, biopsy breast abnormal, breast cancer, breast cancer in situ, breast reconstruction, cholelithiasis, culdoplasty, dyspnoea, haemangioma of liver, . ESTRADERM dosage: 0.05 MG/DAY, TIWCE WEEKLY. During the same period patient was treated with PROVERA, PREMPRO, PREMARIN, ESTRACE. Patient recovered.

Estraderm Side Effects Report #5405626-4
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on July 27, 2007. Female patient, 56 years of age, weighting 160.0 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: biopsy, biopsy breast abnormal, blood cholesterol increased, breast cancer, breast microcalcification, cardiac tamponade, colon polypectomy, colonic polyp, colonoscopy, . ESTRADERM dosage: unknown. During the same period patient was treated with PREMARIN, ESTRATAB, ESTRACE, ESTRATEST, PROVERA, CYCRIN. Patient was hospitalized. Patient recovered.

Premarin Side Effects Report #5391930-5
PREMARIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 13, 2007. Female patient, 52 years of age, weighting 115.0 lb, was diagnosed with menopausal symptoms, menopause and was treated with PREMARIN. After drug was administered, patient experienced the following problems/side effects: basal cell carcinoma, biopsy breast abnormal, blood cholesterol increased, blood triglycerides increased, breast cancer, breast cancer in situ, breast microcalcification, breast reconstruction, cardiac pacemaker replacement, . PREMARIN dosage: unknown. During the same period patient was treated with PROVERA, ESTRADERM, NORLUTATE. Patient recovered.

Estraderm Side Effects Report #5393298-7
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on July 13, 2007. Female patient, 70 years of age, weighting 150.0 lb, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: benign breast neoplasm, biopsy breast abnormal, biopsy breast normal, blood cholesterol increased, blood triglycerides increased, bone densitometry, bone density decreased, breast cancer female, breast cancer in situ, . ESTRADERM dosage: 0.1 MG 1 PATCH 2X PER WEEK. During the same period patient was treated with PREMARIN, FOSAMAX ONCE WEEKLY, PROVERA. Patient recovered.

Premarin Side Effects Report #5391930-5
PREMARIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 13, 2007. Female patient, 52 years of age, weighting 115.0 lb, was diagnosed with menopausal symptoms, menopause and was treated with PREMARIN. After drug was administered, patient experienced the following problems/side effects: basal cell carcinoma, biopsy breast abnormal, blood cholesterol increased, blood triglycerides increased, breast cancer, breast cancer in situ, breast microcalcification, breast reconstruction, cardiac pacemaker replacement, . PREMARIN dosage: unknown. During the same period patient was treated with PROVERA, ESTRADERM, NORLUTATE. Patient recovered.

Estraderm Side Effects Report #5393298-7
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on July 13, 2007. Female patient, 70 years of age, weighting 150.0 lb, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: benign breast neoplasm, biopsy breast abnormal, biopsy breast normal, blood cholesterol increased, blood triglycerides increased, bone densitometry, bone density decreased, breast cancer female, breast cancer in situ, . ESTRADERM dosage: 0.1 MG 1 PATCH 2X PER WEEK. During the same period patient was treated with PREMARIN, FOSAMAX ONCE WEEKLY, PROVERA. Patient recovered.

Estraderm Side Effects Report #5772297-7
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on June 09, 2008. Female patient, weighting 160.0 lb, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: biopsy, biopsy breast abnormal, biopsy endometrium, blood cholesterol increased, breast cancer, cardiac tamponade, chest wall operation, colon polypectomy, colonic polyp, . ESTRADERM dosage: 0.1MG-0.5MG. During the same period patient was treated with PREMARIN, ESTRATAB, ESTRACE, ESTRATEST, PROVERA, CYCRIN. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5780257-5
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on June 16, 2008. Female patient, weighting 128.0 lb, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: aspiration pleural cavity, biopsy breast abnormal, breast cancer, breast cancer in situ, breast lump removal, breast reconstruction, cholelithiasis, culdoplasty, diverticulitis, . ESTRADERM dosage: 0.05 MG/DAY, TIWCE WEEKLY. During the same period patient was treated with PREMARIN, PROVERA, PREMPRO, ESTRACE. Patient recovered.

Estraderm Side Effects Report #5699649-8
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 04, 2008. Female patient, 67 years of age, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: aspiration pleural cavity, biopsy breast abnormal, breast cancer, breast cancer in situ, breast reconstruction, cholelithiasis, culdoplasty, dyspnoea, haemangioma of liver, . ESTRADERM dosage: 0.05 MG/DAY, TIWCE WEEKLY. During the same period patient was treated with PROVERA, PREMPRO, PREMARIN, ESTRACE. Patient recovered.

Estraderm Side Effects Report #5699650-4
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Apr 04, 2008. Female patient, 67 years of age, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: aspiration pleural cavity, biopsy breast abnormal, breast cancer, breast cancer in situ, breast reconstruction, cholelithiasis, culdoplasty, dyspnoea, haemangioma of liver, . ESTRADERM dosage: 0.05 MG/DAY, TIWCE WEEKLY. During the same period patient was treated with PROVERA, PREMPRO, PREMARIN, ESTRACE. Patient recovered.

Estraderm Side Effects Report #5338099-0
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on May 18, 2007. Female patient, 67 years of age, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: aspiration pleural cavity, biopsy breast abnormal, breast cancer, breast cancer in situ, cholelithiasis, dyspnoea, haemangioma of liver, hysterectomy, injury, . ESTRADERM dosage: 0.05 MG/DAY, TIWCE WEEKLY. During the same period patient was treated with PROVERA, PREMPRO, PREMARIN, ESTRACE. Patient recovered.

Vivelle Side Effects Report #5586373-5
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Jan 07, 2008. Female patient, 56 years of age, was diagnosed with menopause and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: accident, back pain, biopsy breast abnormal, biopsy endometrium abnormal, bladder disorder, breast calcifications, breast cancer, cystocele, eye laser surgery, . VIVELLE dosage: 0.05 MG/DAY, UNK. During the same period patient was treated with PREMARIN, PROVERA, ESTRACE, PROMETRIUM. Patient recovered.

Vivelle Side Effects Report #5532758-2
VIVELLE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Female patient, 56 years of age, was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: aspiration breast, benign lung neoplasm, biopsy breast abnormal, biopsy mucosa abnormal, breast cancer, breast cancer stage iii, breast discomfort, breast mass, breast microcalcification, . VIVELLE dosage: 0.0375 MG/DAY. During the same period patient was treated with PREMPHASE, PROVERA, MEDROXYPROGESTERONE. Patient recovered.

Vivelle Side Effects Report #5506078-6
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Oct 30, 2007. Female patient was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: adenocarcinoma, arthroscopy, biopsy breast abnormal, breast cancer, breast hyperplasia, breast mass, depression, hot flush, . VIVELLE dosage: 0.1 MG/DAY, UNK. During the same period patient was treated with ESTRACE, PROVERA, CYCRIN, PREMPRO, PREMARIN. Patient recovered.

Combipatch Side Effects Report #5489537-4
COMBIPATCH problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2007. Female patient, 57 years of age, weighting 201.9 lb, was diagnosed with vulvovaginal dryness and was treated with COMBIPATCH. After drug was administered, patient experienced the following problems/side effects: alopecia, asthenia, biopsy breast abnormal, blood pressure abnormal, breast cancer, breast cancer in situ, deformity, fear, fibrocystic breast disease, . COMBIPATCH dosage: unknown. During the same period patient was treated with PREMPRO, PREMARIN. Patient recovered.

Combipatch Side Effects Report #5409265-0
Consumer or non-health professional from UNITED STATES reported COMBIPATCH problem on Aug 03, 2007. Female patient was diagnosed with menopause, gastrooesophageal reflux disease, hypersensitivity and was treated with COMBIPATCH. After drug was administered, patient experienced the following problems/side effects: anxiety, arthritis, biopsy breast abnormal, breast cancer, breast mass, bundle branch block, cardiac enzymes increased, cardiac failure congestive, cardiomyopathy, . COMBIPATCH dosage: 0.05/0.14 MG/DAY, UNK. During the same period patient was treated with PREMARIN, PREMPRO, ESTRADIOL, PREVACID, NEXIUM, NASACORT AQ. Patient recovered.

Estraderm Side Effects Report #5423331-5
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 17, 2007. Female patient, 51 years of age, weighting 138.0 lb, was diagnosed with menopause, seasonal allergy, menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: arthralgia, biopsy, biopsy breast abnormal, breast cancer, dyspnoea, mammogram abnormal, musculoskeletal pain, nasal septum deviation, osteoporosis, . ESTRADERM dosage: 0.05 MG/DAY, UNK. During the same period patient was treated with VIVELLE, ESTRATEST, PROVERA, PREMARIN, CLARITIN, EFFEXOR. Patient recovered.

Vivelle Side Effects Report #5389872-4
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on July 06, 2007. Female patient, 56 years of age, was diagnosed with menopause and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: accident, back pain, biopsy breast abnormal, biopsy endometrium abnormal, bladder disorder, breast cancer, breast microcalcification, cystocele, . VIVELLE dosage: 0.05 MG/DAY, UNK. During the same period patient was treated with PREMARIN, PROVERA, ESTRACE, PROMETRIUM. Patient recovered.

Vivelle Side Effects Report #5389872-4
VIVELLE problem was reported by a Consumer or non-health professional from UNITED STATES on July 06, 2007. Female patient, 56 years of age, was diagnosed with menopause and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: accident, back pain, biopsy breast abnormal, biopsy endometrium abnormal, bladder disorder, breast cancer, breast microcalcification, cystocele, . VIVELLE dosage: 0.05 MG/DAY, UNK. During the same period patient was treated with PREMARIN, PROVERA, ESTRACE, PROMETRIUM. Patient recovered.

Combipatch Side Effects Report #5763586-0
Consumer or non-health professional from UNITED STATES reported COMBIPATCH problem on May 29, 2008. Female patient, weighting 180.0 lb, was diagnosed with menopause, gastrooesophageal reflux disease, hypersensitivity and was treated with COMBIPATCH. After drug was administered, patient experienced the following problems/side effects: anxiety, arthritis, biopsy breast abnormal, breast cancer, breast mass, bundle branch block, cardiac enzymes increased, cardiac failure congestive, cardiomyopathy, . COMBIPATCH dosage: 0.05/0.14 MG/DAY, UNK. During the same period patient was treated with PREMPRO, PREMARIN, ESTRADIOL, PREVACID, NEXIUM, NASACORT AQ. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5777360-2
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on June 16, 2008. Female patient, weighting 138.0 lb, was diagnosed with menopause, osteoporosis and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: arthralgia, biopsy, biopsy breast abnormal, breast cancer, dyspnoea, mammogram abnormal, musculoskeletal pain, nasal septum deviation, osteoporosis, . ESTRADERM dosage: 0.05 MG/DAY, UNK. During the same period patient was treated with VIVELLE, ESTRATEST, PROVERA, PREMARIN, PREMPRO, FOSAMAX. Patient recovered.

Vivelle Side Effects Report #5778819-4
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on June 16, 2008. Female patient, weighting 157.0 lb, was diagnosed with menopause and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: accident, back pain, biopsy breast abnormal, biopsy endometrium abnormal, bladder disorder, breast cancer, breast lump removal, colon polypectomy, constipation, . VIVELLE dosage: 0.05 MG/DAY, UNK. During the same period patient was treated with PREMARIN, PROVERA, ESTRACE, MEDROXYPROGESTERONE, PROMETRIUM, CLIMARA, ELMIRON. Patient recovered.

Combipatch Side Effects Report #5745633-5
COMBIPATCH problem was reported by a Consumer or non-health professional from UNITED STATES on May 19, 2008. Female patient, 60 years of age, weighting 180.0 lb, was diagnosed with menopause, gastrooesophageal reflux disease, hypersensitivity and was treated with COMBIPATCH. After drug was administered, patient experienced the following problems/side effects: anxiety, arthritis, biopsy breast abnormal, breast cancer, breast mass, bundle branch block, cardiac enzymes increased, cardiac failure congestive, cardiomyopathy, . COMBIPATCH dosage: 0.05/0.14 MG/DAY, UNK. During the same period patient was treated with PREMARIN, PREMPRO, ESTRADIOL, PREVACID, NEXIUM, NASACORT AQ. Patient was hospitalized. Patient recovered.

Vivelle Side Effects Report #5699724-8
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Apr 01, 2008. Female patient, 56 years of age, weighting 157.0 lb, was diagnosed with menopause and was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: accident, back pain, biopsy breast abnormal, biopsy endometrium abnormal, bladder disorder, breast calcifications, breast cancer, breast lump removal, colon polypectomy, . VIVELLE dosage: 0.05 MG/DAY, UNK. During the same period patient was treated with PREMARIN, PROVERA, ESTRACE, PROMETRIUM, CLIMARA, ELMIRON, VIOXX. Patient recovered.

Immune Side Effects Report #5258518-8
IMMUNE GLOBULIN SUBCUTANEOUS problem was reported by a Health Professional from UNITED STATES on Feb 27, 2007. Female patient, 41 years of age, weighting 123.0 lb, was diagnosed with immunodeficiency and was treated with IMMUNE GLOBULIN SUBCUTANEOUS. After drug was administered, patient experienced the following problems/side effects: arthralgia, axillary mass, biopsy breast abnormal, breast mass, condition aggravated, dysgeusia, headache, infusion site pain, nausea, . IMMUNE GLOBULIN SUBCUTANEOUS dosage: unknown. During the same period patient was treated with IMMUNE GLOBULIN SUBCUTANEOUS, IMMUNE GLOBULIN SUBCUTANEOUS, IMMUNE GLOBULIN SUBCUTANEOUS. Patient recovered.

Estraderm Side Effects Report #5259209-X
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on Feb 26, 2007. Female patient, 49 years of age, weighting 148.0 lb, was diagnosed with menopausal symptoms and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: asthenia, barium enema normal, biopsy breast abnormal, bladder disorder, bladder repair, breast cancer, cervical dysplasia, constipation, . ESTRADERM dosage: 0.5 MG, UNK. During the same period patient was treated with PREMARIN. Patient recovered.

Vivelle Side Effects Report #5265909-8
VIVELLE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2007. Female patient, 56 years of age, was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: aspiration breast, benign lung neoplasm, biopsy breast abnormal, biopsy mucosa abnormal, breast cancer, breast cancer female, breast discomfort, cervical stricture, colitis, . VIVELLE dosage: 0.0375 MG/DAY. During the same period patient was treated with PREMPHASE, PROVERA, MEDROXYPROGESTERONE. Patient recovered.

Vivelle Side Effects Report #5281626-2
Consumer or non-health professional from UNITED STATES reported VIVELLE problem on Mar 19, 2007. Female patient, 60 years of age, weighting 180.0 lb, was treated with VIVELLE. After drug was administered, patient experienced the following problems/side effects: adenocarcinoma, arthroscopy, biopsy breast abnormal, breast cancer, breast hyperplasia, breast mass, depression, hot flush, . VIVELLE dosage: 0.1 MG/DAY, UNK. During the same period patient was treated with ESTRACE, PROVERA, CYCRIN, PREMPRO, PREMARIN. Patient recovered.