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Vivelle (Estradiol Transdermal) - Lymphoedema - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Lymphoedema (3)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Vivelle (Estradiol Transdermal) where reactions include lymphoedema. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Vivelle side effects in female

Reported by a physician from United States on 2012-02-10

Patient: female

Reactions: Thrombosis, Asthma, Lymphadenopathy, Hypoglycaemia, Osteomyelitis, Lipids Increased, Cerebrovascular Disorder, Peripheral Sensory Neuropathy, Oedema Peripheral, Uterine Leiomyoma, Irritable Bowel Syndrome, Postmenopausal Haemorrhage, Hypoxia, Breast Cancer, Pneumonia, Pain in Extremity, Mastitis, Breast Mass, Hypoaesthesia, Diverticulum Intestinal, Adenomyosis, Diabetic Neuropathy, Staphylococcal Infection, Nervous System Disorder, Gastric Polyps, non-Hodgkin's Lymphoma, Sleep Apnoea Syndrome, Uterine Haemorrhage, Aphasia, Viith Nerve Paralysis, Fibrocystic Breast Disease, Neuropathy Peripheral, Fibromyalgia, Obesity, Depression, Lymphoedema, Transient Ischaemic Attack, Migraine, Abdominal Pain Lower, Type 2 Diabetes Mellitus, Motor Dysfunction, Urinary Tract Infection, Cognitive Disorder, Cystitis, Amnesia, Cerebrovascular Accident, Anxiety, Osteoarthritis, Dysarthria, Diarrhoea, Arthralgia, Dysuria, Flank Pain, Alopecia, Gait Disturbance, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Estraderm
    Dosage: 0.5 mg, unk
    Indication: Hormone Replacement Therapy
    Start date: 1994-04-01
    End date: 1997-06-01

Vivelle
    Dosage: 0.1 mg, unk
    Indication: Hormone Replacement Therapy
    Start date: 1997-10-01
    End date: 1997-12-01

Provera
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Hormone Replacement Therapy
    Start date: 1994-03-01
    End date: 1994-08-01

Premarin
    Indication: Hormone Replacement Therapy

Medroxyprogesterone Acetate
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Hormone Replacement Therapy
    Start date: 1994-09-01
    End date: 2000-02-16

Estraderm
    Dosage: 0.1 mg, unk
    Start date: 1997-08-01
    End date: 2000-02-01



Possible Vivelle side effects in female

Reported by a lawyer from United States on 2012-01-12

Patient: female

Reactions: Asthma, Thrombosis, Lymphadenopathy, Hypoglycaemia, Cerebrovascular Disorder, Lipids Increased, Peripheral Sensory Neuropathy, Uterine Leiomyoma, Irritable Bowel Syndrome, Hypoxia, Postmenopausal Haemorrhage, Breast Cancer, Pneumonia, Pain in Extremity, Breast Mass, Hypoaesthesia, Diverticulum Intestinal, Adenomyosis, Staphylococcal Infection, Diabetic Neuropathy, Nervous System Disorder, Gastric Polyps, non-Hodgkin's Lymphoma, Sleep Apnoea Syndrome, Uterine Haemorrhage, Aphasia, Viith Nerve Paralysis, Neuropathy Peripheral, Fibrocystic Breast Disease, Fibromyalgia, Obesity, Depression, Lymphoedema, Transient Ischaemic Attack, Migraine, Abdominal Pain Lower, Type 2 Diabetes Mellitus, Motor Dysfunction, Cognitive Disorder, Amnesia, Cerebrovascular Accident, Osteoarthritis, Dysarthria, Anxiety, Arthralgia, Diarrhoea, Gait Disturbance, Hypertension

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Estraderm
    Dosage: 0.5 mg, unk
    Indication: Hormone Replacement Therapy
    Start date: 1994-04-01
    End date: 1997-06-01

Vivelle
    Dosage: 0.1 mg, unk
    Indication: Hormone Replacement Therapy
    Start date: 1997-10-01
    End date: 1997-12-01

Premarin
    Indication: Hormone Replacement Therapy

Provera
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Hormone Replacement Therapy
    Start date: 1994-03-01
    End date: 1994-08-01

Estraderm
    Dosage: 0.1 mg, unk
    Start date: 1997-08-01
    End date: 2000-02-01

Medroxyprogesterone Acetate
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Hormone Replacement Therapy
    Start date: 1994-09-01
    End date: 2000-02-16



Possible Vivelle side effects in female

Reported by a physician from United States on 2011-12-02

Patient: female, weighing 68.0 kg (149.7 pounds)

Reactions: Lymphadenopathy, Uterine Leiomyoma, Oedema Peripheral, Arteriosclerosis, Breast Pain, Breast Cancer, Cellulitis, Cardiac Murmur, Osteopenia, Hirsutism, Cerebral Small Vessel Ischaemic Disease, Metastases To Spine, Uterine Disorder, Scar, Bone Pain, Fall, Metastases To Lymph Nodes, Intervertebral Disc Disorder, Dizziness, Oedema, Abdominal Distension, Metastases To Peritoneum, Lymphoedema, Lymph Node Fibrosis, Breast Disorder, Musculoskeletal Pain, Cerebral Atrophy, Osteoarthritis, Anxiety, Mitral Valve Incompetence, Metastases To Bone, Deep Vein Thrombosis

Drug(s) suspected as cause:
Vivelle
    Dosage: 0.05mg
    Indication: Hormone Replacement Therapy
    Start date: 1998-12-30

Combipatch
    Dosage: 50/140mcg
    Indication: Menopause
    Start date: 1998-12-19

Gynodiol
    Dosage: 1 mg, unk

Vivelle
    Dosage: 0.025mg
    Administration route: Topical

Prometrium
    Dosage: 100mg
    Indication: Hormone Replacement Therapy
    Start date: 1998-12-30

Prempro
    Dosage: 2.5mg
    Indication: Menopause
    Start date: 1998-03-13

Vagifem
    Dosage: 25 ug, unk

Vivelle
    Dosage: .075 mg, unk

Estradiol
    Dosage: 1 mg, unk

Gynodiol
    Dosage: 0.5 mg, unk
    Indication: Hormone Replacement Therapy

Estradiol
    Dosage: 0.5mg
    Indication: Menopause
    Start date: 1999-03-12

Other drugs received by patient: Aldactone; Wellbutrin; Femara; Remeron; Paxil; Dyazide; Spironolactone; Nolvadex; Prozac; Zyban; Xenical; Miacalcin; Aromasin; Alprazolam; Hydrochlorothiazide; Proventil; Zyrtec; Buspar

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