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Provera (Medroxyprogesterone) - Insomnia - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Insomnia (9)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Provera (Medroxyprogesterone) where reactions include insomnia. 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 consumer/non-health professional from United States on 2012-07-23

Patient: female, weighing 102.0 kg (224.4 pounds)

Reactions: Diabetes Mellitus, Drug Ineffective, Pain, Endometrial Hypertrophy, Hunger, Malaise, Fatigue, Palpitations, Dyspepsia, Dizziness, Abdominal Distension, Musculoskeletal Stiffness, Eye Pruritus, Muscle Spasms, Vein Disorder, Chest Discomfort, Pain in Extremity, Drug Intolerance, Eye Pain, Hyperplasia, Arthralgia, Rhinalgia, Insomnia, Dehydration, Vertigo, DRY Eye, Asthenia

Drug(s) suspected as cause:
Provera
    Dosage: 5 mg, unk
    Administration route: Oral
    Indication: Neoplasm Malignant
    Start date: 2012-07-01

Omeprazole

Hyoscyamine

Omeprazole
    Indication: Irritable Bowel Syndrome

Omeprazole
    Dosage: 20 mg, 1x/day
    Indication: Gastrooesophageal Reflux Disease

Hyoscyamine
    Indication: Irritable Bowel Syndrome

Provera
    Dosage: unk
    Administration route: Oral
    Indication: Endometrial Hypertrophy
    Start date: 2010-08-01
    End date: 2010-01-01

Provera
    Dosage: 10 mg, 1x/day
    Administration route: Oral
    Indication: Endometrial Hyperplasia
    Start date: 2012-07-12
    End date: 2012-07-01

Provera
    Dosage: unk
    Administration route: Oral
    Indication: Menorrhagia

Hyoscyamine
    Dosage: 0.125 mg, 1x/day
    Indication: Gastrooesophageal Reflux Disease

Other drugs received by patient: Bactroban



Possible Provera side effects in

Reported by a physician from United States on 2012-07-19

Patient:

Reactions: Abdominal Pain, Lymphadenopathy, Glossodynia, Osteomyelitis, Chronic Obstructive Pulmonary Disease, Colonic Polyp, Abdominal Discomfort, Oral Candidiasis, Pharyngeal Ulceration, Cellulitis, Peptic Ulcer, Oral Infection, Rectal Adenoma, Fungal Infection, Insomnia, Fistula Discharge, Tooth Abscess, Abdominal Pain Upper, Colitis Microscopic, Chest Pain, Blood Cholesterol Increased, Gastrooesophageal Reflux Disease, Drug Hypersensitivity, Haemorrhoids, Dental Caries, Musculoskeletal Pain, Appendix Disorder, Hyperlipidaemia, Anxiety, Osteonecrosis of JAW, Diarrhoea, Sepsis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Actonel
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2008-04-20
    End date: 2010-01-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Start date: 2008-02-12
    End date: 2008-03-01

Fosamax
    Dosage: 70 mg, qw
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2001-01-29
    End date: 2008-03-20

Provera
    Administration route: Oral
    Start date: 2001-01-01



Possible Provera side effects in 58 year old female

Reported by a physician from United States on 2012-05-25

Patient: 58 year old female, weighing 66.0 kg (145.2 pounds)

Reactions: Abdominal Pain, Lymphadenopathy, Glossodynia, Osteomyelitis, Chronic Obstructive Pulmonary Disease, Abdominal Discomfort, Colonic Polyp, Oral Candidiasis, Pharyngeal Ulceration, Cellulitis, Peptic Ulcer, Oral Infection, Rectal Adenoma, Fungal Infection, Insomnia, Fistula Discharge, Tooth Abscess, Abdominal Pain Upper, Colitis Microscopic, Chest Pain, Blood Cholesterol Increased, Gastrooesophageal Reflux Disease, Haemorrhoids, Musculoskeletal Pain, Drug Hypersensitivity, Dental Caries, Appendix Disorder, Anxiety, Hyperlipidaemia, Diarrhoea, Osteonecrosis of JAW, Sepsis, Hypertension

Adverse event resulted in: hospitalization, disablity

Drug(s) suspected as cause:
Fosamax
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2001-01-29
    End date: 2008-03-20

Provera
    Administration route: Oral
    Start date: 2001-01-01

Alendronate Sodium
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2008-02-12
    End date: 2008-01-01

Actonel
    Administration route: Oral
    Indication: Osteoporosis Prophylaxis
    Start date: 2008-04-20
    End date: 2010-01-01



Possible Provera side effects in female

Reported by a consumer/non-health professional from United States on 2012-04-10

Patient: female, weighing 64.4 kg (141.7 pounds)

Reactions: Hot Flush, Insomnia

Drug(s) suspected as cause:
Premarin
    Indication: Menstrual Disorder

Provera
    Dosage: 2.5 mg, daily
    Indication: Endometriosis
    Start date: 1989-01-01
    End date: 2005-01-01

Premarin
    Dosage: 0.625 mg, daily
    Indication: Endometriosis
    Start date: 1989-01-01
    End date: 2005-01-01

Provera
    Indication: Menstrual Disorder



Possible Provera side effects in female

Reported by a consumer/non-health professional from United States on 2012-02-14

Patient: female, weighing 54.0 kg (118.8 pounds)

Reactions: Insomnia

Drug(s) suspected as cause:
Provera
    Dosage: 2.5 mg, 1x/day
    Administration route: Oral
    Start date: 1992-01-01

Premarin
    Dosage: 1.25 mg, 1x/day
    Administration route: Oral
    Indication: Menopause
    Start date: 2002-08-01

Other drugs received by patient: Furomex; Xanax; Acetylsalicylic Acid; Acetylsalicylic Acid



Possible Provera side effects in female

Reported by a individual with unspecified qualification from United States on 2012-01-10

Patient: female, weighing 67.1 kg (147.7 pounds)

Reactions: Abdominal Pain, Metaplasia, Breast Cancer in Situ, Mammogram Abnormal, Breast Cyst, Uterine Leiomyoma, Biliary Dilatation, Emotional Disorder, Breast Hyperplasia, Melanocytic Naevus, Proctalgia, Muscle Spasms, Back Pain, Breast Cancer, Postoperative Adhesion, Intervertebral Disc Protrusion, Pain in Extremity, Anaemia, Breast Mass, General Physical Health Deterioration, Osteopenia, Breast Calcifications, Micturition Urgency, Paraesthesia, Uterine Prolapse, Cerebral Small Vessel Ischaemic Disease, Dilatation Intrahepatic Duct Acquired, Insomnia, Osteoporosis, Pain, Rectal Haemorrhage, Breast Induration, Oral Herpes, Fall, Fibrocystic Breast Disease, Fibroadenoma of Breast, Aortic Arteriosclerosis, Intervertebral Disc Degeneration, Injury, Sinusitis, RIB Fracture, Breast Disorder, Biopsy Breast, Avulsion Fracture, Deformity, Anxiety, Atrophic Vulvovaginitis, Oral Pain, Presyncope, Spinal Disorder, Lymph Nodes Scan Abnormal, Arthritis

Drug(s) suspected as cause:
Hormones
    Indication: Menopause
    Start date: 1988-01-01
    End date: 1989-01-01

Provera
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Menopause
    Start date: 1991-08-18
    End date: 1995-08-29

Prempro
    Dosage: .625/2.5 mg
    Administration route: Oral
    Indication: Menopause
    Start date: 1995-05-01
    End date: 1999-01-12

Premarin
    Dosage: 0.9 mg, unk
    Administration route: Oral
    Indication: Menopause
    Start date: 1991-05-08
    End date: 1991-05-15

Premarin
    Dosage: 0.625 mg, unk
    Administration route: Oral
    Start date: 1991-05-16
    End date: 1995-08-29

Estraderm
    Dosage: 0.1 (units not spec.) 2x weekly
    Indication: Menopause
    Start date: 1991-08-18
    End date: 1991-10-01

Other drugs received by patient: Anusol HC; H2 Blocker ^ratiopharm^



Possible Provera side effects in female

Reported by a physician from United States on 2011-12-01

Patient: female, weighing 68.0 kg (149.6 pounds)

Reactions: Foot Deformity, Abdominal Pain, Endometrial Hyperplasia, Aortic Stenosis, Chronic Obstructive Pulmonary Disease, Vitamin B12 Deficiency, Dyspepsia, Uterine Leiomyoma, Breast Hyperplasia, Metabolic Disorder, Arteriosclerosis, Breast Cancer, Cardiac Murmur, Hiatus Hernia, Ovarian Cyst, Coronary Artery Disease, Breast Mass, Cervical Dysplasia, Insomnia, Pelvic Pain, Fibrocystic Breast Disease, Fatigue, Chest Pain, Liver Function Test Abnormal, Dizziness, Depression, Gastrooesophageal Reflux Disease, Dyspnoea, Nausea, Amnesia, Rectocele, Dysuria, Visual Impairment

Drug(s) suspected as cause:
Premarin
    Dosage: 0.625 mg, unk
    Indication: Menopause
    Start date: 1990-11-26
    End date: 2000-11-01

Provera
    Dosage: 10 mg, unk
    Start date: 1990-11-26

Medroxyprogesterone
    Indication: Menopause
    Start date: 1991-01-01

Provera
    Dosage: 2.5 mg, unk
    End date: 2000-11-01

Ogen

Provera
    Indication: Menopause
    Start date: 1988-01-01
    End date: 1991-01-01

Premarin
    Start date: 1988-01-01
    End date: 1991-01-01

Prempro

Provera
    Start date: 1991-01-01

Premarin
    Administration route: Topical
    Indication: Menopause
    Start date: 1992-03-11
    End date: 1997-11-23

Hormones
    Administration route: Topical
    Indication: Menopause
    Start date: 1991-01-01

Climara

Estraderm
    Indication: Menopause
    Start date: 1991-01-01
    End date: 1993-03-11

Estraderm
    Dosage: 0.05 mg, biw
    Start date: 1992-03-11
    End date: 1993-03-11

Cycrin
    Dosage: 2.5 mg, unk
    Indication: Menopause
    Start date: 1997-11-17
    End date: 1997-12-17

Other drugs received by patient: Calcium Carbonate; Fosamax; Plavix; Prednisone TAB; Tamoxifen Citrate; Zantac; Magnesium Sulfate; Tricor; Methotrexate; Fluconazole; Paxil; Naproxen (Aleve); Aspirin; Prevacid; Macrodantin; Folic Acid; Zoloft



Possible Provera side effects in female

Reported by a lawyer from United States on 2011-10-25

Patient: female, weighing 88.4 kg (194.6 pounds)

Reactions: Economic Problem, Night Sweats, Contusion, Pain, Metastases To Lymph Nodes, Constipation, Hot Flush, Palpitations, Obesity, Oedema Peripheral, Psychiatric Symptom, Fear of Disease, Gastrooesophageal Reflux Disease, Breast Cancer, Migraine, Cellulitis, Rhinorrhoea, Deformity, Hyperlipidaemia, Anxiety, Life Expectancy Shortened, Dysuria, Insomnia, Pollakiuria, Feeling Abnormal, Scar

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Provera
    Dosage: unk
    Indication: Hormone Replacement Therapy
    Start date: 1993-01-28
    End date: 1997-01-09

Estraderm
    Dosage: unk
    Indication: Hormone Replacement Therapy
    Start date: 1994-06-08
    End date: 1997-01-09

Prempro
    Dosage: unk
    Indication: Hormone Replacement Therapy
    Start date: 1997-01-09
    End date: 2002-08-19

Other drugs received by patient: Paxil; Ativan; Metformin HCL; Decadron; Acyclovir; Coumadin; Keflex; Calcium D Sandoz; Effexor; Colace; Zoloft; Arimidex



Possible Provera side effects in female

Reported by a consumer/non-health professional from United States on 2011-10-24

Patient: female, weighing 68.0 kg (149.7 pounds)

Reactions: Abdominal Pain, Lymphadenopathy, Metastases To Liver, Headache, Malaise, Hot Flush, Uterine Leiomyoma, Pneumothorax, Hypoxia, Hepatic Cirrhosis, Muscle Spasms, Back Pain, Intervertebral Disc Protrusion, Pneumonia, Ovarian Cyst, Musculoskeletal Discomfort, Osteopenia, Breast Calcifications, Diverticulum Intestinal, Breast Cancer Stage II, Insomnia, Dermal Cyst, Breast Necrosis, Portal Hypertension, General Physical Condition Abnormal, Impaired Work Ability, Pain, Bone Pain, Pelvic Pain, Pleural Effusion, Depression, Cholecystitis, Splenomegaly, Adrenal Mass, Blood Pressure Increased, Polyp, Dyspnoea, Lung Neoplasm, Rash, Deformity, Ascites, Osteoarthritis, Anxiety, Device Failure, Atrophic Vulvovaginitis, Arthralgia, Leukocytosis

Drug(s) suspected as cause:
Estraderm
    Dosage: .05 mg, qw2
    Indication: Menopause
    Start date: 1999-01-01
    End date: 2000-01-01

Premarin
    Indication: Hormone Replacement Therapy

Cycrin
    Dosage: 2.5 mg, unk
    Administration route: Oral
    Indication: Menopause
    Start date: 1999-01-01
    End date: 2000-01-01

Estrostep
    Dosage: unk
    Indication: Menopause
    End date: 2001-01-01

Prempro
    Dosage: .625/2.5 mg
    Administration route: Oral
    Indication: Menopause
    Start date: 2000-01-01
    End date: 2002-01-01

Medroxyprogesterone Acetate
    Indication: Menopause

Provera
    Indication: Hormone Replacement Therapy

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