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Nexium (Esomeprazole) - Adverse Event Reports - All Cases - Nausea

 



Index of reports > All cases (512) > Cases with Nausea (29)

Below is the selection of adverse event reports related to Nexium (Esomeprazole) that includes all cases where reactions include nausea.

 Reports 1 - 25 of 29   Next >>

Adverse event in female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: female

Adverse reactions / side effects: Asthma, Weight Decreased, Pneumonia, Increased Appetite, Nausea, Early Satiety, Abdominal Pain Upper, Tremor, Injection Site Erythema, Diarrhoea, Abdominal Distension, Violence-Related Symptom, Depressed Mood, Blood Glucose Increased, Decreased Appetite

Suspect drug(s):
Nexium

Prednisone

Ranitidine HCL

Symlin
    Dosage: 120 mcg;tid;sc
    Indication: Diabetes Mellitus
    Start date: 2007-01-01

Other drugs received by patient: Prednisone; Nebulizer Treatment, NOT Specified; Antibiotics; Lantus; Glucovance; Avandia; Maalox



Adverse event in male receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-10-26

Patient: male, weighing 95.3 kg (209.7 pounds)

Adverse reactions / side effects: Vomiting, Blood Iron Abnormal, Nausea, Adverse Drug Reaction, Drug Interaction, Serum Ferritin Increased, Laboratory Test Abnormal, Diarrhoea, Asthenia, Influenza Like Illness

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient possibly interacting with the suspect drug:
Lipitor
    Administration route: Oral
    Indication: Arteriosclerosis

Lipitor
    Indication: Blood Cholesterol

Other drugs received by patient: Ecotrin; Aciphex; Atenolol



Adverse event in female receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-10-19

Patient: female

Adverse reactions / side effects: Weight Decreased, Asthma, Oral Intake Reduced, Increased Appetite, Wheezing, Abdominal Pain Upper, Weight Increased, Injection Site Erythema, Malaise, Glycosylated Haemoglobin Increased, Abdominal Distension, Depression, Blood Glucose Increased, Pneumonia, Dyspnoea, Nausea, Tremor, Diarrhoea, Swelling, Anorexia, Violence-Related Symptom

Suspect drug(s):
Antibiotics
    Start date: 2007-07-25
    End date: 2007-08-01

Avandia
    Dosage: dose: unk
    Start date: 2005-01-01
    End date: 2007-06-01

Drug Used IN Diabetes
    Indication: Diabetes Mellitus
    Start date: 2007-01-01

Lantus
    Indication: Diabetes Mellitus

Lantus
    Start date: 2006-08-01

Nexium
    Dosage: dose: unk
    Start date: 2007-08-01
    End date: 2007-08-07

Prednisone

Prednisone
    Start date: 2007-07-25
    End date: 2007-07-30

Ranitidine HCL
    Dosage: dose: unk
    Start date: 2005-01-01
    End date: 2007-08-01

Other drugs received by patient: Glucovance / 01503701 /; Maalox / 00091001 /; Unknown Drug



Adverse event in female receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-10-17

Patient: female

Adverse reactions / side effects: Weight Decreased, Asthma, Oral Intake Reduced, Increased Appetite, Wheezing, Abdominal Pain Upper, Weight Increased, Injection Site Erythema, Malaise, Glycosylated Haemoglobin Increased, Abdominal Distension, Depression, Blood Glucose Increased, Pneumonia, Dyspnoea, Nausea, Tremor, Diarrhoea, Swelling, Anorexia, Violence-Related Symptom

Suspect drug(s):
Antibiotics
    Start date: 2007-07-25
    End date: 2007-08-01

Avandia
    Dosage: dose: unk
    Start date: 2005-01-01
    End date: 2007-06-01

Drug Used IN Diabetes
    Indication: Diabetes Mellitus
    Start date: 2007-01-01

Lantus
    Indication: Diabetes Mellitus

Lantus
    Start date: 2006-08-01

Nexium
    Dosage: dose: unk
    Start date: 2007-08-01
    End date: 2007-08-07

Prednisone

Prednisone
    Start date: 2007-07-25
    End date: 2007-07-30

Ranitidine HCL
    Dosage: dose: unk
    Start date: 2005-01-01
    End date: 2007-08-01

Other drugs received by patient: Glucovance / 01503701 /; Maalox / 00091001 /; Unknown Drug



Adverse event in 69 year old receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-10-08

Patient: 69 year old , weighing 68.9 kg (151.6 pounds)

Adverse reactions / side effects: Blood Pressure Increased, Nausea, Chest Pain, Atrial Fibrillation, Headache, Abdominal Pain Upper

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient: Levothyroxine Sodium; Warfarin Sodium; Sotalol Hydrochloride; Benazepril Hydrochloride; Calcium



Adverse event in 62 year old female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-07-31

Patient: 62 year old female, weighing 63.0 kg (138.6 pounds)

Adverse reactions / side effects: Weight Decreased, Drug Ineffective, Nausea, Chest Pain, Decreased Appetite

Adverse event resulted in: hospitalization

Suspect drug(s):
Nexium
    Administration route: Oral
    Indication: Barrett's Oesophagus
    Start date: 2007-06-04

Nexium
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2007-06-04



Adverse event in receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from Germany on 2007-07-19

Patient:

Adverse reactions / side effects: Vomiting, Nausea, Blood Potassium Decreased, Dizziness, Hyponatraemia, Unevaluable Event

Adverse event resulted in: hospitalization

Suspect drug(s):
Altace
    Dosage: 10 mg, qd
    Administration route: Oral
    Start date: 2006-09-01

Carbamazepine
    Dosage: 600 mg, qd
    Administration route: Oral
    Start date: 2006-11-27
    End date: 2006-11-27

Carbamazepine
    Dosage: 1100 mg, qd
    Administration route: Oral
    Start date: 2006-11-28
    End date: 2006-11-28

Carbamazepine
    Dosage: 200 mg, qd
    Administration route: Oral
    Start date: 2006-11-29
    End date: 2006-11-29

Disalunil
    Dosage: 50 mg, qd
    Administration route: Oral
    Start date: 2006-09-01
    End date: 2006-11-28

Disalunil
    Dosage: 25 mg, qd
    Administration route: Oral
    Start date: 2006-11-29
    End date: 2006-11-30

Nexium
    Dosage: 20 mg, qd
    Administration route: Oral
    Start date: 2006-11-27

Other drugs received by patient: Trimipramine Maleate; Protaphane MC / 00030504 /; Insulin MC Actrapid



Adverse event in 57 year old male receiving Nexium (Esomeprazole)

Reported by a health professional (non-physician/pharmacist) from Ireland on 2007-07-12

Patient: 57 year old male

Adverse reactions / side effects: Diarrhoea, Nausea, Impaired Work Ability, Pharyngolaryngeal Pain, Headache, Abdominal Pain Upper

Suspect drug(s):
Clonamox
    Dosage: took 3 doses
    Administration route: Oral
    Indication: Helicobacter Infection

Klacid Forte
    Dosage: took 3 doses
    Indication: Helicobacter Infection

Nexium
    Dosage: took 3 doses
    Administration route: Oral
    Indication: Helicobacter Infection



Adverse event in 62 year old female receiving Nexium (Esomeprazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-15

Patient: 62 year old female

Adverse reactions / side effects: Abdominal Pain, Dyspnoea, Blood Potassium Decreased, Nausea, Dehydration, Pain, Pyrexia, Cough, Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Bevacizumab
    Dosage: 2 mg/kg, over 90-30 minutes, day 1, 15 and 29, intravenous
    Indication: Pancreatic Carcinoma
    Start date: 2006-08-23

Celebrex
    Dosage: 100 mg twice daily, oral
    Administration route: Oral

Ibuprofen
    Dosage: 800 mg at bedtime

Nexium
    Dosage: 40 mg daily

SU-011,248 (Suntinib Malate)
    Dosage: 25 mg, day 1 to 28, oral
    Administration route: Oral
    Indication: Pancreatic Carcinoma
    Start date: 2006-08-23

Viokase 16 (Pancrelipase)
    Dosage: 2 tab daily, oral
    Administration route: Oral



Adverse event in 84 year old female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-04-30

Patient: 84 year old female, weighing 77.6 kg (170.7 pounds)

Adverse reactions / side effects: Nausea, Unevaluable Event, Headache, Constipation

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient: High Blood Pressure Medication; Glaucoma; Aspirin; Vitamins



Adverse event in 77 year old male receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-04-30

Patient: 77 year old male, weighing 65.8 kg (144.8 pounds)

Adverse reactions / side effects: Nausea, Palpitations, Dizziness, Disorientation, Asthenia, Tremor, Abdominal Pain Upper

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient: Paxil; Ativan



Adverse event in 64 year old female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-04-30

Patient: 64 year old female, weighing 77.1 kg (169.6 pounds)

Adverse reactions / side effects: Chest Discomfort, Dysphagia, Nausea

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient: Synthroid; Actos; Altace; Vytorin; Paxil



Adverse event in 467 month old male receiving Nexium (Esomeprazole)

Reported by a physician from France on 2007-04-30

Patient: 467 month old male, weighing 61.0 kg (134.2 pounds)

Adverse reactions / side effects: Cheilitis, Gingivitis, Stomatitis, Nausea, Dizziness, Asthenia, Abdominal Pain Upper

Suspect drug(s):
Nexium
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2007-02-28
    End date: 2007-03-02

Nexium
    Administration route: Oral
    Indication: Dysphonia
    Start date: 2007-02-28
    End date: 2007-03-02

Omeprazole
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2007-03-03
    End date: 2007-03-03

Omeprazole
    Administration route: Oral
    Indication: Dysphonia
    Start date: 2007-03-03
    End date: 2007-03-03



Adverse event in 24 year old female receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-04-30

Patient: 24 year old female

Adverse reactions / side effects: Nausea, Dyspepsia, Feeling Hot and Cold, Dizziness

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient: Atenolol; Florane; Prozac



Adverse event in 91 year old female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-04-30

Patient: 91 year old female, weighing 84.4 kg (185.7 pounds)

Adverse reactions / side effects: Abdominal Pain, Malaise, Nausea, Diarrhoea, Faeces Discoloured

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient: Sucralfate



Adverse event in 71 year old female receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-04-30

Patient: 71 year old female, weighing 61.2 kg (134.6 pounds)

Adverse reactions / side effects: Nausea, Dizziness, Blood Pressure Decreased

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient possibly interacting with the suspect drug:
Valium

Other drugs received by patient: Calan



Adverse event in female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-04-30

Patient: female

Adverse reactions / side effects: Sensation of Foreign Body, Nausea, Hiccups

Suspect drug(s):
Nexium
    Administration route: Oral
    Indication: Oesophageal Ulcer

Nexium
    Administration route: Oral
    Indication: Chest Discomfort

Nexium
    Administration route: Oral
    Indication: Musculoskeletal Discomfort

Other drugs received by patient: Lovastatin; Atenolol



Adverse event in female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-04-30

Patient: female

Adverse reactions / side effects: Vomiting, Nausea, Drug Interaction

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient possibly interacting with the suspect drug:
Calcium Chloride



Adverse event in female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from United States on 2007-04-30

Patient: female, weighing 93.2 kg (205.0 pounds)

Adverse reactions / side effects: Vomiting, Nausea, Decreased Appetite

Suspect drug(s):
Actonel
    Start date: 2006-12-01

Byetta
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-05-01
    End date: 2006-06-01

Byetta
    Start date: 2006-06-01
    End date: 2006-12-01

Byetta
    Start date: 2007-01-01

Nexium
    Administration route: Oral
    Start date: 2006-12-01



Adverse event in 39 year old female receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-04-30

Patient: 39 year old female, weighing 54.4 kg (119.7 pounds)

Adverse reactions / side effects: Malaise, Nausea, Drug Exposure During Pregnancy, Dizziness

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient: Vitamin and Mineral Prenatal Supplement W / Folic Acid CAP



Adverse event in 84 year old female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from France on 2007-04-25

Patient: 84 year old female

Adverse reactions / side effects: Nausea, Malnutrition, General Physical Health Deterioration, Hyponatraemia, Impaired Self-Care, Dehydration, Feeling Hot, Insomnia, Anorexia

Adverse event resulted in: hospitalization

Suspect drug(s):
Nexium
    Dosage: 40mg per day
    Administration route: Oral

Preterax
    Dosage: 1unit per day
    Administration route: Oral
    End date: 2006-07-22

Requip
    Dosage: 2mg per day
    Administration route: Oral

Sinemet
    Dosage: 1tab per day
    Administration route: Oral



Adverse event in 89 year old female receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-04-04

Patient: 89 year old female, weighing 73.0 kg (160.6 pounds)

Adverse reactions / side effects: Drug Ineffective, Nausea, Headache, Abdominal Pain Upper, Diarrhoea, Fracture, DRY Mouth, Abdominal Distension, Dizziness, Vision Blurred

Adverse event resulted in: hospitalization

Suspect drug(s):
Nexium
    Administration route: Oral
    Indication: Duodenal Ulcer
    Start date: 2006-01-01
    End date: 2006-01-01

Nexium
    Administration route: Oral
    Indication: Hiatus Hernia
    Start date: 2006-01-01
    End date: 2006-01-01

Nexium
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2006-01-01
    End date: 2006-01-01

Nexium
    Administration route: Oral
    Start date: 2006-01-01

Nexium
    Administration route: Oral
    Start date: 2006-01-01

Nexium
    Administration route: Oral
    Start date: 2006-01-01

Other drugs received by patient: Cozaar; Hydrochlorathiazide; Lorazepam; Colace; Plavix; Toprol-XL; Senna



Adverse event in female receiving Nexium (Esomeprazole)

Reported by a consumer/non-health professional from Brazil on 2007-03-21

Patient: female

Adverse reactions / side effects: Weight Decreased, Nausea, Dizziness, Drug Interaction, Depression, Somnolence, Decreased Appetite, Abdominal Pain Upper

Adverse event resulted in: hospitalization

Suspect drug(s):
Nexium (Esomeprazole)

Other drugs received by patient possibly interacting with the suspect drug:
Bupropion HCL
    Indication: Depression
    Start date: 2007-02-13

Valium
    Administration route: Oral
    Indication: Anxiety
    Start date: 2005-01-01



Adverse event in 89 year old female receiving Nexium (Esomeprazole)

Reported by a individual with unspecified qualification from United States on 2007-03-15

Patient: 89 year old female, weighing 73.0 kg (160.6 pounds)

Adverse reactions / side effects: Drug Ineffective, Nausea, Headache, Abdominal Pain Upper, Fracture, DRY Mouth, Abdominal Distension, Dizziness, Vision Blurred

Adverse event resulted in: hospitalization

Suspect drug(s):
Nexium
    Administration route: Oral
    Indication: Duodenal Ulcer
    Start date: 2006-01-01
    End date: 2006-01-01

Nexium
    Administration route: Oral
    Indication: Hiatus Hernia
    Start date: 2006-01-01
    End date: 2006-01-01

Nexium
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2006-01-01
    End date: 2006-01-01

Nexium
    Administration route: Oral
    Start date: 2006-01-01

Nexium
    Administration route: Oral
    Start date: 2006-01-01

Nexium
    Administration route: Oral
    Start date: 2006-01-01

Other drugs received by patient: Cozaar; Hydrochlorathiazide; Lorazepam; Colace; Plavix; Toprol-XL; Senna



Adverse event in 56 year old female receiving Nexium (Esomeprazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-07

Patient: 56 year old female, weighing 74.8 kg (164.7 pounds)

Adverse reactions / side effects: Somnolence, Hyperhidrosis, Weight Increased, Hypercholesterolaemia, Frequent Bowel Movements, Face Oedema, Fatigue, Oedema Peripheral, Abdominal Distension, Depression, Muscle Spasms, Bowel Movement Irregularity, Vomiting, Nausea, Hyperglycaemia, Condition Aggravated, Hypertension

Suspect drug(s):
Nexium (Esomeprazole)



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