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Index of reports
> Cases resulting in other serious reactions (144)
Below is the selection of adverse event reports related to Nexium (Esomeprazole) that includes cases resulting in other serious reactions.
Reports 1 - 25 of 144 Next >>
Adverse event in 43 year old male receiving Nexium (Esomeprazole)
Reported by a pharmacist from Canada on 2007-10-31
Patient: 43 year old male
Adverse reactions / side effects: Condition Aggravated
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Lyrica; Atenolol; Rabeprazole Sodium
Adverse event in 40 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-31
Patient: 40 year old female
Adverse reactions / side effects: Dyspnoea, Breast Enlargement, Muscular Weakness, Abdominal Pain Upper, Menstrual Disorder, Weight Increased, Fatigue, Dermatitis, Swelling, Myocardial Infarction
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Domperidone
Adverse event in 44 year old female receiving Nexium (Esomeprazole)
Reported by a physician from Germany on 2007-10-31
Patient: 44 year old female, weighing 59.0 kg (129.8 pounds)
Adverse reactions / side effects: Disorientation, Hallucination
Suspect drug(s):
Nexium (Esomeprazole)
Adverse event in 85 year old male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-30
Patient: 85 year old male
Adverse reactions / side effects: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Hepatocellular Damage
Suspect drug(s):
Nexium
Administration route: Oral
Tylenol (Caplet)
Vitalux
Administration route: Oral
Adverse event in male receiving Nexium (Esomeprazole)
Reported by a pharmacist from United States on 2007-10-30
Patient: male, weighing 33.4 kg (73.5 pounds)
Adverse reactions / side effects: Blood Amylase Increased, Pancreatitis, Lipase Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Ativan
Dosage: text:3-4.5mg-freq:q3-4h: prn
Indication: Agitation
Start date: 2007-07-06
End date: 2007-08-03
Clonidine
Indication: Neuralgia
Demerol
Dosage: text:25-50 mg-freq:q2h: prn
Indication: Pain
Start date: 2007-07-30
End date: 2007-08-03
Diazepam
Indication: Agitation
Fluconazole
Indication: Systemic Candida
Start date: 2007-07-29
End date: 2007-08-03
Keppra
Indication: Convulsion
Start date: 2007-07-12
End date: 2007-08-03
Methadone HCL
Administration route: Oral
Indication: Pain
Start date: 2007-07-29
End date: 2007-08-03
Methadone HCL
Indication: Sedation
Nexium
Indication: Gastrooesophageal Reflux Disease
Start date: 2007-07-29
End date: 2007-08-03
Paxil
Dosage: daily dose:15mg
Administration route: Oral
Start date: 2007-07-01
End date: 2007-08-03
Adverse event in 48 year old female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United States on 2007-10-30
Patient: 48 year old female
Adverse reactions / side effects: Pain in Extremity, Fear, Abasia, Nervousness
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Amoxicillin
Adverse event in 79 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-30
Patient: 79 year old female
Adverse reactions / side effects: RED Blood Cell Count Decreased, Anaemia, Dizziness
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Muscle Relaxant; Thyroid TAB
Adverse event in 43 year old female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United Kingdom on 2007-10-30
Patient: 43 year old female, weighing 85.0 kg (187.0 pounds)
Adverse reactions / side effects: Wheezing, Rash, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Augmentin '125'
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-10-03
Citalopram Hydrobromide
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2005-10-01
Levothyroxine Sodium
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2003-01-01
Nexium
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2005-01-01
Adverse event in 29 year old female receiving Nexium (Esomeprazole)
Reported by a pharmacist from Canada on 2007-10-30
Patient: 29 year old female
Adverse reactions / side effects: Breast Discharge
Suspect drug(s):
Nexium (Esomeprazole)
Adverse event in 58 year old male receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: 58 year old male, weighing 76.2 kg (167.6 pounds)
Adverse reactions / side effects: Spinal Disorder, Resorption Bone Increased
Suspect drug(s):
Nexium (Esomeprazole)
Adverse event in female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: female
Adverse reactions / side effects: Oesophageal Operation
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium (Esomeprazole)
Adverse event in 79 year old female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United States on 2007-10-26
Patient: 79 year old female
Adverse reactions / side effects: Asthma, Cataract, Erythema, Neuropathy Peripheral, Staphylococcal Infection, Fungal Infection, Oedema Peripheral, Dehydration, Aspergillosis, Hypertension, Depressed Mood
Adverse event resulted in: disablity
Suspect drug(s):
Alprazolam
Catapres-TTS-1
Edecrin
Isradipine
Nexium
Norvasc
Other drugs received by patient: Metoprolol; Neurontin
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 43 year old female receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-25
Patient: 43 year old female, weighing 85.0 kg (187.0 pounds)
Adverse reactions / side effects: Wheezing, Rash, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Augmentin '250'
Dosage: 625 mg, oral
Administration route: Oral
Start date: 2007-10-03
Citalopram Hydrobromide
Dosage: 20 mg, oral
Administration route: Oral
Start date: 2005-10-01
Levothyroxine Sodium
Dosage: 150 ug, oral
Administration route: Oral
Start date: 2003-01-01
Nexium
Dosage: 40 mg, oral
Administration route: Oral
Start date: 2005-01-01
Adverse event in 866 month old male receiving Nexium (Esomeprazole)
Reported by a physician from Australia on 2007-10-25
Patient: 866 month old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Jaundice Cholestatic
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Cardizem; Tritace
Adverse event in male receiving Nexium (Esomeprazole)
Reported by a physician from South Africa on 2007-10-23
Patient: male, weighing 86.0 kg (189.2 pounds)
Adverse reactions / side effects: Oesophageal Spasm, Chest Pain, Gastric Polyps
Suspect drug(s):
Nexium
Dosage: 20-40 mg daily
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Start date: 2005-01-01
End date: 2007-02-01
Nexium
Administration route: Oral
Start date: 2007-01-01
Other drugs received by patient: Crestor
Adverse event in 66 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-23
Patient: 66 year old female, weighing 80.9 kg (178.0 pounds)
Adverse reactions / side effects: Regurgitation, Pruritus, Drug Ineffective, Swelling, Rash
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Synthroid
Adverse event in 79 year old female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United States on 2007-10-22
Patient: 79 year old female
Adverse reactions / side effects: Asthma, Cataract, Neuropathy Peripheral, Staphylococcal Infection, Fungal Infection, Oedema Peripheral, Dehydration, Aspergillosis, Depressed Mood, Hypertension
Adverse event resulted in: disablity
Suspect drug(s):
Alprazolam
Catapres-TTS-1
Edecrin
Isradipine
Nexium
Norvasc
Other drugs received by patient: Metoprolol; Neurontin
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 71 year old female receiving Nexium (Esomeprazole)
Reported by a physician from Canada on 2007-10-18
Patient: 71 year old female
Adverse reactions / side effects: Haemoglobin Decreased, Drug Interaction, Anaemia Macrocytic
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient possibly interacting with the suspect drug:
Methotrexate
Indication: Rheumatoid Arthritis
Start date: 1999-01-01
Methotrexate
Dosage: increased
Start date: 2007-02-01
End date: 2007-07-16
Methotrexate
Dosage: decreased
Start date: 2007-08-01
Other drugs received by patient: Plaquenil; Prednisone; Pantoprazole Sodium; Metoprolol; Diltiazem HCL; Aspirin; Nitroglycerin; Risedronate Sodium; Calcium; Vitamin D
Adverse event in 43 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-18
Patient: 43 year old female, weighing 85.0 kg (187.0 pounds)
Adverse reactions / side effects: Wheezing, Rash, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Augmentin '125'
Administration route: Oral
Start date: 2007-10-03
Citalopram Hydrobromide
Administration route: Oral
Start date: 2005-10-01
Levothyroxine Sodium
Administration route: Oral
Start date: 2003-01-01
Nexium
Administration route: Oral
Start date: 2005-01-01
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 male receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United States on 2007-10-17
Patient: male, weighing 86.4 kg (190.0 pounds)
Adverse reactions / side effects: Abnormal Dreams, Asthma, Migraine, Polyp, Diarrhoea, Dyspepsia, Dehydration, Bronchospasm
Suspect drug(s):
Chantix
Indication: Smoking Cessation Therapy
Nexium
Other drugs received by patient: Alprazolam; Advair Diskus 100 / 50; Albuterol; Salbutamol
Adverse event in 90 year old male receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from United States on 2007-10-16
Patient: 90 year old male
Adverse reactions / side effects: Death, Electrolyte Imbalance
Adverse event resulted in: death
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: SIX Different Blood Pressure Medications
Adverse event in 71 year old female receiving Nexium (Esomeprazole)
Reported by a physician from Canada on 2007-10-16
Patient: 71 year old female
Adverse reactions / side effects: Haemoglobin Decreased, Drug Interaction, Anaemia Macrocytic
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient possibly interacting with the suspect drug:
Methotrexate
Indication: Rheumatoid Arthritis
Start date: 1999-01-01
Methotrexate
Dosage: increased
Start date: 2007-02-01
End date: 2007-07-16
Methotrexate
Start date: 2007-02-01
Other drugs received by patient: Plaquenil; Prednisone; Pantoprazole Sodium; Metoprolol; Diltiazem Hydrochloride; Aspirin; Nitroglycerin; Risedronate Sodium; Calcium; Vitamin D
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