|
Index of reports
> Cases resulting in life threatening events (22)
Below is the selection of adverse event reports related to Nexium (Esomeprazole) that includes cases resulting in life threatening events.
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 43 year old female receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-29
Patient: 43 year old female
Adverse reactions / side effects: Wheezing, Rash, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Citalopram (Citalopram)
Dosage: 20 mg; oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2005-10-01
Augmentin
Dosage: 625 mg; oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-10-03
Levothyroxine Sodium
Indication: Drug USE FOR Unknown Indication
Start date: 2003-01-01
Nexium
Dosage: 40 mg; oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2005-01-01
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):
Citalopram Hydrobromide
Dosage: 20 mg, oral
Administration route: Oral
Start date: 2005-10-01
Augmentin '250'
Dosage: 625 mg, oral
Administration route: Oral
Start date: 2007-10-03
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 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):
Nexium
Administration route: Oral
Start date: 2005-01-01
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
Adverse event in 64 year old female receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from United States on 2007-10-17
Patient: 64 year old female, weighing 58.5 kg (128.7 pounds)
Adverse reactions / side effects: Back Pain, Flushing, Middle Insomnia, Pain in Extremity, Chest Pain, Hyperhidrosis, Muscle Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Nexium
Indication: Dyspepsia
Start date: 2007-08-30
End date: 2007-09-19
Nexium
Indication: Hiatus Hernia
Start date: 2007-08-30
End date: 2007-09-19
Adverse event in male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-07-31
Patient: male
Adverse reactions / side effects: Pulmonary Embolism
Adverse event resulted in: life threatening event
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Remicade
Indication: Colitis Ulcerative
Start date: 2007-01-01
Other drugs received by patient: Azathioprine Sodium; Previscan; Solu-Medrol
Adverse event in female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-07-17
Patient: female
Adverse reactions / side effects: Hyponatraemia, Convulsion
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
End date: 2007-04-19
Lipanthyl
Administration route: Oral
Indication: Hypercholesterolaemia
End date: 2007-04-19
Betaserc
Administration route: Oral
Indication: Dizziness
Start date: 2007-03-15
End date: 2007-04-19
Tanganil
Administration route: Oral
Indication: Dizziness
Start date: 2007-03-15
End date: 2007-04-19
Other drugs received by patient: Herbal Medicine; Homeopathic Drugs
Adverse event in 35 year old female receiving Nexium (Esomeprazole)
Reported by a physician from Netherlands on 2007-07-06
Patient: 35 year old female
Adverse reactions / side effects: Suicide Attempt
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Oral Contraceptive
Adverse event in 67 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from Spain on 2007-06-25
Patient: 67 year old female
Adverse reactions / side effects: Oedema, Thrombocytopenia, Hepatitis, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lorazepam
Dosage: (1 mg qd oral)
Administration route: Oral
Start date: 2004-01-01
End date: 2007-04-04
Nexium
Dosage: (40 mg qd oral)
Administration route: Oral
Indication: Dyspepsia
Start date: 2007-02-21
End date: 2007-04-04
Dogmatil (Dogmatil) 50 MG (Not Specified)
Dosage: (50 mg prn oral)
Administration route: Oral
Indication: Dizziness
Start date: 2004-01-01
End date: 2004-04-04
Other drugs received by patient: Pantecta
Adverse event in 48 year old male receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from Germany on 2007-06-21
Patient: 48 year old male, weighing 81.0 kg (178.2 pounds)
Adverse reactions / side effects: Crush Syndrome, Rhabdomyolysis, Drug Interaction, Hypokinesia, Renal Failure, Respiratory Failure, Dialysis, Acute Hepatic Failure
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Simvastatin
Dosage: 40 mg, oral
Administration route: Oral
Indication: LOW Density Lipoprotein Increased
Start date: 2007-01-01
End date: 2007-04-01
Allopurinol
Dosage: 300 mg, oral
Administration route: Oral
Indication: Hypernatraemia
Start date: 2007-01-01
End date: 2007-04-01
Nexium
Dosage: 20 mg, oral
Administration route: Oral
Indication: Gastritis
Start date: 2006-12-01
End date: 2007-01-01
Adverse event in 67 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from Spain on 2007-06-19
Patient: 67 year old female
Adverse reactions / side effects: Oedema, Hepatitis, Thrombocytopenia, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Dyspepsia
Start date: 2007-02-21
End date: 2007-04-04
Orfidal Wyeth
Administration route: Oral
Start date: 2004-01-01
End date: 2007-04-04
Dogmatil
Administration route: Oral
Indication: Dizziness
Start date: 2004-01-01
End date: 2007-04-04
Dogmatil
Administration route: Oral
Start date: 2004-01-01
End date: 2007-04-04
Other drugs received by patient: Pantecta
Adverse event in male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-18
Patient: male
Adverse reactions / side effects: Sepsis, Neutropenia, Thrombocytopenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Nexium
Administration route: Oral
Start date: 2007-03-03
End date: 2007-05-02
Sutent
Administration route: Oral
Start date: 2007-01-01
End date: 2007-01-28
Sutent
Administration route: Oral
Start date: 2007-02-01
End date: 2007-03-01
Sutent
Administration route: Oral
Start date: 2007-04-02
End date: 2007-04-27
Adverse event in male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-06-15
Patient: male, weighing 74.0 kg (162.8 pounds)
Adverse reactions / side effects: Respiratory Failure, Depressed Level of Consciousness, Quadriplegia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Reflux Oesophagitis
Metoprolol Succinate
Administration route: Oral
Indication: Hypertension
Jurnista
Administration route: Oral
Indication: Pain
Start date: 2007-06-02
Adverse event in female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-06-11
Patient: female, weighing 81.0 kg (178.2 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Acute Hepatic Failure
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Gastritis
Start date: 2006-12-01
End date: 2007-01-01
Nexium
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-12-01
End date: 2007-01-01
Simvabeta
Administration route: Oral
Indication: Obesity
Start date: 2007-01-01
End date: 2007-04-01
Simvabeta
Administration route: Oral
Indication: LOW Density Lipoprotein Increased
Start date: 2007-01-01
End date: 2007-04-01
Allopurinol
Administration route: Oral
Indication: Hyperuricaemia
Start date: 2007-01-01
End date: 2007-04-01
Adverse event in 35 year old female receiving Nexium (Esomeprazole)
Reported by a physician from Netherlands on 2007-06-07
Patient: 35 year old female
Adverse reactions / side effects: Suicide Attempt
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Oral Contraceptive
Adverse event in female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-25
Patient: female, weighing 58.1 kg (127.7 pounds)
Adverse reactions / side effects: Asthma, Dyspnoea, Lung Neoplasm Malignant
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Nexium (Esomeprazole)
Adverse event in 85 year old male receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from United States on 2007-04-10
Patient: 85 year old male
Adverse reactions / side effects: Cerebrovascular Accident
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Nexium (Esomeprazole)
Adverse event in 92 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-04
Patient: 92 year old female
Adverse reactions / side effects: Autoimmune Thrombocytopenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Inipomp
Administration route: Oral
End date: 2006-09-20
Inipomp
Administration route: Oral
Start date: 2007-01-11
End date: 2007-01-15
Kardegic
Administration route: Oral
End date: 2007-01-24
Nexium
Administration route: Oral
Start date: 2006-09-20
End date: 2007-01-04
Nexium
Administration route: Oral
Start date: 2007-01-15
End date: 2007-01-24
Calciparine
Start date: 2007-01-01
End date: 2007-01-19
Other drugs received by patient: Augmentin '125'; Lasix; Triatec; Amlor; Levothyroxine Sodium
Adverse event in 47 year old male receiving Nexium (Esomeprazole)
Reported by a physician from United States on 2007-02-19
Patient: 47 year old male
Adverse reactions / side effects: Metastatic Neoplasm
Adverse event resulted in: life threatening event
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Barrett's Oesophagus
Prilosec
Administration route: Oral
Indication: Barrett's Oesophagus
Start date: 1998-01-01
Adverse event in 47 year old male receiving Nexium (Esomeprazole)
Reported by a physician from United States on 2007-01-19
Patient: 47 year old male
Adverse reactions / side effects: Metastatic Neoplasm
Adverse event resulted in: life threatening event
Suspect drug(s):
Nexium (Esomeprazole)
Adverse event in 803 month old male receiving Nexium (Esomeprazole)
Reported by a physician from France on 2007-01-12
Patient: 803 month old male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Amyotrophic Lateral Sclerosis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Prophylaxis Against Gastrointestinal Ulcer
Start date: 2005-11-01
End date: 2005-12-01
Nexium
Administration route: Oral
Start date: 2006-02-21
End date: 2006-03-17
Other drugs received by patient: Tilcotil; Tilcotil; Plavix; Lodales; Chondrosulf; Granions DE Cuivre; Granions D'or; Granions DE Selenium; Synedil; Creon; Colchicine
Adverse event in 84 year old male receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from United States on 2007-01-03
Patient: 84 year old male, weighing 70.3 kg (154.7 pounds)
Adverse reactions / side effects: Weight Decreased, Diarrhoea, Asthenia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Prednisone
|
