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Index of reports
> Cases resulting in a serious event (336)
> Cases with Neutropenia (22)
Below is the selection of adverse event reports related to Nexium (Esomeprazole) that includes cases resulting in a serious event where reactions include neutropenia.
Adverse event in 69 year old female receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from United States on 2007-07-25
Patient: 69 year old female, weighing 74.4 kg (163.7 pounds)
Adverse reactions / side effects: Breast Cancer, Cataract, Urinary Incontinence, Urinary Tract Infection, Knee Arthroplasty, Neutropenia, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Chemotherapy
Indication: Breast Cancer
Other drugs received by patient: Benecar; Coreg; Klor-CON; Folic Acid; Zoloft; Prednisone; Cyclobenzaprine HCL; Darvocet; Relafen; Tigan; Oscal; Ascorbic Acid; Boniva
Adverse event in 31 year old male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-27
Patient: 31 year old male, weighing 62.0 kg (136.4 pounds)
Adverse reactions / side effects: Anaemia, Pyrexia, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Rocaltrol; Detensiel; Pyostacine; Sterogyl; Rivotril; Kayexalate; Tramadol HCL
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 23 year old female receiving Nexium (Esomeprazole)
Reported by a physician from France on 2007-06-11
Patient: 23 year old female
Adverse reactions / side effects: Neutropenia
Suspect drug(s):
Nexium (Esomeprazole)
Other drugs received by patient: Interferon; Homeopathy
Adverse event in 45 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-22
Patient: 45 year old female, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Lymphopenia, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Belustine
Indication: Oligodendroglioma
Start date: 2006-05-19
Natulan
Indication: Oligodendroglioma
Start date: 2006-05-19
Oncovin
Indication: Oligodendroglioma
Start date: 2006-05-19
Other drugs received by patient: Depakene; Solupred; Bactrim; Tardyferon; Speciafoldine; Duphalac; Lovenox; Radiotherapy
Adverse event in 82 year old female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from France on 2007-05-01
Patient: 82 year old female
Adverse reactions / side effects: Anaemia, Lymphopenia, Pancreatitis, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Azathioprine Sodium
Dosage: 2.5tab per day
Administration route: Oral
End date: 2007-02-25
Augmentin '125'
Dosage: 1g twice per day
Administration route: Oral
Start date: 2007-02-13
End date: 2007-04-13
Nexium
Administration route: Oral
Start date: 2007-02-25
End date: 2007-03-10
Triflucan
Dosage: 50mg per day
Administration route: Oral
Start date: 2007-02-19
End date: 2007-03-03
Cortancyl
Dosage: 5mg per day
Administration route: Oral
Chronadalate LP
Dosage: 30mg per day
Administration route: Oral
Other drugs received by patient: Lovenox; Actiskenan; Gelox; Novonorm; Cozaar
Adverse event in 82 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-28
Patient: 82 year old female
Adverse reactions / side effects: Anaemia, Lymphopenia, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Triflucan
Augmentin '125'
Nexium
Dosage: daily dose:40mg
Administration route: Oral
Start date: 2007-02-25
End date: 2007-03-10
Azathioprine Sodium
Dosage: text:2 tablets
Administration route: Oral
Indication: Colitis
End date: 2007-02-25
Cortancyl
Indication: Colitis
Chronadalate
Other drugs received by patient: Actiskenan; Lovenox; Gelox; Novonorm; Cozaar
Adverse event in 82 year old female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from France on 2007-04-23
Patient: 82 year old female
Adverse reactions / side effects: Anaemia, Lymphopenia, Pancreatitis, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Azathioprine Sodium
Dosage: 2.5tab per day
Administration route: Oral
End date: 2007-02-25
Augmentin '125'
Dosage: 1g twice per day
Administration route: Oral
Nexium
Administration route: Oral
Start date: 2007-02-25
End date: 2007-03-10
Triflucan
Dosage: 50mg per day
Administration route: Oral
Cortancyl
Dosage: 5mg per day
Administration route: Oral
Chronadalate LP
Dosage: 30mg per day
Administration route: Oral
Other drugs received by patient: Lovenox; Actiskenan; Gelox; Novonorm; Cozaar
Adverse event in 82 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-20
Patient: 82 year old female
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Start date: 2007-02-25
End date: 2007-03-06
Nexium
Administration route: Oral
Start date: 2007-03-07
End date: 2007-03-10
Augmentin '125'
Administration route: Oral
Triflucan
Administration route: Oral
End date: 2007-03-03
Azathioprine Sodium
Administration route: Oral
Indication: Proctocolitis
End date: 2007-02-25
Cortancyl
Administration route: Oral
Indication: Proctocolitis
Chronadalate
Administration route: Oral
Other drugs received by patient: Actiskenan; Lovenox; Gelox; Novonorm; Cozaar
Adverse event in 44 year old male receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from Japan on 2007-04-09
Patient: 44 year old male
Adverse reactions / side effects: Rheumatoid Factor Increased, Neutropenia, Splenomegaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Loxen LP
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Depakene
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Temesta
Dosage: dosage regimen reported as 1 mg, uid/qd
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Lovenox
Dosage: daily dose reported as 1 dose form, uid/qd
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Nexium
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Triatec
Dosage: daily dose as 5 mg, uid/qd
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-19
End date: 2007-01-24
Adverse event in 44 year old male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-02
Patient: 44 year old male
Adverse reactions / side effects: Rheumatoid Factor Increased, Neutropenia, Splenomegaly, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Depakene
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Heparin-Fraction, Sodium Salt
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Ramipril
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-19
End date: 2007-01-24
Lorazepam
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Nexium
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Loxen PR
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-19
End date: 2007-01-24
Adverse event in 65 year old female receiving Nexium (Esomeprazole)
Reported by a consumer/non-health professional from Japan on 2007-03-26
Patient: 65 year old female
Adverse reactions / side effects: Pneumothorax, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Loxen
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-11
End date: 2007-01-16
Acupan
Dosage: form reported as injection. route reported as iv nos.
Indication: Drug USE FOR Unknown Indication
End date: 2007-01-22
Lorazepam
Dosage: route reported as per oral nos.
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2007-01-22
Effexor
Dosage: route reported as per oral nos.
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-11
End date: 2007-01-16
Nexium
Dosage: route reported as per oral nos.
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2007-01-14
Perfalgan
Dosage: route reported as iv nos.
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-11
End date: 2007-01-16
Adverse event in 65 year old female receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification from France on 2007-03-23
Patient: 65 year old female
Adverse reactions / side effects: Histiocytosis Haematophagic, Bone Marrow Failure, Neutropenia, Leukopenia, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Temesta
Dosage: 1 mg q day po
Administration route: Oral
End date: 2007-01-22
Effexor
Dosage: df po
Administration route: Oral
Indication: Depression
Start date: 2007-01-11
End date: 2007-01-16
Acupan
Dosage: df iv
End date: 2007-01-22
Nexium
Dosage: df po
Administration route: Oral
End date: 2007-01-14
Loxen
Dosage: df po
Administration route: Oral
Start date: 2007-01-11
End date: 2007-01-16
Perfalgan
Dosage: 4mg q day iv
Start date: 2007-01-11
End date: 2007-01-16
Adverse event in 44 year old male receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification on 2007-03-22
Patient: 44 year old male
Adverse reactions / side effects: Rheumatoid Factor Increased, Neutropenia, Splenomegaly
Adverse event resulted in: hospitalization
Suspect drug(s):
Lovenox
Start date: 2006-12-19
End date: 2007-01-24
Triatec / 00885601 /
Administration route: Oral
Start date: 2007-01-19
End date: 2007-01-24
Depakene
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Temesta / 00273201 /
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Nexium
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Loxen
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Adverse event in 44 year old male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-03-16
Patient: 44 year old male
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Depakene
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Lorazepam
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Lovenox
Start date: 2006-12-19
End date: 2007-01-24
Nicardipine Hydrochloride
Administration route: Oral
Start date: 2006-12-19
End date: 2007-01-24
Triatec
Administration route: Oral
Start date: 2007-01-19
End date: 2007-01-24
Adverse event in 65 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-03-15
Patient: 65 year old female
Adverse reactions / side effects: Granulocytes Maturation Arrest, Histiocytosis Haematophagic, Bone Marrow Failure, Neutropenia, Leukopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Effexor
Dosage: unknown
Administration route: Oral
Indication: Depression
Start date: 2007-01-11
End date: 2007-01-16
Perfalgan
Dosage: 4 mg total daily
Start date: 2007-01-11
End date: 2007-01-16
Loxen
Dosage: unknown
Administration route: Oral
Start date: 2007-01-11
End date: 2007-01-16
Nexium
Dosage: unknown
Administration route: Oral
End date: 2007-01-14
Acupan
Dosage: unknown
End date: 2007-01-22
Lorazepam
Administration route: Oral
End date: 2007-01-22
Adverse event in female receiving Nexium (Esomeprazole)
Reported by a physician from France on 2007-03-01
Patient: female
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Start date: 2006-08-01
End date: 2006-11-10
Norset
Indication: Depression
Start date: 2006-08-01
End date: 2006-10-01
Other drugs received by patient: Omeprazole; Neurontin; Doliprane
Adverse event in 45 year old female receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-02-26
Patient: 45 year old female, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Lymphopenia, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Belustine
Indication: Oligodendroglioma
Start date: 2006-05-19
Natulan
Indication: Oligodendroglioma
Start date: 2006-05-19
Oncovin
Indication: Oligodendroglioma
Start date: 2006-05-19
Other drugs received by patient: Depakene; Solupred; Bactrim; Tardyferon; Speciafoldine; Duphalac; Lovenox; Radiotherapy
Adverse event in 72 year old male receiving Nexium (Esomeprazole)
Reported by a individual with unspecified qualification on 2007-02-15
Patient: 72 year old male, weighing 71.0 kg (156.2 pounds)
Adverse reactions / side effects: Granulocytopenia, Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Clexane
Start date: 2006-08-31
End date: 2006-10-10
Clexane
Start date: 2006-08-31
End date: 2006-10-10
Tienam
Start date: 2006-08-19
End date: 2006-08-19
Nexium
Administration route: Oral
Start date: 2006-09-02
End date: 2006-09-21
Adverse event in 82 year old male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-31
Patient: 82 year old male
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Start date: 2006-10-16
End date: 2006-11-24
Zyloric
Administration route: Oral
End date: 2006-11-24
Adverse event in 72 year old male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-16
Patient: 72 year old male, weighing 82.0 kg (180.4 pounds)
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Aldactone
Administration route: Oral
Indication: Essential Hypertension
Start date: 2006-11-08
End date: 2006-11-20
Tahor
Administration route: Oral
Indication: Hyperlipidaemia
Triatec
Administration route: Oral
Indication: Essential Hypertension
Start date: 2006-10-25
End date: 2006-11-21
Nexium
Dosage: daily dose:40mg-freq:daily
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-10-25
End date: 2006-11-20
Other drugs received by patient: Plavix; Plavix
Adverse event in 72 year old male receiving Nexium (Esomeprazole)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-12
Patient: 72 year old male, weighing 82.0 kg (180.4 pounds)
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-10-25
End date: 2006-11-20
Nexium
Start date: 2006-11-27
Triatec
Administration route: Oral
Indication: Essential Hypertension
Start date: 2006-10-25
End date: 2006-11-21
Aldactone
Administration route: Oral
Indication: Essential Hypertension
Start date: 2006-11-08
End date: 2006-11-20
Tahor
Administration route: Oral
Indication: Hyperlipidaemia
End date: 2006-11-21
Other drugs received by patient: Plavix; Plavix
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