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Index of reports
> Cases resulting in hospitalization (166)
> Cases with Neutropenia (20)
Below is the selection of adverse event reports related to Nexium (Esomeprazole) that includes cases resulting in hospitalization 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 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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