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Protonix (Pantoprazole) - Adverse Event Reports - Death

 



Index of reports > Cases resulting in death (5)

     Malignant Neoplasm Progression (1)Urinary Tract Infection (1)Blood Count Abnormal (1)Multiple Myeloma (1)Cerebrovascular Accident (1)Cardiac Disorder (1)Sepsis (1)Platelet Count Decreased (1)Myocardial Infarction (1)

Below is the selection of adverse event reports related to Protonix (Pantoprazole) that includes cases resulting in death.

Adverse event in female receiving Protonix (Pantoprazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-26

Patient: female

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Protonix (Pantoprazole)



Adverse event in female receiving Protonix (Pantoprazole)

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

Patient: female

Adverse reactions / side effects: Death

Adverse event resulted in: death

Suspect drug(s):
Protonix (Pantoprazole)



Adverse event in male receiving Protonix (Pantoprazole)

Reported by a physician from United States on 2007-06-15

Patient: male, weighing 65.8 kg (144.8 pounds)

Adverse reactions / side effects: Myocardial Infarction

Adverse event resulted in: death

Suspect drug(s):
Protonix (Pantoprazole)

Other drugs received by patient: Sertraline; Acetylsalicylic Acid SRT



Adverse event in male receiving Protonix (Pantoprazole)

Reported by a physician from United States on 2007-03-16

Patient: male

Adverse reactions / side effects: Urinary Tract Infection, Sepsis, Cerebrovascular Accident

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Protonix (Pantoprazole)

Other drugs received by patient: MS Contin; Allopurinol; Imdur; Prednisone; Coreg; Lasix



Adverse event in 69 year old male receiving Protonix (Pantoprazole)

Reported by a physician from United States on 2007-01-31

Patient: 69 year old male

Adverse reactions / side effects: Malignant Neoplasm Progression, Platelet Count Decreased, Blood Count Abnormal, Multiple Myeloma, Cardiac Disorder

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Actos
    Indication: Drug USE FOR Unknown Indication

Coumadin
    Indication: Drug USE FOR Unknown Indication

Insulin (Insulin)
    Indication: Drug USE FOR Unknown Indication

Lisinopril
    Indication: Drug USE FOR Unknown Indication

Protonix
    Indication: Drug USE FOR Unknown Indication

Revlimid
    Dosage: 25 mg, 3 weeks on, 1 week off, oral
    Administration route: Oral
    Indication: Multiple Myeloma
    Start date: 2006-07-10
    End date: 2006-12-08

Revlimid

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