|
Index of reports
> Cases resulting in other serious reactions (32)
> Cases with Angina Pectoris (4)
Below is the selection of adverse event reports related to Protonix (Pantoprazole) that includes cases resulting in other serious reactions where reactions include angina pectoris.
Adverse event in 57 year old male receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-07-19
Patient: 57 year old male, weighing 69.1 kg (152.0 pounds)
Adverse reactions / side effects: Angina Pectoris, Intestinal Obstruction
Adverse event resulted in: hospitalization
Suspect drug(s):
Toprol-XL
Administration route: Oral
Indication: Hypertension
Xanax
Administration route: Oral
Indication: Sleep Disorder
Placebo
Administration route: Oral
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
Irinotecan HCL
Dosage: 125 mg/m2 day 1 and 8 cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Irinotecan HCL
Start date: 2003-08-18
End date: 2003-08-18
Fluorouracil
Dosage: 500 mg/m2, day 1 and 8 cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Fluorouracil
Start date: 2003-08-18
End date: 2003-08-18
Leucovorin Calcium
Dosage: 20 mg/m2, cycle 1, day 1, and day 8
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Protonix
Administration route: Oral
Ciprofloxacin HCL
Administration route: Oral
Indication: Prophylaxis
Acetylsalicylic Acid SRT
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Amiodarone HCL
Administration route: Oral
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-04-27
Patient: male, weighing 69.0 kg (151.8 pounds)
Adverse reactions / side effects: Angina Pectoris, Blood Chloride Decreased, Platelet Count Increased, Intestinal Obstruction, Constipation, Haemoglobin Decreased, Haematocrit Decreased, RED Blood Cell Count Decreased, Blood Sodium Decreased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix
Administration route: Oral
Toprol-XL
Administration route: Oral
Indication: Hypertension
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Fluorouracil
Dosage: 500 mg/m*2, day 1 and 8 cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Fluorouracil
Dosage: 500 mg/m*2, day 1 and 8 cycle
Start date: 2003-08-18
End date: 2003-08-18
Acetylsalicylic Acid SRT
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Amiodarone HCL
Administration route: Oral
Leucovorin Calcium
Dosage: ^(20 mg/m*2, cycle 1, day 1 and^
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Irinotecan HCL
Dosage: 125 mg/m*2, day 1 and 8, cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Irinotecan HCL
Dosage: 125 mg/m*2, day 1 and 8, cycle
Start date: 2003-08-18
End date: 2003-08-18
Xanax
Administration route: Oral
Indication: Sleep Disorder
Cipro
Indication: Prophylaxis
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-04-24
Patient: male, weighing 68.9 kg (151.7 pounds)
Adverse reactions / side effects: Angina Pectoris, Intestinal Obstruction
Adverse event resulted in: hospitalization
Suspect drug(s):
Amiodarone HCL
Dosage: 200 mg, 2 in 1 day, po
Administration route: Oral
Xanax
Dosage: 0.5 mg, hs, oral
Administration route: Oral
Indication: Sleep Disorder
Placebo
Dosage: 2 in 1 day, po
Administration route: Oral
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
Irinotecan HCL
Dosage: 125mg/m2, day 1+8, iv
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Fluorouracil
Dosage: 500mg/m2, day 1+8, iv
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Leucovorin Calcium
Dosage: 20mg/m2, day 1+8, iv
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Toprol-XL
Dosage: 50 mg, 1 in 1 day, po
Administration route: Oral
Indication: Hypertension
Zetia
Dosage: 10 mg, 1 in 1 day, po
Administration route: Oral
Indication: Blood Cholesterol
Protonix
Dosage: 40 mg, 1 in 1 day, po
Administration route: Oral
Ciprofloxacin
Dosage: 250mg, 1 in 1 day, po
Administration route: Oral
Indication: Prophylaxis
Acetylsalicylic Acid SRT
Dosage: 81 mg, 1 in 1 day, po
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Adverse event in 57 year old male receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-04-16
Patient: 57 year old male, weighing 69.1 kg (152.0 pounds)
Adverse reactions / side effects: Angina Pectoris, Intestinal Obstruction, Constipation
Adverse event resulted in: hospitalization
Suspect drug(s):
Toprol-XL
Administration route: Oral
Indication: Hypertension
Xanax
Administration route: Oral
Indication: Sleep Disorder
Placebo
Administration route: Oral
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
Irinotecan HCL
Dosage: 125 mg/m2 day 1 and 8 cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Fluorouracil
Dosage: 500 mg/m2, day 1 and 8 cycle
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Leucovorin Calcium
Dosage: 20 mg/m2, cycle 1, day 1, and day 8
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Protonix
Administration route: Oral
Ciprofloxacin HCL
Administration route: Oral
Indication: Prophylaxis
Acetylsalicylic Acid SRT
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Amiodarone HCL
Administration route: Oral
|
