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Index of reports
> Cases resulting in hospitalization (37)
> Cases with Abdominal Pain (6)
Below is the selection of adverse event reports related to Protonix (Pantoprazole) that includes cases resulting in hospitalization where reactions include abdominal pain.
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-10-19
Patient: male
Adverse reactions / side effects: Abdominal Pain, Glossodynia, Diverticulitis, Intestinal Resection, Oral Discomfort, Nephrolithiasis, Myalgia, Endodontic Procedure, Oral Candidiasis, Animal Bite, Pharyngolaryngeal Pain, Oedema Mouth, Epistaxis, Post Procedural Infection, Back Pain, Abscess Drainage, Swollen Tongue, Lobar Pneumonia, Burning Sensation, Osteoarthritis, Oral Pain, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor
Indication: Blood Cholesterol Increased
Celebrex
Prednisone
Protonix
Other drugs received by patient: Ambien; Acetylsalicylic Acid; Glucosamine; Chondroitin; ALL Other Therapeutic Products; Chondroitin / Glucosamine / Methylsulfonylmethane; Vitamin E; Centrum Silver; Ginsana; Royal Jelly
Adverse event in 58 year old male receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-07-12
Patient: 58 year old male, weighing 69.0 kg (151.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Angina Pectoris, Intestinal Obstruction, Constipation, Haemoglobin Decreased, Haematocrit Decreased, Enterovesical Fistula, Sleep Disorder, Colorectal Cancer Metastatic, Blood Cholesterol, Bladder Disorder, Blood Sodium Decreased, Arteriosclerosis, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Ciprofloxacin HCL
Dosage: total daily dose: 250 mg unit dose: 250 mg
Administration route: Oral
Indication: Prophylaxis
Aspirin
Dosage: total daily dose: 81 mg unit dose: 81 mg
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Irinotecan HCL
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
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
Xanax
Dosage: total daily dose: 0.5 mg
Administration route: Oral
Indication: Sleep Disorder
Leucovorin Calcium
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Toprol-XL
Dosage: total daily dose: 50 mg
Administration route: Oral
Indication: Hypertension
Zetia
Dosage: total daily dose: 10 mg
Administration route: Oral
Indication: Hypercholesterolaemia
Protonix
Dosage: total daily dose: 40 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Amiodarone HCL
Dosage: total daily dose: 400 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 57 year old male receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-04-26
Patient: 57 year old male
Adverse reactions / side effects: Haemoglobin Decreased, Abdominal Pain, Haematocrit Decreased, Angina Pectoris, Intestinal Obstruction, Constipation, Blood Sodium Decreased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia
Dosage: 10 mg/daily/po
Administration route: Oral
Indication: Blood Cholesterol
Cipro
Dosage: 250 mg/daily
Indication: Prophylaxis
Aspirin
Dosage: 81 mg/daily
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Xanax
Dosage: 0.5 mg/daily/po
Administration route: Oral
Indication: Sleep Disorder
Toprol-XL
Dosage: 50 mg/daily/po
Administration route: Oral
Indication: Hypertension
Protonix
Dosage: 40 mg/daily/po
Administration route: Oral
Indication: Hypertension
Amiodarone HCL
Dosage: 200mg/bid/po
Administration route: Oral
Other drugs received by patient: Fluorouracil; Irinotecan HCL; Leucovorin Calcium
Adverse event in 58 year old male receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-04-17
Patient: 58 year old male, weighing 69.0 kg (151.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Angina Pectoris, Intestinal Obstruction, Constipation
Adverse event resulted in: hospitalization
Suspect drug(s):
Ciprofloxacin HCL
Dosage: total daily dose: 250 mg unit dose: 250 mg
Administration route: Oral
Indication: Prophylaxis
Acetylsalicylic Acid SRT
Dosage: total daily dose: 81 mg unit dose: 81 mg
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Irinotecan HCL
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
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
Xanax
Dosage: total daily dose: 0.5 mg
Administration route: Oral
Indication: Sleep Disorder
Leucovorin Calcium
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Toprol-XL
Dosage: total daily dose: 50 mg
Administration route: Oral
Indication: Hypertension
Zetia
Dosage: total daily dose: 10 mg
Administration route: Oral
Indication: Hypercholesterolaemia
Protonix
Dosage: total daily dose: 40 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Amiodarone HCL
Dosage: total daily dose: 400 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in female receiving Protonix (Pantoprazole)
Reported by a lawyer from United States on 2007-02-14
Patient: female, weighing 85.7 kg (188.5 pounds)
Adverse reactions / side effects: Agitation, Abdominal Pain, Pruritus, Sciatica, Headache, Erythema, Delusion, Duodenitis, Oesophagitis, Uterine Leiomyoma, Blood Pressure Inadequately Controlled, Pneumonitis, Back Pain, Chest Discomfort, Hiatus Hernia, Pain in Extremity, Hyperglycaemia, Coronary Artery Disease, Hypoaesthesia, Dehydration, Disorientation, Myalgia, Chest Pain, Dizziness, Intestinal Polyp, Vomiting, Viral Infection, Nausea, Musculoskeletal Pain, Rash, Purpura, Facial Pain, Hypertensive Crisis, Limb Discomfort, Diarrhoea, Arthralgia, Pollakiuria, Gastroenteritis, Bronchitis, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Procardia XL
Administration route: Oral
Indication: Hypertension
Procardia XL
Administration route: Oral
Start date: 2001-01-22
End date: 2001-02-04
Procardia XL
Administration route: Oral
Start date: 2001-02-05
End date: 2003-08-29
Nifedipine
Administration route: Oral
Indication: Hypertension
Start date: 2004-02-01
End date: 2004-01-01
Vasotec
Start date: 1998-12-13
End date: 1999-03-20
Cozaar
Administration route: Oral
Start date: 1999-12-07
End date: 2001-01-22
Hyzaar
Start date: 1999-12-07
End date: 2000-01-01
Toprol-XL
Start date: 1999-03-20
Paxil
Start date: 1999-03-20
Clonidine
Start date: 1999-03-20
Biaxin
Prilosec
Start date: 2001-12-04
End date: 2003-01-01
Premarin
Start date: 2002-02-25
Diovane
Start date: 2002-02-25
End date: 2002-05-06
Benicar
End date: 2003-08-29
Catapres
Start date: 2001-01-22
End date: 2001-01-01
Oxycodone
Indication: Pain
Start date: 2001-02-05
Lopressor
Start date: 2001-01-01
Protonix
Start date: 2001-01-01
Adalat
Start date: 2001-02-05
Prevacid
Start date: 2000-01-10
Nitrol
Start date: 2002-05-06
Heparin
Start date: 2002-05-06
Aspirin
Start date: 2002-05-06
Vicodin ES
Adverse event in female receiving Protonix (Pantoprazole)
Reported by a lawyer from United States on 2007-01-31
Patient: female, weighing 85.7 kg (188.5 pounds)
Adverse reactions / side effects: Abdominal Pain, Pruritus, Sciatica, Urticaria, Erythema, Delusion, Duodenitis, Oesophagitis, Uterine Leiomyoma, Blood Pressure Inadequately Controlled, Pneumonitis, Back Pain, Chest Discomfort, Hiatus Hernia, Pain in Extremity, Hyperglycaemia, Coronary Artery Disease, Hypoaesthesia, Dehydration, Chest Pain, Dizziness, Intestinal Polyp, Viral Infection, Vomiting, Nausea, Musculoskeletal Pain, Purpura, Facial Pain, Hypertensive Crisis, Limb Discomfort, Diarrhoea, Arthralgia, Gastroenteritis, Bronchitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Procardia XL
Administration route: Oral
Indication: Hypertension
Procardia XL
Administration route: Oral
Start date: 2001-01-22
End date: 2001-02-04
Procardia XL
Administration route: Oral
Start date: 2001-02-05
End date: 2003-08-29
Nifedipine
Administration route: Oral
Indication: Hypertension
Start date: 2004-02-01
End date: 2004-01-01
Vasotec
Start date: 1998-12-13
End date: 1999-03-20
Cozaar
Administration route: Oral
Start date: 1999-12-07
End date: 2001-01-22
Hyzaar
Start date: 1999-12-07
End date: 2000-01-01
Toprol-XL
Start date: 1999-03-20
Paxil
Start date: 1999-03-20
Clonidine
Start date: 1999-03-20
Biaxin
Prilosec
Start date: 2001-12-04
End date: 2003-01-01
Premarin
Start date: 2002-02-25
Diovane
Start date: 2002-02-25
End date: 2002-05-06
Benicar
End date: 2003-08-29
Catapres
Start date: 2001-01-22
End date: 2001-01-01
Oxycodone HCL
Indication: Pain
Start date: 2001-02-05
Lopressor
Start date: 2001-01-01
Protonix
Start date: 2001-01-01
Adalat
Start date: 2001-02-05
Prevacid
Start date: 2000-01-10
Nitrol
Start date: 2002-05-06
Heparin
Start date: 2002-05-06
Aspirin
Start date: 2002-05-06
Vicodin ES
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