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Index of reports
> Cases resulting in hospitalization (37)
Below is the selection of adverse event reports related to Protonix (Pantoprazole) that includes cases resulting in hospitalization.
Reports 1 - 25 of 37 Next >>
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 female receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-10-12
Patient: female, weighing 2.3 kg (5.1 pounds)
Adverse reactions / side effects: Small FOR Dates Baby, Drug Exposure During Pregnancy, Flatulence, Abdominal Distension, Urinary Retention
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix
Dosage: 40mg once daily po
Administration route: Oral
Indication: Dyspepsia
Start date: 2007-06-01
Protonix
Dosage: 40mg once daily po
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Start date: 2007-06-01
Other drugs received by patient: Valtrex
Adverse event in 55 year old female receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-10-11
Patient: 55 year old female
Adverse reactions / side effects: Drug Toxicity, Hydronephrosis, Ureteric Obstruction, Blood Culture Positive, Neutrophil Count Decreased, Escherichia Infection, Calculus Ureteric, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix
Dosage: unknown
Leucovorin Calcium
Dosage: dose and frequency unspecified
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-07
Leucovorin Calcium
Dosage: (400 mg/m2) 744 mg total
Start date: 2007-08-08
Emend
Dosage: unknown
Fluorouracil
Dosage: (400 mg/m2) 2790 mg total
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-07
Marinol
Dosage: unknown
Cetuximab
Dosage: dose and frequency unspecified
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-07
Cetuximab
Dosage: (400 mg/m2) 279 mg total
Start date: 2007-08-08
Oxaliplatin
Dosage: dose and frequency unspecified
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-07
Oxaliplatin
Dosage: (85 mg/m2) 74 mg total
Start date: 2007-08-08
Adverse event in 663 month old female receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-10-02
Patient: 663 month old female
Adverse reactions / side effects: Ureteric Obstruction, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Marinol
Dosage: daily dose: unknown
Administration route: Oral
Indication: Ill-Defined Disorder
Cetuximab
Dosage: daily dose: 279 mg dose on 08 aug 2007
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-08
Leucovorin Calcium
Dosage: daily dose: 744 mg dose on 08 aug 2007
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-08
Fluorouracil
Dosage: daily dose: 2790 mg, bolus omitted on 08 aug 2007 due to toxicity
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-08
Oxaliplatin
Dosage: daily dose: 74 mg dose on 08 aug 2007
Indication: Colon Cancer
Start date: 2007-02-07
End date: 2007-08-08
Emend
Dosage: daily dose: unknown
Indication: Ill-Defined Disorder
Protonix
Dosage: daily dose: unknown
Administration route: Oral
Indication: Ill-Defined Disorder
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 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 40 year old male receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-07-03
Patient: 40 year old male
Adverse reactions / side effects: Drug Interaction, Anticonvulsant Drug Level Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Prevacid
End date: 2007-05-22
Protonix
Dosage: 40 mg, 1 in 1 d, oral
Administration route: Oral
Start date: 2007-05-23
Phenytoin Sodium
Indication: Convulsion
Other drugs received by patient: Multivitamin; Gabapentin
Adverse event in 52 year old female receiving Protonix (Pantoprazole)
Reported by a pharmacist from United States on 2007-06-19
Patient: 52 year old female, weighing 84.0 kg (184.8 pounds)
Adverse reactions / side effects: Pruritus, Angioedema
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix (Pantoprazole)
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-06-11
Patient: male, weighing 127.1 kg (279.7 pounds)
Adverse reactions / side effects: Lacunar Infarction
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix
Administration route: Oral
Indication: Dyspepsia
Start date: 2007-05-02
End date: 2007-05-08
Lunesta
Dosage: 3 mg hs; 5 out of the 7 evenings
Administration route: Oral
Indication: Insomnia
Start date: 2007-05-02
End date: 2007-05-08
Other drugs received by patient: Ibuprofen; Vytorin; Simvastatin; Temazepam; Aggrenox
Adverse event in 26 year old male receiving Protonix (Pantoprazole)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-07
Patient: 26 year old male, weighing 97.5 kg (214.6 pounds)
Adverse reactions / side effects: Agitation, Pain, Headache, Abdominal Pain Upper, Tendon Pain, Myalgia, Overdose, Malaise, Neck Pain, Dizziness, Hallucination, Nightmare, Pain in Extremity, Drug Intolerance, Rash, Eye Pain, Paraesthesia, Panic Attack, Arthralgia, Ear Pain
Adverse event resulted in: hospitalization
Suspect drug(s):
Nexium
Dosage: 40 mg twice a day po
Administration route: Oral
Indication: Crohn's Disease
Start date: 2007-01-01
End date: 2007-06-02
Nexium
Dosage: 40 mg twice a day po
Administration route: Oral
Indication: Hiatus Hernia
Start date: 2007-01-01
End date: 2007-06-02
Nexium
Dosage: 40 mg twice a day po
Administration route: Oral
Indication: Oesophagitis
Start date: 2007-01-01
End date: 2007-06-02
Protonix
Dosage: 40mg 1 a day po
Administration route: Oral
Indication: Crohn's Disease
Start date: 2006-12-23
End date: 2007-01-01
Protonix
Dosage: 40mg 1 a day po
Administration route: Oral
Indication: Hiatus Hernia
Start date: 2006-12-23
End date: 2007-01-01
Protonix
Dosage: 40mg 1 a day po
Administration route: Oral
Indication: Oesophagitis
Start date: 2006-12-23
End date: 2007-01-01
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a pharmacist from United States on 2007-06-06
Patient: male
Adverse reactions / side effects: Drug Interaction, Anticonvulsant Drug Level Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix (Pantoprazole)
Other drugs received by patient possibly interacting with the suspect drug:
Dilantin
Dosage: unknown
Indication: Convulsion
Other drugs received by patient: Gabapentin; Vitamin CAP
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-25
Patient: male, weighing 127.1 kg (279.7 pounds)
Adverse reactions / side effects: Cerebrovascular Accident
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix
Administration route: Oral
Indication: Dyspepsia
Start date: 2007-05-02
End date: 2007-05-09
Lunesta
Dosage: unknown
Administration route: Oral
Start date: 2007-05-02
Adverse event in female receiving Protonix (Pantoprazole)
Reported by a pharmacist from United States on 2007-05-14
Patient: female, weighing 98.0 kg (215.6 pounds)
Adverse reactions / side effects: Mental Status Changes, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix (Pantoprazole)
Adverse event in 69 year old female receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-05-04
Patient: 69 year old female
Adverse reactions / side effects: Back Pain, Rash Generalised, Pruritus, Swelling Face, Drug Ineffective, Head Injury, Hypotension, Chills, Erythema, Syncope, Fatigue, Dehydration, Eye Swelling, Back Injury, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Nitrofurantoin Monohydrate / Macrocrystals
Dosage: see image
Administration route: Oral
Indication: Cystitis
Start date: 2006-11-16
End date: 2006-11-22
Nitrofurantoin Monohydrate / Macrocrystals
Dosage: see image
Administration route: Oral
Indication: Cystitis
Start date: 2006-11-30
End date: 2006-12-05
Nitrofurantoin Monohydrate / Macrocrystals
Dosage: see image
Administration route: Oral
Indication: Cystitis
Start date: 2007-02-06
End date: 2007-02-11
Protonix
Dosage: oral
Administration route: Oral
Start date: 2006-12-10
End date: 2007-01-18
Protonix
Dosage: oral
Administration route: Oral
End date: 2007-04-03
Other drugs received by patient: Levothyroxine Sodium; Alendronate Sodium; Triamterene and Hydrochlorothiazide
Adverse event in 57 year old male receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-04-30
Patient: 57 year old male
Adverse reactions / side effects: Chest Pain, Intestinal Obstruction, Constipation
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Xanax
Administration route: Oral
Indication: Sleep Disorder
Placebo (Unspecified)
Administration route: Oral
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
Irinotecan HCL
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Fluorouracil and Levamisole
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Leucovorin Calcium
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Toprol-XL
Administration route: Oral
Indication: Hypertension
Protonix
Administration route: Oral
Ciprofloxacin HCL
Administration route: Oral
Indication: Prophylaxis
Aspirin
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Amiodarone
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 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 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 male receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-04-24
Patient: male
Adverse reactions / side effects: Colon Cancer
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix
Administration route: Oral
Indication: Hiatus Hernia
Start date: 2003-01-01
End date: 2003-01-01
Protonix
Administration route: Oral
Indication: Pain
Start date: 2006-12-01
Other drugs received by patient: Atenolol; Plavix; Levothyroxine Sodium; Glucotrol; Acetylsalicylic Acid SRT; Actos
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 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
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-04-12
Patient: male, weighing 74.9 kg (164.8 pounds)
Adverse reactions / side effects: Syncope, Vomiting, Coeliac Disease, Diarrhoea
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix
Administration route: Oral
Start date: 2006-11-01
Protonix
Administration route: Oral
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-04-05
Patient: male, weighing 47.7 kg (104.9 pounds)
Adverse reactions / side effects: Weight Gain Poor, Weight Decreased, Joint Dislocation, Coma, Libido Decreased, Gingival Atrophy, Prostatic Disorder, Insomnia, Anorexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix (Pantoprazole)
Other drugs received by patient: Cortisone Acetate; Oxycontin; Oxycontin; Oxycontin
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-03-19
Patient: male, weighing 66.3 kg (145.8 pounds)
Adverse reactions / side effects: Ventricular Arrhythmia
Adverse event resulted in: hospitalization
Suspect drug(s):
Protonix (Pantoprazole)
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
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