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Index of reports
> Cases resulting in other serious reactions (32)
Below is the selection of adverse event reports related to Protonix (Pantoprazole) that includes cases resulting in other serious reactions.
Reports 1 - 25 of 32 Next >>
Adverse event in female receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-10-31
Patient: female
Adverse reactions / side effects: Chills, Liver Function Test Abnormal, Oedema Peripheral, Pyrexia
Suspect drug(s):
Parnate
Dosage: 30mg per day
Administration route: Oral
Indication: Major Depression
Start date: 2006-01-01
Lithium Carbonate
Estradiol
Levoxyl
Bentyl
Protonix
Other drugs received by patient: Risperdal
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 pharmacist from United States on 2007-10-11
Patient: female, weighing 68.0 kg (149.7 pounds)
Adverse reactions / side effects: Skin Exfoliation, Oedema Peripheral, Rash
Suspect drug(s):
Protonix (Pantoprazole)
Adverse event in female receiving Protonix (Pantoprazole)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-05
Patient: female
Adverse reactions / side effects: Renal Failure, Diarrhoea, Pyrexia, Thrombocytopenia, White Blood Cell Count Increased
Suspect drug(s):
Tygacil
Start date: 2007-09-21
End date: 2007-09-26
Protonix
Lovenox
Aspirin
Merrem
Other drugs received by patient: Flagyl; Medrol; Procrit; Norvasc; MAG-OX; Diflucan; Potassium Chloride; Coreg; Levothyroxine Sodium
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 50 year old female receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-07-06
Patient: 50 year old female, weighing 59.0 kg (129.7 pounds)
Adverse reactions / side effects: Arthralgia, Oedema Peripheral, Vision Blurred, Visual Acuity Reduced
Suspect drug(s):
Metoclopramide
Dosage: 1 tablet 4 times/day po
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Start date: 2007-05-18
End date: 2007-06-23
Protonix
Dosage: 1 tablet once a day po
Administration route: Oral
Indication: Oesophagitis
Start date: 2007-05-18
End date: 2007-06-23
Adverse event in 70 year old female receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-06-29
Patient: 70 year old female
Adverse reactions / side effects: Hepatic Steatosis
Suspect drug(s):
Nolvadex
Administration route: Oral
Start date: 2003-01-01
Protonix
Administration route: Oral
Adverse event in 78 year old male receiving Protonix (Pantoprazole)
Reported by a pharmacist from United States on 2007-06-15
Patient: 78 year old male
Adverse reactions / side effects: Thrombocytopenia
Suspect drug(s):
Protonix
Dosage: 40 mg frequency unspecified
Start date: 2007-05-01
End date: 2007-05-01
Protonix
Start date: 2007-05-01
End date: 2007-06-02
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 receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-06-01
Patient:
Adverse reactions / side effects: Pharyngeal Oedema, Drug Interaction, Ulcer
Suspect drug(s):
Diovan
Dosage: 160mg, unk
Protonix
Dosage: unk, unk
Indication: Ulcer
Adverse event in receiving Protonix (Pantoprazole)
Reported by a pharmacist from United States on 2007-05-14
Patient:
Adverse reactions / side effects: Hyperglycaemia
Suspect drug(s):
Protonix (Pantoprazole)
Adverse event in male receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-05-11
Patient: male
Adverse reactions / side effects: Feeling Jittery, Suicidal Ideation, Nervousness
Suspect drug(s):
Protonix (Pantoprazole)
Other drugs received by patient: Xanax; Maxzide; Cymbalta; Benicar; Lotrel
Adverse event in 68 year old female receiving Protonix (Pantoprazole)
Reported by a pharmacist from United States on 2007-05-09
Patient: 68 year old female, weighing 62.6 kg (137.8 pounds)
Adverse reactions / side effects: Pancytopenia
Suspect drug(s):
Protonix (Pantoprazole)
Other drugs received by patient: Catapres; Diflucan; Lantus; Zofran; Tygacil; Morphine; Valium
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 male receiving Protonix (Pantoprazole)
Reported by a pharmacist from United States on 2007-04-24
Patient: male, weighing 130.6 kg (287.4 pounds)
Adverse reactions / side effects: Hyperglycaemia
Suspect drug(s):
Protonix (Pantoprazole)
Other drugs received by patient: Humalog; Lisinopril; Lovastatin; Therapeutic Multivitamin
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 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 female receiving Protonix (Pantoprazole)
Reported by a physician from Germany on 2007-04-19
Patient: female
Adverse reactions / side effects: Abdominal Hernia, Confusional State, Bone Pain, Angina Unstable, Deafness, Hypercholesterolaemia, Fatigue, Malaise, Hypoaesthesia Facial, Transient Ischaemic Attack, Pain in Extremity, Hypoaesthesia, Vision Blurred, Hypertension, Asthenia, Feeling Abnormal
Suspect drug(s):
Protonix
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Atorvastatin Calcium
Administration route: Oral
Indication: Hypercholesterolaemia
Hydrochlorothiazide
Administration route: Oral
Indication: Essential Hypertension
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 female receiving Protonix (Pantoprazole)
Reported by a physician from United States on 2007-04-12
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Abortion Spontaneous
Suspect drug(s):
Rapamune
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Protonix
Dosage: unspecified
Other drugs received by patient: Synthroid; Cyanocobalamin; Vitamins, Other Combinations; Folic Acid; Pyridoxine Hydrochloride; Prograf; Bactrim
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 34 year old female receiving Protonix (Pantoprazole)
Reported by a individual with unspecified qualification from United States on 2007-03-14
Patient: 34 year old female
Adverse reactions / side effects: Abortion Spontaneous
Suspect drug(s):
Truvada
Administration route: Oral
Indication: HIV Infection
Bactrim
Protonix
Other drugs received by patient: Lexiva; Norvir
Adverse event in 49 year old female receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-03-12
Patient: 49 year old female, weighing 62.6 kg (137.7 pounds)
Adverse reactions / side effects: Heart Rate Increased, Drug Interaction, Dizziness, Asthenia, Feeling Abnormal
Suspect drug(s):
Lisinopril
Dosage: 1 tab daily po
Administration route: Oral
Indication: Hypertension
Start date: 2006-10-02
End date: 2006-11-20
Protonix
Dosage: 1 tab daily po
Administration route: Oral
Indication: Abdominal Pain Upper
Start date: 2006-11-13
End date: 2006-12-28
Protonix
Dosage: 1 tab daily po
Administration route: Oral
Indication: Gastrooesophageal Reflux Disease
Start date: 2006-11-13
End date: 2006-12-28
Adverse event in 49 year old female receiving Protonix (Pantoprazole)
Reported by a consumer/non-health professional from United States on 2007-02-20
Patient: 49 year old female, weighing 123.4 kg (271.4 pounds)
Adverse reactions / side effects: Drug Effect Decreased, Scab, Rash Pruritic
Suspect drug(s):
Protonix
Dosage: 1 tablet daily po
Administration route: Oral
Indication: Gastric Disorder
Start date: 2007-01-29
End date: 2007-02-12
Protonix
Dosage: 1 tablet daily po
Administration route: Oral
Indication: Prophylaxis
Start date: 2007-01-29
End date: 2007-02-12
Other drugs received by patient: Ritalin; Imiprimine; Wellbutrin; Neurontin; Risperdal
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