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PROTONIX Safety Reports

Total PROTONIX reports: 68.
PROTONIX FDA safety alerts: 2004 .
Reported deaths: 1    Reported hospitalizations: 32.
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Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Dec 29, 2006. Female patient, 63 years of age, was diagnosed with gastrooesophageal reflux disease, hypercholesterolaemia, essential hypertension and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: angina unstable, transient ischaemic attack. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. During the same period patient was treated with ATORVASTATIN CALCIUM, HYDROCHLOROTHIAZIDE. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 08, 2007. Male patient, 71 years of age, was diagnosed with hiatus hernia, pain and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: chest pain, colon cancer. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with ASPIRIN, ATENOLOL, ACTOS, LEVOXYL, GLUCOTROL. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Jan 11, 2007. Female patient, 38 years of age, weighting 155.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, alcohol poisoning. PROTONIX dosage: 40 MG 1X PER 1DAY, ORAL. During the same period patient was treated with ALCOHOL, AMBIEN, ALPRAZOLAM, COUMADIN, PAROXETINE, HYDROCODONE BITARTRATE, SINGULAIR, DILTIAZEM. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on Jan 25, 2007. Female patient, weighting 150.0 lb, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: pruritus, urticaria. PROTONIX dosage: unknown. During the same period patient was treated with ALBUTEROL, BIRTH CONTROL S. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Jan 30, 2007. Male patient, weighting 146.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: ventricular arrhythmia. PROTONIX dosage: unknown. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on Feb 09, 2007. Female patient was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: somnolence, stomach discomfort. PROTONIX dosage: unknown. During the same period patient was treated with PAROXETINE HYDROCHLORIDE. Patient recovered.

Pharmacist from UNITED STATES reported PROTONIX problem on Feb 08, 2007. Female patient, 18 years of age, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: hypertensive crisis, white blood cell count decreased. PROTONIX dosage: unknown. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on Feb 14, 2007. Female patient, 89 years of age, weighting 110.0 lb, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: blood pressure systolic decreased, burning sensation, pruritus. PROTONIX dosage: 80MG ONE ADMINISTRATION IV. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Feb 20, 2007. Female patient, 49 years of age, weighting 272.0 lb, was diagnosed with gastric disorder, prophylaxis and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: rash pruritic, scab. PROTONIX dosage: unknown. During the same period patient was treated with RITALIN, IMIPRIMINE, WELLBUTRIN, NEURONTIN, RISPERDAL. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Feb 12, 2007. Female patient, weighting 135.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: dyspnoea exertional, iron deficiency anaemia, microcytic anaemia, syncope. PROTONIX dosage: unknown. Patient was hospitalized. Patient recovered.

Pharmacist from UNITED STATES reported PROTONIX problem on Feb 27, 2007. Male patient, 32 years of age, was diagnosed with abdominal pain upper and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: eosinophil count increased, gastroenteritis, rectal haemorrhage. PROTONIX dosage: 40MG DAILY IV. During the same period patient was treated with TEGRETOL. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 07, 2007. Male patient, weighting 146.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: ventricular arrhythmia. PROTONIX dosage: unknown. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Mar 12, 2007. Male patient was diagnosed with insomnia, restless legs syndrome and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: amnesia, eating disorder, sleep walking, weight increased. PROTONIX dosage: unknown. During the same period patient was treated with NORVASC, HYDROCHLOROTHIAZIDE, COZAAR, ATENOLOL, EFFEXOR, WELLBUTRIN, AMBIEN. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2006. Male patient, 50 years of age, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: pancreatitis chronic. PROTONIX dosage: unknown. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on Feb 23, 2006. Male patient, weighting 196.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: angioedema. PROTONIX dosage: unknown. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Mar 28, 2007. Male patient, weighting 105.1 lb, was diagnosed with gastrooesophageal reflux disease, arthralgia, fibromyalgia, arthritis, pain and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: anorexia, coma, gingival atrophy, insomnia, joint dislocation, libido decreased, prostatic disorder, weight decreased, weight gain poor. PROTONIX dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, OXYCONTIN. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Apr 02, 2007. Male patient, weighting 165.1 lb, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: coeliac disease, diarrhoea, syncope, vomiting. PROTONIX dosage: unknown. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Apr 16, 2007. Male patient, weighting 152.1 lb, was diagnosed with hypertension, hypercholesterolaemia, colorectal cancer metastatic, prophylaxis and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: angina pectoris, blood chloride decreased, blood sodium decreased, constipation, haematocrit decreased, haemoglobin decreased, intestinal obstruction, platelet count increased, red blood cell count decreased. PROTONIX dosage: unknown. During the same period patient was treated with TOPROL, ZETIA, FLUOROURACIL, ACETYLSALICYLIC ACID SRT, AMIODARONE, LEUCOVORIN CALCIUM, IRINOTECAN. Patient was hospitalized. Patient recovered.

Pharmacist from UNITED STATES reported PROTONIX problem on Apr 24, 2007. Male patient, weighting 288.0 lb, was diagnosed with gastritis and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: hyperglycaemia. PROTONIX dosage: 40 MG QAM PO. During the same period patient was treated with HUMALOG, LISINOPRIL, LOVASTATIN, THERAPEUTIC VITAMIN. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 20, 2007. Female patient, 53 years of age, was diagnosed with gastrooesophageal reflux disease, abdominal distension and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, cardiac disorder, chest discomfort, dyspnoea, mitral valve prolapse, palpitations. PROTONIX dosage: unknown. During the same period patient was treated with ZELNORM. Patient recovered.

Pharmacist from UNITED STATES reported PROTONIX problem on Aug 01, 2006. Female patient was diagnosed with cough, gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: optic ischaemic neuropathy. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. During the same period patient was treated with LIPITOR, TOPROL. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Apr 07, 2006. Male patient was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: pyrexia. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. Patient was hospitalized. Patient recovered.

Health Professional from UNITED STATES reported PROTONIX problem on Sept 15, 2006. Female patient, 62 years of age, weighting 205.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: angioedema, face oedema, headache, laryngitis. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. During the same period patient was treated with REGLAN, LORCET, SYNTHROID, VYTORIN, ZOLOFT, DIOVAN, HYDROCHLOROTHIAZIDE, NEURONTIN. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Apr 09, 2006. Female patient, weighting 160.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, pollakiuria, thirst. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. During the same period patient was treated with FLUOXETINE. Patient was hospitalized. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on Apr 12, 2006. Female patient, 48 years of age, weighting 180.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, diplopia, extraocular muscle paresis, headache. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 27, 2006. Male patient was diagnosed with prophylaxis and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: white blood cell count decreased. PROTONIX dosage: unknown. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on May 09, 2006. Male patient was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: rhabdomyolysis. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2006. Female patient, 41 years of age, weighting 130.1 lb, was diagnosed with ulcer and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: chest pain, lipids increased, pancreatitis. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. Patient was hospitalized. Patient recovered.

Pharmacist from UNITED STATES reported PROTONIX problem on May 17, 2006. Female patient, 49 years of age, was diagnosed with gastroenteritis and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: chest pain, myocardial infarction. PROTONIX dosage: 40 MG 2X PER 1 DAY ORAL. During the same period patient was treated with ZOFRAN, MAALOX, DILAUDID. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Aug 15, 2006. Female patient, 50 years of age, weighting 160.1 lb, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: pancreatitis. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. During the same period patient was treated with LOPRESSOR, LISINOPRIL, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Sept 11, 2006. Male patient, 39 years of age, weighting 148.1 lb, was diagnosed with gastrooesophageal reflux disease, weight decreased and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, condition aggravated, constipation, dizziness, headache, myalgia, nausea, weight decreased. PROTONIX dosage: 40 MG 1X PER 1 DAY ORAL. During the same period patient was treated with EFFEXOR, REGLAN. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on May 04, 2007. Female patient, 53 years of age, was diagnosed with gastrooesophageal reflux disease, abdominal distension and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, cardiac disorder, chest discomfort, dyspnoea, mitral valve prolapse, palpitations. PROTONIX dosage: unknown. During the same period patient was treated with ZELNORM. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on May 07, 2007. Female patient, 53 years of age, was diagnosed with gastrooesophageal reflux disease, abdominal distension and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, cardiac disorder, cardiac stress test normal, chest discomfort, dyspnoea, mitral valve prolapse, non-cardiac chest pain, palpitations. PROTONIX dosage: unknown. During the same period patient was treated with ZELNORM. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on May 14, 2007. Female patient, weighting 216.1 lb, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: mental status changes, pyrexia. PROTONIX dosage: unknown. Patient was hospitalized. Patient recovered.

Health Professional from UNITED STATES reported PROTONIX problem on May 15, 2007. Male patient, weighting 280.3 lb, was diagnosed with dyspepsia and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident. PROTONIX dosage: unknown. During the same period patient was treated with LUNESTA. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on Jan 23, 2007. Female patient, 68 years of age, weighting 138.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: pancytopenia. PROTONIX dosage: 80 MG 3X PER 1 DAY, INTRAVENOUS. During the same period patient was treated with CATAPRES, DIFLUCAN, LANTUS, ZOFRAN, TYGACIL, MORPHINE, VALIUM. Patient recovered.

Pharmacist from UNITED STATES reported PROTONIX problem on Sept 28, 2006. Female patient, 50 years of age, weighting 98.08 lb, was diagnosed with abdominal pain upper and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: pancytopenia. PROTONIX dosage: unknown. During the same period patient was treated with ALUMINUM HYDROXIDE AND MAGNESIUM TRISILICATE, HEPARIN. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on June 26, 2006. Female patient was diagnosed with gastrointestinal ulcer haemorrhage, prophylaxis and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: gastric ph decreased. PROTONIX dosage: unknown. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on May 30, 2007. Male patient, weighting 280.3 lb, was diagnosed with dyspepsia, insomnia and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: lacunar infarction. PROTONIX dosage: unknown. During the same period patient was treated with IBUPROFEN, VYTORIN, SIMVASTATIN, TEMAZEPAM, LUNESTA, AGGRENOX. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on June 05, 2007. Male patient, 78 years of age, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: thrombocytopenia. PROTONIX dosage: unknown. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on June 07, 2007. Male patient, weighting 145.1 lb, was diagnosed with gastrooesophageal reflux disease, depression and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: myocardial infarction. PROTONIX dosage: unknown. During the same period patient was treated with SERTRALINE, ACETYLSALICYLIC ACID SRT. Patient died on 04/01/2007.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on June 19, 2007. Female patient, 52 years of age, weighting 185.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: angioedema, pruritus. PROTONIX dosage: 40MG DAILY PO. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on June 26, 2006. Female patient, 52 years of age, weighting 145.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, pain in extremity. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with AMBIEN. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on July 17, 2006. Female patient, 35 years of age, weighting 162.9 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: swelling face, throat irritation, wheezing. PROTONIX dosage: unknown. During the same period patient was treated with NEXIUM, ZOLOFT, NASONEX, MIRALAX, ZELNORM, CARAFATE, AMBIEN, PEPCID. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on July 03, 2006. Male patient, 16 years of age, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: chest pain. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on July 27, 2006. Female patient, 35 years of age, weighting 162.9 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: hypersensitivity, swelling face, throat irritation, wheezing. PROTONIX dosage: unknown. During the same period patient was treated with NEXIUM, ZOLOFT, MIRALAX, CARAFATE, PEPCID, NASONEX, ZELNORM, AMBIEN. Patient was hospitalized. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on Aug 02, 2006. Female patient, weighting 287.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: swelling face, urticaria. PROTONIX dosage: 40 MG. During the same period patient was treated with EFFEXOR, LASIX, ALLEGRA, SYNTHROID, LAMICTAL, PROVENTIL. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on July 26, 2006. Female patient, 24 years of age, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: treatment noncompliance, vomiting. PROTONIX dosage: unknown. During the same period patient was treated with ZELNORM. Patient was hospitalized. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Aug 02, 2006. Female patient was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, intestinal gangrene, vomiting. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with MIDODRINE HYDROCHLORIDE, TRAMADOL, ACETYLSALICYLIC ACID SRT, ACETAMINOPHEN, MAALOX. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Aug 02, 2006. Male patient, 65 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: dyspnoea, pruritus, syncope, throat tightness. PROTONIX dosage: unknown. During the same period patient was treated with CELEXA, PROSCAR, ZOCOR, RITALIN, LACTULOSE, CIPRO, FLONASE. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Aug 11, 2006. Female patient, 46 years of age, weighting 152.1 lb, was diagnosed with dyspepsia, gastric disorder and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: coeliac disease, diarrhoea, vomiting. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with MVI, NEURONTIN, FUROSEMIDE, SPIRONOLACTONE, PENTOXIFYLLINE, LEVOXYL, MAGNESIUM. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2006. Female patient, 24 years of age, was diagnosed with nausea, vomiting and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: nausea, treatment noncompliance, vomiting. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. Patient was hospitalized. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on Sept 06, 2006. Female patient, 41 years of age, weighting 147.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: joint stiffness, swollen tongue. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Sept 20, 2006. Female patient, 73 years of age, weighting 140.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: choking, dysarthria, dysphagia, motor neurone disease, nervous system disorder. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with PAXIL, PRAVACHOL. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on Oct 02, 2006. Female patient was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: intestinal gangrene. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with MIDODRINE HYDROCHLORIDE, TRAMADOL, ASPIRIN, ACETAMINOPHEN, ALUMINUM HYDROXIDE AND MAGNESIUM TRISILICATE. Patient was hospitalized. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Sept 26, 2006. Female patient, 29 years of age, weighting 200.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: aphasia, hemiparesis, hemiplegia, hypoaesthesia, muscular weakness. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with WELLBUTRIN, FLEXERIL, HYDROCODONE, CYANOCOBALAMIN, GLUCOPHAGE. Patient was hospitalized and became disabled. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on Oct 30, 2006. Female patient, 42 years of age, weighting 151.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: chest pain, diarrhoea, dizziness, dyspnoea, headache, nausea, uterine dilation and curettage, vomiting. PROTONIX dosage: unknown. During the same period patient was treated with OXYCONTIN. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Oct 19, 2006. Female patient, 73 years of age, weighting 140.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: amyotrophic lateral sclerosis, nuclear magnetic resonance imaging brain abnormal. PROTONIX dosage: 40 MG 1X PER 1 DAY, ORAL. During the same period patient was treated with PAXIL, PRAVACHOL. Patient recovered.

Pharmacist from UNITED STATES reported PROTONIX problem on Oct 20, 2006. Male patient was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: renal failure. PROTONIX dosage: 40 MG DAILY. During the same period patient was treated with VFEND. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 26, 2006. Female patient, 59 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, blister, blood potassium decreased, cellulitis, dyspnoea, pain, skin exfoliation, staphylococcal infection. PROTONIX dosage: 40 MG 1X PER 1 DAY; ORAL. During the same period patient was treated with CELEBREX, VALIUM, PHENERGAN, MS CONTIN, LEXAPRO, SEPTRA, DEPAKOTE, DILAUDID. Patient was hospitalized. Patient recovered.

Physician from UNITED STATES reported PROTONIX problem on Nov 14, 2006. Female patient, 73 years of age, weighting 140.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: amyotrophic lateral sclerosis, choking, dysarthria, dysphagia. PROTONIX dosage: 40 MG 1X PER 1 DAY; ORAL. During the same period patient was treated with PAXIL, PRAVACHOL. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on Nov 27, 2006. Female patient, 70 years of age, was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: colon cancer, polymyositis. PROTONIX dosage: 40 MG DAILY PO IV. During the same period patient was treated with PREVACID. Patient recovered.

Health Professional from UNITED STATES reported PROTONIX problem on Aug 06, 2007. Male patient, child 8 years of age, weighting 83.78 lb, was diagnosed with abdominal discomfort, pneumonia, tracheitis and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: thrombocytopenia. PROTONIX dosage: 40MG ONCE A DAY 042. During the same period patient was treated with CLINDAMYCIN, KLONOPIN, ALBUTEROL, BENADRYL, CEFTAZIDIME. Patient recovered.

PROTONIX problem was reported by a Pharmacist from UNITED STATES on Aug 15, 2007. Female patient, 48 years of age, weighting 145.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: genital herpes. PROTONIX dosage: 40MG DAILY PO. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Aug 30, 2007. Female patient, 34 years of age, weighting 125.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: nausea, optic neuritis, weight decreased. PROTONIX dosage: unknown. Patient recovered.

PROTONIX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 04, 2007. Male patient, 45 years of age, weighting 200.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: haemorrhage, sinus disorder, sinusitis. PROTONIX dosage: unknown. Patient recovered.

Consumer or non-health professional from UNITED STATES reported PROTONIX problem on Sept 11, 2007. Female patient, 20 years of age, weighting 125.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, dysphonia, throat irritation. PROTONIX dosage: 40MG TWICE DAILY PO. During the same period patient was treated with WELLBUTRIN. Patient recovered.

PROTONIX problem was reported by a Physician from UNITED STATES on Sept 17, 2007. Female patient was diagnosed with colon cancer and was treated with PROTONIX. After drug was administered, patient experienced the following problems/side effects: infection, ureteric obstruction. PROTONIX dosage: unknown. During the same period patient was treated with MARINOL, EMEND, FLUOROURACIL, LEUCOVORIN CALCIUM, CETUXIMAB, OXALIPLATIN. Patient was hospitalized. Patient recovered.

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Alrex (loteprednol etabonate)
AltaceThis drug has as active FDA Safety Alert (ramipril)
Ambien (zolpidem tartrate)
AmergeThis drug has as active FDA Safety Alert (naratriptan)
Aminolevulinic acid
AmiodaroneThis drug has as active FDA Safety Alert
Amitiza (lubiprostone)
AmnesteemThis drug has as active FDA Safety Alert (isotretinoin)
Amphadase (hyaluronidase)
luronidase)
Amphetamine saltsThis drug has as active FDA Safety Alert
Amprenavir
AnaproxThis drug has as active FDA Safety Alert (naproxen sodium)
Angiomax (bivalirudin)
Anidulafungin
Antagon (ganirelix acetate)
Anthelios SX (avobenzone, ecamsule, octocrylene)
Apidra (insulin glulisine recombinant)
Apokyn (apomorphine)
Aprepitant
Aprotinin
Aptivus (tipranavir)
AranespThis drug has as active FDA Safety Alert (darbepoetin alpha)
Arava (leflunomide)
Arformoterol

Argatroban
ArediaThis drug has as active FDA Safety Alert (pamidronate)
Aripiprazole
Arixtra (fondaparinux)
Aromasin (exemestane)
Arranon (nelarabine)
Arsenic trioxide
Aspirin
Atacand (candesartan cilexetil)
Atazanavir sulfate
AtomoxetineThis drug has as active FDA Safety Alert
Avastin (bevacizumab)
Avelox (moxifloxacin)
Avobenzone, Ecamsule, Octocrylene
Avodart (dutasteride)
Avonex (interferon beta-1a)
AxertThis drug has as active FDA Safety Alert (almotriptan malate)
Azacitidine
Azilect (rasagiline)
Azopt (brinzolamide)

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B
Balsalazide disodium
Baraclude (entecavir)
BenazeprilThis drug has as active FDA Safety Alert
Benicar (olmesartan medoxomil)
Bevacizumab
Bexarotene
BextraThis drug has as active FDA Safety Alert (valdecoxib)
BiaxinThis drug has as active FDA Safety Alert (clarithromycin)
Bimatoprost
Bivalirudin
BonivaThis drug has as active FDA Safety Alert (ibandronate)
Bortezomib
Brinzolamide
Brovana (arformoterol)
BupropionThis drug has as active FDA Safety Alert
Butisol sodium
Byetta (exenatide)


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C
Calfactant
CampathThis drug has as active FDA Safety Alert (alemtuzumab)
Campral (acamprosate calcium)
Cancidas (caspofungin)
Candesartan cilexetil
Capecitabine
CapotenThis drug has as active FDA Safety Alert (captopril)
CaptoprilThis drug has as active FDA Safety Alert
CarbamazepineThis drug has as active FDA Safety Alert
CarbatrolThis drug has as active FDA Safety Alert (carbamazepine)
Carbrital (pentobarbital and carbromal)
Caspofungin
Cefditoren pivoxil
CefepimeThis drug has as active FDA Safety Alert
CeftriaxoneThis drug has as active FDA Safety Alert
CelebrexThis drug has as active FDA Safety Alert (celecoxib)
CelecoxibThis drug has as active FDA Safety Alert
CelexaThis drug has as active FDA Safety Alert (citalopram hydrobromide)
Cetrorelix acetate
Cetrotide (cetrorelix acetate)
Cetuximab
Cevimeline
ChantixThis drug has as active FDA Safety Alert (varenicline)
Cialis (tadalafil)
Cilostazol
Cinacalcet
Cirlesonide
CitalopramThis drug has as active FDA Safety Alert
ClaravisThis drug has as active FDA Safety Alert (isotretinoin)
ClarithromycinThis drug has as active FDA Safety Alert
Clarinex (desloratadine)
Clolar (clofarabine)
Clofarabine
Clozapine
Clozaril (clozapine)
CodeineThis drug has as active FDA Safety Alert
Colazal (balsalazide disodium)
Colesevelam
ColistimethateThis drug has as active FDA Safety Alert
Coly-Mycin M (colistimethate)This drug has as active FDA Safety Alert
Comtan (entacapone)
Concerta (methylphenidate)
Conivaptan
CordaroneThis drug has as active FDA Safety Alert (amiodarone)
CrestorThis drug has as active FDA Safety Alert (rosuvastatin calcium)
Cubicin (daptomycin)
Curosurf (poractant alfa)
CylertThis drug has as active FDA Safety Alert (pemoline)
CymbaltaThis drug has as active FDA Safety Alert (duloxetine)
CytotecThis drug has as active FDA Safety Alert (misoprostol)

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D
Dacogen (decitabine)
Dalfopristin
Dalmane (flurazepam)
Daptomycin
Darbepoetin alphaThis drug has as active FDA Safety Alert
Darifenacin
Darunavir
Dasatinib
Daytrana (methylphenidate transdermal)
DDAVPThis drug has as active FDA Safety Alert (desmopressin)
DDAVP Nasal SprayThis drug has as active FDA Safety Alert (demopressin)
DDAVP Rhinal TubeThis drug has as active FDA Safety Alert (desmopressin)
DDVPThis drug has as active FDA Safety Alert (desmopressin
Decitabine
Deferasirox
Definity (perflutren lipid microspheres)
DepaconThis drug has as active FDA Safety Alert (valproate)
DepakeneThis drug has as active FDA Safety Alert (valproate)
DepakoteThis drug has as active FDA Safety Alert (valproate)
Desloratadine
DesmopressinThis drug has as active FDA Safety Alert
Detrol (tolterodine tartrate)
terodine tartrate)
Dexedrine (dextroamphetamine sulfate)
Dexmedetomidine
Dexmethylphenidate HCl
> Dextroamphetamine sulfate
Diastat AcuDialThis drug has as active FDA Safety Alert
Diazepam rectal gelThis drug has as active FDA Safety Alert
DidronelThis drug has as active FDA Safety Alert (etidronate)
DiprivanThis drug has as active FDA Safety Alert (propofol)
Dofetilide
Doral (quazepam)
Doxercalcif
Drospirenone
DuloxetineThis drug has as active FDA Safety Alert
DuragesicThis drug has as active FDA Safety Alert (fentanyl transdermal system)
Dutasteride

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E

Eculizumab
Edetate disodium
Efalizumab
Efavirenz
EffexorThis drug has as active FDA Safety Alert (venlafaxine)
Elestat (epinastine)
EletriptanThis drug has as active FDA Safety Alert
Elidel (pimecrolimus)
Ellence (epirubicin)
Eloxatin (oxaliplatin)
Emend (aprepitant)
Emtricitabine
Emtriva (emtricitabine)
Enablex (darifenacin)
Enalapril / EnalaprilatThis drug has as active FDA Safety Alert
Endrate (edetate disodium)
Enfuvirtide
Entacapone
Entecavir
Epinastine
Epirubicin
Eplerenone
Epoetin alfaThis drug has as active FDA Safety Alert
EpogenThis drug has as active FDA Safety Alert (epoetin alfa)
Eptifibatide
EquetroThis drug has as active FDA Safety Alert (carbamazepine)
Eraxis (anidulafungin)
Erbitux (cetuximab)
Ertaczo (sertaconazole)
EscitalopramThis drug has as active FDA Safety Alert
Estazolam
Eszopiclone
Ethchlorvynol

Ethinyl estradiol
EtidronateThis drug has as active FDA Safety Alert
Evoxac (cevimeline)
Exelon (rivastigmine tartrate)
Exenatide
Exjade (deferasirox)
Exemestane
Extraneal (icodextrin)
Ezetimibe
Ezetimibe/simvastatin

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F
Factive (gemifloxacin mesylate)
Faslodex (fulvestrant)
FelbamateThis drug has as active FDA Safety Alert
FelbatolThis drug has as active FDA Safety Alert (felbamate)
Fentanyl buccal tabletsThis drug has as active FDA Safety Alert
Fentanyl citrate
Fentanyl transdermal systemThis drug has as active FDA Safety Alert
FentoraThis drug has as active FDA Safety Alert (fentanyl buccal tablets)
Ferrlecit (sodium ferric gluconate complex)
Fleet Accu-PrepThis drug has as active FDA Safety Alert (sodium phosphate)
Fleet Phospho-SodaThis drug has as active FDA Safety Alert (sodium phosphate)
FluoxetineThis drug has as active FDA Safety Alert
Flurazepam
Fluticasone propionate
FluvoxamineThis drug has as active FDA Safety Alert
Focalin (dexmethylphenidate)
Focalin XR (dexmethylphenidate)
Fomivirsen
Fondaparinux
Foradil (formoterol fumarate)
Formoterol fumarate
FosamaxThis drug has as active FDA Safety Alert (alendronate)
FosinoprilThis drug has as active FDA Safety Alert
FrovaThis drug has as active FDA Safety Alert (frovatriptan succinate)
Frovatriptan succinateThis drug has as active FDA Safety Alert
Fulvestrant
Fuzeon (enfuvirtide)

G
GabapentinThis drug has as active FDA Safety Alert
GabitrilThis drug has as active FDA Safety Alert (tiagabine)
Gadobenate DimeglumineThis drug has as active FDA Safety Alert
GadodiamideThis drug has as active FDA Safety Alert
GadoliniumThis drug has as active FDA Safety Alert
Gadopentetate DimeglumineThis drug has as active FDA Safety Alert
GadoteridolThis drug has as active FDA Safety Alert
GadoversetamideThis drug has as active FDA Safety Alert
GalantamineThis drug has as active FDA Safety Alert
Ganirelix acetate
GatifloxacinThis drug has as active FDA Safety Alert
GefitinibThis drug has as active FDA Safety Alert
Gemifloxacin mesylate
Gemtuzumab ozogamicin
Geodon (ziprasidone)
Gleevec (imatinib mesylate)

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H
Halcion (triazolam)
HaldolThis drug has as active FDA Safety Alert (haloperidol)
Haloperidol
This drug has as active FDA Safety Alert
Hectorol (doxercalcif)
Hepsera (adefovir dipivoxil)
Hyaluronidase
Hydase (hyaluronidase)
Human Secretin

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I
IbandronateThis drug has as active FDA Safety Alert
Ibuprofen
Icodextrin
Iloprost
Imatinib mesylate
Increlex (Mecasermin [rDNA origin]
Infasurf Preservative Free (calfactant)
ImitrexThis drug has as active FDA Safety Alert (sumatriptan)
Innohep (tinzaparin)
Inspra (eplerenone)
Insulin Aspart recombinant
Insulin Detemir recombinant
Insulin Glargine recombinant

Insulin Glulisine recombinant

Intron A (interferon alfa-2b)
Integrilin (eptifibatide)
ifibatide)
Interferon alfa-2b
Interferon beta-1a
Interferon gamma-1bThis drug has as active FDA Safety Alert
Invega (paliperidone)
Iplex  (mecasermin rinfabate)
IressaThis drug has as active FDA Safety Alert (gefitinib)
IsotretinoinThis drug has as active FDA Safety Alert

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J
Januvia (sitagliptin phosphate)

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K
Kaletra (lopinavir; ritonavir)
Kepivance (palifermin)
KeppraThis drug has as active FDA Safety Alert (levetiracetam)
Ketek (telithromycin)
Ketotifen fumarate

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L
LamictalThis drug has as active FDA Safety Alert (lamotrigine)
LamotrigineThis drug has as active FDA Safety Alert
Lantus (insulin glargine recombinant)
Leflunomide
Lenalidomide
Lepirudin recombinant
Levalbuterol
Levemir (insulin detemir recombinant)
LevetiracetamThis drug has as active FDA Safety Alert
Levitra (vardenafil)
Levonorgestrel
Levothyroxine sodium
Levulan Kerastick (aminolevulinic acid)
LexaproThis drug has as active FDA Safety Alert (escitalopram)
Lindane
Linezolid
This drug has as active FDA Safety Alert
LisinoprilThis drug has as active FDA Safety Alert
Lopinavir/ritonavir
Lotemax (loteprednol etabonate)
LotensinThis drug has as active FDA Safety Alert (benazepril)
Loteprednol etabonate
Lotronex (alosetron hydrochloride)
Lubiprostone
Lucentis (ranibizumab)
Lumigan (bimatoprost)
Lunestra (eszopiclone)
LyricaThis drug has as active FDA Safety Alert (pregabalin)

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M
Macugen (pegaptanib)
MagnevistThis drug has as active FDA Safety Alert (gadopentetate dimeglumine)
Maraviroc
MavikThis drug has as active FDA Safety Alert (trandolapril)
MaxaltThis drug has as active FDA Safety Alert (rizatriptan benzoate)
MaxipimeThis drug has as active FDA Safety Alert (cefepime)
Mecasermin [rDNA origin]
Mecasermin-rinfabate
Meloxicam
Memantine
Metadate CD (methylphenidate HCl)
ylphenidate HCl)
Methylphenidate HCl
Methylphenidate transdermal
Mequinol
Micafungin
Micardis (telmisartan)
misartan)
MifeprexThis drug has as active FDA Safety Alert (mifepristone)
MifepristoneThis drug has as active FDA Safety Alert
Miglustat
MinirinThis drug has as active FDA Safety Alert (desmopressin)
MirtazapineThis drug has as active FDA Safety Alert
MisoprostolThis drug has as active FDA Safety Alert
Mobic (meloxicam)
Modafinil
MoexiprilThis drug has as active FDA Safety Alert
MonoprilThis drug has as active FDA Safety Alert (fosinopril)
Moxifloxacin
MultiHanceThis drug has as active FDA Safety Alert (gadobenate dimeglumine)
Mycamine (micafungin)
Mylotarg (gemtuzumab ozogamicin)

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N
Namenda (memantine)
NaprosynThis drug has as active FDA Safety Alert (naproxen)
NaproxenThis drug has as active FDA Safety Alert
Naratriptan
Nesiritide recombinant
Nateglinide
Natrecor (nesiritide recombinant)
NefazodoneThis drug has as active FDA Safety Alert
Nelarabine
NeoTect Kit (technetium Tc 99m depreotide)
Nesiritide recombinant
NeurontinThis drug has as active FDA Safety Alert (gabapentin)
Nexavar (sorafenib)
Nitazoxanide
Nitisinone
Norelgestromin
NovoLog (insulin aspart recombinant)
Noxafil (posaconazole)

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O
Olanzapine
Olanzapine/fluoxetineThis drug has as active FDA Safety Alert
Olmesartan medoxomil
Omacor (omega-3-acid ethyl esters)
OmalizumabThis drug has as active FDA Safety Alert
Omega-3-acid ethyl esters
Omnaris (cirlesonide)
OmniscanThis drug has as active FDA Safety Alert (gadodiamide)
OptiMARK (gadoversetamide)
Optison (perflutren protein-type A microspheres)
Orencia (abatacept)
Orfadin (nitisinone)
Orlistat
Ortho Evra (norelgestromin; ethinyl estradiol)
Oseltamivir phosphate
OsmoprepThis drug has as active FDA Safety Alert (sodium phosphate)
Oxaliplatin
OxcarbazepineThis drug has as active FDA Safety Alert


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P
PaceroneThis drug has as active FDA Safety Alert (amiodarone)
Palifermin
Paliperidone
PamidronateThis drug has as active FDA Safety Alert
Panitumumab
Panretin Gel (alitretinoin)
Pantoprazole
Paricalcitol
ParoxetineThis drug has as active FDA Safety Alert
PaxilThis drug has as active FDA Safety Alert (paroxetine)
Pegaptanib
Pegvisomant

Pemetrexed
PemolineThis drug has as active FDA Safety Alert
Pentobarbital and carbromal
Perflutren lipid microspheres
PerindoprilThis drug has as active FDA Safety Alert
PhenerganThis drug has as active FDA Safety Alert (promethazine)
Pimecrolimus

PioglitazoneThis drug has as active FDA Safety Alert
Placidyl (ethchlorvynol)
Plan B (levonorgestrel)
Pletal (cilostazol)