NEXIUM Side Effects

7022047-1 | Renal Failure Acute
on Sep 21, 2010 Female patient from UNITED STATES , 56 years of age, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure acute. Nexium dosage: .

7022046-X |
Patient was taking Nexium (View Usage). on Sep 21, 2010 from NETHERLANDS Additional patient health information: Female patient , 37 years of age, . Nexium dosage: . During the same period patient was treated with XANAX (View Xanax Review and Xanax Label ), PAROXETINE HYDROCHLORIDE (0.5 Water) (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ).

7020848-7 | Cholecystectomy, Diarrhoea, Gastritis, Haematochezia, Muscle Spasms, Oesophageal Dilatation, Vomiting
Adverse event was reported on Sep 20, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 52 years of age, weighting 162.0 lb, After Nexium was administered, patient had the following side effects: cholecystectomy, diarrhoea, gastritis, haematochezia, muscle spasms, oesophageal dilatation, vomiting. During the same period patient was treated with KEPPRA (View Keppra Review and Keppra Label ), KLONOPIN (View Klonopin Review and Klonopin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), INDICET (View Indicet Review and Indicet Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), PATANOL (View Patanol Review and Patanol Label ). Patient was hospitalized.

7020771-8 | Gastrooesophageal Reflux Disease, Haemoptysis
on Sep 20, 2010 Female patient from UNITED STATES , 42 years of age, was diagnosed with ulcer (What is ulcer?) and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: gastrooesophageal reflux disease, haemoptysis. Nexium dosage: . During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ).


7020444-1 | Toxic Skin Eruption
on Sep 20, 2010 Female patient from FRANCE , 89 years of age, was treated with Nexium (View Usage). Patient had the following side effects: toxic skin eruption. Nexium dosage: . During the same period patient was treated with PERFALGAN (View Perfalgan Review and Perfalgan Label ), FLAGYL (View Flagyl Review and Flagyl Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), LASIX (View Lasix Review and Lasix Label ).

7020096-0 | Body Temperature Increased, Dermatitis, Hypotension, Pain
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: body temperature increased, dermatitis, hypotension, pain (What is pain?) on Sep 20, 2010 from SOUTH AFRICA Additional patient health information: Female patient , 22 years of age, was diagnosed with oesophagitis, stress (What is stress?), contraception and. Nexium dosage: . During the same period patient was treated with MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), RESCUE (View Rescue Review and Rescue Label ), YASMIN (View Yasmin Review and Yasmin Label ). Patient was hospitalized.

7018846-2 | Agitation, Apathy, Apnoea, Arrhythmia, Barrett's Oesophagus, Blood Pressure Fluctuation, Change Of Bowel Habit, Confusional State, Deafness
Adverse event was reported on Sep 16, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with type 2 diabetes mellitus and. Location: UNITED STATES , 53 years of age, Patient experienced the following unwanted or unexpected effects: agitation, apathy, apnoea, arrhythmia (What is arrhythmia?), barrett's oesophagus, blood pressure fluctuation, change of bowel habit, confusional state, deafness. During the same period patient was treated with PRILOSEC (Daily) (View Prilosec Review and Prilosec Label ), NORVASC (View Norvasc Review and Norvasc Label ), JANUVIA (View Januvia Review and Januvia Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), BENICAR (View Benicar Review and Benicar Label ), GLIMEPIRIDE (View Glimepiride Review and Glimepiride Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ). Patient was hospitalized.

7015208-9 | Bronchopneumonia, Cardio-respiratory Arrest, Depression, Dizziness, Dry Mouth, Fibromyalgia, Insomnia, Intervertebral Disc Protrusion, Nausea
on Sep 17, 2010 Female patient from BRAZIL , 54 years of age, weighting 172.0 lb, was diagnosed with gastritis erosive, depression (What is depression?), insomnia, fibromyalgia, hypothyroidism, intervertebral disc protrusion and was treated with Nexium (View Usage). Patient had the following side effects: bronchopneumonia, cardio-respiratory arrest, depression (What is depression?), dizziness (What is dizziness?), dry mouth, fibromyalgia, insomnia, intervertebral disc protrusion, nausea (What is nausea?). Nexium dosage: . During the same period patient was treated with SEROQUEL (View Seroquel Review and Seroquel Label ), LYRICA (View Lyrica Review and Lyrica Label ), PURAN T4 (View Puran T4 Review and Puran T4 Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), PROFENID (View Profenid Review and Profenid Label ), APRAZ (View Apraz Review and Apraz Label ), MORPHINE (View Morphine Review and Morphine Label ). Patient was hospitalized.

7015081-9 | Arthritis, Breast Cancer, Bronchitis, Lung Neoplasm Malignant, Menstrual Disorder, Osteoporosis, Sleep Disorder
on Sep 23, 2010 Female patient from UNITED STATES , 63 years of age, weighting 132.1 lb, was diagnosed with gastrooesophageal reflux disease, myasthenia gravis, pain (What is pain?) and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: arthritis (What is arthritis?), breast cancer (What is breast cancer?), bronchitis (What is bronchitis?), lung neoplasm malignant, menstrual disorder, osteoporosis (What is osteoporosis?), sleep disorder (What is sleep disorder?). Nexium dosage: . During the same period patient was treated with PRILOSEC (Daily) (View Prilosec Review and Prilosec Label ), PULMICORT RESPULES (View Pulmicort Respules Review and Pulmicort Respules Label ), MESTINON (View Mestinon Review and Mestinon Label ), ACTONEL (35 Mg Daily, Dose Frequency Week) (View Actonel Review and Actonel Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), LIDODERM (Daily) (View Lidoderm Review and Lidoderm Label ).

7012595-2 | Hernia Hiatus Repair, Rheumatoid Arthritis
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: hernia hiatus repair, rheumatoid arthritis (What is rheumatoid arthritis?) on Sep 15, 2010 from UNITED STATES Additional patient health information: Male patient , 43 years of age, . Nexium dosage: . During the same period patient was treated with HUMIRA (View Humira Review and Humira Label ). Patient was hospitalized.

7011855-9 | Blister, Diverticulitis, Loss Of Consciousness, Skin Exfoliation
Adverse event was reported on Sep 14, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease, hypertension and. Location: UNITED STATES , 75 years of age, weighting 179.9 lb, Patient had the following side effects: blister, diverticulitis, loss of consciousness, skin exfoliation. During the same period patient was treated with ALENDRONATE SODIUM (View Alendronate Sodium Review and Alendronate Sodium Label ), CADUET (10/20 Daily) (View Caduet Review and Caduet Label ), LISINOPRIL (Bid) (View Lisinopril Review and Lisinopril Label ), FEXOFENADINE HCL (Daily) (View Fexofenadine Hcl Review and Fexofenadine Hcl Label ), VITAMINS (View Vitamins Review and Vitamins Label ). Patient was hospitalized.

7010817-5 | Atrial Fibrillation, Cardiac Disorder, Laboratory Test Interference, Malabsorption, Mobility Decreased, Spinal Compression Fracture
on Sep 23, 2010 Female patient from UNITED STATES , 90 years of age, weighting 175.0 lb, was diagnosed with duodenal ulcer, spinal compression fracture and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), cardiac disorder, laboratory test interference, malabsorption, mobility decreased, spinal compression fracture. Nexium dosage: . During the same period patient was treated with DARVOCET N 100 (View Darvocet-n 100 Review and Darvocet-n 100 Label ). Patient was hospitalized.

7007348-5 | Cytolytic Hepatitis
on Sep 13, 2010 Female patient from FRANCE , 27 years of age, was diagnosed with acinetobacter test positive, pulmonary embolism (What is pulmonary embolism?) and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: cytolytic hepatitis. Nexium dosage: . During the same period patient was treated with CEFTAZIDIME (View Ceftazidime Review and Ceftazidime Label ), PREVISCAN (View Previscan Review and Previscan Label ). Patient was hospitalized.

7001485-7 | Shock
Patient was taking Nexium (View Usage). Patient had the following side effects: shock on Sep 14, 2010 from CHINA Additional patient health information: Male patient , 60 years of age, was diagnosed with stress ulcer and. Nexium dosage: .

7000626-5 | Cough, Dyspnoea, Increased Upper Airway Secretion
Adverse event was reported on Sep 10, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 64 years of age, After Nexium was administered, patient had the following side effects: cough, dyspnoea, increased upper airway secretion. Patient was hospitalized.

6999086-X | Barrett's Oesophagus, Gastrooesophageal Reflux Disease, Myalgia, Nasal Operation, Neck Pain, Pain In Extremity, Periarthritis, Pharyngeal Erythema
on Sep 09, 2010 Male patient from UNITED STATES , 65 years of age, weighting 151.9 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: barrett's oesophagus, gastrooesophageal reflux disease, myalgia, nasal operation, neck pain, pain in extremity, periarthritis, pharyngeal erythema. Nexium dosage: .

6992367-5 | Nephrolithiasis
on Sep 08, 2010 Male patient from UNITED STATES , 70 years of age, weighting 220.0 lb, was diagnosed with gastric ulcer and was treated with Nexium (View Usage). Patient had the following side effects: nephrolithiasis. Nexium dosage: .

6992274-8 | Capsule Issue, Condition Aggravated, Dyspepsia
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: capsule issue, condition aggravated, dyspepsia on Sep 14, 2010 from UNITED STATES Additional patient health information: Female patient , 69 years of age, weighting 150.0 lb, was diagnosed with gastrooesophageal reflux disease and. Nexium dosage: 1 Capsule Twice Daily, At Least 2 Years. During the same period patient was treated with CELEBREX (View Celebrex Review and Celebrex Label ), SINGULAIR (View Singulair Review and Singulair Label ), CRESTOR (View Crestor Review and Crestor Label ), ALENDRONATE SODIUM (View Alendronate Sodium Review and Alendronate Sodium Label ), XOPENEX HFA (View Xopenex Hfa Review and Xopenex Hfa Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ).

6992232-3 | Gastritis, Peptic Ulcer, Precancerous Mucosal Lesion
Adverse event was reported on Sep 08, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) . Location: UNITED STATES , 61 years of age, Patient experienced the following unwanted or unexpected effects: gastritis, peptic ulcer (What is peptic ulcer?), precancerous mucosal lesion.

6987782-X | Asthenia, Decreased Appetite, Headache, Pancreatitis Acute
on Aug 30, 2010 Male patient from FRANCE , 58 years of age, was diagnosed with type 1 diabetes mellitus and was treated with Nexium (View Usage). Patient had the following side effects: asthenia, decreased appetite, headache (What is headache?), pancreatitis acute. Nexium dosage: 40 Mg Daily Oral. During the same period patient was treated with PROPRANOLOL (40 Mg Bid Oral) (View Propranolol Review and Propranolol Label ), CRESTOR (10 Mg Daily Oral) (View Crestor Review and Crestor Label ), TOPIRAMATE (50 Mg Bid Oral) (View Topiramate Review and Topiramate Label ), ESCITALOPRAM (20 Mg Daily Oral) (View Escitalopram Review and Escitalopram Label ), CREON (12000 Iu Oral) (View Creon Review and Creon Label ), DOGMATIL (SULPIRIDE) (50 Mg Bid Oral) (View Dogmatil (sulpiride) Review and Dogmatil (sulpiride) Label ), ACETAMINOPHEN (1 G Tid Oral) (View Acetaminophen Review and Acetaminophen Label ), HUMALOG (32 Iu Bid Subcutaneous) (View Humalog Review and Humalog Label ). Patient was hospitalized.

6987752-1 | Abdominal Discomfort, Abdominal Pain, Blepharitis, Burning Sensation, Chest Discomfort, Chest Pain, Choking, Colitis, Cough
on Sep 07, 2010 Female patient from UNITED STATES , 71 years of age, weighting 130.1 lb, was diagnosed with gastrooesophageal reflux disease, non-cardiac chest pain and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: abdominal discomfort, abdominal pain (What is abdominal pain?), blepharitis, burning sensation, chest discomfort, chest pain (What is chest pain?), choking (What is choking?), colitis, cough. Nexium dosage: . Patient was hospitalized.

6987745-4 | Radius Fracture
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: radius fracture on Sep 07, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 244.9 lb, was diagnosed with prophylaxis against gastrointestinal ulcer, osteoarthritis (What is osteoarthritis?), rheumatoid arthritis (What is rheumatoid arthritis?) and. Nexium dosage: . During the same period patient was treated with CELECOXIB (Three Times A Day) (View Celecoxib Review and Celecoxib Label ), IBUPROFEN (Three Times A Day) (View Ibuprofen Review and Ibuprofen Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), TRAMADOL HYDROCHLORIDE (View Tramadol Hydrochloride Review and Tramadol Hydrochloride Label ), OMEGA 3 TRIGLYCERIDES (View Omega-3 Triglycerides Review and Omega-3 Triglycerides Label ).

6985678-0 | Cytolytic Hepatitis
Adverse event was reported on Sep 06, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) . Location: FRANCE , 76 years of age, Patient had the following side effects: cytolytic hepatitis. During the same period patient was treated with ZOLEDRONIC (View Zoledronic Review and Zoledronic Label ), TOPALGIC (View Topalgic Review and Topalgic Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), DOLIPRANE (View Doliprane Review and Doliprane Label ), TANGANIL (View Tanganil Review and Tanganil Label ), AVLOCARDYL (View Avlocardyl Review and Avlocardyl Label ), METFORMIN (View Metformin Review and Metformin Label ), EZETROL (View Ezetrol Review and Ezetrol Label ). Patient was hospitalized.

6978315-2 | Amnesia, Anxiety, Cerebrovascular Accident, Convulsion
on Sep 01, 2010 Female patient from UNITED STATES , 63 years of age, was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: amnesia, anxiety (What is anxiety?), cerebrovascular accident, convulsion. Nexium dosage: . Patient was hospitalized.

6976338-0 | Abdominal Pain Upper, Abscess, Arthropod Bite, Dysphagia, Infection, Lymphoedema
on Sep 01, 2010 Female patient from UNITED STATES , 56 years of age, was diagnosed with hiatus hernia, anxiety (What is anxiety?), pain (What is pain?), insomnia and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, abscess (What is abscess?), arthropod bite, dysphagia, infection (What is infection?), lymphoedema. Nexium dosage: . During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ), ACIDOPHILUS (View Acidophilus Review and Acidophilus Label ), NORCO (10/325 Mg Daily) (View Norco Review and Norco Label ), PRE NATAL VITAMINS (View Pre-natal Vitamins Review and Pre-natal Vitamins Label ), TRAZODONE HCL (View Trazodone Hcl Review and Trazodone Hcl Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ). Patient was hospitalized.

6975780-1 | Abdominal Pain Upper, Burning Sensation, Cardiac Operation, Dyspepsia, Gastrointestinal Sounds Abnormal, Gastrooesophageal Reflux Disease, Hiccups
Patient was taking Nexium (View Usage). Patient had the following side effects: abdominal pain upper, burning sensation, cardiac operation, dyspepsia, gastrointestinal sounds abnormal, gastrooesophageal reflux disease, hiccups on Aug 31, 2010 from UNITED STATES Additional patient health information: Female patient , 76 years of age, weighting 160.1 lb, was diagnosed with gastrooesophageal reflux disease and. Nexium dosage: . During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ).

6973215-6 | Gastrooesophageal Reflux Disease, Myocardial Infarction
Adverse event was reported on Aug 31, 2010 by a Male patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 89 years of age, After Nexium was administered, patient had the following side effects: gastrooesophageal reflux disease, myocardial infarction. Patient was hospitalized.

6971938-6 | Burning Sensation
on Sep 08, 2010 Female patient from UNITED STATES , 40 years of age, weighting 175.0 lb, was diagnosed with ulcer (What is ulcer?) and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: burning sensation. Nexium dosage: 40mg Bid Po.

6970411-9 | Arthralgia, Gait Disturbance, Muscular Weakness, Myocardial Infarction, Tendon Pain, Weight Decreased
on Aug 30, 2010 Female patient from UNITED STATES , 87 years of age, weighting 89.95 lb, was diagnosed with gastrooesophageal reflux disease, gout (What is gout?) and was treated with Nexium (View Usage). Patient had the following side effects: arthralgia, gait disturbance, muscular weakness, myocardial infarction, tendon pain, weight decreased. Nexium dosage: . During the same period patient was treated with ENTOCORT EC (View Entocort Ec Review and Entocort Ec Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), CARAFATE (View Carafate Review and Carafate Label ).

6970063-8 | Mixed Liver Injury
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: mixed liver injury on Aug 30, 2010 from FRANCE Additional patient health information: Male patient , 49 years of age, . Nexium dosage: . During the same period patient was treated with CIPROFLOXACINE MERCK (View Ciprofloxacine Merck Review and Ciprofloxacine Merck Label ), PIPERACILLINE TAZOBACTAM MYLAN (4g/500mg, 12g, 4g Three Times A Day) (View Piperacilline Tazobactam Mylan Review and Piperacilline Tazobactam Mylan Label ). Patient was hospitalized.

6968953-5 | Myocardial Infarction, Pneumonia, Weight Increased
Adverse event was reported on Aug 27, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 47 years of age, weighting 160.9 lb, Patient experienced the following unwanted or unexpected effects: myocardial infarction, pneumonia (What is pneumonia?), weight increased.

6967509-8 | Fall, Urticaria
on Aug 26, 2010 Female patient from CANADA , 78 years of age, was diagnosed with abdominal pain upper, neuralgia, hypertension, memory impairment, anxiety (What is anxiety?), urticaria and was treated with Nexium (View Usage). Patient had the following side effects: fall (What is fall?), urticaria. Nexium dosage: 40 Mg Daily Am. During the same period patient was treated with TRAMADOL HCL (4x Daily) (View Tramadol Hcl Review and Tramadol Hcl Label ), GABAPENTIN (300 Mg Pm) (View Gabapentin Review and Gabapentin Label ), DIOVAN (80 Mg Am) (View Diovan Review and Diovan Label ), LYRICA (View Lyrica Review and Lyrica Label ), CLONAZEPAM (0.5 Mg Pm) (View Clonazepam Review and Clonazepam Label ), HYDROCORTISONE (Prn Every 4 Hours) (View Hydrocortisone Review and Hydrocortisone Label ), NOVOGESIC FORTE (Prn Every 4-6 Hrs) (View Novogesic Forte Review and Novogesic Forte Label ). Patient was hospitalized.

6965785-9 | Abdominal Adhesions, Ileus
on Aug 25, 2010 Female patient from UNITED STATES , 60 years of age, weighting 175.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: abdominal adhesions, ileus. Nexium dosage: . During the same period patient was treated with SUCRALFATE (View Sucralfate Review and Sucralfate Label ), MAGOX (View Magox Review and Magox Label ), NA BICOARB (View Na Bicoarb Review and Na Bicoarb Label ), LOMOTIL (View Lomotil Review and Lomotil Label ), LOPERAMIDE (View Loperamide Review and Loperamide Label ), HYDROXYZINE HCL (View Hydroxyzine Hcl Review and Hydroxyzine Hcl Label ), POTASSIUM (View Potassium Review and Potassium Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6960507-X | Bladder Cancer, Breast Cancer, Cough, Dyspepsia
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: bladder cancer (What is bladder cancer?), breast cancer (What is breast cancer?), cough, dyspepsia on Aug 23, 2010 from UNITED STATES Additional patient health information: Female patient , 82 years of age, weighting 149.9 lb, was diagnosed with gastrooesophageal reflux disease, barrett's oesophagus, breast cancer (What is breast cancer?) and. Nexium dosage: . During the same period patient was treated with ARIMIDEX (View Arimidex Review and Arimidex Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), AMARYL (View Amaryl Review and Amaryl Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), MIACALCIN (View Miacalcin Review and Miacalcin Label ).

6960160-5 | Toxic Skin Eruption
Adverse event was reported on Aug 23, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: FRANCE , weighting 198.4 lb, Patient had the following side effects: toxic skin eruption. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), SECTRAL (View Sectral Review and Sectral Label ), LOVENOX (View Lovenox Review and Lovenox Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), PRETERAX (View Preterax Review and Preterax Label ). Patient was hospitalized.

6956582-9 | Catheterisation Cardiac, Malaise
on Aug 19, 2010 Male patient from UNITED STATES , 64 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: catheterisation cardiac, malaise. Nexium dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), COQ ENZYME (View Coq Enzyme Review and Coq Enzyme Label ), LOTRIL (View Lotril Review and Lotril Label ), LOVAZA (View Lovaza Review and Lovaza Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), GLUCOSAMIDE CHONDROITIN (View Glucosamide Chondroitin Review and Glucosamide Chondroitin Label ), ZOCOR (View Zocor Review and Zocor Label ), PLAVIX (View Plavix Review and Plavix Label ).

6956099-1 | Abdominal Pain Upper, Cardiac Operation, Dyspepsia, Gastrointestinal Sounds Abnormal, Hiccups, Malaise, Vomiting
on Aug 19, 2010 Female patient from UNITED STATES , 76 years of age, weighting 160.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, cardiac operation, dyspepsia, gastrointestinal sounds abnormal, hiccups, malaise, vomiting. Nexium dosage: . During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ).

6954788-6 | No Adverse Event
Patient was taking Nexium (View Usage). Patient had the following side effects: no adverse event on Aug 18, 2010 from UNITED STATES Additional patient health information: Female patient , 68 years of age, weighting 172.0 lb, was diagnosed with gastrooesophageal reflux disease, gastritis and. Nexium dosage: . During the same period patient was treated with GLYBURIDE (View Glyburide Review and Glyburide Label ), LANTUS (View Lantus Review and Lantus Label ), JANUVIA (View Januvia Review and Januvia Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ).

6945453-X | Cerebrovascular Accident, Depression, Hyperchlorhydria, Myocardial Infarction, Vomiting
Adverse event was reported on Aug 19, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease, bladder disorder and. Location: UNITED STATES , 60 years of age, After Nexium was administered, patient had the following side effects: cerebrovascular accident, depression (What is depression?), hyperchlorhydria, myocardial infarction, vomiting. During the same period patient was treated with TOVAZ (View Tovaz Review and Tovaz Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6942068-4 | Arthralgia, Pneumonia, Tendonitis
on Aug 19, 2010 Male patient from UNITED STATES , 78 years of age, was diagnosed with gastrooesophageal reflux disease, chronic obstructive pulmonary disease and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, pneumonia (What is pneumonia?), tendonitis. Nexium dosage: . During the same period patient was treated with SYMBICORT (640 Mcg Bid) (View Symbicort Review and Symbicort Label ). Patient was hospitalized.

6940370-3 | Abdominal Pain Upper, Atrial Fibrillation, Back Pain, Blood Urine Present, Chest Pain, Chromaturia, Cystitis, Headache, Hepatic Enzyme Increased
on Aug 16, 2010 Female patient from UNITED STATES , 74 years of age, was diagnosed with ulcer (What is ulcer?), hypercholesterolaemia and was treated with Nexium (View Usage). Patient had the following side effects: abdominal pain upper, atrial fibrillation (What is atrial fibrillation?), back pain (What is back pain?), blood urine present, chest pain (What is chest pain?), chromaturia, cystitis, headache (What is headache?), hepatic enzyme increased. Nexium dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

6940254-0 | Amenorrhoea, Liver Injury
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: amenorrhoea, liver injury on Aug 17, 2010 from UNITED STATES Additional patient health information: Female patient , 22 years of age, . Nexium dosage: . During the same period patient was treated with REBIF (44 Mcg, Three In One Week) (View Rebif Review and Rebif Label ), DEXILANT (View Dexilant Review and Dexilant Label ), CARAFATE (View Carafate Review and Carafate Label ), CIPRO (View Cipro Review and Cipro Label ), SINGULAIR (View Singulair Review and Singulair Label ).

6937554-7 | Anaphylactic Reaction, Shock
Adverse event was reported on Aug 23, 2010 by a Male patient taking Nexium (View Usage) (Dosage: 40 Mg Delayed Release 1 Daily Po) was diagnosed with dyspepsia, oesophageal discomfort and. Location: UNITED STATES , weighting 185.0 lb, Patient experienced the following unwanted or unexpected effects: anaphylactic reaction, shock.

6936402-9 | Convulsion, Gastrooesophageal Reflux Disease
on Aug 13, 2010 Female patient from UNITED STATES , 56 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). Patient had the following side effects: convulsion, gastrooesophageal reflux disease. Nexium dosage: . During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ). Patient was hospitalized.

6933651-0 | Muscle Contractions Involuntary, Muscular Weakness, Myalgia
on Aug 11, 2010 Male patient from FRANCE , 39 years of age, was diagnosed with gastrooesophageal reflux disease, migraine (What is migraine?) and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: muscle contractions involuntary, muscular weakness, myalgia. Nexium dosage: . During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), NOCERTONE (View Nocertone Review and Nocertone Label ).

6932253-X | Epilepsy
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: epilepsy (What is epilepsy?) on Aug 11, 2010 from SWITZERLAND Additional patient health information: Female patient , 51 years of age, was diagnosed with gastritis, epilepsy (What is epilepsy?), hypercholesterolaemia and. Nexium dosage: . During the same period patient was treated with TEGRETOL (200 Mg In The Morning And 400 Mg In The Evening) (View Tegretol Review and Tegretol Label ), SORTIS (20) (View Sortis Review and Sortis Label ).

6930809-1 | Hepatitis Fulminant
Adverse event was reported on Aug 09, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with renal abscess and. Location: FRANCE , 56 years of age, Patient had the following side effects: hepatitis fulminant. During the same period patient was treated with CEFTRIAXONE PANPHARMA (View Ceftriaxone Panpharma Review and Ceftriaxone Panpharma Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), SEROPLEX (View Seroplex Review and Seroplex Label ), LEXOMIL (View Lexomil Review and Lexomil Label ), EQUANIL (View Equanil Review and Equanil Label ), HAVLANE (View Havlane Review and Havlane Label ), ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ).

6928158-0 | Enterocolitis Haemorrhagic, International Normalised Ratio Increased, Petechiae
on Aug 12, 2010 Male patient from SWITZERLAND , 72 years of age, was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: enterocolitis haemorrhagic, international normalised ratio increased, petechiae. Nexium dosage: . During the same period patient was treated with SINTROM (View Sintrom Review and Sintrom Label ), DEPAKENE (View Depakene Review and Depakene Label ), PLAVIX (View Plavix Review and Plavix Label ), CIPROFLOXACIN (View Ciprofloxacin Review and Ciprofloxacin Label ), IMIPENEM AND CILASTATIN (View Imipenem And Cilastatin Review and Imipenem And Cilastatin Label ), SORTIS (View Sortis Review and Sortis Label ), FLUANXOL (View Fluanxol Review and Fluanxol Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ).

6926199-0 | Amnesia, Anger
on Aug 13, 2010 Male patient from UNITED STATES , 56 years of age, weighting 238.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: amnesia, anger. Nexium dosage: 40 M Night Before Bed Po.

6923033-X | Abdominal Pain Upper, Hypoaesthesia, Paraesthesia, Quality Of Life Decreased, Suicidal Ideation, Vomiting, Weight Increased
Patient was taking Nexium (View Usage). Patient had the following side effects: abdominal pain upper, hypoaesthesia, paraesthesia, quality of life decreased, suicidal ideation, vomiting, weight increased on Aug 04, 2010 from UNITED STATES Additional patient health information: Female patient , 56 years of age, was diagnosed with nausea (What is nausea?) and. Nexium dosage: . During the same period patient was treated with FISH OIL PILLS (View Fish Oil Pills Review and Fish Oil Pills Label ), MULTI VIT (View Multi Vit Review and Multi Vit Label ), ESTROGEN PATCH (View Estrogen Patch Review and Estrogen Patch Label ).