NEXIUM Side Effects

6918527-7 | Haemorrhagic Anaemia
on Aug 02, 2010 Female patient from FRANCE , weighting 326.3 lb, was diagnosed with agitation and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: haemorrhagic anaemia. Nexium dosage: . During the same period patient was treated with TENORMIN (View Tenormin Review and Tenormin Label ), CIPRALAN (View Cipralan Review and Cipralan Label ). Patient was hospitalized.

6915906-9 | Bone Marrow Failure, Cardio-respiratory Arrest, Cytomegalovirus Test Positive, Haemophilus Infection, Lung Disorder, Sepsis, Staphylococcus Test Positive
Patient was taking Nexium (View Usage). Patient had the following side effects: bone marrow failure, cardio-respiratory arrest, cytomegalovirus test positive, haemophilus infection, lung disorder, sepsis (What is sepsis?), staphylococcus test positive on Aug 05, 2010 from FRANCE Additional patient health information: Male patient , 58 years of age, . Nexium dosage: . During the same period patient was treated with VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), CANCIDAS (View Cancidas Review and Cancidas Label ), PERFALGAN (View Perfalgan Review and Perfalgan Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), PIPERACILLIN AND TAZOBACTAM (View Piperacillin And Tazobactam Review and Piperacillin And Tazobactam Label ), ZOVIRAX (View Zovirax Review and Zovirax Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ), TEGELINE LFB (View Tegeline Lfb Review and Tegeline Lfb Label ). Patient was hospitalized.

6915903-3 | Ammonia Increased, Dizziness, Dyspepsia, Eructation, Flatulence
Adverse event was reported on Aug 02, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 68 years of age, weighting 172.0 lb, After Nexium was administered, patient had the following side effects: ammonia increased, dizziness (What is dizziness?), dyspepsia, eructation, flatulence. 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 HYDROCHLORIDE (View Tramadol Hydrochloride Review and Tramadol Hydrochloride Label ). Patient was hospitalized.

6914505-2 | Atrioventricular Block Second Degree, Cough, Extrasystoles, Presyncope
on Jul 30, 2010 Female patient from UNITED STATES , 61 years of age, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: atrioventricular block second degree, cough, extrasystoles, presyncope. Nexium dosage: . During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), CARDIA (View Cardia Review and Cardia Label ), DILTIAZEM (View Diltiazem Review and Diltiazem Label ), ALLEGRA (View Allegra Review and Allegra Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ), NORVASC (View Norvasc Review and Norvasc Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ). Patient was hospitalized.


6914388-0 | Abdominal Distension, Alopecia, Amnesia, Confusional State, Constipation, Panic Reaction, Product Quality Issue
on Aug 05, 2010 Female patient from UNITED STATES , weighting 120.0 lb, was diagnosed with cholecystectomy, irritable bowel syndrome (What is irritable bowel syndrome?) and was treated with Nexium (View Usage). Patient had the following side effects: abdominal distension, alopecia, amnesia, confusional state, constipation (What is constipation?), panic reaction, product quality issue. Nexium dosage: 1/day Daily.

6914380-6 | Leukaemia
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: leukaemia on Aug 04, 2010 from BULGARIA Additional patient health information: Male patient , 65 years of age, was diagnosed with gastric ulcer and. Nexium dosage: . During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6913721-3 | Chills, Dehydration, Dyspepsia, Fibromyalgia, Headache, Syncope
Adverse event was reported on Jul 30, 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 123.0 lb, Patient experienced the following unwanted or unexpected effects: chills, dehydration, dyspepsia, fibromyalgia, headache (What is headache?), syncope. During the same period patient was treated with EVISTA (View Evista Review and Evista Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), XANAX (View Xanax Review and Xanax Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ).

6910393-9 | Cerebral Ischaemia
on Jul 28, 2010 Male patient from BRAZIL , 54 years of age, weighting 187.4 lb, was diagnosed with gastritis and was treated with Nexium (View Usage). Patient had the following side effects: cerebral ischaemia. Nexium dosage: . Patient was hospitalized.

6906280-2 | Abdominal Pain Lower, Ankle Fracture, Nausea, Vitamin D Decreased
on Jul 26, 2010 Female patient from UNITED STATES , 72 years of age, was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: abdominal pain lower, ankle fracture, nausea (What is nausea?), vitamin d decreased. Nexium dosage: . During the same period patient was treated with CALTRATE (View Caltrate Review and Caltrate Label ).

6906105-5 | Neutropenia, Thrombocytopenia
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: neutropenia, thrombocytopenia on Jul 27, 2010 from FRANCE Additional patient health information: Male patient , 61 years of age, . Nexium dosage: .

6905501-X | Dyskinesia
Adverse event was reported on Jul 29, 2010 by a Male patient taking Nexium (View Usage) (Dosage: ) . Location: UNITED STATES , 32 years of age, Patient had the following side effects: dyskinesia. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ).

6905379-4 | Tinnitus
on Jul 26, 2010 Male patient from IRELAND , 43 years of age, was diagnosed with dyspepsia, gastrooesophageal reflux disease and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: tinnitus (What is tinnitus?). Nexium dosage: . During the same period patient was treated with DIAZEPAM (Rarely Needed, Rarely Take) (View Diazepam Review and Diazepam Label ).

6894601-9 | Colitis Collagenous, Weight Decreased
on Jul 22, 2010 Female patient from FRANCE , 82 years of age, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: colitis collagenous, weight decreased. Nexium dosage: . During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), KREDEX (View Kredex Review and Kredex Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), IMOVANE (View Imovane Review and Imovane Label ), XANAX (Until Two Per Day) (View Xanax Review and Xanax Label ).

6886977-3 | Myocardial Infarction
Patient was taking Nexium (View Usage). Patient had the following side effects: myocardial infarction on Jul 26, 2010 from FRANCE Additional patient health information: Male patient , 81 years of age, . Nexium dosage: . During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), CORVASAL (View Corvasal Review and Corvasal Label ), TEMERIT (View Temerit Review and Temerit Label ), LERCAN (View Lercan Review and Lercan Label ), XATRAL (View Xatral Review and Xatral Label ), TOPALGIC (View Topalgic Review and Topalgic Label ), EQUANIL (View Equanil Review and Equanil Label ).

6882139-4 | Myositis
Adverse event was reported on Jul 20, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) . Location: AUSTRALIA , 47 years of age, After Nexium was administered, patient had the following side effects: myositis (What is myositis?). During the same period patient was treated with AMOXICILLIN TRIHYDRATE (View Amoxicillin Trihydrate Review and Amoxicillin Trihydrate Label ), CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label ), AMOXICILLIN SODIUM (View Amoxicillin Sodium Review and Amoxicillin Sodium Label ). Patient was hospitalized.

6880228-1 | Constipation, Hypotension, Oesophageal Haemorrhage, Somnolence
on Jul 19, 2010 Female patient from UNITED STATES , weighting 126.1 lb, was diagnosed with gastrooesophageal reflux disease, constipation (What is constipation?) and was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: constipation (What is constipation?), hypotension, oesophageal haemorrhage, somnolence. Nexium dosage: . During the same period patient was treated with ARICEPT (View Aricept Review and Aricept Label ), NAMENDA (View Namenda Review and Namenda Label ), GAS X (View Gas-x Review and Gas-x Label ), BOWEL SOFTENER (View Bowel Softener Review and Bowel Softener Label ), LACTULOSE (View Lactulose Review and Lactulose Label ). Patient was hospitalized.

6879855-7 | Cholelithiasis, Hernia Repair, Hysterectomy, Lung Lobectomy, Lung Neoplasm Malignant
on Jul 21, 2010 Female patient from UNITED STATES , 65 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). Patient had the following side effects: cholelithiasis, hernia repair, hysterectomy (What is hysterectomy?), lung lobectomy, lung neoplasm malignant. Nexium dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), PLAVIX (View Plavix Review and Plavix Label ), IMDUR (View Imdur Review and Imdur Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PAXIL (View Paxil Review and Paxil Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ). Patient was hospitalized.

6879796-5 | Blood Creatinine Increased, Condition Aggravated, Dialysis, Nausea, Tubulointerstitial Nephritis
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: blood creatinine increased, condition aggravated, dialysis (What is dialysis?), nausea (What is nausea?), tubulointerstitial nephritis on Jul 19, 2010 from CANADA Additional patient health information: Male patient , 34 years of age, weighting 136.7 lb, . Nexium dosage: . Patient was hospitalized.

6879556-5 | Abasia, Abdominal Pain Upper, Alopecia, Arthritis, Asthenia, Carpal Tunnel Syndrome, Dizziness, Eye Pain, Gait Disturbance
Adverse event was reported on Jul 19, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) . Location: CANADA , 59 years of age, Patient experienced the following unwanted or unexpected effects: abasia, abdominal pain upper, alopecia, arthritis (What is arthritis?), asthenia, carpal tunnel syndrome (What is carpal tunnel syndrome?), dizziness (What is dizziness?), eye pain, gait disturbance. During the same period patient was treated with DIFLUNISAL (View Diflunisal Review and Diflunisal Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREDNISONE (View Prednisone Review and Prednisone Label ).

6879530-9 | Limb Discomfort, Oedema Peripheral, Pain In Extremity, Renal Impairment
on Jul 19, 2010 Female patient from CANADA , 59 years of age, was treated with Nexium (View Usage). Patient had the following side effects: limb discomfort, oedema peripheral, pain in extremity, renal impairment. Nexium dosage: . Patient was hospitalized.

6879529-2 | Activities Of Daily Living Impaired, Asthenia, Dyspnoea, Feeding Disorder, Hepatitis, Myalgia, Ocular Icterus, Vision Blurred, Weight Decreased
on Jul 19, 2010 Male patient from CANADA , 78 years of age, weighting 225.1 lb, was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: activities of daily living impaired, asthenia, dyspnoea, feeding disorder, hepatitis (What is hepatitis?), myalgia, ocular icterus, vision blurred, weight decreased. Nexium dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), APO PREDNISONE (View Apo Prednisone Review and Apo Prednisone Label ), APO AMOXI CLAV (875/125) (View Apo-amoxi Clav Review and Apo-amoxi Clav Label ), ATIVAN (View Ativan Review and Ativan Label ), CELEBREX (View Celebrex Review and Celebrex Label ), RATIO EMTEC 30 (View Ratio-emtec-30 Review and Ratio-emtec-30 Label ), RATIO SALBUTAMOL HFA (View Ratio-salbutamol Hfa Review and Ratio-salbutamol Hfa Label ).

6878048-7 | Back Pain, Eye Haemorrhage
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), eye haemorrhage on Jul 19, 2010 from CANADA Additional patient health information: Female patient , 40 years of age, weighting 157.0 lb, . Nexium dosage: . During the same period patient was treated with MINOCYCLINE (View Minocycline Review and Minocycline Label ).

6875816-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, International Normalised Ratio Increased, Jaundice, Liver Function Test Abnormal
Adverse event was reported on Jul 19, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) . Location: CANADA , 34 years of age, weighting 129.0 lb, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, international normalised ratio increased, jaundice (What is jaundice?), liver function test abnormal. During the same period patient was treated with ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), BENZYDAMINE (View Benzydamine Review and Benzydamine Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ), DIPHENHYDRAMINE (View Diphenhydramine Review and Diphenhydramine Label ), DOCUSATE (View Docusate Review and Docusate Label ), MORPHINE (View Morphine Review and Morphine Label ), MUCOSITIS MOUTHWASH (View Mucositis Mouthwash Review and Mucositis Mouthwash Label ). Patient was hospitalized.

6875815-0 | Breast Swelling
on Jul 19, 2010 Male patient from CANADA , 55 years of age, weighting 179.9 lb, was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: breast swelling. Nexium dosage: . During the same period patient was treated with ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), LUMIGAN (View Lumigan Review and Lumigan Label ).

6875654-0 | Abdominal Pain Upper, Hypertension, Liver Disorder, Pancreatitis, Pyrexia
on Jul 19, 2010 Female patient from CANADA , 52 years of age, weighting 134.9 lb, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, hypertension, liver disorder, pancreatitis, pyrexia. Nexium dosage: . Patient was hospitalized.

6875647-3 | Barrett's Oesophagus, Cerebrovascular Accident, Dyspepsia, Gastritis, Gastrointestinal Motility Disorder, Gastrooesophageal Reflux Disease, Oropharyngeal Pain
Patient was taking Nexium (View Usage). Patient had the following side effects: barrett's oesophagus, cerebrovascular accident, dyspepsia, gastritis, gastrointestinal motility disorder, gastrooesophageal reflux disease, oropharyngeal pain on Jul 16, 2010 from UNITED STATES Additional patient health information: Female patient , 79 years of age, was diagnosed with gastrooesophageal reflux disease, cerebrovascular accident and. Nexium dosage: . During the same period patient was treated with OMEPRAZOLE (Total Daily Dosage 20 Mg) (View Omeprazole Review and Omeprazole Label ), PLAVIX (View Plavix Review and Plavix Label ).

6875646-1 | Implantable Defibrillator Insertion
Adverse event was reported on Jul 16, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with dyspepsia and. Location: UNITED STATES , 41 years of age, weighting 179.9 lb, After Nexium was administered, patient had the following side effects: implantable defibrillator insertion. During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), LEBETALOL (View Lebetalol Review and Lebetalol Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), VITAMINS (View Vitamins Review and Vitamins Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

6870914-1 | Living In Residential Institution, Road Traffic Accident
on Jul 14, 2010 Female patient from UNITED STATES , weighting 134.9 lb, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: living in residential institution, road traffic accident. Nexium dosage: . Patient was hospitalized.

6870839-1 | Crohn's Disease, Dehydration, Diarrhoea, Hypokalaemia, Hypomagnesaemia, Renal Failure Acute
on Jul 14, 2010 Male patient from UNITED STATES , weighting 153.0 lb, was diagnosed with crohn's disease (What is crohn's disease?) and was treated with Nexium (View Usage). Patient had the following side effects: crohn's disease (What is crohn's disease?), dehydration, diarrhoea, hypokalaemia, hypomagnesaemia, renal failure acute. Nexium dosage: . During the same period patient was treated with REMICADE (Eight Infusion) (View Remicade Review and Remicade Label ), IMODIUM (View Imodium Review and Imodium Label ), PEDIALYTE (View Pedialyte Review and Pedialyte Label ), QUESTRAN (View Questran Review and Questran Label ), XIFAXAN (View Xifaxan Review and Xifaxan Label ), CDP 870 (View Cdp-870 Review and Cdp-870 Label ). Patient was hospitalized.

6866779-4 | Asthenia, Blood Glucose Increased, Blood Pressure Increased, Candidiasis, Dysarthria, Dysphagia, Fasciitis, Gastrooesophageal Reflux Disease, Hallucination, Visual
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: asthenia, blood glucose increased, blood pressure increased, candidiasis, dysarthria, dysphagia, fasciitis, gastrooesophageal reflux disease, hallucination, visual on Jul 13, 2010 from UNITED STATES Additional patient health information: Male patient , 35 years of age, weighting 211.0 lb, was diagnosed with gastrooesophageal reflux disease, hypertension, schizoaffective disorder bipolar type and. Nexium dosage: . During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), SEROQUEL (View Seroquel Review and Seroquel Label ), LITHIUM (View Lithium Review and Lithium Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), PROPHENAZINE (View Prophenazine Review and Prophenazine Label ). Patient was hospitalized.

6866114-1 | Dyspnoea, Pulmonary Fibrosis
Adverse event was reported on Jul 19, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) . Location: FRANCE , 47 years of age, Patient experienced the following unwanted or unexpected effects: dyspnoea, pulmonary fibrosis (What is pulmonary fibrosis?). During the same period patient was treated with ALIMTA (View Alimta Review and Alimta Label ), CISPLATIN MYLAN (View Cisplatin Mylan Review and Cisplatin Mylan Label ), BIPROFENID (View Biprofenid Review and Biprofenid Label ), DI ANTALVIC (View Di Antalvic Review and Di Antalvic Label ), IMOVANE (View Imovane Review and Imovane Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), SPECIAFOLDINE (View Speciafoldine Review and Speciafoldine Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ).

6862688-5 | Coronary Arterial Stent Insertion
on Jul 12, 2010 Male patient from UNITED STATES , weighting 200.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Nexium (View Usage). Patient had the following side effects: coronary arterial stent insertion. Nexium dosage: . During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6862387-X | Abdominal Discomfort, Abdominal Pain Upper, Cardiac Operation, Hiccups, Malaise, Vomiting
on Jul 14, 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). After Nexium was administered, patient had the following side effects: abdominal discomfort, abdominal pain upper, cardiac operation, hiccups, malaise, vomiting. Nexium dosage: . During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ).

6862292-9 | Lymphoma
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: lymphoma (What is lymphoma?) on Jul 13, 2010 from UNITED STATES Additional patient health information: Female patient , 88 years of age, weighting 125.0 lb, was diagnosed with gastrooesophageal reflux disease and. Nexium dosage: . During the same period patient was treated with MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ), EVISTA (View Evista Review and Evista Label ), CALCIUM (View Calcium Review and Calcium Label ).

6856025-X | Dyspnoea, Obstructive Airways Disorder, Pruritus, Rash, Swollen Tongue
Adverse event was reported on Jul 16, 2010 by a Female patient taking Nexium (View Usage) (Dosage: 50 Mg) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 53 years of age, weighting 180.0 lb, Patient had the following side effects: dyspnoea, obstructive airways disorder, pruritus, rash (What is rash?), swollen tongue. Patient was hospitalized.

6847456-2 | Hyperaemia, Laryngeal Oedema
on Jul 09, 2010 Female patient from RUSSIAN FEDERATION , 58 years of age, weighting 116.8 lb, was diagnosed with duodenal ulcer and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: hyperaemia, laryngeal oedema. Nexium dosage: 20 Mg, Daily; 6 Months Ago - 12 Tablets, 09-jul-2010 - One Tablet.. Patient was hospitalized.

6844090-5 | Decreased Appetite, Headache, Myalgia, Nausea
on Jul 14, 2010 Female patient from UNITED STATES , 53 years of age, weighting 115.0 lb, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: decreased appetite, headache (What is headache?), myalgia, nausea (What is nausea?). Nexium dosage: 40mg 2x Daily.

6843883-8 | Abdominal Distension, Abdominal Pain Upper, Diarrhoea, Muscle Spasms, Oedema Peripheral, Paraesthesia
Patient was taking Nexium (View Usage). Patient had the following side effects: abdominal distension, abdominal pain upper, diarrhoea, muscle spasms, oedema peripheral, paraesthesia on Jul 14, 2010 from UNITED STATES Additional patient health information: Female patient , 42 years of age, weighting 178.0 lb, was diagnosed with gastrooesophageal reflux disease and. Nexium dosage: 40mg Daily Po.

6839911-6 | Abdominal Discomfort, Abdominal Pain, Blepharitis, Burning Sensation, Chest Discomfort, Chest Pain, Choking, Colitis, Cough
Adverse event was reported on Jul 06, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease, irritable bowel syndrome (What is irritable bowel syndrome?), non-cardiac chest pain and. Location: UNITED STATES , 67 years of age, weighting 130.1 lb, 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. During the same period patient was treated with XANAX (View Xanax Review and Xanax Label ), HYOSCYAMINE (View Hyoscyamine Review and Hyoscyamine Label ), ZANTAC (View Zantac Review and Zantac Label ). Patient was hospitalized.

6839826-3 | Diabetes Mellitus, Gallbladder Disorder, Hypopituitarism, Menstruation Irregular, Oropharyngeal Pain, Road Traffic Accident, Total Lung Capacity Decreased
on Jul 06, 2010 Female patient from UNITED STATES , 48 years of age, weighting 196.0 lb, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: diabetes mellitus, gallbladder disorder, hypopituitarism, menstruation irregular, oropharyngeal pain, road traffic accident, total lung capacity decreased. Nexium dosage: . During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), SUDAFED 12 HOUR (View Sudafed 12 Hour Review and Sudafed 12 Hour Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), GLIPIZIDE (View Glipizide Review and Glipizide Label ), METFORMIN (View Metformin Review and Metformin Label ). Patient was hospitalized.

6839427-7 | Thoracic Vertebral Fracture
on Jul 06, 2010 Male patient from AUSTRALIA , weighting 196.2 lb, was treated with Nexium (View Usage). Patient had the following side effects: thoracic vertebral fracture. Nexium dosage: . During the same period patient was treated with LYRICA (Twice Daily) (View Lyrica Review and Lyrica Label ), TRAMOR (Twice Daily) (View Tramor Review and Tramor Label ), PANADINE FORTE (When Required) (View Panadine Forte Review and Panadine Forte Label ), SULMLEATE (View Sulmleate Review and Sulmleate Label ).

6835774-3 | Condition Aggravated, Gastrooesophageal Reflux Disease
Patient was taking Nexium (View Usage). After Nexium was administered, patient had the following side effects: condition aggravated, gastrooesophageal reflux disease on Jul 12, 2010 from UNITED STATES Additional patient health information: Male patient , 26 years of age, weighting 250.0 lb, was diagnosed with gastrooesophageal reflux disease and. Nexium dosage: 40 Mg Daily Po. During the same period patient was treated with CYMBALTA (View Cymbalta Review and Cymbalta Label ), PROZAC (View Prozac Review and Prozac Label ), NUVIGIL (View Nuvigil Review and Nuvigil Label ).

6835634-8 | Abdominal Discomfort, Abdominal Pain Upper, Blood Glucose Abnormal, Dry Mouth, Dysgeusia, Insomnia, Ocular Hyperaemia
Adverse event was reported on Jul 07, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 72 years of age, weighting 175.0 lb, Patient experienced the following unwanted or unexpected effects: abdominal discomfort, abdominal pain upper, blood glucose abnormal, dry mouth, dysgeusia, insomnia, ocular hyperaemia. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6832051-1 | Hepatocellular Injury, Pancreatic Enzymes Increased
on Jul 01, 2010 Male patient from SWITZERLAND , 24 years of age, was treated with Nexium (View Usage). Patient had the following side effects: hepatocellular injury, pancreatic enzymes increased. Nexium dosage: . During the same period patient was treated with ROCEPHIN (View Rocephin Review and Rocephin Label ), FLAGYL (View Flagyl Review and Flagyl Label ), TAZOBAC (View Tazobac Review and Tazobac Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ), TORADOL (View Toradol Review and Toradol Label ), CLEXAN (View Clexan Review and Clexan Label ).

6826098-9 | Cataract
on Jul 02, 2010 Female patient from SPAIN , 78 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: cataract (What is cataract?). Nexium dosage: 20 Mg, 28 Tablets. During the same period patient was treated with AMARYL (30 Tablets) (View Amaryl Review and Amaryl Label ), ACETILCISTEINA (View Acetilcisteina Review and Acetilcisteina Label ), PLUSVENT (50/250 Mg Powder For Inhalation 1x60) (View Plusvent Review and Plusvent Label ), SOMAZINA (10 Bags Of 10 Ml) (View Somazina Review and Somazina Label ).

6826061-8 | Arthralgia, Bone Marrow Oedema
Patient was taking Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, bone marrow oedema on Jul 02, 2010 from VENEZUELA Additional patient health information: Male patient , 55 years of age, weighting 233.7 lb, was diagnosed with gastrooesophageal reflux disease and. Nexium dosage: .

6822383-5 | Haemolytic Anaemia, Microangiopathic Haemolytic Anaemia, Thrombocytopenia
Adverse event was reported on Jul 02, 2010 by a Female patient taking Nexium (View Usage) (Dosage: ) . Location: FRANCE , 47 years of age, Patient had the following side effects: haemolytic anaemia, microangiopathic haemolytic anaemia, thrombocytopenia. During the same period patient was treated with ENDOXAN (View Endoxan Review and Endoxan Label ), BACTRIM (View Bactrim Review and Bactrim Label ). Patient was hospitalized.

6822217-9 | Leukaemia
on Jun 30, 2010 Male patient from BULGARIA , 65 years of age, was diagnosed with gastric ulcer and was treated with Nexium (View Usage). After Nexium was administered, patient had the following side effects: leukaemia. Nexium dosage: . During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6820098-0 | Myositis
on Jun 28, 2010 Female patient from AUSTRALIA , 47 years of age, was treated with Nexium (View Usage). Patient experienced the following unwanted or unexpected effects: myositis (What is myositis?). Nexium dosage: . During the same period patient was treated with AMOXICILLIN TRIHYDRATE (View Amoxicillin Trihydrate Review and Amoxicillin Trihydrate Label ), CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label ). Patient was hospitalized.

6820000-1 | Abdominal Discomfort, Atrial Fibrillation, Chromaturia, Haematuria, Palpitations
Patient was taking Nexium (View Usage). Patient had the following side effects: abdominal discomfort, atrial fibrillation (What is atrial fibrillation?), chromaturia, haematuria, palpitations on Jun 28, 2010 from UNITED STATES Additional patient health information: Female patient , 74 years of age, weighting 164.9 lb, was diagnosed with depression (What is depression?), blood cholesterol, hypertension and. Nexium dosage: . During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), COUMADIN (View Coumadin Review and Coumadin Label ), SERTRALINE (View Sertraline Review and Sertraline Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.