ZEGERID Side Effects

7019573-8 | Abdominal Pain Upper, Decreased Appetite, Dizziness, Dyspepsia, Early Satiety, Fatigue, Gastrooesophageal Reflux Disease, Impaired Work Ability
on Sep 28, 2010 Female patient from UNITED STATES , weighting 100.0 lb, was diagnosed with gastritis and was treated with Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, decreased appetite, dizziness (What is dizziness?), dyspepsia, early satiety, fatigue, gastrooesophageal reflux disease, impaired work ability. Zegerid dosage: One Pill Once A Day Po.

6867093-3 | Blood Amylase Decreased, Blood Calcium Decreased, Blood Creatinine Decreased, Blood Glucose Increased, Blood Magnesium Decreased, Blood Phosphorus Decreased, Blood Potassium Decreased, Blood Urea Decreased, Cardiac Failure Congestive
Patient was taking Zegerid (View Usage). Patient had the following side effects: blood amylase decreased, blood calcium decreased, blood creatinine decreased, blood glucose increased, blood magnesium decreased, blood phosphorus decreased, blood potassium decreased, blood urea decreased, cardiac failure congestive on Jul 28, 2008 from UNITED STATES Additional patient health information: Female patient , 61 years of age, was diagnosed with ill-defined disorder, restless legs syndrome and. Zegerid dosage: . During the same period patient was treated with LYRICA (50mg Per Day) (View Lyrica Review and Lyrica Label ), DYAZIDE (View Dyazide Review and Dyazide Label ), QUININE (View Quinine Review and Quinine Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), COLACE (View Colace Review and Colace Label ), PREMARIN (.625mg Per Day) (View Premarin Review and Premarin Label ), DILTIAZEM (View Diltiazem Review and Diltiazem Label ), ISOSORBIDE (View Isosorbide Review and Isosorbide Label ). Patient was hospitalized.

6774098-X | Back Pain, Cardiac Disorder, Chest Pain, Headache, Neck Pain, Tinnitus
Adverse event was reported on Jun 15, 2010 by a Female patient taking Zegerid (View Usage) (Dosage: 40 Mg Daily Oral) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 63 years of age, weighting 180.3 lb, After Zegerid was administered, patient had the following side effects: back pain (What is back pain?), cardiac disorder, chest pain (What is chest pain?), headache (What is headache?), neck pain, tinnitus (What is tinnitus?).

6742853-8 | Anaphylactic Reaction, Balance Disorder, Blood Pressure Increased, Clonus, Confusional State, Convulsion, Coprolalia, Disturbance In Attention, Facial Pain
on Apr 29, 2010 Female patient from UNITED STATES , 81 years of age, was diagnosed with excoriation and was treated with Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic reaction, balance disorder, blood pressure increased, clonus, confusional state, convulsion, coprolalia, disturbance in attention, facial pain. Zegerid dosage: 40 Mg;qd;po. During the same period patient was treated with ACTOS (View Actos Review and Actos Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ). Patient was hospitalized.


6732978-5 | Anaphylactic Reaction, Blood Pressure Increased, Confusional State, Epilepsy, Tardive Dyskinesia, Vomiting
on Apr 29, 2010 Female patient from UNITED STATES , 81 years of age, was diagnosed with excoriation, oesophageal disorder and was treated with Zegerid (View Usage). Patient had the following side effects: anaphylactic reaction, blood pressure increased, confusional state, epilepsy (What is epilepsy?), tardive dyskinesia, vomiting. Zegerid dosage: Po. Patient was hospitalized.

6570150-2 | Gastritis, Gastrointestinal Disorder, Weight Decreased
Patient was taking Zegerid (View Usage). After Zegerid was administered, patient had the following side effects: gastritis, gastrointestinal disorder, weight decreased on Feb 02, 2010 from UNITED STATES Additional patient health information: Male patient , 61 years of age, weighting 162.0 lb, was diagnosed with gastrooesophageal reflux disease and. Zegerid dosage: I Packet In Water, Per Label Hs Po. During the same period patient was treated with PEPCID COMPLETE (2 Tabs Hs Po) (View Pepcid Complete Review and Pepcid Complete Label ).

6399968-6 | Pancreatitis Acute
Adverse event was reported on Oct 08, 2009 by a Male patient taking Zegerid (View Usage) (Dosage: 40 Mg Daily Po) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 56 years of age, weighting 305.0 lb, Patient experienced the following unwanted or unexpected effects: pancreatitis acute. Patient was hospitalized.

6194907-5 | Diarrhoea, Vomiting
on May 15, 2009 Male patient from UNITED STATES , 73 years of age, weighting 200.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Zegerid (View Usage). Patient had the following side effects: diarrhoea, vomiting. Zegerid dosage: One Pill Daily Po. Patient was hospitalized.

6163692-5 | Agitation, Hypoaesthesia Eye, Hypoaesthesia Facial, Insomnia, Muscular Weakness, Paraesthesia
on Apr 20, 2009 Female patient from UNITED STATES , 42 years of age, weighting 107.0 lb, was diagnosed with gastrooesophageal reflux disease, ulcer (What is ulcer?) and was treated with Zegerid (View Usage). After Zegerid was administered, patient had the following side effects: agitation, hypoaesthesia eye, hypoaesthesia facial, insomnia, muscular weakness, paraesthesia. Zegerid dosage: 1 Daily Po.

6148876-4 | Blood Homocysteine Increased, Coronary Artery Stenosis, Stent Occlusion
Patient was taking Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: blood homocysteine increased, coronary artery stenosis, stent occlusion on Mar 23, 2009 from UNITED STATES Additional patient health information: Female patient , 60 years of age, was diagnosed with gastrooesophageal reflux disease and. Zegerid dosage: 40 Mg; Bid; Po. During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), CRESTOR (View Crestor Review and Crestor Label ), PREMPRO (View Prempro Review and Prempro Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6107928-5 | Erythema, Nocturia, Paraesthesia
Adverse event was reported on Mar 05, 2009 by a Male patient taking Zegerid (View Usage) (Dosage: 40-1100 Bid Po) was diagnosed with dyspepsia and. Location: UNITED STATES , 62 years of age, weighting 147.0 lb, Patient had the following side effects: erythema, nocturia, paraesthesia.

6017211-4 | Abdominal Pain Upper, Arthralgia, Blood Lead Increased, Burning Sensation Mucosal, Clostridium Difficile Colitis, Dysphonia, Glossodynia, Headache
on Dec 05, 2008 Female patient from UNITED STATES , 58 years of age, weighting 140.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Zegerid (View Usage). After Zegerid was administered, patient had the following side effects: abdominal pain upper, arthralgia, blood lead increased, burning sensation mucosal, clostridium difficile colitis, dysphonia, glossodynia, headache (What is headache?). Zegerid dosage: 40 Mg; Qd; Po. During the same period patient was treated with OXYCONTIN (View Oxycontin Review and Oxycontin Label ), FENTANYL 100 (View Fentanyl-100 Review and Fentanyl-100 Label ), OXYCODONE (View Oxycodone Review and Oxycodone Label ), DURASEGIC (View Durasegic Review and Durasegic Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), TRAZODONE (View Trazodone Review and Trazodone Label ), THYROID TAB (View Thyroid Tab Review and Thyroid Tab Label ). Patient was hospitalized.

5958971-8 | Chronic Obstructive Pulmonary Disease, Hypocalcaemia, Hypokalaemia, Hypomagnesaemia, Hypophosphataemia, No Therapeutic Response, Oedema Peripheral
on Oct 31, 2008 Female patient from UNITED KINGDOM , 78 years of age, was diagnosed with diverticulum, duodenitis, hiatus hernia and was treated with Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: chronic obstructive pulmonary disease, hypocalcaemia, hypokalaemia, hypomagnesaemia, hypophosphataemia, no therapeutic response, oedema peripheral. Zegerid dosage: . During the same period patient was treated with SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), BUMETANIDE (View Bumetanide Review and Bumetanide Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ), ACETAMINOPHEN W/ CODEINE (View Acetaminophen W/ Codeine Review and Acetaminophen W/ Codeine Label ), HYOSCINE HBR HYT (View Hyoscine Hbr Hyt Review and Hyoscine Hbr Hyt Label ). Patient was hospitalized.

5958970-6 | Atrial Flutter, Blood Parathyroid Hormone Abnormal, Bradycardia, Fall, Hypocalcaemia, Hypokalaemia, Hypomagnesaemia, Hypotension, Urinary Tract Infection
Patient was taking Zegerid (View Usage). Patient had the following side effects: atrial flutter, blood parathyroid hormone abnormal, bradycardia, fall (What is fall?), hypocalcaemia, hypokalaemia, hypomagnesaemia, hypotension, urinary tract infection (What is urinary tract infection?) on Oct 31, 2008 from UNITED KINGDOM Additional patient health information: Male patient , 81 years of age, . Zegerid dosage: . During the same period patient was treated with ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), QUININE (View Quinine Review and Quinine Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), OLMESARTAN (View Olmesartan Review and Olmesartan Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

5924907-9 | Asthenia, Dizziness, Headache, Joint Swelling, Nausea
Adverse event was reported on Oct 17, 2008 by a Female patient taking Zegerid (View Usage) (Dosage: 40mg Daily Po) was diagnosed with barrett's oesophagus, gastrooesophageal reflux disease and. Location: UNITED STATES , 32 years of age, weighting 92.50 lb, After Zegerid was administered, patient had the following side effects: asthenia, dizziness (What is dizziness?), headache (What is headache?), joint swelling, nausea (What is nausea?).

5852862-9 | Convulsion
on Sep 07, 2007 Male patient from UNITED STATES , child 4 years of age, was treated with Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion. Zegerid dosage: 10 Mg;bid;po. Patient was hospitalized.

5847721-1 | Dysgeusia, Hyperhidrosis, Influenza Like Illness, Nausea, Palpitations, Tremor
on Aug 15, 2008 Female patient from UNITED STATES , weighting 135.0 lb, was diagnosed with ulcer (What is ulcer?) and was treated with Zegerid (View Usage). Patient had the following side effects: dysgeusia, hyperhidrosis, influenza like illness, nausea (What is nausea?), palpitations, tremor. Zegerid dosage: One Capsule 2x Daily Mouth. During the same period patient was treated with PYLORA (View Pylora Review and Pylora Label ).

5753672-3 | Cardiac Failure Congestive
Patient was taking Zegerid (View Usage). After Zegerid was administered, patient had the following side effects: cardiac failure congestive on May 09, 2008 from UNITED STATES Additional patient health information: Female patient , 70 years of age, was diagnosed with gastrooesophageal reflux disease and. Zegerid dosage: 40 Mg;qd;po. During the same period patient was treated with HYZAAR (View Hyzaar Review and Hyzaar Label ). Patient was hospitalized.

5745951-0 | Agitation, Amnesia, Confusional State, Dehydration, Delirium, Hyperreflexia, Hyponatraemic Encephalopathy, Inappropriate Antidiuretic Hormone Secretion, Rhabdomyolysis
Adverse event was reported on May 05, 2008 by a Male patient taking Zegerid (View Usage) (Dosage: ) . Location: UNITED STATES , 46 years of age, Patient experienced the following unwanted or unexpected effects: agitation, amnesia, confusional state, dehydration, delirium, hyperreflexia, hyponatraemic encephalopathy, inappropriate antidiuretic hormone secretion, rhabdomyolysis. Patient was hospitalized.

5650530-X | Heart Rate Increased, Paraesthesia
on Mar 04, 2008 Female patient from UNITED STATES , weighting 130.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Zegerid (View Usage). Patient had the following side effects: heart rate increased, paraesthesia. Zegerid dosage: 1 Capsule 1/2 Hour In Am Po.

5501315-6 | Dyspnoea, Formication, Meralgia Paraesthetica, Nerve Compression, Weight Increased
on Oct 11, 2007 Female patient from UNITED STATES , 56 years of age, weighting 111.0 lb, was diagnosed with gastritis and was treated with Zegerid (View Usage). After Zegerid was administered, patient had the following side effects: dyspnoea, formication, meralgia paraesthetica, nerve compression, weight increased. Zegerid dosage: 40 Mg; Qd; Po. During the same period patient was treated with PROLASTIN (View Prolastin Review and Prolastin Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), ATROVENT (View Atrovent Review and Atrovent Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ), DUONEB (View Duoneb Review and Duoneb Label ), XANAX (View Xanax Review and Xanax Label ).

5272597-3 | Arthralgia, Burning Sensation, Cholelithiasis, Condition Aggravated, Dyspepsia, Pain In Extremity
Patient was taking Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, burning sensation, cholelithiasis, condition aggravated, dyspepsia, pain in extremity on Mar 20, 2007 from UNITED STATES Additional patient health information: Female patient , 50 years of age, weighting 190.0 lb, was diagnosed with gastrooesophageal reflux disease and. Zegerid dosage: 40 Mg 1 Capsule A Day Po.

5268632-9 | Anxiety, Blood Pressure Increased
Adverse event was reported on Mar 15, 2007 by a Male patient taking Zegerid (View Usage) (Dosage: 40mg Daily Po) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 225.0 lb, Patient had the following side effects: anxiety (What is anxiety?), blood pressure increased.

5171377-7 | Dyspnoea, Hyperhidrosis, Oedema Peripheral, Syncope
on Dec 08, 2006 Female patient from UNITED STATES , 68 years of age, weighting 160.0 lb, was diagnosed with dyspepsia and was treated with Zegerid (View Usage). After Zegerid was administered, patient had the following side effects: dyspnoea, hyperhidrosis, oedema peripheral, syncope. Zegerid dosage: 1 Pac In H20 Daily.

4922700-7 | Anorexia, Blood Creatine Phosphokinase Increased, C-reactive Protein Increased, Dermatomyositis, Lethargy, Pyrexia, Rash Erythematous, Rash Papular, Rash Pruritic
on Feb 02, 2006 Female patient from AUSTRALIA , 81 years of age, was diagnosed with reflux oesophagitis and was treated with Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: anorexia, blood creatine phosphokinase increased, c-reactive protein increased, dermatomyositis, lethargy, pyrexia, rash erythematous, rash papular, rash pruritic. Zegerid dosage: 40 Mg; Qd; Po. During the same period patient was treated with MELOXICAM (View Meloxicam Review and Meloxicam Label ), PROCHLORPERAZINE MALEATE (View Prochlorperazine Maleate Review and Prochlorperazine Maleate Label ), DOCUSATE SODIUM (View Docusate Sodium Review and Docusate Sodium Label ).

4897548-2 | Abdominal Pain, Diarrhoea, Flatulence
Patient was taking Zegerid (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), diarrhoea, flatulence on Jan 30, 2006 from UNITED STATES Additional patient health information: Female patient , 51 years of age, weighting 128.0 lb, was diagnosed with gastrooesophageal reflux disease and. Zegerid dosage: 20 Mg Once Daily X 2 Weeks. During the same period patient was treated with NEXIUM (20 Mg Once Daily X 2 Weeks) (View Nexium Review and Nexium Label ).

4894843-8 | Abdominal Pain, Diarrhoea
Adverse event was reported on Jan 26, 2006 by a Female patient taking Zegerid (View Usage) (Dosage: 20 Mg Once Daily X 2 Weeks) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 51 years of age, weighting 128.0 lb, After Zegerid was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), diarrhoea. During the same period patient was treated with NEXIUM (20 Mg Once Daily X 2 Weeks) (View Nexium Review and Nexium Label ).

4803502-9 | Parainfluenzae Virus Infection, Sepsis
on Sep 27, 2005 Female patient from UNITED STATES , child 4 years of age, weighting 44.09 lb, was diagnosed with prophylaxis against gastrointestinal ulcer and was treated with Zegerid (View Usage). Patient experienced the following unwanted or unexpected effects: parainfluenzae virus infection, sepsis (What is sepsis?). Zegerid dosage: 1 Mg/kg; 1x; Ngt.

4772529-8 | Arrhythmia, Supraventricular Tachycardia, Ventricular Extrasystoles
on Sep 16, 2005 Male patient from UNITED STATES , 58 years of age, weighting 186.0 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Zegerid (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), supraventricular tachycardia, ventricular extrasystoles. Zegerid dosage: 20mg 1 Bid Po.

4763907-1 | Bradycardia, Dizziness, Hot Flush, Hyperhidrosis, Loss Of Consciousness
Patient was taking Zegerid (View Usage). After Zegerid was administered, patient had the following side effects: bradycardia, dizziness (What is dizziness?), hot flush, hyperhidrosis, loss of consciousness on Aug 26, 2005 from UNITED STATES Additional patient health information: Male patient , 50 years of age, was diagnosed with gastrooesophageal reflux disease and. Zegerid dosage: 40 Mg; Qd; Po. During the same period patient was treated with VITAMINS (View Vitamins Review and Vitamins Label ). Patient was hospitalized.

4750919-7 | Abdominal Pain Upper, Back Pain, Chest Pain, Constipation, Haematocrit Decreased, Hydronephrosis, Kidney Infection, Nephrolithiasis
Adverse event was reported on Aug 06, 2005 by a Male patient taking Zegerid (View Usage) (Dosage: 40 Mg;qd;po) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 33 years of age, Patient experienced the following unwanted or unexpected effects: abdominal pain upper, back pain (What is back pain?), chest pain (What is chest pain?), constipation (What is constipation?), haematocrit decreased, hydronephrosis, kidney infection, nephrolithiasis. Patient was hospitalized.

4711409-0 | Diplopia, Haemorrhage Intracranial, Optic Nerve Disorder, Vision Blurred
on Jun 26, 2005 Male patient from UNITED STATES , 38 years of age, weighting 192.0 lb, was diagnosed with dyspepsia and was treated with Zegerid (View Usage). Patient had the following side effects: diplopia, haemorrhage intracranial, optic nerve disorder, vision blurred. Zegerid dosage: 40 Mg; Qd; Po. During the same period patient was treated with ALLEGRA (View Allegra Review and Allegra Label ).