PROTONIX Side Effects

7023388-4 | Chronic Obstructive Pulmonary Disease, Emphysema, Pain
on Sep 29, 2010 Male patient from UNITED STATES , weighting 155.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: chronic obstructive pulmonary disease, emphysema, pain (What is pain?). Protonix dosage: . During the same period patient was treated with DIAZEPAM (View Diazepam Review and Diazepam Label ).

7004022-6 | Mean Cell Volume Increased, Vitamin B Complex Deficiency
Patient was taking Protonix (View Usage). Patient had the following side effects: mean cell volume increased, vitamin b complex deficiency on Jan 25, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 181.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with LOVASTATIN (View Lovastatin Review and Lovastatin Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ).

7003920-7 | Chest Pain, Hypoaesthesia, Hypoaesthesia Facial
Adverse event was reported on Dec 17, 2009 by a Male patient taking Protonix (View Usage) (Dosage: ) was diagnosed with barrett's oesophagus, anxiety (What is anxiety?) and. Location: UNITED STATES , weighting 155.1 lb, After Protonix was administered, patient had the following side effects: chest pain (What is chest pain?), hypoaesthesia, hypoaesthesia facial. During the same period patient was treated with PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), ERGOCALCIFEROL (View Ergocalciferol Review and Ergocalciferol Label ), CYANOCOBALAMIN (View Cyanocobalamin Review and Cyanocobalamin Label ), SUCRALFATE (View Sucralfate Review and Sucralfate Label ), LORAZEPAM (Daily As Needed) (View Lorazepam Review and Lorazepam Label ). Patient was hospitalized.

7003914-1 | Abdominal Distension
on Dec 15, 2009 Male patient from UNITED STATES , weighting 170.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal distension. Protonix dosage: . During the same period patient was treated with DILANTIN (View Dilantin Review and Dilantin Label ).


7003899-8 | Abdominal Distension, Anxiety, Chest Discomfort, Condition Aggravated, Eructation, Flatulence, Nervousness
on Jan 04, 2010 Female patient from UNITED STATES , weighting 150.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient had the following side effects: abdominal distension, anxiety (What is anxiety?), chest discomfort, condition aggravated, eructation, flatulence, nervousness. Protonix dosage: . During the same period patient was treated with XANAX (View Xanax Review and Xanax Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ).

7003891-3 | Hair Colour Changes
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: hair colour changes on Dec 15, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 170.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with NEURONTIN (View Neurontin Review and Neurontin Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), AVAPRO (View Avapro Review and Avapro Label ), ESTRACE (View Estrace Review and Estrace Label ).

7003838-X | Contusion, Urine Colour Abnormal
Adverse event was reported on Dec 01, 2009 by a Male patient taking Protonix (View Usage) (Dosage: 40 Mg, Frequency Not Specified) . Location: UNITED STATES , 62 years of age, Patient experienced the following unwanted or unexpected effects: contusion, urine colour abnormal.

7003756-7 | Oesophageal Pain, Rash Erythematous, Rash Pruritic, Throat Irritation
on Sep 15, 2009 Female patient from UNITED STATES , weighting 132.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient had the following side effects: oesophageal pain, rash erythematous, rash pruritic, throat irritation. Protonix dosage: . During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

7003755-5 | Ageusia, Dysgeusia
on Nov 13, 2009 Female patient from UNITED STATES , weighting 128.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: ageusia, dysgeusia. Protonix dosage: . During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), TRIAMTERENE (View Triamterene Review and Triamterene Label ), LOTREL (View Lotrel Review and Lotrel Label ).

7003752-X | Dizziness, Dysgeusia, Product Quality Issue, Somnolence, Vision Blurred
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), dysgeusia, product quality issue, somnolence, vision blurred on Oct 19, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 150.1 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: .

7003738-5 | Abdominal Distension, Dyspnoea, Flatulence
Adverse event was reported on Nov 04, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease, transient ischaemic attack and. Location: UNITED STATES , weighting 193.2 lb, Patient had the following side effects: abdominal distension, dyspnoea, flatulence. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), NORVASC (View Norvasc Review and Norvasc Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), PLAVIX (View Plavix Review and Plavix Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ).

7003730-0 | Salmonellosis
on Sep 23, 2009 Male patient from UNITED STATES , weighting 160.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: salmonellosis. Protonix dosage: . During the same period patient was treated with ZETIA (View Zetia Review and Zetia Label ), CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ), ERGOCALCIFEROL (View Ergocalciferol Review and Ergocalciferol Label ), LUNESTA (View Lunesta Review and Lunesta Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), CRESTOR (View Crestor Review and Crestor Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ).

7003720-8 | Abdominal Distension
on Sep 10, 2009 Female patient from UNITED STATES , weighting 135.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal distension. Protonix dosage: . During the same period patient was treated with BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), FELODIPINE (View Felodipine Review and Felodipine Label ), METOPROLOL (View Metoprolol Review and Metoprolol Label ).

7003719-1 | Abdominal Pain Upper, Constipation, Decreased Appetite, Headache, Weight Decreased
Patient was taking Protonix (View Usage). Patient had the following side effects: abdominal pain upper, constipation (What is constipation?), decreased appetite, headache (What is headache?), weight decreased on Oct 07, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 140.1 lb, was diagnosed with abdominal distension, gastrooesophageal reflux disease, flatulence and. Protonix dosage: . During the same period patient was treated with PREMARIN (View Premarin Review and Premarin Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

7003707-5 | Micturition Urgency, Urethral Pain, Urinary Tract Disorder
Adverse event was reported on Jun 16, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with erosive oesophagitis and. Location: UNITED STATES , weighting 150.1 lb, After Protonix was administered, patient had the following side effects: micturition urgency, urethral pain, urinary tract disorder. During the same period patient was treated with THYROID TAB (View Thyroid Tab Review and Thyroid Tab Label ).

7003706-3 | Increased Upper Airway Secretion, Swollen Tongue, Throat Irritation
on Jul 20, 2009 Female patient from UNITED STATES , weighting 170.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: increased upper airway secretion, swollen tongue, throat irritation. Protonix dosage: .

7003704-X | Abdominal Distension, Abdominal Pain Upper, Blood Glucose Decreased, Herpes Zoster, Weight Decreased
on Apr 13, 2009 Female patient from UNITED STATES , weighting 130.1 lb, was diagnosed with gastritis and was treated with Protonix (View Usage). Patient had the following side effects: abdominal distension, abdominal pain upper, blood glucose decreased, herpes zoster, weight decreased. Protonix dosage: ^40 Mg Off And On^. During the same period patient was treated with XANAX (View Xanax Review and Xanax Label ).

7003702-6 | Condition Aggravated, Dyspepsia, Gastritis, Oesophagitis, Weight Decreased
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: condition aggravated, dyspepsia, gastritis, oesophagitis, weight decreased on Oct 19, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 130.1 lb, was diagnosed with gastritis, oesophagitis, oropharyngeal pain, dysphonia and. Protonix dosage: .

7003701-4 | Abdominal Distension, Abdominal Pain
Adverse event was reported on Mar 09, 2009 by a Male patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 145.1 lb, Patient experienced the following unwanted or unexpected effects: abdominal distension, abdominal pain (What is abdominal pain?). During the same period patient was treated with VITAMIN TAB (View Vitamin Tab Review and Vitamin Tab Label ).

7003699-9 | Dry Throat, Nausea, Oesophageal Pain
on Apr 07, 2009 Female patient from UNITED STATES , weighting 130.1 lb, was diagnosed with abdominal discomfort, flatulence and was treated with Protonix (View Usage). Patient had the following side effects: dry throat, nausea (What is nausea?), oesophageal pain. Protonix dosage: . During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

7003689-6 | Blood Iron Decreased
on Oct 22, 2009 Male patient from UNITED STATES , weighting 190.2 lb, was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: blood iron decreased. Protonix dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), PLAVIX (View Plavix Review and Plavix Label ), DIGOXIN (View Digoxin Review and Digoxin Label ).

7003679-3 | Jaundice
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: jaundice (What is jaundice?) on Mar 05, 2009 from UNITED STATES Additional patient health information: Female patient , 42 years of age, weighting 150.1 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ).

7003677-X | Abdominal Pain Upper, Defaecation Urgency, Diarrhoea, Product Quality Issue
Adverse event was reported on Jul 31, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 164.2 lb, Patient had the following side effects: abdominal pain upper, defaecation urgency, diarrhoea, product quality issue.

7003675-6 | Faeces Pale
on May 21, 2009 Female patient from UNITED STATES , weighting 110.1 lb, was diagnosed with oesophagitis and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: faeces pale. Protonix dosage: . During the same period patient was treated with CENTRUM (View Centrum Review and Centrum Label ), SINGULAIR (View Singulair Review and Singulair Label ).

7003674-4 | Osteopenia
on Sep 02, 2009 Male patient from UNITED STATES , weighting 164.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: osteopenia. Protonix dosage: . During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), RHINOCORT (View Rhinocort Review and Rhinocort Label ).

7003667-7 | Condition Aggravated, Dizziness, Dyspnoea Exertional, Wheezing
Patient was taking Protonix (View Usage). Patient had the following side effects: condition aggravated, dizziness (What is dizziness?), dyspnoea exertional, wheezing on Mar 09, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 170.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with CLARINEX (View Clarinex Review and Clarinex Label ), MECLIZINE (View Meclizine Review and Meclizine Label ).

7003662-8 | Glossodynia, Hypersensitivity, Oral Lichen Planus, Rash Erythematous, Rash Pruritic
Adverse event was reported on Apr 15, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastric ulcer and. Location: UNITED STATES , weighting 179.2 lb, After Protonix was administered, patient had the following side effects: glossodynia, hypersensitivity, oral lichen planus, rash erythematous, rash pruritic. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

7003661-6 | Abdominal Pain Upper, Gastric Ph Decreased
on Jul 22, 2009 Female patient from UNITED STATES , weighting 197.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, gastric ph decreased. Protonix dosage: . During the same period patient was treated with LIBRAX (View Librax Review and Librax Label ), DIOVAN (View Diovan Review and Diovan Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), LASIX (View Lasix Review and Lasix Label ), CARAFATE (View Carafate Review and Carafate Label ), PLAVIX (View Plavix Review and Plavix Label ).

7003658-6 | Abdominal Distension
on Jun 18, 2009 Male patient from UNITED STATES , 41 years of age, was diagnosed with gastritis, gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient had the following side effects: abdominal distension. Protonix dosage: .

7003651-3 | Dry Eye, Eye Swelling
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: dry eye, eye swelling on Aug 14, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 160.1 lb, was diagnosed with oesophagitis and. Protonix dosage: .

7003645-8 | Coeliac Disease
Adverse event was reported on Apr 28, 2009 by a Male patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 200.2 lb, Patient experienced the following unwanted or unexpected effects: coeliac disease.

7003636-7 | Rash Erythematous
on Aug 11, 2009 Female patient from UNITED STATES , weighting 124.1 lb, was diagnosed with abdominal discomfort and was treated with Protonix (View Usage). Patient had the following side effects: rash erythematous. Protonix dosage: . During the same period patient was treated with TYLENOL (View Tylenol Review and Tylenol Label ). Patient was hospitalized.

7003635-5 | Bleeding Time Prolonged, Contusion, Diarrhoea
on Sep 01, 2009 Male patient from UNITED STATES , weighting 188.0 lb, was diagnosed with prophylaxis against gastrointestinal ulcer and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: bleeding time prolonged, contusion, diarrhoea. Protonix dosage: . During the same period patient was treated with ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), ROSUVASTATIN (View Rosuvastatin Review and Rosuvastatin Label ), QUINAPRIL (View Quinapril Review and Quinapril Label ), AMLODIPINE BESILATE (View Amlodipine Besilate Review and Amlodipine Besilate Label ), PLAVIX (View Plavix Review and Plavix Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

7003633-1 | Fall, Upper Respiratory Tract Infection
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), upper respiratory tract infection on Jun 12, 2009 from UNITED STATES Additional patient health information: Female patient , 74 years of age, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: Began 40 Mg Daily 5-7 Years Ago. During the same period patient was treated with ALLEGRA (View Allegra Review and Allegra Label ).

7003624-0 | Product Quality Issue
Adverse event was reported on Jun 26, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 150.1 lb, Patient had the following side effects: product quality issue. During the same period patient was treated with PREMARIN (View Premarin Review and Premarin Label ).

7003623-9 | Sensation Of Pressure
on Mar 05, 2009 Female patient from UNITED STATES , weighting 173.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: sensation of pressure. Protonix dosage: .

7003622-7 | Decreased Appetite, Eructation, Increased Upper Airway Secretion
on Feb 13, 2009 Male patient from UNITED STATES , weighting 154.1 lb, was diagnosed with gastritis and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: decreased appetite, eructation, increased upper airway secretion. Protonix dosage: . During the same period patient was treated with HYDROCODONE BITARTRATE + ACETAMINOPHEN (View Hydrocodone Bitartrate + Acetaminophen Review and Hydrocodone Bitartrate + Acetaminophen Label ), ZESTRIL (View Zestril Review and Zestril Label ), ASTELIN (View Astelin Review and Astelin Label ).

7003619-7 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Vomiting
Patient was taking Protonix (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, vomiting on Mar 23, 2009 from UNITED STATES Additional patient health information: Female patient , 84 years of age, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . Patient was hospitalized.

7003616-1 | Constipation, Faeces Hard, Flatulence
Adverse event was reported on Feb 03, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 189.2 lb, After Protonix was administered, patient had the following side effects: constipation (What is constipation?), faeces hard, flatulence. During the same period patient was treated with MAGNESIUM (View Magnesium Review and Magnesium Label ), VYTORIN (View Vytorin Review and Vytorin Label ), PREMPRO (View Prempro Review and Prempro Label ).

7003614-8 | Paraesthesia Oral
on Feb 24, 2009 Female patient from UNITED STATES , 75 years of age, weighting 180.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: paraesthesia oral. Protonix dosage: . During the same period patient was treated with RANITIDINE (View Ranitidine Review and Ranitidine Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), LIPITOR (View Lipitor Review and Lipitor Label ).

6997603-7 | Abdominal Pain Upper
on Nov 30, 2009 Male patient from UNITED STATES , weighting 135.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient had the following side effects: abdominal pain upper. Protonix dosage: . During the same period patient was treated with VIAGRA (View Viagra Review and Viagra Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), ZANTAC (View Zantac Review and Zantac Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), TYLENOL (View Tylenol Review and Tylenol Label ), TUMS (View Tums Review and Tums Label ), PREDNISONE (View Prednisone Review and Prednisone Label ).

6993134-9 | Convulsion, Respiratory Arrest, Respiratory Depression, Unresponsive To Stimuli
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: convulsion, respiratory arrest, respiratory depression, unresponsive to stimuli on Sep 07, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 170.2 lb, was diagnosed with gastrooesophageal reflux disease, anxiety (What is anxiety?), nephrolithiasis, prophylaxis, depression (What is depression?), pain (What is pain?) and. Protonix dosage: . During the same period patient was treated with CLONOPIN (0.5 Mg Daily Prn) (View Clonopin Review and Clonopin Label ), TAMSULOSIN HCL (View Tamsulosin Hcl Review and Tamsulosin Hcl Label ), PAXIL (View Paxil Review and Paxil Label ), FENTANYL (View Fentanyl Review and Fentanyl Label ), BUPROPION HYDROCHLORIDE (View Bupropion Hydrochloride Review and Bupropion Hydrochloride Label ). Patient was hospitalized.

6984090-8 | Abdominal Pain Upper
Adverse event was reported on May 27, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with ulcer (What is ulcer?), gastrooesophageal reflux disease and. Location: UNITED STATES , 62 years of age, Patient experienced the following unwanted or unexpected effects: abdominal pain upper. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), REGLAN (View Reglan Review and Reglan Label ).

6977227-8 | Blood Iron Decreased, Body Temperature Increased, Chronic Myeloid Leukaemia, Condition Aggravated, Diabetes Mellitus, Discomfort, Epistaxis
on Aug 30, 2010 Female patient from UNITED STATES , weighting 117.1 lb, was diagnosed with oesophageal disorder, gastrointestinal haemorrhage, diabetes mellitus and was treated with Protonix (View Usage). Patient had the following side effects: blood iron decreased, body temperature increased, chronic myeloid leukaemia, condition aggravated, diabetes mellitus, discomfort, epistaxis. Protonix dosage: . During the same period patient was treated with BENICAR (View Benicar Review and Benicar Label ), ZITHROMAX (View Zithromax Review and Zithromax Label ), IRON (View Iron Review and Iron Label ), METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ), GLYBURIDE (5 Mg Bid, Plus 2.5 Mg Once Daily) (View Glyburide Review and Glyburide Label ), NORVASC (View Norvasc Review and Norvasc Label ).

6976344-6 | Diarrhoea
on Apr 16, 2009 Male patient from UNITED STATES , 87 years of age, was diagnosed with tracheostomy and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: diarrhoea. Protonix dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), IRON (View Iron Review and Iron Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), TIZANIDINE HCL (View Tizanidine Hcl Review and Tizanidine Hcl Label ), MAGNESIUM (View Magnesium Review and Magnesium Label ), PAXIL (View Paxil Review and Paxil Label ), CHOLESTYRAMINE (View Cholestyramine Review and Cholestyramine Label ).

6974986-5 | Gastric Ph Increased
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: gastric ph increased on Jan 21, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 210.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6974904-X | Product Quality Issue
Adverse event was reported on Jan 05, 2009 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with dyspepsia and. Location: UNITED STATES , weighting 220.2 lb, Patient had the following side effects: product quality issue.

6974771-4 | Haematospermia
on Dec 15, 2008 Male patient from UNITED STATES , weighting 206.2 lb, was diagnosed with abdominal discomfort and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: haematospermia. Protonix dosage: . During the same period patient was treated with TYLENOL (View Tylenol Review and Tylenol Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ).

6974760-X | Condition Aggravated, Gastrooesophageal Reflux Disease, Ileus Spastic
on Dec 11, 2008 Female patient from UNITED STATES , weighting 106.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, gastrooesophageal reflux disease, ileus spastic. Protonix dosage: . During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ), DICYCLOVERINE HYDROCHLORIDE (View Dicycloverine Hydrochloride Review and Dicycloverine Hydrochloride Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ).

6974745-3 | Blood Glucose Increased
Patient was taking Protonix (View Usage). Patient had the following side effects: blood glucose increased on Nov 25, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 175.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with PROZAC (View Prozac Review and Prozac Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).