PROTONIX Side Effects

6974627-7 | Blood Iron Decreased, Haematocrit Decreased, Haemoglobin Decreased, Red Blood Cell Count Decreased
on Nov 12, 2008 Female patient from UNITED STATES , 57 years of age, weighting 120.1 lb, was diagnosed with gastrointestinal haemorrhage and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: blood iron decreased, haematocrit decreased, haemoglobin decreased, red blood cell count decreased. Protonix dosage: . During the same period patient was treated with DIAZEPAM (View Diazepam Review and Diazepam Label ), CALCIUM (View Calcium Review and Calcium Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), FLEXERIL (View Flexeril Review and Flexeril Label ).

6974619-8 | Abdominal Pain, Alcohol Interaction, Diarrhoea, Dyspepsia, Nausea
Patient was taking Protonix (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), alcohol interaction, diarrhoea, dyspepsia, nausea (What is nausea?) on Nov 14, 2008 from UNITED STATES Additional patient health information: Female patient , 37 years of age, weighting 150.1 lb, was diagnosed with hiatus hernia and. Protonix dosage: . During the same period patient was treated with ZANTAC (View Zantac Review and Zantac Label ), ALCOHOL (View Alcohol Review and Alcohol Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ).

6974600-9 | Faeces Discoloured
Adverse event was reported on Jul 31, 2008 by a Male patient taking Protonix (View Usage) (Dosage: ) was diagnosed with peptic ulcer (What is peptic ulcer?) and. Location: UNITED STATES , 75 years of age, weighting 185.2 lb, After Protonix was administered, patient had the following side effects: faeces discoloured.

6974588-0 | Decreased Appetite, Dyspepsia, Throat Irritation, Weight Decreased
on Aug 20, 2008 Male patient from UNITED STATES , 65 years of age, weighting 197.2 lb, was diagnosed with nausea (What is nausea?) and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: decreased appetite, dyspepsia, throat irritation, weight decreased. Protonix dosage: .


6974586-7 | Saliva Altered
on Aug 12, 2008 Male patient from UNITED STATES , weighting 190.2 lb, was diagnosed with reflux laryngitis, gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient had the following side effects: saliva altered. Protonix dosage: .

6974577-6 | Blood Potassium Decreased
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: blood potassium decreased on Nov 04, 2008 from UNITED STATES Additional patient health information: Female patient , 64 years of age, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), CONJUGATED ESTROGENS (View Conjugated Estrogens Review and Conjugated Estrogens Label ), COZAAR (View Cozaar Review and Cozaar Label ), BUSPAR (View Buspar Review and Buspar Label ).

6974565-X | Euphoric Mood
Adverse event was reported on Oct 10, 2008 by a Male patient taking Protonix (View Usage) (Dosage: ) . Location: UNITED STATES , 90 years of age, Patient experienced the following unwanted or unexpected effects: euphoric mood.

6974553-3 | Blister, Glossodynia, Local Swelling, Lymphadenopathy, Oropharyngeal Pain, Rash Pruritic, Skin Discolouration, Skin Exfoliation
on Nov 06, 2008 Female patient from UNITED STATES , weighting 180.2 lb, was diagnosed with gastric ulcer and was treated with Protonix (View Usage). Patient had the following side effects: blister, glossodynia, local swelling, lymphadenopathy, oropharyngeal pain, rash pruritic, skin discolouration, skin exfoliation. Protonix dosage: . During the same period patient was treated with NYSTATIN (View Nystatin Review and Nystatin Label ), AMBIEN (View Ambien Review and Ambien Label ).

6974549-1 | Osteoporosis
on Aug 06, 2008 Male patient from UNITED STATES , 58 years of age, weighting 170.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: osteoporosis (What is osteoporosis?). Protonix dosage: . During the same period patient was treated with METHOCARBAMOL (View Methocarbamol Review and Methocarbamol Label ), CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ).

6974546-6 | Urine Alcohol Test Positive
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: urine alcohol test positive on Jul 29, 2008 from UNITED STATES Additional patient health information: Male patient , 16 years of age, was diagnosed with gastric disorder and. Protonix dosage: .

6974539-9 | Condition Aggravated, Hallucination, Vertigo
Adverse event was reported on Aug 19, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with urinary retention, dysuria and. Location: UNITED STATES , 87 years of age, Patient had the following side effects: condition aggravated, hallucination, vertigo. During the same period patient was treated with FLOMAX (View Flomax Review and Flomax Label ). Patient was hospitalized.

6974536-3 | Dysgeusia, Glossodynia
on Aug 26, 2008 Female patient from UNITED STATES , weighting 165.1 lb, was diagnosed with abdominal pain (What is abdominal pain?) and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: dysgeusia, glossodynia. Protonix dosage: .

6974524-7 | Dizziness, Hypersensitivity, Presyncope
on Sep 16, 2008 Male patient from UNITED STATES , 55 years of age, was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), hypersensitivity, presyncope. Protonix dosage: . During the same period patient was treated with MAALOX (1-2 Tablets Every 4-6 Hours) (View Maalox Review and Maalox Label ).

6974521-1 | Alopecia, Pain, Rash Erythematous, Skin Mass
Patient was taking Protonix (View Usage). Patient had the following side effects: alopecia, pain (What is pain?), rash erythematous, skin mass on Aug 29, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 160.1 lb, was diagnosed with abdominal pain upper and. Protonix dosage: . During the same period patient was treated with ACTONEL (View Actonel Review and Actonel Label ), PREMARIN (View Premarin Review and Premarin Label ).

6974518-1 | Faeces Discoloured, Haemoglobin Decreased, Pain Of Skin, Skin Discolouration
Adverse event was reported on Jul 17, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 150.1 lb, After Protonix was administered, patient had the following side effects: faeces discoloured, haemoglobin decreased, pain of skin, skin discolouration. During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ).

6974488-6 | Faeces Discoloured
on Jul 30, 2008 Male patient from UNITED STATES , 72 years of age, was diagnosed with dyspepsia and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: faeces discoloured. Protonix dosage: . During the same period patient was treated with MAALOX ANTACID/ANTIGAS MAXIMUM STRENGTH MULTI SYMPTOM (6 Tsp Every 1 Day; Cumulative Dose To Event: 30 Tsp) (View Maalox Antacid/antigas Maximum Strength Multi Symptom Review and Maalox Antacid/antigas Maximum Strength Multi Symptom Label ).

6974486-2 | Faeces Discoloured
on Jul 18, 2008 Male 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: faeces discoloured. Protonix dosage: . During the same period patient was treated with METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), LOVASTATIN (View Lovastatin Review and Lovastatin Label ).

6974473-4 | Bone Density Decreased
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: bone density decreased on Aug 18, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 115.1 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with FISH OIL, HYDROGENATED (View Fish Oil, Hydrogenated Review and Fish Oil, Hydrogenated Label ), CALTRATE (View Caltrate Review and Caltrate Label ), CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ), CELEBREX (View Celebrex Review and Celebrex Label ), ESTRADIOL (View Estradiol Review and Estradiol Label ).

6974448-5 | Osteoporosis
Adverse event was reported on Mar 04, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 130.1 lb, Patient experienced the following unwanted or unexpected effects: osteoporosis (What is osteoporosis?). During the same period patient was treated with METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), EVISTA (View Evista Review and Evista Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), LOVASTATIN (View Lovastatin Review and Lovastatin Label ).

6974446-1 | Abdominal Distension, Flatulence, Headache
on Jul 25, 2008 Female patient from UNITED STATES , 74 years of age, weighting 120.1 lb, was diagnosed with gastric ulcer haemorrhage, oesophageal stenosis, hiatus hernia and was treated with Protonix (View Usage). Patient had the following side effects: abdominal distension, flatulence, headache (What is headache?). Protonix dosage: .

6974445-X | Abdominal Distension, Diarrhoea
on May 14, 2008 Female patient from UNITED STATES , weighting 130.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: abdominal distension, diarrhoea. Protonix dosage: .

6974442-4 | Nail Growth Abnormal, Onychoclasis
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: nail growth abnormal, onychoclasis on May 16, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 105.1 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ).

6974441-2 | Bone Pain, Burning Sensation, Chapped Lips, Dizziness, Lip Dry, Paraesthesia, Pyrexia, Visual Impairment, Weight Decreased
Adverse event was reported on Jul 01, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 48 years of age, weighting 135.1 lb, Patient had the following side effects: bone pain, burning sensation, chapped lips, dizziness (What is dizziness?), lip dry, paraesthesia, pyrexia, visual impairment, weight decreased.

6974440-0 | Dysphagia, Saliva Altered
on Jun 11, 2008 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: dysphagia, saliva altered. Protonix dosage: . During the same period patient was treated with PROSCAR (View Proscar Review and Proscar Label ), ENALAPRIL (View Enalapril Review and Enalapril Label ).

6974438-2 | Dry Mouth, Incorrect Dose Administered
on Mar 10, 2008 Male patient from UNITED STATES , weighting 160.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: dry mouth, incorrect dose administered. Protonix dosage: .

6974433-3 | Amnesia, Disturbance In Attention, Vitamin B12 Deficiency
Patient was taking Protonix (View Usage). Patient had the following side effects: amnesia, disturbance in attention, vitamin b12 deficiency on Apr 03, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 214.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with ENBREL (View Enbrel Review and Enbrel Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), NORTRIPTYLINE HCL (View Nortriptyline Hcl Review and Nortriptyline Hcl Label ), EFFEXOR XR (View Effexor Xr Review and Effexor Xr Label ).

6974428-X | Coeliac Disease
Adverse event was reported on Jun 02, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 72 years of age, weighting 137.1 lb, After Protonix was administered, patient had the following side effects: coeliac disease. During the same period patient was treated with CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ).

6974427-8 | Alopecia, Fluid Retention, Weight Loss Poor
on Mar 14, 2008 Female patient from UNITED STATES , weighting 186.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: alopecia, fluid retention, weight loss poor. Protonix dosage: .

6974417-5 | Vitamin D Deficiency
on May 29, 2008 Female patient from UNITED STATES , 80 years of age, weighting 108.1 lb, was treated with Protonix (View Usage). Patient had the following side effects: vitamin d deficiency. Protonix dosage: 40. During the same period patient was treated with CENTRUM SILVER (1 Tablet Sporadically) (View Centrum Silver Review and Centrum Silver Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), PLENDIL (View Plendil Review and Plendil Label ), CALCIUM CARBONATE (1 Tablet Sporadically) (View Calcium Carbonate Review and Calcium Carbonate Label ), ACTONEL (View Actonel Review and Actonel Label ).

6974416-3 | Abdominal Discomfort, Bowel Movement Irregularity
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: abdominal discomfort, bowel movement irregularity on Apr 15, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 200.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: .

6974392-3 | Umbilical Hernia
Adverse event was reported on Mar 07, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , 72 years of age, weighting 135.1 lb, Patient experienced the following unwanted or unexpected effects: umbilical hernia.

6974382-0 | Hepatitis
on May 12, 2008 Female patient from UNITED STATES , 31 years of age, was diagnosed with gastrooesophageal reflux disease, depression (What is depression?), anxiety (What is anxiety?) and was treated with Protonix (View Usage). Patient had the following side effects: hepatitis (What is hepatitis?). Protonix dosage: . During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LABETALOL HCL (View Labetalol Hcl Review and Labetalol Hcl Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), CLONAZEPAM (0.5 Mg Prn) (View Clonazepam Review and Clonazepam Label ).

6974381-9 | Gait Disturbance, Pain In Extremity
on Mar 10, 2008 Female patient from UNITED STATES , 69 years of age, weighting 150.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: gait disturbance, pain in extremity. Protonix dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), OMACOR (View Omacor Review and Omacor Label ), DIOVAN (View Diovan Review and Diovan Label ).

6974362-5 | Intentional Overdose
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: intentional overdose on Apr 07, 2008 from UNITED STATES Additional patient health information: Male patient , 55 years of age, weighting 180.2 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: 40 Mg Qid (overdose Amount). During the same period patient was treated with PERCOCET (View Percocet Review and Percocet Label ), VICODIN (View Vicodin Review and Vicodin Label ), BENICAR (View Benicar Review and Benicar Label ), ACTOS (View Actos Review and Actos Label ).

6974360-1 | Abdominal Distension, Condition Aggravated, Dysphagia, Flatulence, Gastrooesophageal Reflux Disease, Headache, Sensation Of Foreign Body
Adverse event was reported on May 28, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 140.1 lb, Patient had the following side effects: abdominal distension, condition aggravated, dysphagia, flatulence, gastrooesophageal reflux disease, headache (What is headache?), sensation of foreign body. During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), ACTONEL (View Actonel Review and Actonel Label ).

6974359-5 | Abdominal Distension, Flatulence
on Jul 01, 2008 Female patient from UNITED STATES , 66 years of age, weighting 117.1 lb, was diagnosed with dyspepsia and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: abdominal distension, flatulence. Protonix dosage: .

6974296-6 | Myalgia, Osteoporosis
on Jul 01, 2008 Female patient from UNITED STATES , weighting 132.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: myalgia, osteoporosis (What is osteoporosis?). Protonix dosage: . During the same period patient was treated with VITAMINS (View Vitamins Review and Vitamins Label ).

6974295-4 | Condition Aggravated, Osteoporosis
Patient was taking Protonix (View Usage). Patient had the following side effects: condition aggravated, osteoporosis (What is osteoporosis?) on Mar 18, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 115.1 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), FOSAMAX (View Fosamax Review and Fosamax Label ).

6974294-2 | Abdominal Pain Upper, Diarrhoea, Gastrointestinal Sounds Abnormal, Vomiting
Adverse event was reported on Mar 20, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 225.2 lb, After Protonix was administered, patient had the following side effects: abdominal pain upper, diarrhoea, gastrointestinal sounds abnormal, vomiting. During the same period patient was treated with LORAZEPAM (View Lorazepam Review and Lorazepam Label ).

6974292-9 | Aspiration, Choking, Cough
on Mar 03, 2008 Female patient from UNITED STATES , weighting 167.2 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: aspiration, choking (What is choking?), cough. Protonix dosage: . During the same period patient was treated with ALTACE (View Altace Review and Altace Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), HYDROCODONE (View Hydrocodone Review and Hydrocodone Label ), NORVASC (View Norvasc Review and Norvasc Label ), LASIX (View Lasix Review and Lasix Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), BENICAR (View Benicar Review and Benicar Label ).

6974255-3 | Arthralgia, Asthenia, Dry Eye, Dry Mouth, Fatigue, Headache, Hypoaesthesia, Myalgia, Paraesthesia
on Mar 20, 2008 Female patient from UNITED STATES , weighting 161.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient had the following side effects: arthralgia, asthenia, dry eye, dry mouth, fatigue, headache (What is headache?), hypoaesthesia, myalgia, paraesthesia. Protonix dosage: . During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ATACAND (View Atacand Review and Atacand Label ).

6974247-4 | Chills, Dyspepsia, Gastric Polyps, Headache
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: chills, dyspepsia, gastric polyps, headache (What is headache?) on Apr 04, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 148.1 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ).

6974246-2 | Abdominal Distension, Chest Pain, Eructation, Flatulence
Adverse event was reported on Jul 01, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with abdominal distension, abdominal pain (What is abdominal pain?) and. Location: UNITED STATES , 65 years of age, Patient experienced the following unwanted or unexpected effects: abdominal distension, chest pain (What is chest pain?), eructation, flatulence. During the same period patient was treated with CALCIUM (View Calcium Review and Calcium Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ).

6974245-0 | Back Pain, Chills, Cough, Dysphagia, Ear Pain, Oral Pruritus, Oropharyngeal Pain, Rhinorrhoea
on May 20, 2008 Female patient from UNITED STATES , weighting 140.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient had the following side effects: back pain (What is back pain?), chills, cough, dysphagia, ear pain, oral pruritus, oropharyngeal pain, rhinorrhoea. Protonix dosage: 40 Mg Once. During the same period patient was treated with LORATADINE (View Loratadine Review and Loratadine Label ).

6974244-9 | Pain, Pain In Extremity, Sensation Of Heaviness
on Jun 02, 2008 Female patient from UNITED STATES , weighting 95.09 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: pain (What is pain?), pain in extremity, sensation of heaviness. Protonix dosage: .

6974243-7 | Burning Sensation, Rash
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: burning sensation, rash (What is rash?) on Jul 01, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 135.1 lb, was diagnosed with gastrooesophageal reflux disease and. Protonix dosage: . During the same period patient was treated with ALENDRONATE SODIUM (View Alendronate Sodium Review and Alendronate Sodium Label ).

6974228-0 | Abdominal Distension, Swelling, Weight Increased
Adverse event was reported on May 09, 2008 by a Female patient taking Protonix (View Usage) (Dosage: ) was diagnosed with gastrooesophageal reflux disease and. Location: UNITED STATES , weighting 194.2 lb, Patient had the following side effects: abdominal distension, swelling, weight increased.

6974227-9 | Enamel Anomaly
on Apr 17, 2008 Male patient from UNITED STATES , 61 years of age, was diagnosed with dyspepsia and was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: enamel anomaly. Protonix dosage: . During the same period patient was treated with ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ).

6974216-4 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Cholesterol Increased, Blood Triglycerides Increased, High Density Lipoprotein Increased, Low Density Lipoprotein Increased
on Jul 01, 2008 Female patient from UNITED STATES , weighting 150.1 lb, was diagnosed with gastrooesophageal reflux disease and was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood cholesterol increased, blood triglycerides increased, high density lipoprotein increased, low density lipoprotein increased. Protonix dosage: . During the same period patient was treated with SEROQUEL (View Seroquel Review and Seroquel Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), PERCOCET (5mg/325) (View Percocet Review and Percocet Label ), FENTANYL CITRATE (10 Mcg) (View Fentanyl Citrate Review and Fentanyl Citrate Label ), ESTRADIOL (1 Mg) (View Estradiol Review and Estradiol Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), FLONASE (View Flonase Review and Flonase Label ), ZYRTEC (10 Mg) (View Zyrtec Review and Zyrtec Label ). Patient was hospitalized.

6974215-2 | Anxiety, Flatulence, Psychomotor Hyperactivity
Patient was taking Protonix (View Usage). Patient had the following side effects: anxiety (What is anxiety?), flatulence, psychomotor hyperactivity on Feb 12, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 185.2 lb, was diagnosed with gastroenteritis (What is gastroenteritis?) and. Protonix dosage: . During the same period patient was treated with DARVOCET N 100 (View Darvocet-n 100 Review and Darvocet-n 100 Label ), ZOCOR (View Zocor Review and Zocor Label ), AMBIEN (View Ambien Review and Ambien Label ), ATIVAN (View Ativan Review and Ativan Label ), INDERAL (View Inderal Review and Inderal Label ).