Protonix Side Effects|
|
Did You Have a Protonix Side Effect? How Effective is Protonix for You? |
Protonix ForumI was taking Protonix for an ulcer and severe gastritis. I am ...Keep Reading I had been on Protonix for the second time and had started having the ...Keep Reading I have been on the protonix for about 4 months now for Barrets esophogus ...Keep Reading I have been on protonix for about 3-4 months. I recently have been feeling ...Keep Reading I have been on Protonix for about 2 weeks now. It is the ...Keep Reading My doctor prescribed protonix after HPylori infection and then caused severe gastritis. I ...Keep Reading At first it was a little burning in my nose, ears ringing and ...Keep Reading not sure what's tegretol or other new meds but extreme night sweats and loss ...Keep Reading <span style="color: #808080;"><b>Describe Your Injection site swelling from INFLUENZA ...Keep Reading I HAVE BEEN ON PROTONIX FOR 1 MONTH IN HALF I HAVE EXPERIENCED RASH ...Keep Reading RASHES AND HIVES developed. I am allergic to the medicine might different experience ...Keep Reading I was prescribed Protonix by my doctor due to GERD. I took it ...Keep Reading protonix 40mg qd, is it ok to take with heart problem ...Keep Reading |
Protonix Adverse Effect Reports (FDA)
Showing 1-25 of 1180 Next Page >
Liver Function Test Abnormal, Liver Injury (8573048-3)
on Oct 05, 2009 Female patient from UNITED STATES , 28 years of age, was treated with Protonix ^wyeth-ayerst^ (pantoprazole Sodium)(View Usage). Patient experienced the following unwanted or unexpected effects: liver function test abnormal, liver injury. Protonix ^wyeth-ayerst^ (pantoprazole Sodium) dosage: N/A.
Patient was taking other medications:
Breast Cancer (8572339-X)
Patient was taking Protonix (View Usage). Patient had the following side effects: breast cancer (breast cancer Questions) on Jul 20, 2010 from UNITED STATES Additional patient health information: Female patient , 53 years of age, . Protonix dosage: N/A.
Patient was taking other medications:
White Blood Cell Count Decreased, Pneumonia (8519974-2)
Adverse event was reported on Sep 21, 2009 by a Male patient taking Protonix (View Usage) (Dosage: N/A) . Location: UNITED STATES , 78 years of age, After Protonix was administered, patient had the following side effects: white blood cell count decreased, pneumonia (pneumonia Questions).
Patient was taking other medications:
Myalgia, Arthralgia, Fatigue (8509853-9)
on Jun 26, 2009 Female patient from UNITED STATES , 59 years of age, weighting 110.0 lb, was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: myalgia, arthralgia, fatigue. Protonix dosage: N/A.
Patient was taking other medications:
Spondylitis, Spinal Osteoarthritis, Influenza Like Illness, Bone Pain (8504174-2)
on Jul 30, 2009 Female patient from UNITED STATES , 66 years of age, weighting 97.89 lb, was treated with Protonix(View Usage). Patient had the following side effects: spondylitis, spinal osteoarthritis, influenza like illness, bone pain. Protonix dosage: N/A.
Patient was taking other medications:
Adverse Event, Underdose, Cholecystitis Acute, Thrombotic Thrombocytopenic Purpura, Haemolytic Uraemic Syndrome, Nephritis, Abdominal Discomfort (8480206-5)
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: adverse event, underdose, cholecystitis acute, thrombotic thrombocytopenic purpura, haemolytic uraemic syndrome, nephritis, abdominal discomfort on Jun 22, 2012 from UNITED STATES Additional patient health information: Female patient , 40 years of age, was diagnosed with
Gastric Polyps, Gastric Disorder, Dyspnoea, Dyspepsia, Abdominal Discomfort, Cardiac Disorder (8477919-8)
Adverse event was reported on Jun 27, 2012 by a Male patient taking Protonix (View Usage) (Dosage: 40 Mg, Daily) was diagnosed with
Patient was taking other medications:
Chest Discomfort, Chest Pain (8477139-7)
on Jun 18, 2012 Female patient from UNITED STATES , weighting 150.0 lb, was diagnosed with
Patient was taking other medications:
Uterine Perforation, Device Dislocation, Pelvic Pain, Back Pain (8473505-4)
on Jun 22, 2012 Female patient from CANADA , 32 years of age, weighting 150.0 lb, was treated with Protonix(View Usage). After Protonix was administered, patient had the following side effects: uterine perforation, device dislocation, pelvic pain (pelvic pain Questions), back pain (back pain Questions). Protonix dosage: N/A.
Patient was taking other medications:
Atrial Fibrillation (8472426-0)
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: atrial fibrillation (atrial fibrillation Questions) on Aug 25, 2011 from UNITED STATES Additional patient health information: Male patient , 78 years of age, weighting 252.0 lb, was diagnosed with
Patient was taking other medications:
No Adverse Event (8471948-6)
Adverse event was reported on Jun 20, 2012 by a Female patient taking Protonix (View Usage) (Dosage: Unk) . Location: UNITED STATES , weighting 123.0 lb, Patient had the following side effects: no adverse event.
Patient was taking other medications:
Dyspnoea, Bone Marrow Failure, Thrombocytopenia, Anaemia, Myelofibrosis, Pneumonia, Disease Progression (8471846-8)
on Dec 13, 2011 Female patient from UNITED STATES , 59 years of age, was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: dyspnoea, bone marrow failure, thrombocytopenia, anaemia, myelofibrosis, pneumonia (pneumonia Questions), disease progression. Protonix dosage: N/A.
Patient was taking other medications:
Pneumonia (8471616-0)
on Dec 06, 2011 Male patient from UNITED STATES , 65 years of age, weighting 380.0 lb, was treated with Protonix(View Usage). Patient experienced the following unwanted or unexpected effects: pneumonia (pneumonia Questions). Protonix dosage: N/A.
Patient was taking other medications:
Creatinine Renal Clearance Decreased, Anaemia (8470448-7)
Patient was taking Protonix (View Usage). Patient had the following side effects: creatinine renal clearance decreased, anaemia on Nov 30, 2011 from UNITED STATES Additional patient health information: Male patient , 61 years of age, . Protonix dosage: N/A.
Patient was taking other medications:
Glaucoma, Chronic Obstructive Pulmonary Disease, Emphysema (8469385-3)
Adverse event was reported on Jun 22, 2012 by a Female patient taking Protonix (View Usage) (Dosage: 40 Mg, Daily) was diagnosed with
Patient was taking other medications:
Vomiting, Oesophageal Ulcer, Dyspepsia, Gastrooesophageal Reflux Disease, Pain (8465542-0)
on Jun 11, 2012 Male patient from UNITED STATES , 54 years of age, was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: vomiting, oesophageal ulcer, dyspepsia, gastrooesophageal reflux disease, pain (pain Questions). Protonix dosage: N/A.
Patient was taking other medications:
No Adverse Event (8461502-4)
on Jun 20, 2012 Female patient from UNITED STATES , weighting 123.0 lb, was treated with Protonix(View Usage). Patient had the following side effects: no adverse event. Protonix dosage: Unk.
Patient was taking other medications:
Tremor (8461455-9)
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: tremor on Jun 19, 2012 from UNITED STATES Additional patient health information: Female patient , weighting 135.0 lb, was diagnosed with
Gastric Disorder, Dyspnoea, Cardiac Disorder, Abdominal Discomfort, Dyspepsia, Gastric Polyps (8459430-3)
Adverse event was reported on Jun 20, 2012 by a Male patient taking Protonix (View Usage) (Dosage: 40 Mg, Daily) was diagnosed with
Patient was taking other medications:
Vomiting, Gastrointestinal Pain, Gastric Disorder, Nausea (8456816-8)
on Jun 18, 2012 Female patient from UNITED STATES , weighting 202.8 lb, was diagnosed with
Patient was taking other medications:
Impaired Healing, Swollen Tongue, Oral Discomfort, Gingival Swelling, Oral Mucosal Erythema, Diabetes Mellitus (8455063-3)
on Jun 15, 2012 Female patient from UNITED STATES , 75 years of age, weighting 146.1 lb, was treated with Protonix(View Usage). After Protonix was administered, patient had the following side effects: impaired healing, swollen tongue, oral discomfort, gingival swelling, oral mucosal erythema, diabetes mellitus. Protonix dosage: 1 40 Mg. Tab Daily Daily Po.
Nausea, Ill-defined Disorder, Decreased Appetite, Headache, Weight Increased, Tachycardia (8452103-2)
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: nausea (nausea Questions), ill-defined disorder, decreased appetite, headache (headache Questions), weight increased, tachycardia on Jun 13, 2012 from UNITED STATES Additional patient health information: Male patient , 45 years of age, weighting 260.6 lb, . Protonix dosage: N/A.
Patient was taking other medications:
Dyspepsia, Gastrooesophageal Reflux Disease (8448175-1)
Adverse event was reported on Jun 12, 2012 by a Female patient taking Protonix (View Usage) (Dosage: N/A) . Location: UNITED STATES , 56 years of age, Patient had the following side effects: dyspepsia, gastrooesophageal reflux disease.
Patient was taking other medications:
Mantle Cell Lymphoma (8446548-4)
on Jun 13, 2012 Male patient from UNITED STATES , weighting 157.0 lb, was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: mantle cell lymphoma. Protonix dosage: Unk.
Patient was taking other medications:
Cardiac Murmur, Pyrexia, Decreased Appetite, Tinnitus, Fungal Sepsis, Foot Operation, Dehydration, Goitre, Chills (8446323-0)
on Apr 04, 2012 Female patient from UNITED STATES , weighting 212.0 lb, was treated with Protonix(View Usage). Patient experienced the following unwanted or unexpected effects: cardiac murmur, pyrexia, decreased appetite, tinnitus (tinnitus Questions), fungal sepsis, foot operation, dehydration, goitre, chills. Protonix dosage: Unk.
Patient was taking other medications:
on Oct 05, 2009 Female patient from UNITED STATES , 28 years of age, was treated with Protonix ^wyeth-ayerst^ (pantoprazole Sodium)(View Usage). Patient experienced the following unwanted or unexpected effects: liver function test abnormal, liver injury. Protonix ^wyeth-ayerst^ (pantoprazole Sodium) dosage: N/A.
Patient was taking other medications:
- EXJADE (500 Mg, Bid, Oral) (View Exjade Review and Exjade Label )
Breast Cancer (8572339-X)
Patient was taking Protonix (View Usage). Patient had the following side effects: breast cancer (breast cancer Questions) on Jul 20, 2010 from UNITED STATES Additional patient health information: Female patient , 53 years of age, . Protonix dosage: N/A.
Patient was taking other medications:
- DARVOCET (View Darvocet Review and Darvocet Label )
- ESTRADERM (0.05mg, Transdermal) (View Estraderm Review and Estraderm Label )
White Blood Cell Count Decreased, Pneumonia (8519974-2)
Adverse event was reported on Sep 21, 2009 by a Male patient taking Protonix (View Usage) (Dosage: N/A) . Location: UNITED STATES , 78 years of age, After Protonix was administered, patient had the following side effects: white blood cell count decreased, pneumonia (pneumonia Questions).
Patient was taking other medications:
- PLAVIX (View Plavix Review and Plavix Label )
- ASPIRIN (View Aspirin Review and Aspirin Label )
- LASIX (View Lasix Review and Lasix Label )
- TASIGNA (400 Mg, Am. 200 Mg Pm, Daily, Oral, 200 Mg, Bid, Oral) (View Tasigna Review and Tasigna Label )
- CRESTOR (View Crestor Review and Crestor Label )
- DIGOXIN (View Digoxin Review and Digoxin Label )
- RANEXA (View Ranexa Review and Ranexa Label )
- ISMO (View Ismo Review and Ismo Label )
Myalgia, Arthralgia, Fatigue (8509853-9)
on Jun 26, 2009 Female patient from UNITED STATES , 59 years of age, weighting 110.0 lb, was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: myalgia, arthralgia, fatigue. Protonix dosage: N/A.
Patient was taking other medications:
- VERAPAMIL (View Verapamil Review and Verapamil Label )
- AMBIEN (View Ambien Review and Ambien Label )
- RECLAST (5 Mg, Unk, Intravenous) (View Reclast Review and Reclast Label )
- PREMARIN (View Premarin Review and Premarin Label )
Spondylitis, Spinal Osteoarthritis, Influenza Like Illness, Bone Pain (8504174-2)
on Jul 30, 2009 Female patient from UNITED STATES , 66 years of age, weighting 97.89 lb, was treated with Protonix(View Usage). Patient had the following side effects: spondylitis, spinal osteoarthritis, influenza like illness, bone pain. Protonix dosage: N/A.
Patient was taking other medications:
- TORADOL (View Toradol Review and Toradol Label )
- ESTRADIOL (View Estradiol Review and Estradiol Label )
- TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label )
- RECLAST (5mg Iv Once Yearly) (View Reclast Review and Reclast Label )
Adverse Event, Underdose, Cholecystitis Acute, Thrombotic Thrombocytopenic Purpura, Haemolytic Uraemic Syndrome, Nephritis, Abdominal Discomfort (8480206-5)
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: adverse event, underdose, cholecystitis acute, thrombotic thrombocytopenic purpura, haemolytic uraemic syndrome, nephritis, abdominal discomfort on Jun 22, 2012 from UNITED STATES Additional patient health information: Female patient , 40 years of age, was diagnosed with
- abdominal pain upper
- osteopenia
- anxiety (anxiety Questions)
Gastric Polyps, Gastric Disorder, Dyspnoea, Dyspepsia, Abdominal Discomfort, Cardiac Disorder (8477919-8)
Adverse event was reported on Jun 27, 2012 by a Male patient taking Protonix (View Usage) (Dosage: 40 Mg, Daily) was diagnosed with
- gastrooesophageal reflux disease
- hypertension
Patient was taking other medications:
- HYDROCHLOROTHIAZIDE (10 Mg, Daily) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label )
- TOPROL XL (100 Mg, Daily) (View Toprol-xl Review and Toprol-xl Label )
Chest Discomfort, Chest Pain (8477139-7)
on Jun 18, 2012 Female patient from UNITED STATES , weighting 150.0 lb, was diagnosed with
- gastrooesophageal reflux disease
- asthma (asthma Questions)
Patient was taking other medications:
- ADVAIR DISKUS 100/50 (500/50 Mg, Unk) (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label )
- FUZEON (Unk) (View Fuzeon Review and Fuzeon Label )
- THORAZINE (50 Mg, Daily At Bed Time) (View Thorazine Review and Thorazine Label )
Uterine Perforation, Device Dislocation, Pelvic Pain, Back Pain (8473505-4)
on Jun 22, 2012 Female patient from CANADA , 32 years of age, weighting 150.0 lb, was treated with Protonix(View Usage). After Protonix was administered, patient had the following side effects: uterine perforation, device dislocation, pelvic pain (pelvic pain Questions), back pain (back pain Questions). Protonix dosage: N/A.
Patient was taking other medications:
- RHINOCORT (View Rhinocort Review and Rhinocort Label )
- MIRENA (20 Mcg/24hr, Cont) (View Mirena Review and Mirena Label )
- ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label )
- PROPYLENE GLYCOL (View Propylene Glycol Review and Propylene Glycol Label )
- AZELEX (View Azelex Review and Azelex Label )
Atrial Fibrillation (8472426-0)
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: atrial fibrillation (atrial fibrillation Questions) on Aug 25, 2011 from UNITED STATES Additional patient health information: Male patient , 78 years of age, weighting 252.0 lb, was diagnosed with
- gastric ulcer haemorrhage
Patient was taking other medications:
- TADOR (30 Meq, Qd) (View Tador Review and Tador Label )
- ABIRATERONE ACETATE (View Abiraterone Acetate Review and Abiraterone Acetate Label )
- GABAPENTIN (300 Mg, Bid) (View Gabapentin Review and Gabapentin Label )
- PREDNISONE TAB (15 Mg, Qd) (View Prednisone Tab Review and Prednisone Tab Label )
- PROCRIT (Unk, Qwk) (View Procrit Review and Procrit Label )
No Adverse Event (8471948-6)
Adverse event was reported on Jun 20, 2012 by a Female patient taking Protonix (View Usage) (Dosage: Unk) . Location: UNITED STATES , weighting 123.0 lb, Patient had the following side effects: no adverse event.
Patient was taking other medications:
- PLAVIX (Unk) (View Plavix Review and Plavix Label )
- LIPITOR (Unk) (View Lipitor Review and Lipitor Label )
Dyspnoea, Bone Marrow Failure, Thrombocytopenia, Anaemia, Myelofibrosis, Pneumonia, Disease Progression (8471846-8)
on Dec 13, 2011 Female patient from UNITED STATES , 59 years of age, was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: dyspnoea, bone marrow failure, thrombocytopenia, anaemia, myelofibrosis, pneumonia (pneumonia Questions), disease progression. Protonix dosage: N/A.
Patient was taking other medications:
- TEGRETOL (View Tegretol Review and Tegretol Label )
- RISPERDAL (View Risperdal Review and Risperdal Label )
- CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label )
- DETROL (View Detrol Review and Detrol Label )
- VICODIN (View Vicodin Review and Vicodin Label )
- MEGACE (View Megace Review and Megace Label )
- KEFLEX (View Keflex Review and Keflex Label )
- LANTUS (View Lantus Review and Lantus Label )
Pneumonia (8471616-0)
on Dec 06, 2011 Male patient from UNITED STATES , 65 years of age, weighting 380.0 lb, was treated with Protonix(View Usage). Patient experienced the following unwanted or unexpected effects: pneumonia (pneumonia Questions). Protonix dosage: N/A.
Patient was taking other medications:
- LOVENOX (View Lovenox Review and Lovenox Label )
- DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label )
- VELCADE (View Velcade Review and Velcade Label )
- COUMADIN (View Coumadin Review and Coumadin Label )
- TORSEMIDE (View Torsemide Review and Torsemide Label )
- VALACYCLOVIR (VALACICLOVIR HYDROCHLORIDE) (View Valacyclovir (valaciclovir Hydrochloride) Review and Valacyclovir (valaciclovir Hydrochloride) Label )
- TAMSULOSIN ER (TAMSULOSIN) (View Tamsulosin Er (tamsulosin) Review and Tamsulosin Er (tamsulosin) Label )
- MORPHINE (View Morphine Review and Morphine Label )
Creatinine Renal Clearance Decreased, Anaemia (8470448-7)
Patient was taking Protonix (View Usage). Patient had the following side effects: creatinine renal clearance decreased, anaemia on Nov 30, 2011 from UNITED STATES Additional patient health information: Male patient , 61 years of age, . Protonix dosage: N/A.
Patient was taking other medications:
- ZESTRIL (View Zestril Review and Zestril Label )
- DECADRON (View Decadron Review and Decadron Label )
- ASPIRIN (ACETYLSALCYCLIC ACID) (View Aspirin (acetylsalcyclic Acid) Review and Aspirin (acetylsalcyclic Acid) Label )
- NITROSTAT (View Nitrostat Review and Nitrostat Label )
- LENALIDOMIDE (25 Mg, Daily For 21/28 Days, Po ; 25 Mg, Daily For 21/28 Days, Po) (View Lenalidomide Review and Lenalidomide Label )
Glaucoma, Chronic Obstructive Pulmonary Disease, Emphysema (8469385-3)
Adverse event was reported on Jun 22, 2012 by a Female patient taking Protonix (View Usage) (Dosage: 40 Mg, Daily) was diagnosed with
- gastrooesophageal reflux disease
- glaucoma (glaucoma Questions)
- diabetes mellitus
- neuropathy peripheral
Patient was taking other medications:
- XALATAN (Unk, Daily) (View Xalatan Review and Xalatan Label )
- METFORMIN (500 Mg, 2x/day) (View Metformin Review and Metformin Label )
- LYRICA (75 Mg, 2x/day) (View Lyrica Review and Lyrica Label )
Vomiting, Oesophageal Ulcer, Dyspepsia, Gastrooesophageal Reflux Disease, Pain (8465542-0)
on Jun 11, 2012 Male patient from UNITED STATES , 54 years of age, was treated with Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: vomiting, oesophageal ulcer, dyspepsia, gastrooesophageal reflux disease, pain (pain Questions). Protonix dosage: N/A.
Patient was taking other medications:
- NEXIUM (View Nexium Review and Nexium Label )
No Adverse Event (8461502-4)
on Jun 20, 2012 Female patient from UNITED STATES , weighting 123.0 lb, was treated with Protonix(View Usage). Patient had the following side effects: no adverse event. Protonix dosage: Unk.
Patient was taking other medications:
- PLAVIX (Unk) (View Plavix Review and Plavix Label )
Tremor (8461455-9)
Patient was taking Protonix (View Usage). After Protonix was administered, patient had the following side effects: tremor on Jun 19, 2012 from UNITED STATES Additional patient health information: Female patient , weighting 135.0 lb, was diagnosed with
- ulcer (ulcer Questions)
- gastrooesophageal reflux disease
Gastric Disorder, Dyspnoea, Cardiac Disorder, Abdominal Discomfort, Dyspepsia, Gastric Polyps (8459430-3)
Adverse event was reported on Jun 20, 2012 by a Male patient taking Protonix (View Usage) (Dosage: 40 Mg, Daily) was diagnosed with
- gastrooesophageal reflux disease
- hypertension
Patient was taking other medications:
- HYDROCHLOROTHIAZIDE (10 Mg, Daily) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label )
- TOPROL XL (100 Mg, Daily) (View Toprol-xl Review and Toprol-xl Label )
Vomiting, Gastrointestinal Pain, Gastric Disorder, Nausea (8456816-8)
on Jun 18, 2012 Female patient from UNITED STATES , weighting 202.8 lb, was diagnosed with
- gastric disorder
- convulsion
Patient was taking other medications:
- DILANTIN (Unk) (View Dilantin Review and Dilantin Label )
- PHENOBARBITAL (Unk) (View Phenobarbital Review and Phenobarbital Label )
- ATENOLOL (25 Mg, 1x/day) (View Atenolol Review and Atenolol Label )
- DIAZEPAM (Unk) (View Diazepam Review and Diazepam Label )
Impaired Healing, Swollen Tongue, Oral Discomfort, Gingival Swelling, Oral Mucosal Erythema, Diabetes Mellitus (8455063-3)
on Jun 15, 2012 Female patient from UNITED STATES , 75 years of age, weighting 146.1 lb, was treated with Protonix(View Usage). After Protonix was administered, patient had the following side effects: impaired healing, swollen tongue, oral discomfort, gingival swelling, oral mucosal erythema, diabetes mellitus. Protonix dosage: 1 40 Mg. Tab Daily Daily Po.
Nausea, Ill-defined Disorder, Decreased Appetite, Headache, Weight Increased, Tachycardia (8452103-2)
Patient was taking Protonix (View Usage). Patient experienced the following unwanted or unexpected effects: nausea (nausea Questions), ill-defined disorder, decreased appetite, headache (headache Questions), weight increased, tachycardia on Jun 13, 2012 from UNITED STATES Additional patient health information: Male patient , 45 years of age, weighting 260.6 lb, . Protonix dosage: N/A.
Patient was taking other medications:
- ALDACTONE (25mg Per Day) (View Aldactone Review and Aldactone Label )
- REVATIO (20mg Three Times Per Day) (View Revatio Review and Revatio Label )
- TRACLEER (62.5mg Twice Per Day) (View Tracleer Review and Tracleer Label )
- LASIX (60mg Twice Per Day) (View Lasix Review and Lasix Label )
- NEURONTIN (View Neurontin Review and Neurontin Label )
- METOLAZONE (View Metolazone Review and Metolazone Label )
- COREG (View Coreg Review and Coreg Label )
- FLOLAN (View Flolan Review and Flolan Label )
Dyspepsia, Gastrooesophageal Reflux Disease (8448175-1)
Adverse event was reported on Jun 12, 2012 by a Female patient taking Protonix (View Usage) (Dosage: N/A) . Location: UNITED STATES , 56 years of age, Patient had the following side effects: dyspepsia, gastrooesophageal reflux disease.
Patient was taking other medications:
- NEXIUM (View Nexium Review and Nexium Label )
- SYMBICORT (View Symbicort Review and Symbicort Label )
- GAVISCON (View Gaviscon Review and Gaviscon Label )
Mantle Cell Lymphoma (8446548-4)
on Jun 13, 2012 Male patient from UNITED STATES , weighting 157.0 lb, was treated with Protonix (View Usage). After Protonix was administered, patient had the following side effects: mantle cell lymphoma. Protonix dosage: Unk.
Patient was taking other medications:
- DDAVP (0.1 Mg, Unk) (View Ddavp Review and Ddavp Label )
- LANTUS (View Lantus Review and Lantus Label )
- ZANTAC (200) (View Zantac Review and Zantac Label )
- XANAX (View Xanax Review and Xanax Label )
- SOMATROPIN (0.5 Mg, Daily (1/d)) (View Somatropin Review and Somatropin Label )
- MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label )
- PREDNISONE (10 Mg, Unk) (View Prednisone Review and Prednisone Label )
- LEVOTHYROXINE SODIUM (0.75 Mg, Unk) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label )
Cardiac Murmur, Pyrexia, Decreased Appetite, Tinnitus, Fungal Sepsis, Foot Operation, Dehydration, Goitre, Chills (8446323-0)
on Apr 04, 2012 Female patient from UNITED STATES , weighting 212.0 lb, was treated with Protonix(View Usage). Patient experienced the following unwanted or unexpected effects: cardiac murmur, pyrexia, decreased appetite, tinnitus (tinnitus Questions), fungal sepsis, foot operation, dehydration, goitre, chills. Protonix dosage: Unk.
Patient was taking other medications:
- METHOTREXATE SODIUM (View Methotrexate Sodium Review and Methotrexate Sodium Label )
- SYNTHROID (Unk) (View Synthroid Review and Synthroid Label )
- NORVASC (Unk) (View Norvasc Review and Norvasc Label )
- RESTORIL (Unk) (View Restoril Review and Restoril Label )
- ENBREL (50 Mg, Qwk) (View Enbrel Review and Enbrel Label )
- PREMARIN (Unk) (View Premarin Review and Premarin Label )
Showing 1-25 of 1180 Next Page >
Share Your Experience, Discuss with Others
Protonix InformationAlternative PROTONIX Names:PANTOPRAZ Substance:PANTOPRAZ Protonix Dosage, Warnings, Usage. Side Effects reported to FDA: 1180. View FDA Adverse Reports Protonix safety alerts: 2004 Reported deaths: 43 Reported hospitalizations: 371
| ||||||||||||||||||||||