About this FactMed analysis covering adverse side effect reports of ALIZAPRIDE patients who developed GASTROENTERITIS.

FactMed provides MD-approved analysis to help both patients, researchers, and physicians accurately assess the risk profile for more than 20,000 different pharmaceutical products. The below report offers compiled information from Food & Drug Administration and FactMed user submissions. Between January 2004 and October 2012, 2 individuals taking ALIZAPRIDE reported GASTROENTERITIS to the FDA. A total of 102 ALIZAPRIDE drug adverse event reaction reports were made with the FDA during this time period. Often the FDA only receives reports of the most critical and severe cases; these numbers may therefore underrepresent the complication rate of the medication.

FDA Research Report

Introduction This page is designed to help you determine the relationship, if any, between ALIZAPRIDE and GASTROENTERITIS. In doing so, we compare ALIZAPRIDE with other drugs that cause GASTROENTERITIS, to help you evaluate whether or not ALIZAPRIDE causes GASTROENTERITIS. Likewise, this page shows the most highly-reported side effects of ALIZAPRIDE, so you can see if GASTROENTERITIS ranks among ALIZAPRIDE's most well-known side effects.
Summary Statistics
Reports of ALIZAPRIDE causing GASTROENTERITIS: 2
Reports of any side effect of ALIZAPRIDE : 102
Percentage of ALIZAPRIDE patients where GASTROENTERITIS is a reported side effect: 1.9608%

FDA reports of any drug causing GASTROENTERITIS : 6305
Average percentage for all medicated patients where GASTROENTERITIS is reported as a complication: 0.0395%

Physician opinion on ALIZAPRIDE as adverse event culprit:

Overall opinion for all reports of this drug:
Most frequent diagnoses/indications for prescribing ALIZAPRIDE:
DRUG USE FOR UNKNOWN INDICATION ( 14 patients )
NAUSEA ( 14 patients )
PRODUCT USED FOR UNKNOWN INDICATION ( 3 patients )
PREMEDICATION ( 2 patients )
VOMITING ( 2 patients )
ANTIEMETIC SUPPORTIVE CARE ( 2 patients )
PROPHYLAXIS ( 1 patients )
PROPHYLAXIS OF NAUSEA AND VOMITING ( 1 patients )
( 0 patients )
Drugs with high FDA adverse event association with GASTROENTERITIS:

ACCUTANE (1026 patients)
VIOXX (854 patients)
FOSAMAX (825 patients)
ASPIRIN (662 patients)
REMICADE (502 patients)
PREDNISOLONE (436 patients)
PREDNISONE (411 patients)
SEROQUEL (381 patients)
METHOTREXATE (284 patients)
NEXIUM (281 patients)
LASIX (280 patients)
LIPITOR (275 patients)
FOLIC ACID (267 patients)
OMEPRAZOLE (263 patients)
ACETAMINOPHEN (261 patients)
FUROSEMIDE (235 patients)
LISINOPRIL (221 patients)
XANAX (220 patients)
AMBIEN (216 patients)
SIMVASTATIN (216 patients)
COUMADIN (214 patients)
HUMIRA (210 patients)
ZOMETA (205 patients)
PRILOSEC (199 patients)
SYNTHROID (198 patients)
PROTONIX (197 patients)
ZOCOR (194 patients)
NORVASC (193 patients)
PREDNISONE TAB (192 patients)
BIOFERMIN R (192 patients)
MYCOPHENOLATE MOFETIL (187 patients)
NEURONTIN (186 patients)
ZOLOFT (180 patients)
LEVOTHYROXINE SODIUM (178 patients)
LEVAQUIN (178 patients)
PREVACID (177 patients)
IBUPROFEN (175 patients)
METFORMIN HCL (172 patients)
TOCILIZUMAB (170 patients)
MEIACT (162 patients)
DIGOXIN (159 patients)
PLAVIX (157 patients)
ATENOLOL (157 patients)
CELEBREX (153 patients)
ALLOPURINOL (150 patients)
PREMARIN (149 patients)
HEPARIN SODIUM INJECTION (146 patients)
ZOFRAN (146 patients)
LORAZEPAM (145 patients)
REVLIMID (142 patients)
ALBUTEROL (142 patients)
CYCLOSPORINE (142 patients)
FORTEO (141 patients)
HYDROCHLOROTHIAZIDE (141 patients)
POTASSIUM CHLORIDE (137 patients)
VICODIN (136 patients)
ATIVAN (136 patients)
AREDIA (127 patients)
BYETTA (122 patients)
FOSAMAX PLUS D (122 patients)
TOPROL-XL (121 patients)
DIOVAN (118 patients)
LEXAPRO (117 patients)
LYRICA (116 patients)
TACROLIMUS (116 patients)
LANTUS (115 patients)
NEVIRAPINE (115 patients)
ZITHROMAX (115 patients)
SYNAGIS (114 patients)
PROZAC (114 patients)
PAXIL (111 patients)
ZYRTEC (110 patients)
MULTI-VITAMINS (110 patients)
KLARICID:DRYSYRUP (108 patients)
REGLAN (108 patients)
ZYPREXA (107 patients)
DEXAMETHASONE (107 patients)
CLONAZEPAM (106 patients)
AMLODIPINE (106 patients)
FLAGYL (105 patients)
CYCLOPHOSPHAMIDE (104 patients)
CELEXA (103 patients)
CALCIUM (101 patients)
COMPAZINE (100 patients)
GLUCOPHAGE (100 patients)
PERCOCET (99 patients)
ENALAPRIL MALEATE (98 patients)
VITAMIN D (98 patients)
NITROGLYCERIN (97 patients)
VITAMIN E (96 patients)
LANSOPRAZOLE (96 patients)
RISPERDAL (96 patients)
AMOXICILLIN (95 patients)
PREDONINE (94 patients)
METHYLPREDNISOLONE (94 patients)
MULTI-VITAMIN (94 patients)
FLUOROURACIL (94 patients)
ACTONEL (94 patients)
ALDACTONE (94 patients)
METOPROLOL TARTRATE (93 patients)
ZANTAC (93 patients)
OXYCONTIN (93 patients)
NEORAL (91 patients)
METOCLOPRAMIDE (90 patients)
LORTAB (90 patients)
CALCIUM CARBONATE (90 patients)
SIROLIMUS (90 patients)
ALPRAZOLAM (89 patients)
ALENDRONATE SODIUM (89 patients)
YASMIN (88 patients)
EFFEXOR (87 patients)
TRAMADOL HCL (86 patients)
INSULIN (85 patients)
GABAPENTIN (83 patients)
SINGULAIR (83 patients)
METFORMIN (82 patients)
TYLENOL (82 patients)
LAMIVUDINE (82 patients)
PANTOPRAZOLE (81 patients)
IMODIUM (81 patients)
KLONOPIN (80 patients)
TYLENOL (CAPLET) (80 patients)
FLONASE (79 patients)
BACTRIM (79 patients)
[THERAPY UNSPECIFIED] (79 patients)
ADVAIR DISKUS 100/50 (79 patients)
RAMIPRIL (78 patients)
BERACHIN:SYRUP (78 patients)
SPIRONOLACTONE (77 patients)
ELAVIL (77 patients)
SODIUM CHLORIDE (76 patients)
PROGRAF (76 patients)
FLOMAX (76 patients)
RIBAVIRIN (76 patients)
RANITIDINE (76 patients)
AVONEX (76 patients)
CYMBALTA (75 patients)
COREG (74 patients)
ZIDOVUDINE (74 patients)
BENADRYL (73 patients)
FAMOTIDINE (73 patients)
CLARITIN (73 patients)
ULTRAM (72 patients)
ENBREL (71 patients)
CIPROFLOXACIN (71 patients)
SANDOSTATIN LAR (70 patients)
PHENERGAN (70 patients)
HYDROCORTISONE (70 patients)
CARVEDILOL (70 patients)
FLUCONAZOLE (69 patients)
COZAAR (69 patients)
CRESTOR (69 patients)
PANTOPRAZOLE SODIUM (68 patients)
VITAMINS (UNSPECIFIED) (68 patients)
CLOZARIL (68 patients)
ATORVASTATIN CALCIUM (68 patients)
MUCOSOLVAN DS FOR PEDIATRIC (66 patients)
DILAUDID (66 patients)
MORPHINE (66 patients)
CELLCEPT (66 patients)
CLONIDINE (66 patients)
DIFLUCAN (65 patients)
ALLEGRA (65 patients)
ROCEPHIN (64 patients)
OXYCODONE HCL (64 patients)
NYSTATIN (64 patients)
ORTHO TRI-CYCLEN (63 patients)
REMERON (63 patients)
ANTIHISTAMINES (63 patients)
METOPROLOL SUCCINATE (63 patients)
TYSABRI (62 patients)
CYANOCOBALAMIN (62 patients)
FLEXERIL (62 patients)
WARFARIN SODIUM (62 patients)
TRAZODONE HCL (61 patients)
COLACE (60 patients)
LOPRESSOR (60 patients)
DIPHENHYDRAMINE HCL (60 patients)
MAGNESIUM OXIDE (60 patients)
LEUCOVORIN CALCIUM (60 patients)
DECADRON (60 patients)
INFLIXIMAB (60 patients)
METRONIDAZOLE (60 patients)
PEPCID (60 patients)
DURAGESIC-100 (60 patients)
PLACEBO (60 patients)
GOLIMUMAB (60 patients)
SOMA (60 patients)
EXJADE (59 patients)
VENTOLIN (59 patients)
IRON (59 patients)
AVASTIN (59 patients)
DIAZEPAM (58 patients)
RITUXIMAB (58 patients)
WELLBUTRIN (58 patients)
PROMETHAZINE (58 patients)
NAPROXEN (58 patients)
REBIF (58 patients)
AVANDIA (56 patients)
ARICEPT (56 patients)
GLIPIZIDE (56 patients)
VOLTAREN (56 patients)
VALIUM (56 patients)
ACYCLOVIR (56 patients)
MIRALAX (56 patients)
MUCODYNE (55 patients)
PREMPRO (55 patients)
COMBIVIR (55 patients)
MOTRIN (55 patients)
ACTOS (54 patients)
Most common side effects for patients taking ALIZAPRIDE:
DIARRHOEA (16 patients)
PYREXIA (16 patients)
VOMITING (10 patients)
FATIGUE (9 patients)
HYPOKALAEMIA (9 patients)
DEHYDRATION (8 patients)
NAUSEA (7 patients)
ANAEMIA (6 patients)
ASTHENIA (6 patients)
BRONCHOPNEUMONIA (6 patients)
DRUG INTERACTION (6 patients)
DYSPNOEA (6 patients)
HYPOTENSION (6 patients)
PNEUMONIA (6 patients)
GENERAL PHYSICAL HEALTH DETERIORATION (5 patients)
HAEMORRHAGE (5 patients)
HYPOMAGNESAEMIA (5 patients)
HYPOPHOSPHATAEMIA (5 patients)
JAUNDICE (5 patients)
RESPIRATORY FAILURE (5 patients)
SOMNOLENCE (5 patients)
TACHYCARDIA (5 patients)
ABDOMINAL PAIN (4 patients)
ADVERSE DRUG REACTION (4 patients)
FALL (4 patients)
HAEMODIALYSIS (4 patients)
HAEMOGLOBIN DECREASED (4 patients)
INTESTINAL OBSTRUCTION (4 patients)
MALAISE (4 patients)
SLEEP APNOEA SYNDROME (4 patients)
SUPRAVENTRICULAR TACHYCARDIA (4 patients)
THROMBOCYTHAEMIA (4 patients)
THROMBOCYTOPENIA (4 patients)
WHITE BLOOD CELL COUNT DECREASED (4 patients)
ACUTE RESPIRATORY DISTRESS SYNDROME (3 patients)
BACTERIAL SEPSIS (3 patients)
BLOOD BILIRUBIN INCREASED (3 patients)
BLOOD CREATININE INCREASED (3 patients)
DECREASED APPETITE (3 patients)
DERMATITIS EXFOLIATIVE (3 patients)
DEVICE DISLOCATION (3 patients)
ENTERITIS (3 patients)
FEBRILE NEUTROPENIA (3 patients)
FIBRIN D DIMER INCREASED (3 patients)
FUSOBACTERIUM INFECTION (3 patients)
HAEMOPTYSIS (3 patients)
HYPOXIA (3 patients)
ILEUS (3 patients)
LEUKAEMIA RECURRENT (3 patients)
MUCOSAL INFLAMMATION (3 patients)
NEUROTOXICITY (3 patients)
NEUTROPENIA (3 patients)
OVERDOSE (3 patients)
PRESYNCOPE (3 patients)
PROTEUS INFECTION (3 patients)
RASH (3 patients)
RENAL FAILURE ACUTE (3 patients)
SEPTIC SHOCK (3 patients)
SUPERINFECTION (3 patients)
TONGUE DISORDER (3 patients)
ACUTE PULMONARY OEDEMA (2 patients)
AGRANULOCYTOSIS (2 patients)
ATRIAL FIBRILLATION (2 patients)
BLOOD FIBRINOGEN INCREASED (2 patients)
BLOOD GLUCOSE INCREASED (2 patients)
BONE MARROW DEPRESSION (2 patients)
BONE MARROW FAILURE (2 patients)
BRONCHOPULMONARY ASPERGILLOSIS (2 patients)
C-REACTIVE PROTEIN INCREASED (2 patients)
CHILLS (2 patients)
COLITIS ISCHAEMIC (2 patients)
CONSTIPATION (2 patients)
CONVULSION (2 patients)
CORONARY ARTERY DISEASE (2 patients)
DEAFNESS (2 patients)
DIZZINESS (2 patients)
DRUG ADMINISTRATION ERROR (2 patients)
DYSPHAGIA (2 patients)
DYSURIA (2 patients)
EJECTION FRACTION DECREASED (2 patients)
ERYSIPELAS (2 patients)
FACIAL PALSY (2 patients)
FEBRILE BONE MARROW APLASIA (2 patients)
FLATULENCE (2 patients)
GASTROENTERITIS (2 patients)
HAEMATOCRIT DECREASED (2 patients)
HYPERSENSITIVITY (2 patients)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION (2 patients)
INFECTION (2 patients)
KLEBSIELLA SEPSIS (2 patients)
LEUKOPENIA (2 patients)
LYMPHANGITIS (2 patients)
LYMPHOCYTE COUNT INCREASED (2 patients)
NERVOUS SYSTEM DISORDER (2 patients)
NEUTROPHIL COUNT DECREASED (2 patients)
OEDEMA MUCOSAL (2 patients)
OTITIS MEDIA (2 patients)
PANCYTOPENIA (2 patients)
PARTIAL SEIZURES (2 patients)
PLATELET COUNT DECREASED (2 patients)
PULMONARY EMBOLISM (2 patients)
RED BLOOD CELL COUNT DECREASED (2 patients)
RENAL FAILURE (2 patients)
RHINORRHOEA (2 patients)
SHOCK (2 patients)
STREPTOCOCCAL SEPSIS (2 patients)
SUDDEN CARDIAC DEATH (2 patients)
URTICARIA (2 patients)
ACCIDENTAL OVERDOSE (1 patients)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE (1 patients)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN (1 patients)
AGITATION (1 patients)
ALVEOLITIS (1 patients)
ANOREXIA (1 patients)
ANXIETY (1 patients)
APHASIA (1 patients)
APHTHOUS STOMATITIS (1 patients)
ARACHNOIDITIS (1 patients)
BLOOD CULTURE POSITIVE (1 patients)
CALCULUS URINARY (1 patients)
CANDIDA SEPSIS (1 patients)
CANDIDIASIS (1 patients)
CARDIO-RESPIRATORY ARREST (1 patients)
CENTRAL NERVOUS SYSTEM LEUKAEMIA (1 patients)
CEREBRAL HAEMORRHAGE (1 patients)
CHEST PAIN (1 patients)
COLITIS (1 patients)
CONFUSIONAL STATE (1 patients)
COUGH (1 patients)
CYANOSIS (1 patients)
DIARRHOEA INFECTIOUS (1 patients)
DISEASE PROGRESSION (1 patients)
DISLOCATION OF VERTEBRA (1 patients)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG (1 patients)
DRUG HYPERSENSITIVITY (1 patients)
DRUG TOXICITY (1 patients)
DRY SKIN (1 patients)
ENCEPHALOPATHY (1 patients)
EPILEPSY (1 patients)
ERYTHEMA (1 patients)
FLUSHING (1 patients)
GAMMA-GLUTAMYLTRANSFERASE INCREASED (1 patients)
GENERAL PHYSICAL CONDITION ABNORMAL (1 patients)
GRAFT VERSUS HOST DISEASE (1 patients)
HAEMATURIA (1 patients)
HEADACHE (1 patients)
HYPERBILIRUBINAEMIA (1 patients)
HYPERTENSIVE CRISIS (1 patients)
HYPOACUSIS (1 patients)
HYPOAESTHESIA (1 patients)
HYPOCALCAEMIA (1 patients)
HYPOMANIA (1 patients)
HYPOVOLAEMIC SHOCK (1 patients)
KLEBSIELLA INFECTION (1 patients)
LACTOSE INTOLERANCE (1 patients)
LEUKAEMIA PLASMACYTIC (1 patients)
METASTATIC NEOPLASM (1 patients)
MULTI-ORGAN FAILURE (1 patients)
MULTIPLE MYELOMA (1 patients)
MUSCULAR WEAKNESS (1 patients)
MYALGIA (1 patients)
MYOGLOBIN BLOOD INCREASED (1 patients)
NEOPLASM (1 patients)
NEURALGIA (1 patients)
OEDEMA (1 patients)
OEDEMA PERIPHERAL (1 patients)
PAIN (1 patients)
PARESIS (1 patients)
PNEUMONIA KLEBSIELLA (1 patients)
PNEUMONITIS (1 patients)
PRODUCTIVE COUGH (1 patients)
PRURITUS (1 patients)
PULMONARY ALVEOLAR HAEMORRHAGE (1 patients)
PULMONARY HYPERTENSION (1 patients)
RADIUS FRACTURE (1 patients)
RASH GENERALISED (1 patients)
RASH MACULAR (1 patients)
RASH MACULO-PAPULAR (1 patients)
RENAL COLIC (1 patients)
RESPIRATORY DISTRESS (1 patients)
RIGHT VENTRICULAR DYSFUNCTION (1 patients)
SEPSIS (1 patients)
SKIN LESION (1 patients)
SPUTUM PURULENT (1 patients)
STAPHYLOCOCCAL BACTERAEMIA (1 patients)
STEM CELL TRANSPLANT (1 patients)
STOMATITIS (1 patients)
THROMBOSIS (1 patients)
THROMBOTIC MICROANGIOPATHY (1 patients)
TOXICITY TO VARIOUS AGENTS (1 patients)
ULNA FRACTURE (1 patients)
WEIGHT DECREASED (1 patients)

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