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

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, 1 individuals taking ALIZAPRIDE reported HAEMATURIA 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 HAEMATURIA. In doing so, we compare ALIZAPRIDE with other drugs that cause HAEMATURIA, to help you evaluate whether or not ALIZAPRIDE causes HAEMATURIA. Likewise, this page shows the most highly-reported side effects of ALIZAPRIDE, so you can see if HAEMATURIA ranks among ALIZAPRIDE's most well-known side effects.
Summary Statistics
Reports of ALIZAPRIDE causing HAEMATURIA: 1
Reports of any side effect of ALIZAPRIDE : 102
Percentage of ALIZAPRIDE patients where HAEMATURIA is a reported side effect: 0.9804%

FDA reports of any drug causing HAEMATURIA : 12065
Average percentage for all medicated patients where HAEMATURIA is reported as a complication: 0.0756%

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 HAEMATURIA:

FOSAMAX (1788 patients)
ASPIRIN (1689 patients)
VIOXX (1138 patients)
ZOMETA (832 patients)
WARFARIN SODIUM (768 patients)
COUMADIN (692 patients)
LIPITOR (644 patients)
LASIX (579 patients)
PREDNISONE (566 patients)
FUROSEMIDE (475 patients)
OMEPRAZOLE (473 patients)
AREDIA (468 patients)
PLAVIX (452 patients)
PRADAXA (452 patients)
SIMVASTATIN (448 patients)
LISINOPRIL (439 patients)
DIGOXIN (411 patients)
ZOCOR (407 patients)
NEXIUM (395 patients)
ATENOLOL (382 patients)
HEPARIN SODIUM INJECTION (363 patients)
NEURONTIN (360 patients)
PROTONIX (358 patients)
ALLOPURINOL (357 patients)
LOVENOX (354 patients)
OXYCONTIN (353 patients)
PREDNISOLONE (353 patients)
ACETAMINOPHEN (346 patients)
IMMUCYST (338 patients)
NORVASC (330 patients)
PRILOSEC (329 patients)
VICODIN (327 patients)
LEVAQUIN (326 patients)
METHOTREXATE (321 patients)
FOLIC ACID (309 patients)
PERCOCET (308 patients)
ZOLOFT (307 patients)
DEXAMETHASONE (302 patients)
AMBIEN (297 patients)
IBUPROFEN (294 patients)
CELEBREX (289 patients)
POTASSIUM CHLORIDE (282 patients)
ACTOS (280 patients)
METFORMIN HCL (277 patients)
CYCLOSPORINE (274 patients)
SEROQUEL (270 patients)
ZYPREXA (268 patients)
ZOFRAN (265 patients)
SYNTHROID (265 patients)
HYDROCHLOROTHIAZIDE (261 patients)
ALBUTEROL (258 patients)
DECADRON (257 patients)
FLOMAX (256 patients)
CYCLOPHOSPHAMIDE (253 patients)
CRESTOR (245 patients)
XANAX (240 patients)
NEORAL (239 patients)
LORAZEPAM (239 patients)
PREDNISONE TAB (238 patients)
AUGMENTIN '125' (232 patients)
SOLIRIS (229 patients)
ARANESP (222 patients)
ATIVAN (222 patients)
REMICADE (217 patients)
AMOXICILLIN (217 patients)
OXYCODONE HCL (214 patients)
LEVOTHYROXINE SODIUM (213 patients)
TOPROL-XL (212 patients)
METOPROLOL TARTRATE (208 patients)
HEPARIN (207 patients)
MULTI-VITAMINS (203 patients)
CIPROFLOXACIN (202 patients)
COLACE (195 patients)
REVLIMID (194 patients)
CARBOPLATIN (192 patients)
ADVAIR DISKUS 100/50 (192 patients)
ZITHROMAX (192 patients)
VITAMIN D (190 patients)
AVASTIN (189 patients)
INSULIN (187 patients)
ZANTAC (186 patients)
MYCOPHENOLATE MOFETIL (186 patients)
DIOVAN (185 patients)
AMLODIPINE (184 patients)
PREMARIN (182 patients)
ACCUTANE (182 patients)
PROZAC (182 patients)
HUMIRA (181 patients)
EXJADE (177 patients)
CASODEX (176 patients)
FINASTERIDE (173 patients)
LYRICA (173 patients)
ALENDRONATE SODIUM (173 patients)
LANTUS (172 patients)
VANCOMYCIN (172 patients)
THALIDOMIDE (171 patients)
MORPHINE (166 patients)
FLUOROURACIL (164 patients)
GLEEVEC (164 patients)
CALCIUM CARBONATE (161 patients)
CALCIUM (160 patients)
GABAPENTIN (159 patients)
RANITIDINE (156 patients)
PAXIL (155 patients)
PREVACID (153 patients)
FORTEO (152 patients)
SPIRIVA (152 patients)
LEXAPRO (152 patients)
PROCRIT /00909301/ (151 patients)
TAXOTERE (151 patients)
BACTRIM (149 patients)
ACTONEL (147 patients)
SUTENT (146 patients)
WELLBUTRIN (145 patients)
FENTANYL (144 patients)
LANSOPRAZOLE (143 patients)
VELCADE (143 patients)
COREG (143 patients)
CLONAZEPAM (143 patients)
COMPAZINE (143 patients)
CYMBALTA (142 patients)
FLUCONAZOLE (142 patients)
ASCORBIC ACID (142 patients)
CEPHALEXIN (141 patients)
GLIPIZIDE (140 patients)
ACYCLOVIR (140 patients)
ALLEGRA (139 patients)
PEPCID (139 patients)
DILAUDID (139 patients)
EFFEXOR (138 patients)
CHEMOTHERAPEUTICS NOS (138 patients)
TAXOL (136 patients)
CELEXA (135 patients)
ALPRAZOLAM (134 patients)
ENBREL (134 patients)
SINGULAIR (134 patients)
SPIRONOLACTONE (133 patients)
LORTAB (133 patients)
NITROGLYCERIN (132 patients)
METOPROLOL (132 patients)
NEUPOGEN (132 patients)
GLUCOPHAGE (130 patients)
TRAMADOL HCL (130 patients)
AMARYL (129 patients)
RAMIPRIL (129 patients)
WARFARIN (129 patients)
SANDOSTATIN LAR (128 patients)
LUPRON (127 patients)
TYLENOL (CAPLET) (125 patients)
CARVEDILOL (125 patients)
ROCEPHIN (124 patients)
LOPRESSOR (123 patients)
GLYBURIDE (123 patients)
XELODA (122 patients)
NPLATE (122 patients)
DURAGESIC-100 (121 patients)
NEXAVAR (121 patients)
MORPHINE SULFATE (121 patients)
MULTI-VITAMIN (121 patients)
FERROUS SULFATE TAB (121 patients)
BENADRYL (120 patients)
CHLORHEXIDINE GLUCONATE (120 patients)
FISH OIL (120 patients)
LIDOCAINE (118 patients)
ZYRTEC (118 patients)
METHYLPREDNISOLONE (117 patients)
VITAMIN B-12 (116 patients)
FLEXERIL (115 patients)
ELAVIL (114 patients)
MS CONTIN (114 patients)
CALCIUM (UNSPECIFIED) (114 patients)
CISPLATIN (112 patients)
AZITHROMYCIN (112 patients)
KEFLEX (112 patients)
ENALAPRIL MALEATE (111 patients)
CIPRO (110 patients)
CLOPIDOGREL (110 patients)
RIBAVIRIN (109 patients)
RADIATION THERAPY (109 patients)
METOPROLOL SUCCINATE (109 patients)
TYLENOL (109 patients)
METRONIDAZOLE (109 patients)
NYSTATIN (109 patients)
DIFLUCAN (108 patients)
IRON (108 patients)
ENOXAPARIN SODIUM (107 patients)
SOLU-MEDROL (107 patients)
COZAAR (107 patients)
VITAMIN E (107 patients)
FOSAMAX PLUS D (106 patients)
CLARITIN (106 patients)
VALTREX (105 patients)
PREVISCAN (105 patients)
CYTOXAN (104 patients)
PROSCAR (104 patients)
METFORMIN (102 patients)
HYDROCODONE (101 patients)
ZETIA (100 patients)
FAMOTIDINE (100 patients)
MOTRIN (99 patients)
AMIODARONE HCL (99 patients)
CYTARABINE (99 patients)
PHENERGAN (99 patients)
ALDACTONE (98 patients)
FLONASE (97 patients)
TRAZODONE HCL (97 patients)
DIAZEPAM (97 patients)
PANTOPRAZOLE (96 patients)
CLONIDINE (95 patients)
REGLAN (95 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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