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

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, 5 individuals taking ALIZAPRIDE reported HAEMORRHAGE 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 HAEMORRHAGE. In doing so, we compare ALIZAPRIDE with other drugs that cause HAEMORRHAGE, to help you evaluate whether or not ALIZAPRIDE causes HAEMORRHAGE. Likewise, this page shows the most highly-reported side effects of ALIZAPRIDE, so you can see if HAEMORRHAGE ranks among ALIZAPRIDE's most well-known side effects.
Summary Statistics
Reports of ALIZAPRIDE causing HAEMORRHAGE: 5
Reports of any side effect of ALIZAPRIDE : 102
Percentage of ALIZAPRIDE patients where HAEMORRHAGE is a reported side effect: 4.9020%

FDA reports of any drug causing HAEMORRHAGE : 25320
Average percentage for all medicated patients where HAEMORRHAGE is reported as a complication: 0.1587%

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 HAEMORRHAGE:

ASPIRIN (2495 patients)
HEPARIN SODIUM INJECTION (1680 patients)
COUMADIN (1484 patients)
PRADAXA (1316 patients)
WARFARIN SODIUM (1267 patients)
PLAVIX (1084 patients)
FOSAMAX (1041 patients)
VIOXX (1016 patients)
MISOPROSTOL (979 patients)
HUMIRA (848 patients)
LASIX (824 patients)
LISINOPRIL (785 patients)
LIPITOR (756 patients)
PREDNISONE (735 patients)
FORTEO (718 patients)
FUROSEMIDE (705 patients)
CELEBREX (674 patients)
LOVENOX (669 patients)
NEXIUM (649 patients)
ZOMETA (649 patients)
AVONEX (644 patients)
REVLIMID (625 patients)
DOXYCYCLINE (581 patients)
OMEPRAZOLE (581 patients)
REMICADE (542 patients)
ATENOLOL (536 patients)
HEPARIN (521 patients)
DEXAMETHASONE (517 patients)
SIMVASTATIN (492 patients)
SYNTHROID (488 patients)
DIGOXIN (486 patients)
FOLIC ACID (482 patients)
MIFEPRISTONE TABLETS, 200 MG (DANCO LABS) (445 patients)
ACETAMINOPHEN (440 patients)
METHOTREXATE (426 patients)
NORVASC (423 patients)
POTASSIUM CHLORIDE (417 patients)
PREDNISOLONE (415 patients)
HEPARIN SODIUM (415 patients)
LEVOTHYROXINE SODIUM (414 patients)
ACCUTANE (407 patients)
MIFEPRISTONE (MIFEPREX) (396 patients)
ALLOPURINOL (387 patients)
AREDIA (370 patients)
VITAMIN D (360 patients)
PRILOSEC (357 patients)
PROTONIX (355 patients)
OXYCONTIN (346 patients)
XANAX (333 patients)
ZOCOR (332 patients)
SEROQUEL (329 patients)
NPLATE (328 patients)
NEURONTIN (325 patients)
ZOLOFT (324 patients)
ARIXTRA (316 patients)
ALBUTEROL (316 patients)
LYRICA (313 patients)
METOPROLOL TARTRATE (311 patients)
TOPROL-XL (311 patients)
IBUPROFEN (310 patients)
AMBIEN (306 patients)
CRESTOR (306 patients)
PREDNISONE TAB (303 patients)
HYDROCHLOROTHIAZIDE (300 patients)
PREVACID (298 patients)
ENBREL (293 patients)
DIOVAN (283 patients)
MORPHINE (282 patients)
LORAZEPAM (281 patients)
LANTUS (281 patients)
VICODIN (276 patients)
CLOPIDOGREL (274 patients)
MULTI-VITAMINS (272 patients)
PREMARIN (265 patients)
CALCIUM (264 patients)
CYMBALTA (263 patients)
LEVAQUIN (263 patients)
EXJADE (252 patients)
METFORMIN HCL (252 patients)
MIRENA (252 patients)
INSULIN (251 patients)
WARFARIN (250 patients)
FENTANYL (242 patients)
ENOXAPARIN SODIUM (241 patients)
CLONAZEPAM (240 patients)
TRACLEER (240 patients)
METOPROLOL (237 patients)
LANSOPRAZOLE (236 patients)
SUTENT (231 patients)
ZOFRAN (229 patients)
DIANEAL (228 patients)
PAXIL (222 patients)
ATIVAN (220 patients)
AMLODIPINE (220 patients)
TYLENOL (CAPLET) (219 patients)
SPIRONOLACTONE (217 patients)
AVASTIN (212 patients)
LETAIRIS (212 patients)
ADVAIR DISKUS 100/50 (211 patients)
XARELTO (210 patients)
TYLENOL (209 patients)
GABAPENTIN (209 patients)
CYCLOPHOSPHAMIDE (209 patients)
VANCOMYCIN (208 patients)
DECADRON (206 patients)
PEGASYS (203 patients)
FLUCONAZOLE (202 patients)
ZYPREXA (201 patients)
LEXAPRO (200 patients)
ARANESP (199 patients)
COREG (198 patients)
BENADRYL (194 patients)
GLEEVEC (193 patients)
OXYCODONE HCL (190 patients)
CELEXA (187 patients)
NITROGLYCERIN (186 patients)
PERCOCET (184 patients)
MULTI-VITAMIN (184 patients)
VITAMIN E (181 patients)
FLUOROURACIL (180 patients)
REBIF (179 patients)
ASCORBIC ACID (178 patients)
RAMIPRIL (178 patients)
FERROUS SULFATE TAB (177 patients)
TRAMADOL HCL (176 patients)
XIGRIS (176 patients)
CISPLATIN (175 patients)
HUMALOG (175 patients)
CIPROFLOXACIN (175 patients)
ACETYLSALICYLIC ACID SRT (174 patients)
ENALAPRIL MALEATE (173 patients)
BEXTRA (173 patients)
ZANTAC (172 patients)
ALDACTONE (171 patients)
ANGIOMAX (171 patients)
FAMOTIDINE (168 patients)
IRON (167 patients)
RANITIDINE (167 patients)
SOLU-MEDROL (166 patients)
FISH OIL (166 patients)
VINCRISTINE (165 patients)
REFACTO (165 patients)
RITUXIMAB (164 patients)
GLYBURIDE (162 patients)
DIAZEPAM (161 patients)
ALPRAZOLAM (161 patients)
SINGULAIR (160 patients)
VITAMIN B-12 (160 patients)
CALCIUM CARBONATE (158 patients)
ZETIA (157 patients)
KOGENATE FS (156 patients)
DIFLUCAN (156 patients)
ZYRTEC (154 patients)
PANTOPRAZOLE (153 patients)
DURAGESIC-100 (151 patients)
SANDOSTATIN LAR (151 patients)
NAPROXEN (151 patients)
NOVOSEVEN (151 patients)
BYETTA (150 patients)
PROZAC (148 patients)
KEPPRA (148 patients)
VELCADE (148 patients)
VOLTAREN (147 patients)
METOPROLOL SUCCINATE (147 patients)
AMIODARONE HCL (145 patients)
MORPHINE SULFATE (145 patients)
CLONIDINE (145 patients)
SPIRIVA (143 patients)
CYTARABINE (143 patients)
NEXAVAR (143 patients)
FLOMAX (142 patients)
BACTRIM (142 patients)
COLACE (141 patients)
LOPRESSOR (141 patients)
AMOXICILLIN (140 patients)
CHANTIX (140 patients)
TYSABRI (139 patients)
METHYLPREDNISOLONE (138 patients)
RIBAVIRIN (137 patients)
XELODA (136 patients)
ADVATE (136 patients)
CARVEDILOL (133 patients)
ACYCLOVIR (133 patients)
THALOMID (133 patients)
PROMETHAZINE (131 patients)
HEPARIN SODIUM 1,000 UNITS AND SODIUM CHLORIDE 0.9% (130 patients)
COZAAR (130 patients)
CITALOPRAM HYDROBROMIDE (130 patients)
REGLAN (129 patients)
HYDROCORTISONE (129 patients)
RADIATION THERAPY (128 patients)
DILAUDID (128 patients)
CARBOPLATIN (127 patients)
HEPARIN SODIUM 5,000 UNITS IN DEXTROSE 5% (125 patients)
COMPAZINE (125 patients)
ZITHROMAX (124 patients)
OXYCODONE (124 patients)
PLAN B ONE-STEP (124 patients)
LORTAB (124 patients)
DEPO-PROVERA (123 patients)
PEPCID (123 patients)
CYCLOSPORINE (122 patients)
PANTOPRAZOLE SODIUM (122 patients)
TAXOTERE (121 patients)
MYCOPHENOLATE MOFETIL (121 patients)
ALEVE (120 patients)
EFFEXOR XR (120 patients)
REOPRO (120 patients)
EPOGEN (119 patients)
MOBIC (118 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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