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

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

FDA reports of any drug causing THROMBOSIS : 28460
Average percentage for all medicated patients where THROMBOSIS is reported as a complication: 0.1784%

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 THROMBOSIS:

VIOXX (7390 patients)
YASMIN (2326 patients)
YAZ (2278 patients)
ASPIRIN (1782 patients)
HEPARIN SODIUM INJECTION (1545 patients)
AVONEX (1415 patients)
COUMADIN (1385 patients)
CELEBREX (1110 patients)
BEXTRA (969 patients)
FOSAMAX (844 patients)
PREDNISONE (824 patients)
PLAVIX (783 patients)
FORTEO (780 patients)
PREMARIN (759 patients)
LIPITOR (746 patients)
REVLIMID (745 patients)
HUMIRA (707 patients)
SYNTHROID (686 patients)
NUVARING (668 patients)
NEXIUM (636 patients)
LASIX (633 patients)
WARFARIN SODIUM (626 patients)
ORTHO EVRA (620 patients)
SEROQUEL (542 patients)
LISINOPRIL (540 patients)
IBUPROFEN (536 patients)
LOVENOX (498 patients)
PREMPRO (491 patients)
ZOLOFT (487 patients)
DROSPIRENONE AND ETHINYL ESTRADIOL (485 patients)
AVANDIA (480 patients)
METHOTREXATE (464 patients)
REMICADE (443 patients)
FOLIC ACID (441 patients)
NEURONTIN (425 patients)
OMEPRAZOLE (423 patients)
ATENOLOL (422 patients)
TYSABRI (420 patients)
TOPROL-XL (401 patients)
NORVASC (396 patients)
PROTONIX (393 patients)
XANAX (390 patients)
FUROSEMIDE (389 patients)
REBIF (389 patients)
PRILOSEC (386 patients)
ZOCOR (385 patients)
SIMVASTATIN (384 patients)
DEXAMETHASONE (379 patients)
ALBUTEROL (375 patients)
ACETAMINOPHEN (374 patients)
PREDNISONE TAB (374 patients)
HEPARIN SODIUM (369 patients)
VICODIN (365 patients)
AMBIEN (364 patients)
HYDROCHLOROTHIAZIDE (357 patients)
HEPARIN (351 patients)
POTASSIUM CHLORIDE (345 patients)
ZOMETA (345 patients)
ENBREL (343 patients)
LEXAPRO (342 patients)
PROVERA (331 patients)
LYRICA (323 patients)
PREVACID (323 patients)
PERCOCET (303 patients)
METFORMIN HCL (296 patients)
LEVOTHYROXINE SODIUM (296 patients)
MORPHINE (294 patients)
DIOVAN (291 patients)
VITAMIN D (291 patients)
TYLENOL (CAPLET) (288 patients)
DIANEAL (279 patients)
INSULIN (275 patients)
LANTUS (267 patients)
CYMBALTA (255 patients)
ALLOPURINOL (255 patients)
PREDNISOLONE (254 patients)
ZYPREXA (254 patients)
[THERAPY UNSPECIFIED] (248 patients)
ADVAIR DISKUS 100/50 (247 patients)
MOTRIN (246 patients)
NPLATE (241 patients)
AREDIA (240 patients)
METOPROLOL TARTRATE (234 patients)
CRESTOR (234 patients)
LEVAQUIN (234 patients)
OXYCONTIN (233 patients)
LORAZEPAM (230 patients)
FLUOROURACIL (227 patients)
CYCLOPHOSPHAMIDE (226 patients)
THALOMID (226 patients)
CALCIUM (226 patients)
ASCORBIC ACID (225 patients)
DIGOXIN (214 patients)
SINGULAIR (213 patients)
CISPLATIN (211 patients)
PROZAC (207 patients)
ATIVAN (207 patients)
ZOFRAN (206 patients)
METOPROLOL (206 patients)
GABAPENTIN (200 patients)
DURAGESIC-100 (199 patients)
EFFEXOR (199 patients)
GLUCOPHAGE (198 patients)
MULTI-VITAMIN (197 patients)
FLEXERIL (195 patients)
CLONAZEPAM (195 patients)
TYLENOL (194 patients)
EVISTA (194 patients)
XARELTO (194 patients)
NITROGLYCERIN (193 patients)
AVASTIN (192 patients)
COREG (192 patients)
BETASERON (189 patients)
KLONOPIN (189 patients)
LORTAB (188 patients)
ALLEGRA (186 patients)
PAXIL (184 patients)
PRADAXA (183 patients)
VINCRISTINE (182 patients)
SOLIRIS (171 patients)
ALPRAZOLAM (170 patients)
WELLBUTRIN (169 patients)
TACROLIMUS (169 patients)
HUMALOG (168 patients)
MULTI-VITAMINS (166 patients)
CHANTIX (166 patients)
ANGIOMAX (164 patients)
VITAMIN B-12 (163 patients)
TOPAMAX (163 patients)
PEGASYS (161 patients)
SANDOSTATIN LAR (161 patients)
XELODA (161 patients)
ARANESP (161 patients)
HEPARIN SODIUM 5,000 UNITS IN DEXTROSE 5% (160 patients)
MIRENA (159 patients)
BACLOFEN (158 patients)
LOPRESSOR (157 patients)
WARFARIN (157 patients)
EXJADE (154 patients)
BYETTA (154 patients)
RANITIDINE (154 patients)
SPIRONOLACTONE (153 patients)
ACCUTANE (153 patients)
ULTRAM (153 patients)
TAXOTERE (152 patients)
COLACE (152 patients)
TRAMADOL HCL (151 patients)
ARIMIDEX (150 patients)
VALIUM (150 patients)
ZYRTEC (148 patients)
CLARITIN (148 patients)
NOVOSEVEN (147 patients)
DECADRON (147 patients)
HYDROCODONE BITARTRATE (146 patients)
ALENDRONATE SODIUM (146 patients)
FENTANYL (146 patients)
OXYCODONE HCL (145 patients)
RIBAVIRIN (145 patients)
CARBOPLATIN (144 patients)
BEVACIZUMAB (143 patients)
ENALAPRIL MALEATE (142 patients)
DARVOCET (142 patients)
VITAMIN E (140 patients)
CELEXA (140 patients)
OCELLA (139 patients)
AMLODIPINE (139 patients)
CALCIUM CARBONATE (137 patients)
NAPROXEN (137 patients)
HALDOL (136 patients)
ARIXTRA (135 patients)
ANTIBIOTICS (134 patients)
BENADRYL (134 patients)
LEVOXYL (134 patients)
IMITREX (132 patients)
SPIRIVA (132 patients)
GLIPIZIDE (132 patients)
ZANTAC (132 patients)
FLUCONAZOLE (130 patients)
IRON (130 patients)
VELCADE (128 patients)
DILAUDID (127 patients)
ZITHROMAX (127 patients)
TRACLEER (127 patients)
ACTONEL (127 patients)
DOXORUBICIN HCL (126 patients)
GLYBURIDE (126 patients)
TRAZODONE HCL (125 patients)
MEDROXYPROGESTERONE ACETATE (124 patients)
TOCILIZUMAB (123 patients)
PROCRIT (122 patients)
METOPROLOL SUCCINATE (121 patients)
BONIVA (120 patients)
CEPHALEXIN (120 patients)
RITUXIMAB (120 patients)
ENOXAPARIN SODIUM (119 patients)
AMOXICILLIN (119 patients)
RAMIPRIL (118 patients)
EFFEXOR XR (118 patients)
PANTOPRAZOLE (117 patients)
ACETYLSALICYLIC ACID SRT (117 patients)
PROMETHAZINE (117 patients)
CAPECITABINE (117 patients)
REGLAN (115 patients)
CORTICOSTEROIDS (115 patients)
ACTOS (114 patients)
THALIDOMIDE (113 patients)
MORPHINE SULFATE (112 patients)
TAMOXIFEN CITRATE (112 patients)
HYDROXYZINE (112 patients)
HYDROCODONE (109 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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