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

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

FDA reports of any drug causing SHOCK : 9995
Average percentage for all medicated patients where SHOCK is reported as a complication: 0.0626%

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 SHOCK:

HEPARIN SODIUM INJECTION (1007 patients)
ASPIRIN (721 patients)
LASIX (467 patients)
PREDNISOLONE (396 patients)
REMICADE (368 patients)
FUROSEMIDE (338 patients)
VOLTAREN (336 patients)
ACETAMINOPHEN (320 patients)
PREDNISONE (275 patients)
FLUOROURACIL (268 patients)
METHOTREXATE (252 patients)
OMEPRAZOLE (246 patients)
SOLU-MEDROL (238 patients)
ATENOLOL (226 patients)
HEPARIN (220 patients)
METFORMIN HCL (220 patients)
ALLOPURINOL (215 patients)
NORVASC (214 patients)
LISINOPRIL (208 patients)
DIGOXIN (204 patients)
FAMOTIDINE (194 patients)
WARFARIN SODIUM (187 patients)
DECADRON (171 patients)
AMLODIPINE (171 patients)
PLAVIX (169 patients)
LIPITOR (167 patients)
DIPRIVAN (164 patients)
DIOVAN (164 patients)
LEVOTHYROXINE SODIUM (162 patients)
VANCOMYCIN (159 patients)
LANSOPRAZOLE (158 patients)
SEROQUEL (154 patients)
SIMVASTATIN (150 patients)
AVASTIN (150 patients)
CISPLATIN (149 patients)
CYCLOPHOSPHAMIDE (148 patients)
VIOXX (146 patients)
OXALIPLATIN (144 patients)
ROCEPHIN (138 patients)
NEXIUM (136 patients)
HEPARIN SODIUM 1,000 UNITS AND SODIUM CHLORIDE 0.9% (134 patients)
POTASSIUM CHLORIDE (134 patients)
ENALAPRIL MALEATE (133 patients)
ALDACTONE (129 patients)
HEPARIN SODIUM (124 patients)
MUCOSTA (124 patients)
HYDROCHLOROTHIAZIDE (122 patients)
INSULIN (121 patients)
MORPHINE (120 patients)
HEPARIN SODIUM 5,000 UNITS IN DEXTROSE 5% (119 patients)
ZANTAC (119 patients)
PREDONINE (115 patients)
FOLIC ACID (115 patients)
CYTARABINE (114 patients)
TRAMADOL HCL (113 patients)
CARVEDILOL (111 patients)
HUMIRA (111 patients)
NIFEDIPINE (110 patients)
METOPROLOL TARTRATE (110 patients)
CARBOPLATIN (109 patients)
FOSAMAX (108 patients)
LOXONIN (108 patients)
IBUPROFEN (106 patients)
GLUCOPHAGE (106 patients)
LEVOFLOXACIN (104 patients)
PROPOFOL (104 patients)
ZOFRAN (101 patients)
CLOZARIL (101 patients)
ALBUTEROL (101 patients)
XYLOCAINE (101 patients)
LANTUS (101 patients)
AVELOX (100 patients)
CLARITHROMYCIN (100 patients)
PROGRAF (100 patients)
PAXIL (100 patients)
FLUCONAZOLE (99 patients)
MAGNESIUM OXIDE (97 patients)
CELEBREX (97 patients)
PREDNISONE TAB (97 patients)
KYTRIL (96 patients)
ZYPREXA (96 patients)
PROTONIX (96 patients)
ZOLOFT (95 patients)
DEXAMETHASONE (95 patients)
COUMADIN (93 patients)
TAXOTERE (93 patients)
GLEEVEC (92 patients)
NEORECORMON (91 patients)
NITROGLYCERIN (89 patients)
CLONAZEPAM (89 patients)
DIAZEPAM (88 patients)
ZOCOR (88 patients)
RAMIPRIL (88 patients)
XANAX (88 patients)
VELCADE (87 patients)
SYNTHROID (87 patients)
ZITHROMAX (85 patients)
AMLODIPINE BESYLATE (84 patients)
CYCLOSPORINE (84 patients)
SOLU-CORTEF (84 patients)
PRILOSEC (83 patients)
TEGRETOL (83 patients)
PEPCID (83 patients)
DIFLUCAN (82 patients)
BISOPROLOL FUMARATE (81 patients)
SPIRONOLACTONE (81 patients)
NEORAL (81 patients)
BLOPRESS (81 patients)
TENORMIN (81 patients)
TAXOL (80 patients)
NEURONTIN (80 patients)
ATARAX (78 patients)
AUGMENTIN '125' (78 patients)
TAMIFLU (77 patients)
OLMESARTAN MEDOXOMIL (77 patients)
LOVENOX (77 patients)
LORAZEPAM (77 patients)
AMARYL (76 patients)
TACROLIMUS (76 patients)
ARIXTRA (76 patients)
CRESTOR (76 patients)
DICLOFENAC SODIUM (75 patients)
CORDARONE (75 patients)
DEPAKENE (74 patients)
MORPHINE SULFATE (74 patients)
ISOSORBIDE MONONITRATE (73 patients)
FOSCAVIR (73 patients)
ENBREL (73 patients)
PACLITAXEL (72 patients)
LOPRESSOR (72 patients)
METHYLPREDNISOLONE (71 patients)
RISPERDAL (70 patients)
PRADAXA (70 patients)
TYLENOL (69 patients)
AVONEX (68 patients)
DEPAS (68 patients)
COREG (68 patients)
FENTANYL (67 patients)
RENAGEL (67 patients)
ARICEPT (67 patients)
COZAAR (66 patients)
CIPROFLOXACIN (66 patients)
LAMICTAL (65 patients)
OXYCONTIN (65 patients)
PARACETAMOL (65 patients)
LEVAQUIN (65 patients)
FERROUS SULFATE TAB (65 patients)
THYMOGLOBULIN (64 patients)
DOPAMINE HCL (64 patients)
ALPRAZOLAM (64 patients)
SELBEX (64 patients)
ELPLAT (64 patients)
CELLCEPT (63 patients)
AMIODARONE HCL (63 patients)
MIDAZOLAM HCL (63 patients)
ETOPOSIDE (63 patients)
XELODA (63 patients)
ADALAT (63 patients)
ALBUMIN (HUMAN) (62 patients)
GABAPENTIN (62 patients)
MEROPENEM (62 patients)
BISOPROLOL (61 patients)
LYRICA (61 patients)
BACTRIM (61 patients)
VERAPAMIL (60 patients)
TOPROL-XL (59 patients)
CANDESARTAN CILEXETIL (59 patients)
ACETYLSALICYLIC ACID SRT (59 patients)
RABEPRAZOLE SODIUM (58 patients)
MYCOPHENOLATE MOFETIL (58 patients)
SANDOSTATIN (57 patients)
AMOXICILLIN (57 patients)
AMN107 AMN+CAP (57 patients)
AVANDIA (56 patients)
DILTIAZEM HYDROCHLORIDE (56 patients)
CITALOPRAM HYDROBROMIDE (56 patients)
AMIODARONE (56 patients)
CYMBALTA (55 patients)
REGLAN (55 patients)
PANTOPRAZOLE SODIUM (55 patients)
VALIUM (55 patients)
GASTER (54 patients)
KALETRA (54 patients)
PREVISCAN (54 patients)
MUCODYNE (54 patients)
ZOLPIDEM TARTRATE (54 patients)
METOCLOPRAMIDE (53 patients)
ATORVASTATIN CALCIUM (53 patients)
GLYBURIDE (53 patients)
WARFARIN (53 patients)
RANITIDINE (53 patients)
MICARDIS (53 patients)
ELOXATIN (53 patients)
LEUCOVORIN CALCIUM (53 patients)
PROPRANOLOL (53 patients)
LIDOCAINE (53 patients)
ARAVA (52 patients)
AMITRIPTYLINE HCL (52 patients)
LACTULOSE (52 patients)
SINGULAIR (52 patients)
RHEUMATREX (52 patients)
TRACLEER (51 patients)
DIANEAL (51 patients)
MAGNESIUM SULFATE (51 patients)
CLOZAPINE (51 patients)
ZOSYN (51 patients)
EXJADE (51 patients)
METFORMIN (50 patients)
PROHANCE (50 patients)
VERAPAMIL HCL (50 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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