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

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, 3 individuals taking ALIZAPRIDE reported PRESYNCOPE 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 PRESYNCOPE. In doing so, we compare ALIZAPRIDE with other drugs that cause PRESYNCOPE, to help you evaluate whether or not ALIZAPRIDE causes PRESYNCOPE. Likewise, this page shows the most highly-reported side effects of ALIZAPRIDE, so you can see if PRESYNCOPE ranks among ALIZAPRIDE's most well-known side effects.
Summary Statistics
Reports of ALIZAPRIDE causing PRESYNCOPE: 3
Reports of any side effect of ALIZAPRIDE : 102
Percentage of ALIZAPRIDE patients where PRESYNCOPE is a reported side effect: 2.9412%

FDA reports of any drug causing PRESYNCOPE : 5749
Average percentage for all medicated patients where PRESYNCOPE is reported as a complication: 0.0360%

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 PRESYNCOPE:

FOSAMAX (793 patients)
ASPIRIN (736 patients)
DIGOXIN (441 patients)
LISINOPRIL (389 patients)
LASIX (333 patients)
COUMADIN (316 patients)
LIPITOR (295 patients)
FUROSEMIDE (249 patients)
BYETTA (241 patients)
FORTEO (234 patients)
SIMVASTATIN (213 patients)
HYDROCHLOROTHIAZIDE (209 patients)
SEROQUEL (205 patients)
ATENOLOL (202 patients)
PLAVIX (197 patients)
ZOMETA (193 patients)
MIRENA (190 patients)
PRILOSEC (187 patients)
OMEPRAZOLE (187 patients)
METFORMIN HCL (185 patients)
XANAX (180 patients)
LYRICA (180 patients)
COREG (179 patients)
PREDNISONE (178 patients)
REMICADE (178 patients)
CYMBALTA (170 patients)
NEXIUM (170 patients)
TOPROL-XL (170 patients)
AMBIEN (168 patients)
NORVASC (168 patients)
POTASSIUM CHLORIDE (168 patients)
FOLIC ACID (167 patients)
SYNTHROID (165 patients)
DIOVAN (164 patients)
ALBUTEROL (163 patients)
METOPROLOL TARTRATE (156 patients)
LEVAQUIN (156 patients)
AREDIA (156 patients)
WARFARIN SODIUM (154 patients)
VITAMIN D (152 patients)
ZOCOR (149 patients)
CALCIUM (144 patients)
PERCOCET (144 patients)
LEVOTHYROXINE SODIUM (143 patients)
LANTUS (142 patients)
LORAZEPAM (140 patients)
REVLIMID (138 patients)
PROTONIX (136 patients)
CHANTIX (136 patients)
NEURONTIN (133 patients)
NITROGLYCERIN (133 patients)
CELEBREX (132 patients)
ACETAMINOPHEN (127 patients)
SPIRONOLACTONE (127 patients)
ALPRAZOLAM (126 patients)
HUMIRA (125 patients)
ZYRTEC (124 patients)
FISH OIL (123 patients)
FLOMAX (122 patients)
MULTI-VITAMINS (121 patients)
IBUPROFEN (120 patients)
ZOLOFT (120 patients)
VITAMIN B-12 (118 patients)
GABAPENTIN (116 patients)
KETEK (115 patients)
ALLOPURINOL (115 patients)
RAMIPRIL (114 patients)
NUVARING (112 patients)
HEPARIN SODIUM INJECTION (111 patients)
PROZAC (107 patients)
ADVAIR DISKUS 100/50 (107 patients)
CLONIDINE (107 patients)
LORTAB (106 patients)
LEXAPRO (106 patients)
ATIVAN (101 patients)
PREDNISONE TAB (101 patients)
PREVACID (99 patients)
METHOTREXATE (99 patients)
VICODIN (97 patients)
METOPROLOL (97 patients)
GLUCOPHAGE (97 patients)
ENBREL (97 patients)
ALENDRONATE SODIUM (96 patients)
DEXAMETHASONE (94 patients)
LOVENOX (94 patients)
AVANDIA (94 patients)
SPIRIVA (94 patients)
CARVEDILOL (92 patients)
CALCIUM CARBONATE (91 patients)
KLOR-CON (90 patients)
COLACE (89 patients)
ALDACTONE (89 patients)
EFFEXOR (88 patients)
RIBAVIRIN (87 patients)
CLONAZEPAM (87 patients)
FOSAMAX PLUS D (87 patients)
TYSABRI (85 patients)
PREMARIN (85 patients)
SINGULAIR (85 patients)
LOPRESSOR (84 patients)
DECADRON (83 patients)
DILTIAZEM (82 patients)
TRAMADOL HCL (81 patients)
MULTI-VITAMIN (81 patients)
CRESTOR (80 patients)
CIPROFLOXACIN (79 patients)
FLONASE (79 patients)
ACTOS (79 patients)
ENALAPRIL MALEATE (79 patients)
OXYCODONE HCL (79 patients)
AMOXICILLIN (79 patients)
WELLBUTRIN (77 patients)
NIASPAN (76 patients)
AMLODIPINE (76 patients)
ZETIA (75 patients)
ZOFRAN (75 patients)
ALLEGRA (75 patients)
ZYPREXA (74 patients)
EFFEXOR XR (73 patients)
MAGNESIUM (73 patients)
POTASSIUM (72 patients)
CLARITIN (72 patients)
ASCORBIC ACID (71 patients)
RANITIDINE (71 patients)
TEMAZEPAM (71 patients)
VITAMIN E (70 patients)
HUMALOG (70 patients)
AMARYL (69 patients)
GLIPIZIDE (69 patients)
NAPROXEN (68 patients)
DIAZEPAM (67 patients)
ZESTRIL (66 patients)
PEPCID (65 patients)
AVELOX (64 patients)
VIAGRA (64 patients)
CHEMOTHERAPEUTICS NOS (64 patients)
COMPAZINE (63 patients)
NOVOLOG (62 patients)
BONIVA (62 patients)
INSULIN (62 patients)
ACYCLOVIR (61 patients)
ALTACE (61 patients)
FLUCONAZOLE (61 patients)
CITALOPRAM HYDROBROMIDE (60 patients)
VYTORIN (60 patients)
CYCLOPHOSPHAMIDE (59 patients)
AMIODARONE HCL (59 patients)
REGLAN (59 patients)
KLONOPIN (59 patients)
CELEXA (58 patients)
CARDIZEM (58 patients)
NASONEX (58 patients)
GILENYA (58 patients)
BENADRYL (57 patients)
TRACLEER (57 patients)
ZITHROMAX (57 patients)
VERAPAMIL (57 patients)
CYCLOBENZAPRINE (57 patients)
AMITRIPTYLINE HCL (57 patients)
PAXIL (57 patients)
DOXYCYCLINE (56 patients)
VALIUM (55 patients)
HYDROCODONE (55 patients)
LANOXIN (55 patients)
PANTOPRAZOLE (55 patients)
GLYBURIDE (54 patients)
GEODON (54 patients)
PROCRIT /00909301/ (54 patients)
ACTONEL (53 patients)
PREDNISOLONE (53 patients)
FLEXERIL (53 patients)
METOPROLOL SUCCINATE (53 patients)
COZAAR (52 patients)
YASMIN (52 patients)
CEPHALEXIN (52 patients)
MAGNEVIST (52 patients)
VALSARTAN (51 patients)
TRAZODONE HCL (51 patients)
THALIDOMIDE (51 patients)
ARICEPT (51 patients)
PRAVACHOL (51 patients)
FEMARA (50 patients)
K-DUR (50 patients)
FERROUS SULFATE TAB (50 patients)
BENICAR (49 patients)
MORPHINE (49 patients)
METRONIDAZOLE (49 patients)
REQUIP (49 patients)
ZANTAC (48 patients)
REBIF (48 patients)
YAZ (47 patients)
SYMBICORT (47 patients)
IRON (46 patients)
ALLI (46 patients)
KEFLEX (45 patients)
CISPLATIN (45 patients)
METOCLOPRAMIDE (45 patients)
FLUOXETINE (44 patients)
AVONEX (44 patients)
DULCOLAX (44 patients)
PRINIVIL (43 patients)
PEG-INTRON (43 patients)
MEDROL (43 patients)
RESTORIL (43 patients)
LOVAZA (43 patients)
TRICOR (43 patients)
PROMETHAZINE (43 patients)
ACIPHEX (42 patients)
AUGMENTIN '125' (42 patients)
MECLIZINE (41 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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