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

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

FDA reports of any drug causing CYANOSIS : 8275
Average percentage for all medicated patients where CYANOSIS is reported as a complication: 0.0519%

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 CYANOSIS:

REMICADE (624 patients)
HEPARIN SODIUM INJECTION (505 patients)
PAXIL (485 patients)
ASPIRIN (444 patients)
ZOLOFT (405 patients)
ALBUTEROL (270 patients)
SYNAGIS (267 patients)
VITAMIN TAB (259 patients)
LASIX (250 patients)
ACETAMINOPHEN (247 patients)
FUROSEMIDE (246 patients)
FOLIC ACID (223 patients)
OMEPRAZOLE (202 patients)
DIGOXIN (202 patients)
PAROXETINE HCL (195 patients)
VIOXX (192 patients)
PREDNISONE (178 patients)
METHOTREXATE (175 patients)
COUMADIN (173 patients)
LORAZEPAM (167 patients)
PAXIL CR (163 patients)
OXYCONTIN (159 patients)
LISINOPRIL (155 patients)
PREDNISOLONE (153 patients)
ATENOLOL (152 patients)
NEXIUM (148 patients)
TYLENOL (147 patients)
TRAMADOL HCL (144 patients)
DIAZEPAM (137 patients)
PRENATAL VITAMINS (136 patients)
BENADRYL (136 patients)
HUMIRA (135 patients)
CLOZARIL (134 patients)
IBUPROFEN (134 patients)
POTASSIUM CHLORIDE (133 patients)
AMOXICILLIN (132 patients)
HYDROCHLOROTHIAZIDE (131 patients)
DEXAMETHASONE (130 patients)
FENTANYL (128 patients)
LEVOTHYROXINE SODIUM (122 patients)
MORPHINE (119 patients)
TYLENOL (CAPLET) (118 patients)
HEPARIN SODIUM (117 patients)
ZOFRAN (115 patients)
SPIRONOLACTONE (115 patients)
PLAVIX (113 patients)
ALLOPURINOL (111 patients)
CLONAZEPAM (109 patients)
ALPRAZOLAM (107 patients)
SYNTHROID (106 patients)
TRACLEER (104 patients)
CARBOPLATIN (104 patients)
SOLU-MEDROL (103 patients)
XANAX (102 patients)
ZANTAC (102 patients)
HEPARIN (100 patients)
MORPHINE SULFATE (100 patients)
MYOZYME (99 patients)
AVELOX (98 patients)
REGLAN (98 patients)
MULTI-VITAMINS (94 patients)
EFFEXOR (94 patients)
LIPITOR (93 patients)
PROPOFOL (93 patients)
NORVASC (93 patients)
SEROQUEL (92 patients)
ATIVAN (91 patients)
GAMMAGARD LIQUID (91 patients)
PERCOCET (91 patients)
METOPROLOL TARTRATE (91 patients)
PACLITAXEL (90 patients)
NEURONTIN (90 patients)
RISPERDAL (90 patients)
SIMVASTATIN (90 patients)
SINGULAIR (90 patients)
LYRICA (89 patients)
ADVAIR DISKUS 100/50 (89 patients)
PROZAC (89 patients)
RANITIDINE (88 patients)
WARFARIN SODIUM (88 patients)
VICODIN (88 patients)
PREVACID (87 patients)
ATROVENT (87 patients)
YASMIN (85 patients)
PREDNISONE TAB (84 patients)
LEXAPRO (81 patients)
XOLAIR (81 patients)
LOVENOX (81 patients)
TOPROL-XL (80 patients)
IRON (79 patients)
CLARITIN (79 patients)
AMBIEN (79 patients)
PROTONIX (78 patients)
DIOVAN (78 patients)
TEGRETOL (77 patients)
ONDANSETRON (77 patients)
FLUOROURACIL (77 patients)
DURAGESIC-100 (77 patients)
CEPHALEXIN (76 patients)
OXYGEN (76 patients)
ENALAPRIL MALEATE (75 patients)
ZYPREXA (75 patients)
CISPLATIN (74 patients)
DECADRON (74 patients)
ZITHROMAX (74 patients)
ROCEPHIN (73 patients)
AMITRIPTYLINE HCL (72 patients)
AUGMENTIN '125' (71 patients)
ZYRTEC (70 patients)
FERROUS SULFATE TAB (69 patients)
CYMBALTA (68 patients)
PARACETAMOL (68 patients)
CLOZAPINE (68 patients)
ALLEGRA (68 patients)
LAMOTRIGINE (68 patients)
VANCOMYCIN (67 patients)
STRATTERA (67 patients)
EFFEXOR XR (67 patients)
SEREVENT (66 patients)
CYCLOPHOSPHAMIDE (66 patients)
INSULIN (65 patients)
CAPTOPRIL (65 patients)
LEVAQUIN (65 patients)
ALDACTONE (64 patients)
MIRTAZAPINE (64 patients)
ZOLPIDEM (64 patients)
SPIRIVA (64 patients)
PRILOSEC (63 patients)
NITROGLYCERIN (63 patients)
RAMIPRIL (63 patients)
METFORMIN HCL (63 patients)
LORTAB (62 patients)
LANSOPRAZOLE (62 patients)
FLONASE (62 patients)
ULTRAVIST 300 (61 patients)
LIDOCAINE (61 patients)
CRESTOR (61 patients)
LAMICTAL (60 patients)
TAXOTERE (60 patients)
LANTUS (59 patients)
METRONIDAZOLE (59 patients)
KEPPRA (59 patients)
AZITHROMYCIN (59 patients)
VALPROATE SODIUM (59 patients)
OXYCODONE HCL (58 patients)
FOSAMAX (58 patients)
CELEBREX (58 patients)
PHENERGAN HCL (57 patients)
NIFEDIPINE (57 patients)
PROPRANOLOL (57 patients)
VOLTAREN (56 patients)
CELEXA (56 patients)
ATARAX (55 patients)
FLEXERIL (55 patients)
FLUCONAZOLE (54 patients)
GABAPENTIN (54 patients)
TOPAMAX (54 patients)
MAGNESIUM SULFATE (54 patients)
MEDROL (54 patients)
CARBAMAZEPINE (53 patients)
DIPRIVAN (53 patients)
GLEEVEC (53 patients)
KYTRIL (53 patients)
COREG (53 patients)
MIDAZOLAM HCL (52 patients)
CITALOPRAM HYDROBROMIDE (51 patients)
AVASTIN (50 patients)
ZOCOR (50 patients)
ZOMETA (49 patients)
GLUCOPHAGE (49 patients)
SANDOSTATIN LAR (49 patients)
HYDROCORTISONE (48 patients)
AMLODIPINE (48 patients)
WELLBUTRIN (47 patients)
MULTI-VITAMIN (47 patients)
FAMOTIDINE (47 patients)
ERBITUX (47 patients)
BACTRIM (47 patients)
CONCERTA (47 patients)
TRAZODONE HCL (46 patients)
VITAMIN B-12 (46 patients)
FLOVENT (46 patients)
VENTOLIN (46 patients)
DURAGESIC (46 patients)
GEMZAR (46 patients)
TYSABRI (46 patients)
CARVEDILOL (46 patients)
PROMETHAZINE (45 patients)
PANTOPRAZOLE (45 patients)
VERAPAMIL (44 patients)
MOTRIN (44 patients)
HALOPERIDOL (44 patients)
VITAMIN D (44 patients)
SUDAFED 12 HOUR (44 patients)
QUETIAPINE (44 patients)
CLONIDINE (44 patients)
PHENERGAN (43 patients)
CIPROFLOXACIN (43 patients)
CALCIUM CARBONATE (43 patients)
PEPCID (43 patients)
TAXOL (43 patients)
COMBIVENT (43 patients)
AFINITOR (43 patients)
DOMPERIDONE (43 patients)
RISPERIDONE (43 patients)
OXALIPLATIN (42 patients)
MAGNEVIST (42 patients)
RITALIN (42 patients)
LEVETIRACETAM (42 patients)
EPINEPHRINE (42 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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