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

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

FDA reports of any drug causing URTICARIA : 36582
Average percentage for all medicated patients where URTICARIA is reported as a complication: 0.2293%

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 URTICARIA:

REMICADE (1991 patients)
ASPIRIN (1911 patients)
HUMIRA (1642 patients)
FOSAMAX (1264 patients)
TYSABRI (1220 patients)
ENBREL (1216 patients)
MAGNEVIST (1073 patients)
PREDNISONE (939 patients)
BENADRYL (931 patients)
AVELOX (880 patients)
SYNTHROID (841 patients)
ULTRAVIST 300 (814 patients)
METHOTREXATE (806 patients)
LISINOPRIL (797 patients)
LIPITOR (770 patients)
NEXIUM (646 patients)
CHANTIX (640 patients)
ZYRTEC (604 patients)
NIASPAN (593 patients)
CELEBREX (583 patients)
ACETAMINOPHEN (570 patients)
SINGULAIR (560 patients)
OMEPRAZOLE (559 patients)
ALBUTEROL (556 patients)
ATENOLOL (545 patients)
AVONEX (542 patients)
HYDROCHLOROTHIAZIDE (540 patients)
LYRICA (530 patients)
VIOXX (528 patients)
FOLIC ACID (526 patients)
XOLAIR (503 patients)
IBUPROFEN (488 patients)
SIMVASTATIN (487 patients)
ADVAIR DISKUS 100/50 (472 patients)
LEVOTHYROXINE SODIUM (469 patients)
CRESTOR (463 patients)
XANAX (459 patients)
METFORMIN HCL (455 patients)
VITAMIN D (449 patients)
ZOLOFT (442 patients)
LEVAQUIN (441 patients)
ULTRAVIST 150 (434 patients)
PLAVIX (434 patients)
BYETTA (432 patients)
LAMICTAL (423 patients)
LASIX (419 patients)
CYMBALTA (419 patients)
ALEVE (382 patients)
PREDNISONE TAB (378 patients)
SPIRIVA (376 patients)
AMOXICILLIN (370 patients)
LEXAPRO (368 patients)
ULTRAVIST 370 (357 patients)
ALEVE (CAPLET) (355 patients)
PREDNISOLONE (355 patients)
WELLBUTRIN (352 patients)
ALLEGRA (349 patients)
PRILOSEC (348 patients)
NEURONTIN (343 patients)
ULTRAVIST (PHARMACY BULK) (341 patients)
NORVASC (339 patients)
CALCIUM (322 patients)
TOPROL-XL (320 patients)
PREVACID (319 patients)
ZOCOR (317 patients)
PREMARIN (312 patients)
GAMMAGARD LIQUID (310 patients)
LANTUS (309 patients)
AUGMENTIN '125' (309 patients)
DIOVAN (302 patients)
ZOMETA (302 patients)
FUROSEMIDE (299 patients)
AMBIEN (293 patients)
COPAXONE (293 patients)
HEPARIN SODIUM INJECTION (292 patients)
PAXIL (287 patients)
MIRENA (285 patients)
GABAPENTIN (281 patients)
ZANTAC (278 patients)
COUMADIN (275 patients)
FORTEO (270 patients)
PROTONIX (269 patients)
LORAZEPAM (263 patients)
FISH OIL (263 patients)
MULTI-VITAMIN (262 patients)
SEROQUEL (261 patients)
WELLBUTRIN XL (258 patients)
VICODIN (258 patients)
MULTI-VITAMINS (256 patients)
ATIVAN (245 patients)
SOLU-MEDROL (242 patients)
ALLOPURINOL (241 patients)
ALPRAZOLAM (231 patients)
PERCOCET (227 patients)
TYLENOL (CAPLET) (224 patients)
MORPHINE (222 patients)
EFFEXOR (219 patients)
RANITIDINE (218 patients)
ZETIA (216 patients)
TEGRETOL (215 patients)
ZITHROMAX (214 patients)
REVLIMID (213 patients)
AMLODIPINE (212 patients)
CIPROFLOXACIN (209 patients)
EXJADE (208 patients)
CLONAZEPAM (206 patients)
FLONASE (206 patients)
PROZAC (206 patients)
METFORMIN (205 patients)
METOPROLOL TARTRATE (204 patients)
OXYCONTIN (202 patients)
LEVOXYL (201 patients)
VOLTAREN (199 patients)
CLARITIN (197 patients)
ZOFRAN (196 patients)
POTASSIUM CHLORIDE (196 patients)
LANSOPRAZOLE (195 patients)
ASCORBIC ACID (195 patients)
TRAMADOL HCL (192 patients)
SYMBICORT (191 patients)
GLUCOPHAGE (190 patients)
BEXTRA (190 patients)
WARFARIN SODIUM (188 patients)
VITAMIN E (185 patients)
DEXAMETHASONE (183 patients)
TYLENOL (182 patients)
SIMCOR (181 patients)
AREDIA (180 patients)
HYDROXYZINE (180 patients)
MULTIHANCE (178 patients)
INSULIN (178 patients)
KLONOPIN (176 patients)
VENTOLIN (175 patients)
NO CONCURRENT MEDICATION (175 patients)
FLUOROURACIL (175 patients)
DECADRON (174 patients)
ATARAX (174 patients)
ACTONEL (173 patients)
JANUVIA (170 patients)
LORATADINE (169 patients)
REBIF (169 patients)
OXYCODONE HCL (168 patients)
ACCUTANE (167 patients)
TRAZODONE HCL (165 patients)
DIGOXIN (165 patients)
ADVIL (164 patients)
CIMZIA (163 patients)
EFFEXOR XR (163 patients)
NAPROXEN (162 patients)
GLEEVEC (162 patients)
TOPAMAX (160 patients)
COZAAR (160 patients)
CELEXA (159 patients)
VITAMIN B-12 (159 patients)
METOPROLOL (157 patients)
CLONIDINE (157 patients)
DURAGESIC-100 (156 patients)
BACTRIM (156 patients)
FENTANYL (154 patients)
ALENDRONATE SODIUM (153 patients)
DEFINITY (153 patients)
BENICAR (149 patients)
HUMALOG (149 patients)
FLOMAX (149 patients)
CALCIUM CARBONATE (146 patients)
ACETYLSALICYLIC ACID SRT (146 patients)
ZYBAN (145 patients)
VALTREX (145 patients)
ERBITUX (144 patients)
VICTOZA (144 patients)
TRICOR (142 patients)
RAMIPRIL (141 patients)
NASONEX (141 patients)
DIAZEPAM (141 patients)
BONIVA (140 patients)
ALTACE (140 patients)
PRADAXA (139 patients)
NEULASTA (139 patients)
VALIUM (139 patients)
VANCOMYCIN (138 patients)
ROCEPHIN (138 patients)
LOVENOX (138 patients)
COREG (137 patients)
LORTAB (137 patients)
GLIPIZIDE (136 patients)
GADAVIST (136 patients)
LAMISIL (136 patients)
CARBOPLATIN (136 patients)
PEGASYS (135 patients)
FAMOTIDINE (134 patients)
MOBIC (134 patients)
AZITHROMYCIN (134 patients)
CYCLOPHOSPHAMIDE (134 patients)
HYDROCORTISONE (132 patients)
PRAVASTATIN (131 patients)
PARACETAMOL (131 patients)
BETASERON (131 patients)
PLAQUENIL (130 patients)
AVANDIA (130 patients)
RIBAVIRIN (130 patients)
FLOVENT (129 patients)
ALLI (127 patients)
FLUOXETINE (126 patients)
ENALAPRIL MALEATE (125 patients)
CETIRIZINE HCL (123 patients)
ACYCLOVIR (123 patients)
FOSAMAX PLUS D (122 patients)
MEDROL (122 patients)
OPTIRAY 350 (122 patients)
DIPHENHYDRAMINE HCL (121 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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