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

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, 8 individuals taking ALIZAPRIDE reported DEHYDRATION 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 DEHYDRATION. In doing so, we compare ALIZAPRIDE with other drugs that cause DEHYDRATION, to help you evaluate whether or not ALIZAPRIDE causes DEHYDRATION. Likewise, this page shows the most highly-reported side effects of ALIZAPRIDE, so you can see if DEHYDRATION ranks among ALIZAPRIDE's most well-known side effects.
Summary Statistics
Reports of ALIZAPRIDE causing DEHYDRATION: 8
Reports of any side effect of ALIZAPRIDE : 102
Percentage of ALIZAPRIDE patients where DEHYDRATION is a reported side effect: 7.8431%

FDA reports of any drug causing DEHYDRATION : 51306
Average percentage for all medicated patients where DEHYDRATION is reported as a complication: 0.3216%

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 DEHYDRATION:

ASPIRIN (4930 patients)
LASIX (2777 patients)
FOSAMAX (2721 patients)
CISPLATIN (2627 patients)
LISINOPRIL (2455 patients)
PREDNISONE (2354 patients)
FUROSEMIDE (2149 patients)
AVONEX (1976 patients)
OMEPRAZOLE (1955 patients)
DEXAMETHASONE (1940 patients)
VIOXX (1899 patients)
LIPITOR (1863 patients)
ZOMETA (1861 patients)
CARBOPLATIN (1841 patients)
FLUOROURACIL (1836 patients)
ZOFRAN (1765 patients)
NEXIUM (1763 patients)
COUMADIN (1666 patients)
FOLIC ACID (1637 patients)
ACETAMINOPHEN (1576 patients)
HEPARIN SODIUM INJECTION (1574 patients)
ATENOLOL (1559 patients)
SEROQUEL (1554 patients)
DIGOXIN (1534 patients)
SYNTHROID (1534 patients)
HYDROCHLOROTHIAZIDE (1517 patients)
SIMVASTATIN (1475 patients)
POTASSIUM CHLORIDE (1419 patients)
PROTONIX (1403 patients)
PRILOSEC (1374 patients)
RIBAVIRIN (1362 patients)
FORTEO (1351 patients)
HUMIRA (1329 patients)
ALLOPURINOL (1319 patients)
METFORMIN HCL (1317 patients)
REVLIMID (1310 patients)
NEURONTIN (1291 patients)
XANAX (1270 patients)
AMBIEN (1269 patients)
PLAVIX (1262 patients)
OXYCONTIN (1260 patients)
REMICADE (1234 patients)
NORVASC (1231 patients)
LEVOTHYROXINE SODIUM (1228 patients)
COMPAZINE (1220 patients)
LORAZEPAM (1218 patients)
ATIVAN (1218 patients)
ZOLOFT (1176 patients)
ZOCOR (1173 patients)
PEG-INTRON (1164 patients)
OXALIPLATIN (1098 patients)
DECADRON (1088 patients)
IBUPROFEN (1063 patients)
CAPECITABINE (1060 patients)
ACCUTANE (1059 patients)
LANTUS (1015 patients)
ALBUTEROL (1004 patients)
TOPROL-XL (1000 patients)
PREDNISOLONE (989 patients)
VITAMIN D (976 patients)
LEXAPRO (973 patients)
PREVACID (972 patients)
SPIRONOLACTONE (956 patients)
METHOTREXATE (955 patients)
XELODA (947 patients)
DIANEAL (943 patients)
AVASTIN (939 patients)
METOPROLOL TARTRATE (936 patients)
PACLITAXEL (926 patients)
BEVACIZUMAB (926 patients)
PERCOCET (923 patients)
PREDNISONE TAB (922 patients)
CETUXIMAB (897 patients)
MORPHINE (893 patients)
OXYCODONE HCL (889 patients)
LYRICA (879 patients)
VICODIN (876 patients)
DIOVAN (870 patients)
BYETTA (861 patients)
AREDIA (836 patients)
LEVAQUIN (835 patients)
DOCETAXEL (809 patients)
CELEBREX (809 patients)
TAXOL (805 patients)
AMLODIPINE (803 patients)
TYSABRI (789 patients)
RADIATION THERAPY (787 patients)
WARFARIN SODIUM (777 patients)
GABAPENTIN (777 patients)
CALCIUM (775 patients)
DURAGESIC-100 (774 patients)
CYMBALTA (769 patients)
ALDACTONE (765 patients)
MULTI-VITAMINS (762 patients)
CYCLOPHOSPHAMIDE (756 patients)
VELCADE (749 patients)
COREG (740 patients)
TAXOTERE (734 patients)
INSULIN (725 patients)
PAXIL (722 patients)
RAMIPRIL (719 patients)
ONDANSETRON (716 patients)
METOCLOPRAMIDE (710 patients)
CRESTOR (708 patients)
FENTANYL (705 patients)
VITAMIN B-12 (701 patients)
ALPRAZOLAM (695 patients)
EXJADE (682 patients)
LEUCOVORIN CALCIUM (680 patients)
IMODIUM (656 patients)
ENALAPRIL MALEATE (653 patients)
TRAMADOL HCL (643 patients)
MULTI-VITAMIN (642 patients)
LANSOPRAZOLE (641 patients)
GLUCOPHAGE (641 patients)
ZYPREXA (640 patients)
PEGASYS (633 patients)
METOPROLOL (633 patients)
EFFEXOR (626 patients)
MORPHINE SULFATE (626 patients)
BENADRYL (621 patients)
REGLAN (614 patients)
SUTENT (603 patients)
LORTAB (598 patients)
ZANTAC (598 patients)
LOVENOX (596 patients)
CLONAZEPAM (595 patients)
COLACE (593 patients)
ADVAIR DISKUS 100/50 (589 patients)
CIPROFLOXACIN (587 patients)
NITROGLYCERIN (586 patients)
DILAUDID (584 patients)
FLUCONAZOLE (582 patients)
ALTACE (579 patients)
MEGACE (577 patients)
ARANESP (575 patients)
RISPERDAL (569 patients)
PROZAC (548 patients)
BACTRIM (545 patients)
RANITIDINE (537 patients)
ACYCLOVIR (534 patients)
LOPRESSOR (533 patients)
SANDOSTATIN LAR (530 patients)
IRINOTECAN HCL (530 patients)
ENBREL (526 patients)
LOMOTIL (526 patients)
COZAAR (526 patients)
REBIF (525 patients)
PREMARIN (522 patients)
TRAZODONE HCL (517 patients)
SPIRIVA (517 patients)
ERBITUX (515 patients)
DOXORUBICIN HCL (515 patients)
NEXAVAR (513 patients)
METFORMIN (509 patients)
CALCIUM CARBONATE (507 patients)
FLOMAX (505 patients)
PEPCID (502 patients)
CELEXA (500 patients)
TYLENOL (499 patients)
FERROUS SULFATE TAB (496 patients)
PANTOPRAZOLE (494 patients)
AMOXICILLIN (488 patients)
ACTOS (482 patients)
REBETOL (481 patients)
WELLBUTRIN (478 patients)
FAMOTIDINE (474 patients)
NYSTATIN (473 patients)
GLYBURIDE (472 patients)
NOVOLOG (460 patients)
ASCORBIC ACID (458 patients)
CARVEDILOL (454 patients)
SINGULAIR (453 patients)
VINCRISTINE (453 patients)
PROMETHAZINE (453 patients)
NEUPOGEN (452 patients)
MIRALAX (451 patients)
LACTULOSE (451 patients)
HUMALOG (449 patients)
GLIPIZIDE (449 patients)
AMITRIPTYLINE HCL (443 patients)
MS CONTIN (443 patients)
PHENERGAN (442 patients)
VALIUM (441 patients)
PROCHLORPERAZINE (433 patients)
MYCOPHENOLATE MOFETIL (432 patients)
MAGNESIUM OXIDE (431 patients)
PANITUMUMAB (430 patients)
IRON (429 patients)
CIPRO (422 patients)
LAPATINIB (421 patients)
EXELON (419 patients)
METOPROLOL SUCCINATE (416 patients)
ALLEGRA (414 patients)
DIFLUCAN (411 patients)
CYCLOSPORINE (411 patients)
FLEXERIL (410 patients)
ACTONEL (407 patients)
TYLENOL (CAPLET) (407 patients)
DIAZEPAM (406 patients)
ZYRTEC (405 patients)
SORAFENIB (398 patients)
CLOZARIL (396 patients)
KLONOPIN (393 patients)
PANTOPRAZOLE SODIUM (393 patients)
GEMCITABINE (392 patients)
ARICEPT (388 patients)
SODIUM CHLORIDE (385 patients)
DEXAMETHASONE TAB (384 patients)
CLONIDINE (383 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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