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

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, 6 individuals taking ALIZAPRIDE reported HYPOTENSION 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 HYPOTENSION. In doing so, we compare ALIZAPRIDE with other drugs that cause HYPOTENSION, to help you evaluate whether or not ALIZAPRIDE causes HYPOTENSION. Likewise, this page shows the most highly-reported side effects of ALIZAPRIDE, so you can see if HYPOTENSION ranks among ALIZAPRIDE's most well-known side effects.
Summary Statistics
Reports of ALIZAPRIDE causing HYPOTENSION: 6
Reports of any side effect of ALIZAPRIDE : 102
Percentage of ALIZAPRIDE patients where HYPOTENSION is a reported side effect: 5.8824%

FDA reports of any drug causing HYPOTENSION : 58738
Average percentage for all medicated patients where HYPOTENSION is reported as a complication: 0.3681%

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 HYPOTENSION:

HEPARIN SODIUM INJECTION (11518 patients)
ASPIRIN (7072 patients)
LASIX (3520 patients)
LISINOPRIL (3197 patients)
FUROSEMIDE (2722 patients)
DIGOXIN (2664 patients)
VIOXX (2535 patients)
FOSAMAX (2470 patients)
PREDNISONE (2256 patients)
ACETAMINOPHEN (2228 patients)
LIPITOR (2179 patients)
PLAVIX (2157 patients)
ATENOLOL (2155 patients)
SIMVASTATIN (2135 patients)
HEPARIN SODIUM (2114 patients)
OMEPRAZOLE (2049 patients)
COUMADIN (2038 patients)
POTASSIUM CHLORIDE (1734 patients)
HYDROCHLOROTHIAZIDE (1617 patients)
ALLOPURINOL (1607 patients)
NEXIUM (1567 patients)
FOLIC ACID (1543 patients)
REMICADE (1533 patients)
SYNTHROID (1522 patients)
METOPROLOL TARTRATE (1493 patients)
WARFARIN SODIUM (1483 patients)
DIANEAL (1404 patients)
DIOVAN (1400 patients)
PROTONIX (1399 patients)
COREG (1357 patients)
ZOFRAN (1348 patients)
LEVOTHYROXINE SODIUM (1338 patients)
METFORMIN HCL (1333 patients)
DEXAMETHASONE (1325 patients)
TOPROL-XL (1310 patients)
ALBUTEROL (1296 patients)
NORVASC (1289 patients)
ZOCOR (1288 patients)
PRILOSEC (1266 patients)
AMLODIPINE (1266 patients)
SEROQUEL (1264 patients)
LORAZEPAM (1250 patients)
MORPHINE (1245 patients)
METHOTREXATE (1213 patients)
AMBIEN (1174 patients)
ZOMETA (1146 patients)
NEURONTIN (1138 patients)
NITROGLYCERIN (1138 patients)
INSULIN (1127 patients)
FENTANYL (1116 patients)
IBUPROFEN (1100 patients)
XANAX (1100 patients)
ATIVAN (1097 patients)
CYCLOPHOSPHAMIDE (1067 patients)
HEPARIN (1062 patients)
RAMIPRIL (1037 patients)
VANCOMYCIN (988 patients)
METOPROLOL (976 patients)
SPIRONOLACTONE (974 patients)
AVONEX (972 patients)
CARBOPLATIN (965 patients)
VELCADE (950 patients)
DECADRON (926 patients)
REVLIMID (923 patients)
LEVAQUIN (917 patients)
LOVENOX (914 patients)
PREVACID (912 patients)
LANTUS (910 patients)
GABAPENTIN (908 patients)
PREDNISONE TAB (900 patients)
PREDNISOLONE (883 patients)
LYRICA (880 patients)
CISPLATIN (878 patients)
VICODIN (873 patients)
CARVEDILOL (866 patients)
ZOLOFT (861 patients)
PERCOCET (811 patients)
HEPARIN SODIUM 5,000 UNITS IN DEXTROSE 5% (809 patients)
FORTEO (808 patients)
OXYCONTIN (806 patients)
CLONAZEPAM (798 patients)
CELEBREX (781 patients)
ENALAPRIL MALEATE (777 patients)
LOPRESSOR (774 patients)
ALDACTONE (770 patients)
ALTACE (765 patients)
PROPOFOL (762 patients)
VITAMIN D (760 patients)
OXYCODONE HCL (755 patients)
FLUOROURACIL (753 patients)
CYTARABINE (746 patients)
BENADRYL (746 patients)
CLONIDINE (742 patients)
PAXIL (742 patients)
CYMBALTA (733 patients)
LEXAPRO (727 patients)
ALPRAZOLAM (724 patients)
ACYCLOVIR (722 patients)
HUMIRA (717 patients)
DIAZEPAM (702 patients)
PANTOPRAZOLE (699 patients)
TYSABRI (697 patients)
ADVAIR DISKUS 100/50 (692 patients)
CALCIUM (685 patients)
FLUCONAZOLE (683 patients)
COLACE (683 patients)
MORPHINE SULFATE (666 patients)
AMIODARONE HCL (661 patients)
RANITIDINE (656 patients)
ZANTAC (642 patients)
CRESTOR (642 patients)
CLOZARIL (631 patients)
ZYPREXA (628 patients)
FLOMAX (628 patients)
TRAMADOL HCL (618 patients)
METOPROLOL SUCCINATE (608 patients)
MULTI-VITAMINS (606 patients)
AREDIA (602 patients)
REGLAN (597 patients)
NIFEDIPINE (596 patients)
RISPERDAL (594 patients)
CIPROFLOXACIN (594 patients)
COZAAR (587 patients)
AVELOX (580 patients)
ETOPOSIDE (579 patients)
SPIRIVA (575 patients)
SINGULAIR (575 patients)
TYLENOL (574 patients)
VERAPAMIL (568 patients)
ONDANSETRON (566 patients)
LORTAB (561 patients)
EFFEXOR (558 patients)
PEPCID (548 patients)
DURAGESIC-100 (546 patients)
CITALOPRAM HYDROBROMIDE (545 patients)
MULTI-VITAMIN (543 patients)
FERROUS SULFATE TAB (541 patients)
COMPAZINE (540 patients)
ARANESP (533 patients)
HYDROCORTISONE (532 patients)
TYLENOL (CAPLET) (531 patients)
EPOGEN (524 patients)
LANSOPRAZOLE (522 patients)
IRON (512 patients)
SANDOSTATIN LAR (510 patients)
DILTIAZEM (510 patients)
TRACLEER (506 patients)
VITAMIN B-12 (503 patients)
GLIPIZIDE (498 patients)
BACTRIM (497 patients)
BISOPROLOL FUMARATE (496 patients)
SOLU-MEDROL (495 patients)
GLYBURIDE (494 patients)
AMOXICILLIN (493 patients)
CLOPIDOGREL (493 patients)
TEMAZEPAM (491 patients)
TAXOTERE (484 patients)
ATORVASTATIN CALCIUM (480 patients)
VINCRISTINE (478 patients)
CELEXA (474 patients)
KLONOPIN (465 patients)
METFORMIN (462 patients)
TAXOL (456 patients)
AUGMENTIN '125' (454 patients)
CALCIUM CARBONATE (454 patients)
BACLOFEN (453 patients)
ASCORBIC ACID (453 patients)
PREMARIN (451 patients)
HEPARIN SODIUM 1,000 UNITS AND SODIUM CHLORIDE 0.9% (451 patients)
METOCLOPRAMIDE (450 patients)
DOCETAXEL (447 patients)
TRAZODONE HCL (446 patients)
ACETYLSALICYLIC ACID SRT (445 patients)
METHYLPREDNISOLONE (442 patients)
PROZAC (438 patients)
PANTOPRAZOLE SODIUM (436 patients)
LIDOCAINE (436 patients)
OXYGEN (433 patients)
DIFLUCAN (432 patients)
PROMETHAZINE (431 patients)
VALIUM (428 patients)
GLUCOPHAGE (427 patients)
DILAUDID (427 patients)
FAMOTIDINE (426 patients)
AMITRIPTYLINE HCL (425 patients)
AMLODIPINE BESYLATE (425 patients)
ERBITUX (424 patients)
ZETIA (424 patients)
WELLBUTRIN (420 patients)
LACTULOSE (420 patients)
CYCLOSPORINE (419 patients)
MIRTAZAPINE (417 patients)
BENICAR (416 patients)
NYSTATIN (415 patients)
METRONIDAZOLE (415 patients)
DIOVAN HCT (411 patients)
OXALIPLATIN (408 patients)
ZYRTEC (406 patients)
POTASSIUM (404 patients)
MIDAZOLAM HCL (402 patients)
CARDIZEM (401 patients)
PACLITAXEL (400 patients)
ALLEGRA (400 patients)
FLAGYL (399 patients)
HYDROCODONE (397 patients)
RENAGEL (397 patients)
ATACAND (396 patients)
RITUXIMAB (396 patients)
ATROVENT (396 patients)
ENBREL (396 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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