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

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, 5 individuals taking ALIZAPRIDE reported HYPOMAGNESAEMIA 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 HYPOMAGNESAEMIA. In doing so, we compare ALIZAPRIDE with other drugs that cause HYPOMAGNESAEMIA, to help you evaluate whether or not ALIZAPRIDE causes HYPOMAGNESAEMIA. Likewise, this page shows the most highly-reported side effects of ALIZAPRIDE, so you can see if HYPOMAGNESAEMIA ranks among ALIZAPRIDE's most well-known side effects.
Summary Statistics
Reports of ALIZAPRIDE causing HYPOMAGNESAEMIA: 5
Reports of any side effect of ALIZAPRIDE : 102
Percentage of ALIZAPRIDE patients where HYPOMAGNESAEMIA is a reported side effect: 4.9020%

FDA reports of any drug causing HYPOMAGNESAEMIA : 3891
Average percentage for all medicated patients where HYPOMAGNESAEMIA is reported as a complication: 0.0244%

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 HYPOMAGNESAEMIA:

OMEPRAZOLE (925 patients)
HEPARIN SODIUM INJECTION (558 patients)
ASPIRIN (464 patients)
CISPLATIN (443 patients)
FOSAMAX (357 patients)
PANITUMUMAB (345 patients)
FLUOROURACIL (310 patients)
CARBOPLATIN (288 patients)
FUROSEMIDE (279 patients)
CETUXIMAB (249 patients)
LISINOPRIL (234 patients)
ERBITUX (231 patients)
POTASSIUM CHLORIDE (230 patients)
LASIX (222 patients)
VIOXX (220 patients)
ATENOLOL (214 patients)
ZOFRAN (201 patients)
SYNTHROID (185 patients)
ZOMETA (181 patients)
LANSOPRAZOLE (179 patients)
DEXAMETHASONE (177 patients)
NEXIUM (174 patients)
DECADRON (171 patients)
SIMVASTATIN (166 patients)
COUMADIN (163 patients)
HYDROCHLOROTHIAZIDE (159 patients)
PROTONIX (154 patients)
PRILOSEC (154 patients)
AMLODIPINE (149 patients)
DIGOXIN (148 patients)
SEROQUEL (148 patients)
TAXOL (145 patients)
PREDNISONE (145 patients)
MAGNESIUM SULFATE (144 patients)
AREDIA (143 patients)
PANTOPRAZOLE (138 patients)
MAGNESIUM OXIDE (137 patients)
RANITIDINE (137 patients)
ONDANSETRON (136 patients)
LORAZEPAM (133 patients)
METFORMIN HCL (131 patients)
DOCETAXEL (129 patients)
REVLIMID (129 patients)
LIPITOR (127 patients)
ACETAMINOPHEN (127 patients)
AVASTIN (127 patients)
NORVASC (126 patients)
IRINOTECAN HCL (126 patients)
SORAFENIB (124 patients)
ATIVAN (122 patients)
ACYCLOVIR (120 patients)
FOLIC ACID (119 patients)
ALLOPURINOL (119 patients)
LEVOTHYROXINE SODIUM (118 patients)
OXALIPLATIN (116 patients)
AMBIEN (115 patients)
PACLITAXEL (112 patients)
PREVACID (107 patients)
XANAX (106 patients)
LEUCOVORIN CALCIUM (106 patients)
ZOLOFT (105 patients)
BENADRYL (101 patients)
MAGNESIUM (101 patients)
MORPHINE (99 patients)
GABAPENTIN (94 patients)
VITAMIN D (93 patients)
PERCOCET (93 patients)
SPIRONOLACTONE (92 patients)
LEVAQUIN (91 patients)
METOPROLOL TARTRATE (91 patients)
LYRICA (89 patients)
REGLAN (88 patients)
CLONIDINE (88 patients)
COMPAZINE (87 patients)
NEURONTIN (87 patients)
ZOCOR (87 patients)
CALCIUM (87 patients)
VELCADE (86 patients)
BEVACIZUMAB (86 patients)
TRAZODONE HCL (85 patients)
TAXOTERE (85 patients)
COLACE (83 patients)
TOPROL-XL (83 patients)
CIPROFLOXACIN (83 patients)
IMODIUM (82 patients)
PLAVIX (82 patients)
LOVENOX (82 patients)
ZANTAC (82 patients)
CALCIUM CARBONATE (81 patients)
WARFARIN SODIUM (79 patients)
CYTARABINE (79 patients)
OXYCONTIN (79 patients)
METHOTREXATE (78 patients)
ARANESP (77 patients)
VICODIN (77 patients)
VANCOMYCIN (77 patients)
FENTANYL (76 patients)
PANTOPRAZOLE SODIUM (76 patients)
TACROLIMUS (75 patients)
RADIATION THERAPY (75 patients)
INSULIN (73 patients)
XELODA (72 patients)
OXYCODONE HCL (71 patients)
ALBUTEROL (71 patients)
PREDNISOLONE (70 patients)
ATORVASTATIN CALCIUM (69 patients)
VECTIBIX (69 patients)
DIOVAN (69 patients)
FLUCONAZOLE (69 patients)
CYCLOPHOSPHAMIDE (68 patients)
RABEPRAZOLE SODIUM (68 patients)
CELEBREX (67 patients)
MORPHINE SULFATE (67 patients)
AMOXICILLIN (66 patients)
KLOR-CON (64 patients)
METOCLOPRAMIDE (64 patients)
NEXAVAR (63 patients)
RAMIPRIL (62 patients)
NEUPOGEN (62 patients)
BENDROFLUMETHIAZIDE (62 patients)
PROGRAF (61 patients)
VITAMIN E (61 patients)
ZYRTEC (61 patients)
METOPROLOL (61 patients)
ALLEGRA (61 patients)
COZAAR (60 patients)
PREDNISONE TAB (60 patients)
PREMARIN (60 patients)
LANTUS (59 patients)
LORTAB (59 patients)
LOPRESSOR (59 patients)
NITROGLYCERIN (59 patients)
FERROUS SULFATE TAB (58 patients)
ALENDRONATE SODIUM (58 patients)
HEPARIN (58 patients)
DURAGESIC-100 (58 patients)
LEXAPRO (57 patients)
GLIPIZIDE (57 patients)
VITAMIN B-12 (57 patients)
DOMPERIDONE (56 patients)
KLONOPIN (56 patients)
FLOMAX (55 patients)
PROMETHAZINE (54 patients)
SENOKOT (54 patients)
LEVOFLOXACIN (54 patients)
GLUCOPHAGE (53 patients)
NAVELBINE (53 patients)
MULTI-VITAMINS (53 patients)
CYCLOSPORINE (52 patients)
ADVAIR DISKUS 100/50 (51 patients)
POTASSIUM (51 patients)
LOMOTIL (51 patients)
CORTICOSTEROIDS (51 patients)
VERAPAMIL (50 patients)
SPIRIVA (50 patients)
ASCORBIC ACID (50 patients)
TYLENOL (50 patients)
CITALOPRAM HYDROBROMIDE (49 patients)
ACCUTANE (49 patients)
SERTRALINE HYDROCHLORIDE (49 patients)
DILAUDID (49 patients)
NPLATE (48 patients)
CRESTOR (48 patients)
MULTI-VITAMIN (48 patients)
ISOSORBIDE MONONITRATE (47 patients)
ANTIHISTAMINES (46 patients)
CHEMOTHERAPEUTICS NOS (46 patients)
ALTACE (46 patients)
ATORVASTATIN (45 patients)
IBUPROFEN (45 patients)
ENALAPRIL MALEATE (45 patients)
ERLOTINIB HYDROCHLORIDE (45 patients)
GLYBURIDE (45 patients)
PROCHLORPERAZINE (44 patients)
BENICAR (44 patients)
LOSEC (44 patients)
ALPRAZOLAM (44 patients)
NYSTATIN (44 patients)
WELLBUTRIN (43 patients)
ALOXI (43 patients)
METFORMIN (42 patients)
DIFLUCAN (42 patients)
FAMOTIDINE (42 patients)
FISH OIL (42 patients)
COREG (42 patients)
MEGACE (41 patients)
BACTRIM (41 patients)
THYMOGLOBULIN (41 patients)
VERSED (41 patients)
DEXAMETHASONE ACETATE (41 patients)
FLAGYL (41 patients)
GUAIFENESIN (41 patients)
PHENERGAN (41 patients)
LOPERAMIDE (40 patients)
TYLENOL (CAPLET) (40 patients)
VALIUM (40 patients)
SOLU-MEDROL (39 patients)
AMARYL (39 patients)
CLARITIN (38 patients)
ETOPOSIDE (38 patients)
CAPECITABINE (38 patients)
LACTULOSE (38 patients)
AMIODARONE HCL (37 patients)
EFFEXOR (37 patients)
DOXORUBICIN HCL (37 patients)
PARACETAMOL (37 patients)
URSODIOL (37 patients)
TRAMADOL HCL (37 patients)
SODIUM CHLORIDE (37 patients)
GLIMEPIRIDE (36 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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