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

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

FDA reports of any drug causing TACHYCARDIA : 30429
Average percentage for all medicated patients where TACHYCARDIA is reported as a complication: 0.1907%

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 TACHYCARDIA:

HEPARIN SODIUM INJECTION (2104 patients)
ASPIRIN (2006 patients)
CLOZARIL (1705 patients)
VIOXX (1633 patients)
FOSAMAX (1557 patients)
REMICADE (1415 patients)
SEROQUEL (1257 patients)
PREDNISONE (1092 patients)
ACETAMINOPHEN (1069 patients)
LASIX (936 patients)
LORAZEPAM (869 patients)
OMEPRAZOLE (841 patients)
DIGOXIN (815 patients)
LISINOPRIL (782 patients)
FUROSEMIDE (779 patients)
METHOTREXATE (744 patients)
LIPITOR (727 patients)
COUMADIN (702 patients)
ZOMETA (701 patients)
ALBUTEROL (695 patients)
CLOZAPINE (693 patients)
NEXIUM (693 patients)
FOLIC ACID (668 patients)
ATIVAN (663 patients)
IBUPROFEN (655 patients)
SYNTHROID (648 patients)
ATENOLOL (633 patients)
XANAX (620 patients)
SIMVASTATIN (614 patients)
DEXAMETHASONE (599 patients)
PROTONIX (599 patients)
ZOLOFT (598 patients)
LEVOTHYROXINE SODIUM (597 patients)
HYDROCHLOROTHIAZIDE (588 patients)
POTASSIUM CHLORIDE (583 patients)
ZOFRAN (564 patients)
PREDNISOLONE (559 patients)
NEURONTIN (526 patients)
PAXIL (519 patients)
LYRICA (519 patients)
RISPERDAL (515 patients)
AMBIEN (514 patients)
HEPARIN SODIUM (501 patients)
METOPROLOL TARTRATE (501 patients)
CYMBALTA (488 patients)
MORPHINE (484 patients)
DIAZEPAM (484 patients)
ZYPREXA (479 patients)
CYCLOPHOSPHAMIDE (474 patients)
CLONAZEPAM (471 patients)
PRILOSEC (468 patients)
ZOCOR (466 patients)
ALLOPURINOL (465 patients)
AREDIA (460 patients)
WARFARIN SODIUM (453 patients)
TOPROL-XL (451 patients)
VANCOMYCIN (446 patients)
FENTANYL (443 patients)
CARBOPLATIN (433 patients)
HUMIRA (431 patients)
PREDNISONE TAB (429 patients)
OLANZAPINE (425 patients)
SPIRIVA (424 patients)
LEVAQUIN (416 patients)
PLAVIX (413 patients)
BENADRYL (410 patients)
TRAMADOL HCL (406 patients)
NORVASC (401 patients)
VICODIN (400 patients)
METFORMIN HCL (395 patients)
CELEBREX (393 patients)
OXYCONTIN (390 patients)
PREVACID (372 patients)
MIRTAZAPINE (368 patients)
LEXAPRO (367 patients)
PROPOFOL (365 patients)
CITALOPRAM HYDROBROMIDE (364 patients)
DECADRON (363 patients)
INSULIN (354 patients)
CIPROFLOXACIN (351 patients)
DIOVAN (349 patients)
AVELOX (347 patients)
SINGULAIR (344 patients)
ADVAIR DISKUS 100/50 (339 patients)
RISPERIDONE (339 patients)
ALPRAZOLAM (338 patients)
STRATTERA (338 patients)
OXYCODONE HCL (335 patients)
FLUCONAZOLE (328 patients)
CISPLATIN (325 patients)
GABAPENTIN (323 patients)
FLUOROURACIL (320 patients)
RANITIDINE (315 patients)
EFFEXOR (313 patients)
AMITRIPTYLINE HCL (312 patients)
FORTEO (312 patients)
AMLODIPINE (310 patients)
LOVENOX (304 patients)
LOPRESSOR (304 patients)
COREG (304 patients)
ALLEGRA (295 patients)
MULTI-VITAMINS (292 patients)
PERCOCET (290 patients)
RAMIPRIL (287 patients)
VITAMIN D (286 patients)
HEPARIN (286 patients)
HYDROCORTISONE (284 patients)
SOLU-MEDROL (284 patients)
ABILIFY (278 patients)
METOPROLOL (277 patients)
ENALAPRIL MALEATE (277 patients)
TRAZODONE HCL (276 patients)
ACYCLOVIR (275 patients)
AMOXICILLIN (275 patients)
VELCADE (274 patients)
COLACE (272 patients)
YAZ (272 patients)
CALCIUM (266 patients)
CYTARABINE (266 patients)
VALPROATE SODIUM (263 patients)
CRESTOR (263 patients)
WELLBUTRIN (260 patients)
REGLAN (260 patients)
ACCUTANE (260 patients)
DURAGESIC-100 (258 patients)
DEPAKOTE (257 patients)
MORPHINE SULFATE (256 patients)
CONCERTA (256 patients)
LANTUS (255 patients)
TEMAZEPAM (255 patients)
METHYLPREDNISOLONE (254 patients)
COMPAZINE (254 patients)
BACTRIM (254 patients)
PANTOPRAZOLE (253 patients)
LANSOPRAZOLE (252 patients)
PARACETAMOL (251 patients)
PAROXETINE HCL (250 patients)
NITROGLYCERIN (250 patients)
TAXOL (248 patients)
ENBREL (245 patients)
SANDOSTATIN LAR (244 patients)
AUGMENTIN '125' (243 patients)
CELEXA (242 patients)
PROZAC (239 patients)
ZANTAC (236 patients)
MULTI-VITAMIN (236 patients)
LAMOTRIGINE (235 patients)
FLEXERIL (235 patients)
ETOPOSIDE (234 patients)
METOCLOPRAMIDE (234 patients)
TYLENOL (233 patients)
PREMARIN (230 patients)
TYLENOL (CAPLET) (230 patients)
FLUOXETINE (229 patients)
PACLITAXEL (228 patients)
AVASTIN (227 patients)
PROMETHAZINE (226 patients)
AVONEX (226 patients)
ONDANSETRON (226 patients)
METOPROLOL SUCCINATE (225 patients)
NAPROXEN (224 patients)
METRONIDAZOLE (224 patients)
PEPCID (221 patients)
DIPHENHYDRAMINE HCL (219 patients)
HALDOL (216 patients)
SPIRONOLACTONE (216 patients)
GLUCOPHAGE (214 patients)
CLONIDINE (213 patients)
HALOPERIDOL (212 patients)
LAMICTAL (210 patients)
COMBIVENT (209 patients)
CLARITHROMYCIN (208 patients)
AVANDIA (206 patients)
YASMIN (205 patients)
ASCORBIC ACID (205 patients)
SYMBICORT (204 patients)
VALIUM (204 patients)
ULTRAM (204 patients)
HEPARIN SODIUM 5,000 UNITS IN DEXTROSE 5% (203 patients)
ALCOHOL (203 patients)
FLAGYL (203 patients)
AZITHROMYCIN (200 patients)
ZYRTEC (199 patients)
BACLOFEN (198 patients)
FERROUS SULFATE TAB (197 patients)
LORTAB (197 patients)
NUVARING (197 patients)
LIDOCAINE (196 patients)
ZITHROMAX (196 patients)
ALTACE (196 patients)
REVLIMID (195 patients)
DILAUDID (195 patients)
GAMMAGARD LIQUID (195 patients)
ALENDRONATE SODIUM (195 patients)
ATROVENT (194 patients)
KLONOPIN (193 patients)
ALDACTONE (193 patients)
CYCLOSPORINE (192 patients)
TAXOTERE (191 patients)
VENLAFAXINE HCL (191 patients)
CARBAMAZEPINE (190 patients)
FLOMAX (189 patients)
CARVEDILOL (188 patients)
CLARITIN (188 patients)
COZAAR (186 patients)
REMERON (186 patients)
CALCIUM CARBONATE (184 patients)
VITAMIN B-12 (184 patients)
NEUPOGEN (183 patients)
CARDIZEM (181 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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