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

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

FDA reports of any drug causing PNEUMONIA : 82141
Average percentage for all medicated patients where PNEUMONIA is reported as a complication: 0.5148%

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 PNEUMONIA:

ASPIRIN (6898 patients)
FOSAMAX (5009 patients)
PREDNISONE (4778 patients)
REMICADE (4394 patients)
LASIX (4370 patients)
METHOTREXATE (4357 patients)
REVLIMID (4246 patients)
AVONEX (4193 patients)
HUMIRA (4133 patients)
VIOXX (3996 patients)
PREDNISOLONE (3820 patients)
HEPARIN SODIUM INJECTION (3232 patients)
FOLIC ACID (3005 patients)
FUROSEMIDE (2976 patients)
FORTEO (2972 patients)
DEXAMETHASONE (2962 patients)
ZOMETA (2933 patients)
NEXIUM (2845 patients)
OMEPRAZOLE (2722 patients)
COUMADIN (2681 patients)
ENBREL (2641 patients)
ALBUTEROL (2605 patients)
LIPITOR (2588 patients)
LISINOPRIL (2478 patients)
SPIRIVA (2420 patients)
SEROQUEL (2404 patients)
ADVAIR DISKUS 100/50 (2339 patients)
ACETAMINOPHEN (2204 patients)
PROTONIX (2065 patients)
TYSABRI (2047 patients)
PREDNISONE TAB (2030 patients)
DIGOXIN (2009 patients)
POTASSIUM CHLORIDE (1995 patients)
PLAVIX (1969 patients)
SIMVASTATIN (1965 patients)
NORVASC (1927 patients)
SYNTHROID (1904 patients)
NEURONTIN (1893 patients)
CYCLOPHOSPHAMIDE (1880 patients)
ALLOPURINOL (1857 patients)
OXYCONTIN (1821 patients)
DIANEAL (1761 patients)
PRILOSEC (1691 patients)
ZOLOFT (1621 patients)
DECADRON (1608 patients)
EXJADE (1607 patients)
AREDIA (1599 patients)
HYDROCHLOROTHIAZIDE (1597 patients)
VELCADE (1572 patients)
AMBIEN (1542 patients)
ATENOLOL (1521 patients)
LEVOTHYROXINE SODIUM (1517 patients)
LEVAQUIN (1502 patients)
XANAX (1492 patients)
LETAIRIS (1467 patients)
WARFARIN SODIUM (1456 patients)
LORAZEPAM (1437 patients)
VITAMIN D (1431 patients)
LANTUS (1415 patients)
ATIVAN (1387 patients)
CELEBREX (1365 patients)
ZOCOR (1340 patients)
LYRICA (1340 patients)
CISPLATIN (1335 patients)
MORPHINE (1334 patients)
SINGULAIR (1318 patients)
ZOFRAN (1299 patients)
GABAPENTIN (1296 patients)
METFORMIN HCL (1270 patients)
TOPROL-XL (1268 patients)
TRACLEER (1266 patients)
VICODIN (1265 patients)
AMLODIPINE (1264 patients)
DIOVAN (1259 patients)
PERCOCET (1244 patients)
OXYCODONE HCL (1233 patients)
GOLIMUMAB (1230 patients)
REBIF (1196 patients)
INSULIN (1194 patients)
METOPROLOL TARTRATE (1191 patients)
CARBOPLATIN (1159 patients)
CLOZARIL (1154 patients)
CALCIUM (1146 patients)
PREVACID (1138 patients)
DURAGESIC-100 (1108 patients)
ACYCLOVIR (1086 patients)
SYMBICORT (1084 patients)
IBUPROFEN (1083 patients)
PAXIL (1049 patients)
ZYPREXA (1042 patients)
LANSOPRAZOLE (1017 patients)
CYMBALTA (1006 patients)
RITUXIMAB (1006 patients)
RISPERDAL (1000 patients)
MYCOPHENOLATE MOFETIL (991 patients)
LEXAPRO (987 patients)
MULTI-VITAMINS (987 patients)
VANCOMYCIN (971 patients)
CLONAZEPAM (969 patients)
COMBIVENT (965 patients)
FLUCONAZOLE (942 patients)
MULTI-VITAMIN (936 patients)
FAMOTIDINE (931 patients)
COREG (926 patients)
VINCRISTINE (906 patients)
CYCLOSPORINE (905 patients)
LORTAB (900 patients)
FENTANYL (899 patients)
SPIRONOLACTONE (894 patients)
CRESTOR (890 patients)
COLACE (889 patients)
FLUOROURACIL (885 patients)
THALOMID (883 patients)
LOVENOX (873 patients)
ZANTAC (870 patients)
OXYGEN (864 patients)
NITROGLYCERIN (854 patients)
THALIDOMIDE (845 patients)
HEPARIN (835 patients)
ALPRAZOLAM (833 patients)
CIPROFLOXACIN (833 patients)
XOLAIR (821 patients)
MAGNESIUM OXIDE (821 patients)
VITAMIN B-12 (813 patients)
LEVOFLOXACIN (803 patients)
CALCIUM CARBONATE (790 patients)
NEUPOGEN (788 patients)
TRAMADOL HCL (787 patients)
FLOMAX (786 patients)
AMOXICILLIN (781 patients)
CLOZAPINE (775 patients)
MORPHINE SULFATE (774 patients)
ATROVENT (772 patients)
COMPAZINE (766 patients)
PREMARIN (765 patients)
ZITHROMAX (757 patients)
METOPROLOL (755 patients)
DIFLUCAN (752 patients)
DIAZEPAM (747 patients)
CYTARABINE (745 patients)
CELEXA (745 patients)
TACROLIMUS (743 patients)
PANTOPRAZOLE (743 patients)
DOXORUBICIN HCL (741 patients)
REGLAN (736 patients)
ALENDRONATE SODIUM (735 patients)
VIDAZA (734 patients)
BACLOFEN (733 patients)
DILAUDID (724 patients)
CARVEDILOL (721 patients)
ETOPOSIDE (721 patients)
COZAAR (719 patients)
LOPRESSOR (718 patients)
ALDACTONE (714 patients)
METHYLPREDNISOLONE (713 patients)
RANITIDINE (712 patients)
RAMIPRIL (712 patients)
ARANESP (704 patients)
FERROUS SULFATE TAB (704 patients)
ASCORBIC ACID (703 patients)
ENALAPRIL MALEATE (701 patients)
EFFEXOR (694 patients)
BACTRIM (692 patients)
PROZAC (689 patients)
TYLENOL (CAPLET) (688 patients)
RIBAVIRIN (686 patients)
AVANDIA (685 patients)
VENTOLIN (679 patients)
TAXOTERE (677 patients)
PROGRAF (675 patients)
GLEEVEC (668 patients)
TOCILIZUMAB (665 patients)
HUMALOG (660 patients)
PEPCID (658 patients)
NYSTATIN (654 patients)
SANDOSTATIN LAR (651 patients)
DOCETAXEL (648 patients)
AVELOX (647 patients)
TRAZODONE HCL (646 patients)
NEORAL (642 patients)
KLONOPIN (642 patients)
PREDONINE (634 patients)
AMITRIPTYLINE HCL (629 patients)
ZYRTEC (628 patients)
TYLENOL (627 patients)
LACTULOSE (615 patients)
FLEXERIL (615 patients)
BYETTA (612 patients)
AMIODARONE HCL (611 patients)
PACLITAXEL (610 patients)
ONDANSETRON (609 patients)
AZITHROMYCIN (605 patients)
SOLU-MEDROL (605 patients)
GLUCOPHAGE (603 patients)
WELLBUTRIN (603 patients)
AVASTIN (597 patients)
KLOR-CON (596 patients)
GLYBURIDE (595 patients)
MS CONTIN (590 patients)
SYNAGIS (590 patients)
BENADRYL (590 patients)
FLONASE (587 patients)
DEXAMETHASONE TAB (582 patients)
VALIUM (582 patients)
ACTOS (576 patients)
RHEUMATREX (575 patients)
AUGMENTIN '125' (573 patients)
FLOVENT (572 patients)
GLIPIZIDE (571 patients)
TAXOL (564 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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