Please choose an event type to view the corresponding MedsFacts report:

DRUG INTERACTION ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
POST PROCEDURAL NAUSEA ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE NEOPLASM MALIGNANT ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMA ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LISTERIA SEPSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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