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

ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
BLOOD UREA INCREASED ( 10 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
ENCEPHALOPATHY ( 9 FDA reports)
HALLUCINATION, VISUAL ( 9 FDA reports)
TREMOR ( 9 FDA reports)
CHEST PAIN ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
ATROPHY ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
CEREBRAL ATROPHY ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
EYE MOVEMENT DISORDER ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RASH ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CLEFT LIP AND PALATE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELIVERY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSLALIA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FALL ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
LEUKOENCEPHALOMYELITIS ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INJURY ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SKIN BLEEDING ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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