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

DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
COMA ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
MALAISE ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
ABNORMAL BEHAVIOUR ( 8 FDA reports)
ASCITES ( 8 FDA reports)
ATELECTASIS ( 8 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
MECHANICAL VENTILATION ( 8 FDA reports)
MEDIASTINAL SHIFT ( 8 FDA reports)
MICTURITION FREQUENCY DECREASED ( 8 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 8 FDA reports)
SPLENOMEGALY ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
VENOOCCLUSIVE DISEASE ( 8 FDA reports)
DEHYDRATION ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLOOD LACTIC ACID DECREASED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
MUTISM ( 4 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SINOATRIAL BLOCK ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
SEDATION ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FLUID REPLACEMENT ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 1 FDA reports)
CYSTIC LYMPHANGIOMA ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HYGROMA COLLI ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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