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

RENAL FAILURE ACUTE ( 75 FDA reports)
OLIGURIA ( 49 FDA reports)
HAEMATURIA ( 46 FDA reports)
PRODUCT QUALITY ISSUE ( 29 FDA reports)
LYMPHOPENIA ( 28 FDA reports)
BLOOD CREATININE INCREASED ( 24 FDA reports)
DRUG INTERACTION ( 20 FDA reports)
CARDIAC ARREST ( 19 FDA reports)
HYPOTENSION ( 18 FDA reports)
ANAPHYLACTIC REACTION ( 16 FDA reports)
OXYGEN SATURATION DECREASED ( 16 FDA reports)
BRADYCARDIA ( 15 FDA reports)
PROPOFOL INFUSION SYNDROME ( 14 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
VENTRICULAR FIBRILLATION ( 12 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
AGITATION ( 8 FDA reports)
CONFUSIONAL STATE ( 8 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
HAEMOLYSIS ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
SEROTONIN SYNDROME ( 7 FDA reports)
ALKALOSIS ( 6 FDA reports)
ANAESTHETIC COMPLICATION ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
OCULOGYRIC CRISIS ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BRADYCARDIA NEONATAL ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HYPERCAPNIA ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
PCO2 DECREASED ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RASH ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
TREMOR ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
COMA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
COUGH ( 3 FDA reports)
CRYSTAL URINE ( 3 FDA reports)
CYANOSIS NEONATAL ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
FIBRINOLYSIS ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INJECTION SITE THROMBOSIS ( 3 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAIN ( 3 FDA reports)
PARALYSIS FLACCID ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POST PROCEDURAL HAEMATURIA ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SKIN TEST POSITIVE ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALLERGIC MYOCARDITIS ( 2 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 2 FDA reports)
ANURIA ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PENILE VASCULAR DISORDER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TRYPTASE ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
MYOTONIA CONGENITA ( 1 FDA reports)
NEONATAL RESPIRATORY ALKALOSIS ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA OF GENITAL FEMALE ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY PNEUMATOCELE ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL LIPOMATOSIS ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINOMA ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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