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BLOOD PRESSURE DECREASED ( 61 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 48 FDA reports)
ANAESTHETIC COMPLICATION ( 47 FDA reports)
CONVULSION ( 40 FDA reports)
DRUG INEFFECTIVE ( 40 FDA reports)
SPINAL CORD INFARCTION ( 33 FDA reports)
MOVEMENT DISORDER ( 31 FDA reports)
DRUG TOXICITY ( 29 FDA reports)
NERVE INJURY ( 27 FDA reports)
HYPOAESTHESIA ( 25 FDA reports)
POST PROCEDURAL COMPLICATION ( 24 FDA reports)
SENSORIMOTOR DISORDER ( 24 FDA reports)
DIPLEGIA ( 20 FDA reports)
LOSS OF CONSCIOUSNESS ( 20 FDA reports)
MEDICATION ERROR ( 18 FDA reports)
PYREXIA ( 17 FDA reports)
SENSORY DISTURBANCE ( 17 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 16 FDA reports)
PULMONARY INFARCTION ( 16 FDA reports)
SHOCK ( 16 FDA reports)
MONOPLEGIA ( 15 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 14 FDA reports)
RESPIRATORY ARREST ( 14 FDA reports)
HYPOPNOEA ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
WOUND COMPLICATION ( 12 FDA reports)
PAIN ( 11 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 10 FDA reports)
CAUDA EQUINA SYNDROME ( 10 FDA reports)
MUSCLE RIGIDITY ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
SPINAL CORD COMPRESSION ( 10 FDA reports)
BRADYCARDIA ( 9 FDA reports)
FEELING COLD ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
PO2 DECREASED ( 9 FDA reports)
POST PROCEDURAL PAIN ( 9 FDA reports)
PROCEDURAL COMPLICATION ( 9 FDA reports)
ACCIDENTAL OVERDOSE ( 8 FDA reports)
ANORECTAL DISORDER ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK ( 8 FDA reports)
BLOOD DISORDER ( 8 FDA reports)
CARDIAC MASSAGE ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
PARALYSIS ( 8 FDA reports)
PARALYSIS FLACCID ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SINOATRIAL BLOCK ( 8 FDA reports)
SINUS ARRHYTHMIA ( 8 FDA reports)
ADAMS-STOKES SYNDROME ( 7 FDA reports)
BLADDER DISORDER ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RESPIRATORY DEPRESSION ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
CLONIC CONVULSION ( 6 FDA reports)
DRUG EFFECT INCREASED ( 6 FDA reports)
LUMBAR RADICULOPATHY ( 6 FDA reports)
PERONEAL NERVE PALSY ( 6 FDA reports)
PROCEDURAL PAIN ( 6 FDA reports)
RESPIRATORY ACIDOSIS ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
SUBDURAL EFFUSION ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GLOSSOPTOSIS ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BEDRIDDEN ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DRUG EFFECT PROLONGED ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARACHNOIDITIS ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SPINAL ANAESTHESIA ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
WOUND ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CHOKING ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KELOID SCAR ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POISONING ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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