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

MULTIPLE DRUG OVERDOSE ( 26 FDA reports)
CONVULSION ( 21 FDA reports)
HYPOTENSION ( 18 FDA reports)
SOMNOLENCE ( 16 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 16 FDA reports)
UNRESPONSIVE TO STIMULI ( 16 FDA reports)
TACHYCARDIA ( 15 FDA reports)
OVERDOSE ( 14 FDA reports)
SUICIDE ATTEMPT ( 12 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
COMA ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
RESPIRATORY ARREST ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 7 FDA reports)
VOMITING ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DRUG ABUSE ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 4 FDA reports)
CYANOSIS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
POISONING ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
SEDATION ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
AEROPHAGIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ULCER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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