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

ALCOHOL USE ( 13 FDA reports)
SUICIDE ATTEMPT ( 13 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 7 FDA reports)
DEPRESSION ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
AGGRESSION ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
AGITATION ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERNIG'S SIGN ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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