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COMPLETED SUICIDE ( 41 FDA reports)
CARDIAC ARREST ( 15 FDA reports)
MULTIPLE DRUG OVERDOSE ( 15 FDA reports)
CARDIO-RESPIRATORY ARREST ( 14 FDA reports)
OVERDOSE ( 14 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 12 FDA reports)
DRUG TOXICITY ( 11 FDA reports)
RESPIRATORY ARREST ( 11 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
AGGRESSION ( 7 FDA reports)
DRUG ABUSER ( 7 FDA reports)
HYPOTENSION ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
POISONING ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
AGITATION ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
DRUG SCREEN POSITIVE ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
COMA ( 3 FDA reports)
DEATH ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
FALL ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATORENAL FAILURE ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BIPOLAR I DISORDER ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOANAL ATRESIA ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLINODACTYLY ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DELAYED FONTANELLE CLOSURE ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSMORPHISM ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ENCOPRESIS ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EXCESSIVE MASTURBATION ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE AMPHETAMINE POSITIVE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABNORMAL PALMAR/PLANTAR CREASES ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APATHY ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL NAIL DISORDER ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HIGH ARCHED PALATE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LABIA ENLARGED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW SET EARS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAPILLARY MUSCLE HAEMORRHAGE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RASH ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SINGLE UMBILICAL ARTERY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEETH BRITTLE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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