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SUICIDE ATTEMPT ( 22 FDA reports)
DRUG INTERACTION ( 19 FDA reports)
NAUSEA ( 17 FDA reports)
VOMITING ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
COMA ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DEPRESSION ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
FALL ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
JAW FRACTURE ( 4 FDA reports)
LACERATION ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
POISONING ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTROENTERITIS SALMONELLA ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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