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DIABETES MELLITUS ( 14 FDA reports)
DEPRESSION ( 9 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
SUICIDE ATTEMPT ( 8 FDA reports)
AGITATION ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
ANXIETY ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
AKATHISIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DIAPHRAGMATIC INJURY ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
GUN SHOT WOUND ( 4 FDA reports)
HEPATIC TRAUMA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MANIA ( 4 FDA reports)
OBESITY ( 4 FDA reports)
PAIN ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANGER ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BILIARY TRACT DISORDER ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
COMA ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POLYTRAUMATISM ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL INJURY ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
LACERATION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TRAUMATIC SHOCK ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY DYSMORPHIC DISORDER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PLEUROTHOTONUS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SUSPICIOUSNESS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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