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

ELECTROCARDIOGRAM QT PROLONGED ( 12 FDA reports)
MALAISE ( 11 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
SUICIDE ATTEMPT ( 10 FDA reports)
NAUSEA ( 9 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
CATATONIA ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
AGGRESSION ( 7 FDA reports)
LICHEN PLANUS ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
COMA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
DYSPHEMIA ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
SCHIZOPHRENIA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TIC ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
ORAL LICHEN PLANUS ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
SEDATION ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALCOHOL DETOXIFICATION ( 2 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FALL ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FOETAL ALCOHOL SYNDROME ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
POISONING ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE ABNORMAL ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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