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

COMPLETED SUICIDE ( 8 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
FALL ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
IDIOSYNCRATIC ALCOHOL INTOXICATION ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ACTIVATION SYNDROME ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COMA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATOBILIARY INFECTION ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER ENLARGEMENT ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAROVARIAN CYST ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SCAR ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONGUE BLACK HAIRY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use