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

CONFUSIONAL STATE ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
FALL ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
SOPOR ( 3 FDA reports)
5'NUCLEOTIDASE INCREASED ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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