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

DEATH ( 5 FDA reports)
TACHYCARDIA ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
AGEUSIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
APATHY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
FALL ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHROLEUKAEMIA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
JAUNDICE ACHOLURIC ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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