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

DIARRHOEA ( 7 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIFFICULTY IN WALKING ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
ANGER ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
MOTION SICKNESS ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
AGGRESSION ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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