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

VOMITING ( 6 FDA reports)
CHOKING ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
FALL ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACROPHOBIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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