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

FLUSHING ( 6 FDA reports)
DIARRHOEA ( 5 FDA reports)
PAIN ( 5 FDA reports)
INSOMNIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
NECK PAIN ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GOUT ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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