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

RASH ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EPISTAXIS ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE UNSPECIFIED ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
COUGH ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABASIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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