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

PARAESTHESIA ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
VASCULITIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
NAIL BED BLEEDING ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOMNOLENCE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
GASTRITIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)

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