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

GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
VOMITING ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DYSPNOEA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)

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