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

HYPERKALAEMIA ( 3 FDA reports)
CLEFT LIP AND PALATE ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
TERATOGENICITY ( 1 FDA reports)

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