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

NEUTROPHIL COUNT DECREASED ( 13 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 10 FDA reports)
PNEUMONIA ( 9 FDA reports)
ANOREXIA ( 8 FDA reports)
STEVENS-JOHNSON SYNDROME ( 8 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
OTITIS EXTERNA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
RASH ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DEATH ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
ENCEPHALITIS POST MEASLES ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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