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

BLOOD PRESSURE DECREASED ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
ABSCESS ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
MELAENA ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ANOREXIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 2 FDA reports)
MALAISE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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