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

ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
BIOPSY LIVER ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FALL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
COMA ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
VOMITING ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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