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

PYREXIA ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ASPIRATION ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EXOPHTHALMOS ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEDIASTINUM NEOPLASM ( 2 FDA reports)
METASTASES TO EYE ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
FALL ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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