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INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
POLYMYOSITIS ( 8 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
GALLBLADDER POLYP ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
AIDS ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
PURPURA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)

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