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PLATELET COUNT DECREASED ( 22 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
RASH ( 9 FDA reports)
STATUS ASTHMATICUS ( 8 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
TREMOR ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
DEATH ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
SHOCK ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
ASPERGILLOMA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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