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

PYREXIA ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
INFECTION ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH ( 2 FDA reports)
SHOCK ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
THIRST ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
VIRAL SKIN INFECTION ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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