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HEPATITIS FULMINANT ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
X-RAY ABNORMAL ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
DYSTONIA ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
COMA ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
SWELLING ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
RASH ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
ILEUS ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
PAIN ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NAUSEA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
SHOCK ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)

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