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DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
TREMOR ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOSTHENURIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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