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

COMPLETED SUICIDE ( 17 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
RESPIRATORY ARREST ( 9 FDA reports)
ACUTE PULMONARY OEDEMA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
FALL ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
PHLEBITIS ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PERITONEAL CARCINOMA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POISONING ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
ACCELERATED HYPERTENSION ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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