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BLOOD GLUCOSE INCREASED ( 5 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
UNDERDOSE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
BLEEDING TIME SHORTENED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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