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

CEREBRAL INFARCTION ( 4 FDA reports)
INJECTION SITE NECROSIS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
SEPSIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HEPATITIS C RNA POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPAPLASTIN DECREASED ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MELAENA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
RASH ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA RECURRENT ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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