MedsFacts Reports covering ADENOSINE TRIPHOSPHATE, DISODIUM SALT
Directory listing ordered by most common adverse events for ADENOSINE TRIPHOSPHATE, DISODIUM SALT
Please choose an event type to view the corresponding MedsFacts report:
NAUSEA ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)