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

PNEUMONIA ( 5 FDA reports)
VOMITING ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
ODYNOPHAGIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
SYNCOPE ( 3 FDA reports)
RHONCHI ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CYANOSIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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