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

FEBRILE NEUTROPENIA ( 18 FDA reports)
BACTERAEMIA ( 14 FDA reports)
GRAFT VERSUS HOST DISEASE ( 12 FDA reports)
ABNORMAL DREAMS ( 10 FDA reports)
INFECTION ( 9 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
DRY MOUTH ( 7 FDA reports)
FLATULENCE ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
AMNESIA ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
FALL ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
INITIAL INSOMNIA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
SECRETION DISCHARGE ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
PAIN ( 5 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
THINKING ABNORMAL ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
TYPHUS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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