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

PYREXIA ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
LEUKOPENIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
BURN OF INTERNAL ORGANS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
VOMITING ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
SEPSIS ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
ASCITES ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
LYMPHOCELE ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
GUM NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ILEUS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VAGINAL OEDEMA ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
SHOCK ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
POST PROCEDURAL URINE LEAK ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INFECTED NEOPLASM ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
INDURATION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)

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