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

LEUKOPENIA ( 9 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
NEPHROPATHY TOXIC ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYDROURETER ( 2 FDA reports)
LITHOTRIPSY ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SPLENIC ARTERY ANEURYSM ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
URETEROCELE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENCEPHALITIS ALLERGIC ( 1 FDA reports)
ENCEPHALITIS POST MEASLES ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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