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

PYREXIA ( 10 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
HYPERCAPNIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 2 FDA reports)
APLASIA PURE RED CELL ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
BK VIRUS INFECTION ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CHEST TUBE INSERTION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
ORCHITIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MASS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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