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

HYPOGLYCAEMIA ( 6 FDA reports)
PNEUMONIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
IMMUNOGLOBULINS DECREASED ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
PHLEBITIS DEEP ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEATH ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)

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