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

BRONCHOSTENOSIS ( 16 FDA reports)
LASER THERAPY ( 16 FDA reports)
LUNG OPERATION ( 16 FDA reports)
PULMONARY ARTERY THERAPEUTIC PROCEDURE ( 16 FDA reports)
TRACHEOSTOMY ( 16 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 16 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
NECROTISING FASCIITIS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PROTEIN URINE PRESENT ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
INFECTION ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RENAL TUBULAR DISORDER ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BREATH SOUNDS DECREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
LIFE SUPPORT ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORTHOPNOEA ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
SHOCK ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
ABORTION ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLISTER ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPILATION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ADRENALITIS ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)

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