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

INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
ANAEMIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
AKINESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUTISM ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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