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

DYSPNOEA ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
VOMITING ( 10 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
ASCITES ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
ILEUS ( 6 FDA reports)
TOOTH ABSCESS ( 6 FDA reports)
TACHYCARDIA ( 5 FDA reports)
ABSCESS DRAINAGE ( 4 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SHOCK ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BONE OPERATION ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
TALIPES ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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