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

HAEMOGLOBIN DECREASED ( 16 FDA reports)
FALL ( 15 FDA reports)
APLASIA PURE RED CELL ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
HYPOGLYCAEMIA ( 11 FDA reports)
SUBDURAL HAEMATOMA ( 11 FDA reports)
FATIGUE ( 10 FDA reports)
SUBDURAL HAEMORRHAGE ( 10 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 9 FDA reports)
ARTHRALGIA ( 9 FDA reports)
CEREBRAL HAEMORRHAGE ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MELAENA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
THERAPY NON-RESPONDER ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PROSTATIC DISORDER ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
DRUG DISPENSING ERROR ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
VITREOUS OPACITIES ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
IMMUNOGLOBULINS DECREASED ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER PERFORATION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRAIN TUMOUR OPERATION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIGLOTTIC OEDEMA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS HYPERTROPHIC ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PSEUDOHYPERKALAEMIA ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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