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

CEREBRAL HAEMORRHAGE ( 50 FDA reports)
PNEUMONIA ( 48 FDA reports)
PYREXIA ( 44 FDA reports)
CEREBRAL INFARCTION ( 43 FDA reports)
DEATH ( 41 FDA reports)
VOMITING ( 41 FDA reports)
ANAEMIA ( 39 FDA reports)
DEEP VEIN THROMBOSIS ( 37 FDA reports)
BONE DISORDER ( 36 FDA reports)
DYSPNOEA ( 36 FDA reports)
OSTEOMYELITIS ( 35 FDA reports)
PAIN ( 35 FDA reports)
ANXIETY ( 34 FDA reports)
PAIN IN JAW ( 31 FDA reports)
MYOCARDIAL INFARCTION ( 30 FDA reports)
GAIT DISTURBANCE ( 29 FDA reports)
HYPOPHAGIA ( 29 FDA reports)
NAUSEA ( 29 FDA reports)
HAEMORRHAGE ( 28 FDA reports)
ASTHENIA ( 27 FDA reports)
FATIGUE ( 27 FDA reports)
THROMBOCYTOPENIA ( 27 FDA reports)
CEREBROVASCULAR ACCIDENT ( 26 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 26 FDA reports)
HYPERTENSION ( 26 FDA reports)
HYPOAESTHESIA ( 26 FDA reports)
CELLULITIS ( 25 FDA reports)
PULMONARY EMBOLISM ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
TOOTH LOSS ( 25 FDA reports)
WEIGHT DECREASED ( 25 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 24 FDA reports)
NEUROPATHY PERIPHERAL ( 24 FDA reports)
DYSPHAGIA ( 23 FDA reports)
BACK PAIN ( 22 FDA reports)
HYPOTENSION ( 22 FDA reports)
OSTEONECROSIS OF JAW ( 21 FDA reports)
PARAESTHESIA ( 21 FDA reports)
SPINAL OSTEOARTHRITIS ( 21 FDA reports)
CORONARY ARTERY DISEASE ( 20 FDA reports)
GASTRITIS ( 20 FDA reports)
INSOMNIA ( 20 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 19 FDA reports)
COMPRESSION FRACTURE ( 19 FDA reports)
LOOSE TOOTH ( 19 FDA reports)
NECK PAIN ( 19 FDA reports)
OEDEMA PERIPHERAL ( 19 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
IMPAIRED HEALING ( 18 FDA reports)
JAW DISORDER ( 18 FDA reports)
ORAL PAIN ( 18 FDA reports)
SINUS DISORDER ( 18 FDA reports)
TOOTH EXTRACTION ( 18 FDA reports)
CHILLS ( 17 FDA reports)
CONFUSIONAL STATE ( 17 FDA reports)
PRIMARY SEQUESTRUM ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
BLOOD POTASSIUM DECREASED ( 16 FDA reports)
BONE LESION ( 16 FDA reports)
ISCHAEMIC STROKE ( 16 FDA reports)
OSTEONECROSIS ( 16 FDA reports)
ANGINA PECTORIS ( 15 FDA reports)
ANGIOEDEMA ( 15 FDA reports)
BLOOD CALCIUM DECREASED ( 15 FDA reports)
BLOOD GLUCOSE INCREASED ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
SWELLING ( 15 FDA reports)
URINARY INCONTINENCE ( 15 FDA reports)
ABSCESS JAW ( 14 FDA reports)
ACTINOMYCOSIS ( 14 FDA reports)
ARTHRALGIA ( 14 FDA reports)
BLOOD ALBUMIN DECREASED ( 14 FDA reports)
DENTAL FISTULA ( 14 FDA reports)
JAW FRACTURE ( 14 FDA reports)
JUGULAR VEIN THROMBOSIS ( 14 FDA reports)
LEUKOENCEPHALOPATHY ( 14 FDA reports)
OCULAR HYPERTENSION ( 14 FDA reports)
ODYNOPHAGIA ( 14 FDA reports)
OESOPHAGITIS ULCERATIVE ( 14 FDA reports)
OSTEITIS ( 14 FDA reports)
PARAPLEGIA ( 14 FDA reports)
PERIODONTAL DISEASE ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
TENDONITIS ( 14 FDA reports)
TONGUE INJURY ( 14 FDA reports)
AGITATION ( 13 FDA reports)
APHASIA ( 13 FDA reports)
ARTHRITIS ( 13 FDA reports)
EDENTULOUS ( 13 FDA reports)
FAECAL INCONTINENCE ( 13 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 13 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 13 FDA reports)
MOBILITY DECREASED ( 13 FDA reports)
ANAPHYLACTOID SHOCK ( 12 FDA reports)
ARTERIOSCLEROSIS ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
COMA ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
MUSCULAR WEAKNESS ( 12 FDA reports)
PROSTHESIS USER ( 12 FDA reports)
PULMONARY HYPERTENSION ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
SKIN DISORDER ( 12 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 12 FDA reports)
TACHYCARDIA ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 11 FDA reports)
CUBITAL TUNNEL SYNDROME ( 11 FDA reports)
DEFORMITY ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 11 FDA reports)
HAEMORRHAGIC STROKE ( 11 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 11 FDA reports)
HYDROCEPHALUS ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 11 FDA reports)
PRURITUS GENERALISED ( 11 FDA reports)
SWELLING FACE ( 11 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 11 FDA reports)
ACUTE CORONARY SYNDROME ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
DISCOMFORT ( 10 FDA reports)
FALL ( 10 FDA reports)
HEMIPLEGIA ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
LEUKOCYTOSIS ( 10 FDA reports)
MULTI-ORGAN FAILURE ( 10 FDA reports)
OEDEMA ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
BRAIN HERNIATION ( 9 FDA reports)
BRAIN OEDEMA ( 9 FDA reports)
CEREBRAL HAEMATOMA ( 9 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
COLONIC POLYP ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DECREASED INTEREST ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
DYSGEUSIA ( 9 FDA reports)
ENCEPHALOPATHY ( 9 FDA reports)
FISTULA ( 9 FDA reports)
HAEMATOMA ( 9 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
HEMIPARESIS ( 9 FDA reports)
INJURY ( 9 FDA reports)
LIFE EXPECTANCY SHORTENED ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
METASTATIC NEOPLASM ( 9 FDA reports)
OSTEOARTHRITIS ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PULMONARY HAEMORRHAGE ( 9 FDA reports)
RADICULOPATHY ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
SEQUESTRECTOMY ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
WHEELCHAIR USER ( 9 FDA reports)
AGGRESSION ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
BONE OPERATION ( 8 FDA reports)
BREAST CANCER METASTATIC ( 8 FDA reports)
CATARACT ( 8 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 8 FDA reports)
DEBRIDEMENT ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DEMENTIA ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
EMBOLISM ( 8 FDA reports)
HIATUS HERNIA ( 8 FDA reports)
INFECTION ( 8 FDA reports)
JOINT CONTRACTURE ( 8 FDA reports)
LACERATION ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
METASTASES TO BONE ( 8 FDA reports)
METASTASES TO LIVER ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
OBESITY ( 8 FDA reports)
PARALYSIS ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
RASH MACULAR ( 8 FDA reports)
SEDATION ( 8 FDA reports)
SENSORY DISTURBANCE ( 8 FDA reports)
SKIN TIGHTNESS ( 8 FDA reports)
SUBDURAL HAEMATOMA ( 8 FDA reports)
TRANSFUSION ( 8 FDA reports)
VERBAL ABUSE ( 8 FDA reports)
VISUAL IMPAIRMENT ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BONE DEBRIDEMENT ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
CAROTID BRUIT ( 7 FDA reports)
CATARACT OPERATION ( 7 FDA reports)
CERVICAL SPINAL STENOSIS ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
CORONARY ARTERY BYPASS ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
GOITRE ( 7 FDA reports)
HEART RATE INCREASED ( 7 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 7 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 7 FDA reports)
HYPERGLYCAEMIA ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 7 FDA reports)
JAW OPERATION ( 7 FDA reports)
LIMB DISCOMFORT ( 7 FDA reports)
LUMBAR SPINAL STENOSIS ( 7 FDA reports)
NEUTROPENIC INFECTION ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
TOOTH ABSCESS ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
WOUND DRAINAGE ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
DEAFNESS ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
KLEBSIELLA SEPSIS ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
RETINAL DETACHMENT ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VENOUS OCCLUSION ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ADENOCARCINOMA ( 5 FDA reports)
ASCITES ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
BONE LOSS ( 5 FDA reports)
BRAIN MIDLINE SHIFT ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
EXTRADURAL HAEMATOMA ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
LIP SWELLING ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 5 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 5 FDA reports)
METASTASES TO LUNG ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
MYOCARDIAL STRAIN ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PLEURECTOMY ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 4 FDA reports)
ATAXIA ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BONE EROSION ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
EMPYEMA ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FIBROSIS ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEPATIC CYST ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
RALES ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SEPSIS SYNDROME ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN FIBROSIS ( 4 FDA reports)
SKIN HYPERTROPHY ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
THROMBOCYTOSIS ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TRACHEAL OBSTRUCTION ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ANURIA ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
APHONIA ( 3 FDA reports)
APNOEA ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACTERIAL DISEASE CARRIER ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BONE FRAGMENTATION ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CATHETER THROMBOSIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EMBOLIC STROKE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
ESCHERICHIA BACTERAEMIA ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EXPOSED BONE IN JAW ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERPLASIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
JOINT EFFUSION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYOCARDIAL RUPTURE ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
ORAL CAVITY FISTULA ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOLYSIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RENAL VEIN THROMBOSIS ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SCAR ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VENA CAVA THROMBOSIS ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANEURYSM ARTERIOVENOUS ( 2 FDA reports)
ANEURYSM RUPTURED ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APATHY ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BASAL GANGLIA INFARCTION ( 2 FDA reports)
BASILAR ARTERY OCCLUSION ( 2 FDA reports)
BENIGN GASTRIC NEOPLASM ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CEREBELLAR HAEMORRHAGE ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EXTREMITY CONTRACTURE ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
FEAR ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GENITAL ABSCESS ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
IMPLANT SITE NECROSIS ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MEDIASTINAL HAEMATOMA ( 2 FDA reports)
MESENTERIC HAEMORRHAGE ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PUNCTURE SITE INFECTION ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
REPERFUSION INJURY ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TRACHEAL DEVIATION ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VERTEBRAL ARTERY DISSECTION ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE MATERIAL OPACIFICATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFUSE AXONAL INJURY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIC FASCIITIS ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL PLAQUE ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
THYROID HAEMORRHAGE ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE CHLORIDE DECREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VASCULAR COMPRESSION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VOCAL CORD THICKENING ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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