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

PNEUMONIA ( 233 FDA reports)
DYSPNOEA ( 211 FDA reports)
PYREXIA ( 209 FDA reports)
RENAL FAILURE ( 158 FDA reports)
HYPOTENSION ( 156 FDA reports)
DIARRHOEA ( 149 FDA reports)
RESPIRATORY FAILURE ( 137 FDA reports)
NAUSEA ( 128 FDA reports)
RENAL FAILURE ACUTE ( 119 FDA reports)
SEPSIS ( 109 FDA reports)
ANAEMIA ( 105 FDA reports)
DIZZINESS ( 102 FDA reports)
ABDOMINAL PAIN ( 101 FDA reports)
FATIGUE ( 95 FDA reports)
VOMITING ( 94 FDA reports)
OEDEMA PERIPHERAL ( 93 FDA reports)
HEPATIC FAILURE ( 92 FDA reports)
MYOCARDIAL INFARCTION ( 91 FDA reports)
PAIN ( 91 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 91 FDA reports)
COUGH ( 90 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 89 FDA reports)
ANXIETY ( 86 FDA reports)
ASTHENIA ( 86 FDA reports)
DEATH ( 85 FDA reports)
THROMBOCYTOPENIA ( 84 FDA reports)
ATRIAL FIBRILLATION ( 83 FDA reports)
CONDITION AGGRAVATED ( 83 FDA reports)
HYPOKALAEMIA ( 83 FDA reports)
DEHYDRATION ( 82 FDA reports)
HYPERTENSION ( 82 FDA reports)
PLEURAL EFFUSION ( 81 FDA reports)
STEVENS-JOHNSON SYNDROME ( 80 FDA reports)
SOMNOLENCE ( 78 FDA reports)
DRUG INTERACTION ( 77 FDA reports)
RASH ( 77 FDA reports)
HAEMOGLOBIN DECREASED ( 73 FDA reports)
PULMONARY OEDEMA ( 71 FDA reports)
SEPTIC SHOCK ( 70 FDA reports)
CARDIAC ARREST ( 68 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 67 FDA reports)
BLOOD CREATININE INCREASED ( 66 FDA reports)
TACHYCARDIA ( 66 FDA reports)
MULTI-ORGAN FAILURE ( 65 FDA reports)
CHEST PAIN ( 64 FDA reports)
LOSS OF CONSCIOUSNESS ( 63 FDA reports)
WEIGHT DECREASED ( 62 FDA reports)
BRADYCARDIA ( 61 FDA reports)
FALL ( 61 FDA reports)
CARDIAC FAILURE ( 60 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 60 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 59 FDA reports)
OVERDOSE ( 59 FDA reports)
PRURITUS ( 58 FDA reports)
DEEP VEIN THROMBOSIS ( 57 FDA reports)
SYNCOPE ( 57 FDA reports)
CONFUSIONAL STATE ( 56 FDA reports)
MEDICATION ERROR ( 56 FDA reports)
DRUG INEFFECTIVE ( 55 FDA reports)
BACK PAIN ( 54 FDA reports)
CONVULSION ( 54 FDA reports)
URINARY TRACT INFECTION ( 54 FDA reports)
DEPRESSION ( 53 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 53 FDA reports)
PULMONARY EMBOLISM ( 53 FDA reports)
HEADACHE ( 52 FDA reports)
AGITATION ( 51 FDA reports)
INFECTION ( 50 FDA reports)
CORONARY ARTERY DISEASE ( 49 FDA reports)
ERYTHEMA ( 49 FDA reports)
HAEMATOMA ( 49 FDA reports)
RENAL IMPAIRMENT ( 49 FDA reports)
GAIT DISTURBANCE ( 48 FDA reports)
HEART RATE INCREASED ( 47 FDA reports)
ARTHRALGIA ( 45 FDA reports)
CELLULITIS ( 45 FDA reports)
CEREBROVASCULAR ACCIDENT ( 45 FDA reports)
LIVER CARCINOMA RUPTURED ( 45 FDA reports)
CONSTIPATION ( 44 FDA reports)
MALAISE ( 44 FDA reports)
NEPHROPATHY TOXIC ( 44 FDA reports)
NEUTROPENIA ( 44 FDA reports)
INJURY ( 43 FDA reports)
ARRHYTHMIA ( 42 FDA reports)
SINUSITIS ( 42 FDA reports)
CHILLS ( 41 FDA reports)
DYSPHAGIA ( 41 FDA reports)
HYPERHIDROSIS ( 41 FDA reports)
BRONCHITIS ( 40 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 38 FDA reports)
EMOTIONAL DISTRESS ( 38 FDA reports)
FEBRILE NEUTROPENIA ( 38 FDA reports)
HYPERKALAEMIA ( 38 FDA reports)
HYPONATRAEMIA ( 38 FDA reports)
PANCYTOPENIA ( 38 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 37 FDA reports)
JAUNDICE ( 37 FDA reports)
RHABDOMYOLYSIS ( 37 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 36 FDA reports)
OXYGEN SATURATION DECREASED ( 36 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 35 FDA reports)
EMPHYSEMA ( 35 FDA reports)
HAEMORRHAGE ( 35 FDA reports)
MITRAL VALVE INCOMPETENCE ( 35 FDA reports)
PARAESTHESIA ( 35 FDA reports)
HYPOXIA ( 34 FDA reports)
UNEVALUABLE EVENT ( 34 FDA reports)
CARDIAC DISORDER ( 33 FDA reports)
CARDIOMYOPATHY ( 33 FDA reports)
PAIN IN EXTREMITY ( 33 FDA reports)
TREMOR ( 33 FDA reports)
DRUG TOXICITY ( 32 FDA reports)
HAEMOPTYSIS ( 32 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 32 FDA reports)
BLISTER ( 31 FDA reports)
DISTURBANCE IN ATTENTION ( 31 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 31 FDA reports)
OSTEOARTHRITIS ( 31 FDA reports)
POST PROCEDURAL COMPLICATION ( 31 FDA reports)
PULMONARY HYPERTENSION ( 31 FDA reports)
HYPOGLYCAEMIA ( 30 FDA reports)
LUNG INFILTRATION ( 30 FDA reports)
RENAL FAILURE CHRONIC ( 30 FDA reports)
CARDIOVASCULAR DISORDER ( 29 FDA reports)
DIABETES MELLITUS ( 29 FDA reports)
DISEASE PROGRESSION ( 29 FDA reports)
ENCEPHALOPATHY ( 29 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 29 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 28 FDA reports)
ANGINA PECTORIS ( 28 FDA reports)
BLOOD PRESSURE INCREASED ( 28 FDA reports)
BLOOD SODIUM DECREASED ( 28 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 28 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 28 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 28 FDA reports)
PNEUMONIA ASPIRATION ( 28 FDA reports)
ASTHMA ( 27 FDA reports)
EPISTAXIS ( 27 FDA reports)
HAEMATOCHEZIA ( 27 FDA reports)
INSOMNIA ( 27 FDA reports)
THROMBOSIS ( 27 FDA reports)
ATELECTASIS ( 26 FDA reports)
AZOTAEMIA ( 26 FDA reports)
COMA ( 26 FDA reports)
DECREASED APPETITE ( 26 FDA reports)
FAECAL INCONTINENCE ( 26 FDA reports)
HAEMATOCRIT DECREASED ( 26 FDA reports)
HYPERSENSITIVITY ( 26 FDA reports)
LEUKOPENIA ( 26 FDA reports)
BLOOD GLUCOSE INCREASED ( 25 FDA reports)
BLOOD PRESSURE DECREASED ( 25 FDA reports)
CLOSTRIDIAL INFECTION ( 25 FDA reports)
HAEMODIALYSIS ( 25 FDA reports)
HEPATIC ENCEPHALOPATHY ( 25 FDA reports)
RESPIRATORY TRACT INFECTION ( 25 FDA reports)
VENTRICULAR FIBRILLATION ( 25 FDA reports)
VISION BLURRED ( 25 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 25 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 24 FDA reports)
ILEUS ( 24 FDA reports)
LUNG DISORDER ( 24 FDA reports)
LYMPHADENOPATHY ( 24 FDA reports)
SPEECH DISORDER ( 24 FDA reports)
URINARY INCONTINENCE ( 24 FDA reports)
ANGIOEDEMA ( 23 FDA reports)
BLOOD BILIRUBIN INCREASED ( 23 FDA reports)
CARDIO-RESPIRATORY ARREST ( 23 FDA reports)
CEREBRAL HAEMORRHAGE ( 23 FDA reports)
DISORIENTATION ( 23 FDA reports)
INFLAMMATION ( 23 FDA reports)
LIVER DISORDER ( 23 FDA reports)
MEMORY IMPAIRMENT ( 23 FDA reports)
MENTAL STATUS CHANGES ( 23 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 23 FDA reports)
OSTEOPOROSIS ( 23 FDA reports)
RESPIRATORY DISTRESS ( 23 FDA reports)
RIB FRACTURE ( 23 FDA reports)
AGRANULOCYTOSIS ( 22 FDA reports)
BACTERIAL INFECTION ( 22 FDA reports)
FEAR ( 22 FDA reports)
LUNG INFECTION ( 22 FDA reports)
OSTEONECROSIS OF JAW ( 22 FDA reports)
PRODUCTIVE COUGH ( 22 FDA reports)
CARDIOGENIC SHOCK ( 21 FDA reports)
DELIRIUM ( 21 FDA reports)
DYSPEPSIA ( 21 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 21 FDA reports)
GRAND MAL CONVULSION ( 21 FDA reports)
LEUKOCYTOSIS ( 21 FDA reports)
MUSCLE SPASMS ( 21 FDA reports)
PERITONITIS ( 21 FDA reports)
PLATELET COUNT DECREASED ( 21 FDA reports)
SLEEP DISORDER ( 21 FDA reports)
URTICARIA ( 21 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 20 FDA reports)
COGNITIVE DISORDER ( 20 FDA reports)
HALLUCINATION ( 20 FDA reports)
HEPATOTOXICITY ( 20 FDA reports)
HYPERGLYCAEMIA ( 20 FDA reports)
INTERSTITIAL LUNG DISEASE ( 20 FDA reports)
NASAL POLYPS ( 20 FDA reports)
TACHYPNOEA ( 20 FDA reports)
ABDOMINAL PAIN UPPER ( 19 FDA reports)
CYANOSIS ( 19 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 19 FDA reports)
KYPHOSIS ( 19 FDA reports)
MUSCULAR WEAKNESS ( 19 FDA reports)
NEUROPATHY PERIPHERAL ( 19 FDA reports)
STAPHYLOCOCCAL INFECTION ( 19 FDA reports)
SUICIDE ATTEMPT ( 19 FDA reports)
ANOREXIA ( 18 FDA reports)
BONE PAIN ( 18 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 18 FDA reports)
CEREBRAL INFARCTION ( 18 FDA reports)
EMBOLISM ( 18 FDA reports)
HYPOAESTHESIA ( 18 FDA reports)
INCORRECT DOSE ADMINISTERED ( 18 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 18 FDA reports)
JOINT SWELLING ( 18 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 18 FDA reports)
LOOSE TOOTH ( 18 FDA reports)
OSTEOMYELITIS ACUTE ( 18 FDA reports)
PSYCHOTIC DISORDER ( 18 FDA reports)
PULMONARY FIBROSIS ( 18 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 18 FDA reports)
ABDOMINAL DISTENSION ( 17 FDA reports)
ABSCESS JAW ( 17 FDA reports)
ARTHRITIS ( 17 FDA reports)
BLOOD UREA INCREASED ( 17 FDA reports)
BONE LESION ( 17 FDA reports)
CARDIOMEGALY ( 17 FDA reports)
CHOLESTASIS ( 17 FDA reports)
CHRONIC SINUSITIS ( 17 FDA reports)
DEFORMITY ( 17 FDA reports)
DIASTOLIC DYSFUNCTION ( 17 FDA reports)
ECONOMIC PROBLEM ( 17 FDA reports)
FEELING ABNORMAL ( 17 FDA reports)
GASTRIC ULCER ( 17 FDA reports)
GENERALISED OEDEMA ( 17 FDA reports)
HYPERVENTILATION ( 17 FDA reports)
INFUSION RELATED REACTION ( 17 FDA reports)
NIKOLSKY'S SIGN ( 17 FDA reports)
OFF LABEL USE ( 17 FDA reports)
PANCREATITIS ( 17 FDA reports)
POLYNEUROPATHY ( 17 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 17 FDA reports)
RESTLESSNESS ( 17 FDA reports)
SHOCK ( 17 FDA reports)
SUICIDAL IDEATION ( 17 FDA reports)
TRANSAMINASES INCREASED ( 17 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
VENTRICULAR TACHYCARDIA ( 17 FDA reports)
VISUAL ACUITY REDUCED ( 17 FDA reports)
ASCITES ( 16 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 16 FDA reports)
BONE DEFORMITY ( 16 FDA reports)
BONE NEOPLASM MALIGNANT ( 16 FDA reports)
CATARACT ( 16 FDA reports)
CHROMATURIA ( 16 FDA reports)
CIRCULATORY COLLAPSE ( 16 FDA reports)
COMPRESSION FRACTURE ( 16 FDA reports)
DIALYSIS ( 16 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 16 FDA reports)
EXPOSED BONE IN JAW ( 16 FDA reports)
GASTROINTESTINAL DISORDER ( 16 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 16 FDA reports)
JAW FRACTURE ( 16 FDA reports)
MASTICATION DISORDER ( 16 FDA reports)
MENINGIOMA ( 16 FDA reports)
METABOLIC ACIDOSIS ( 16 FDA reports)
METASTASES TO SPINE ( 16 FDA reports)
MULTIPLE MYELOMA ( 16 FDA reports)
OEDEMA ( 16 FDA reports)
OSTEOLYSIS ( 16 FDA reports)
OSTEORADIONECROSIS ( 16 FDA reports)
PALLOR ( 16 FDA reports)
PHYSICAL DISABILITY ( 16 FDA reports)
PLASMACYTOMA ( 16 FDA reports)
RESPIRATORY ARREST ( 16 FDA reports)
SKIN DISCOLOURATION ( 16 FDA reports)
SKIN ULCER ( 16 FDA reports)
SYNOVIAL CYST ( 16 FDA reports)
TIBIA FRACTURE ( 16 FDA reports)
TOOTH LOSS ( 16 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 16 FDA reports)
ACIDOSIS ( 15 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 15 FDA reports)
AGGRESSION ( 15 FDA reports)
BRONCHOPNEUMONIA ( 15 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 15 FDA reports)
CARDIAC VALVE DISEASE ( 15 FDA reports)
CHOLELITHIASIS ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
DRUG HYPERSENSITIVITY ( 15 FDA reports)
DRY MOUTH ( 15 FDA reports)
DUODENAL ULCER ( 15 FDA reports)
GASTRITIS ( 15 FDA reports)
HAEMANGIOMA ( 15 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 15 FDA reports)
MALNUTRITION ( 15 FDA reports)
MELAENA ( 15 FDA reports)
OBESITY ( 15 FDA reports)
PNEUMOTHORAX ( 15 FDA reports)
PSEUDOMONAS INFECTION ( 15 FDA reports)
PULMONARY CONGESTION ( 15 FDA reports)
STATUS EPILEPTICUS ( 15 FDA reports)
STRESS ( 15 FDA reports)
UNRESPONSIVE TO STIMULI ( 15 FDA reports)
WOUND SECRETION ( 15 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 14 FDA reports)
ADRENAL INSUFFICIENCY ( 14 FDA reports)
BALANCE DISORDER ( 14 FDA reports)
BLOOD POTASSIUM DECREASED ( 14 FDA reports)
BRONCHOSPASM ( 14 FDA reports)
CUSHINGOID ( 14 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 14 FDA reports)
ENTEROCOCCAL INFECTION ( 14 FDA reports)
HYPERBILIRUBINAEMIA ( 14 FDA reports)
HYPOCALCAEMIA ( 14 FDA reports)
IMPAIRED HEALING ( 14 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 14 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 14 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
LYMPHOCELE ( 14 FDA reports)
NEUROLOGICAL SYMPTOM ( 14 FDA reports)
PNEUMONITIS ( 14 FDA reports)
RASH MACULO-PAPULAR ( 14 FDA reports)
SLEEP APNOEA SYNDROME ( 14 FDA reports)
SUDDEN DEATH ( 14 FDA reports)
VISUAL DISTURBANCE ( 14 FDA reports)
BENCE JONES PROTEINURIA ( 13 FDA reports)
BLOOD POTASSIUM INCREASED ( 13 FDA reports)
COAGULOPATHY ( 13 FDA reports)
CORONARY ARTERY STENOSIS ( 13 FDA reports)
CYTOLYTIC HEPATITIS ( 13 FDA reports)
INTENTIONAL OVERDOSE ( 13 FDA reports)
MYALGIA ( 13 FDA reports)
NASOPHARYNGITIS ( 13 FDA reports)
NERVOUS SYSTEM DISORDER ( 13 FDA reports)
RESPIRATORY DISORDER ( 13 FDA reports)
SINUS TACHYCARDIA ( 13 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 13 FDA reports)
ACCIDENTAL OVERDOSE ( 12 FDA reports)
ACUTE PRERENAL FAILURE ( 12 FDA reports)
ACUTE RESPIRATORY FAILURE ( 12 FDA reports)
ANAPHYLACTIC REACTION ( 12 FDA reports)
ANAPHYLACTIC SHOCK ( 12 FDA reports)
ATRIAL FLUTTER ( 12 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 12 FDA reports)
CHEST DISCOMFORT ( 12 FDA reports)
DEMENTIA ( 12 FDA reports)
DIPLOPIA ( 12 FDA reports)
EAR PAIN ( 12 FDA reports)
FLUID OVERLOAD ( 12 FDA reports)
GASTROENTERITIS ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
HEPATIC ENZYME INCREASED ( 12 FDA reports)
LUMBAR SPINAL STENOSIS ( 12 FDA reports)
LUNG NEOPLASM MALIGNANT ( 12 FDA reports)
LYMPHOPENIA ( 12 FDA reports)
MUCOSAL INFLAMMATION ( 12 FDA reports)
OSTEONECROSIS ( 12 FDA reports)
OSTEOSCLEROSIS ( 12 FDA reports)
PERICARDIAL EFFUSION ( 12 FDA reports)
PETECHIAE ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
RESPIRATORY DEPRESSION ( 12 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 12 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 12 FDA reports)
URINE COLOUR ABNORMAL ( 12 FDA reports)
ACUTE CORONARY SYNDROME ( 11 FDA reports)
ANURIA ( 11 FDA reports)
AORTIC ANEURYSM ( 11 FDA reports)
ARTERIOSCLEROSIS ( 11 FDA reports)
ASCITES INFECTION ( 11 FDA reports)
CONJUNCTIVITIS ( 11 FDA reports)
DERMATITIS EXFOLIATIVE ( 11 FDA reports)
DIVERTICULITIS ( 11 FDA reports)
ENDOTRACHEAL INTUBATION ( 11 FDA reports)
EPILEPSY ( 11 FDA reports)
FLUSHING ( 11 FDA reports)
HAEMOLYSIS ( 11 FDA reports)
HEAD INJURY ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
HEPATIC NECROSIS ( 11 FDA reports)
HERPES ZOSTER ( 11 FDA reports)
HYPOPHAGIA ( 11 FDA reports)
ILL-DEFINED DISORDER ( 11 FDA reports)
INFLUENZA ( 11 FDA reports)
JOINT STIFFNESS ( 11 FDA reports)
PANIC ATTACK ( 11 FDA reports)
SKIN LESION ( 11 FDA reports)
TACHYARRHYTHMIA ( 11 FDA reports)
TORSADE DE POINTES ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 11 FDA reports)
ANAPHYLACTOID REACTION ( 10 FDA reports)
ANHEDONIA ( 10 FDA reports)
AORTIC VALVE INCOMPETENCE ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 10 FDA reports)
CARDIAC OUTPUT DECREASED ( 10 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 10 FDA reports)
CARDIOPULMONARY FAILURE ( 10 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 10 FDA reports)
CEREBELLAR ISCHAEMIA ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
DYSGEUSIA ( 10 FDA reports)
ESCHERICHIA INFECTION ( 10 FDA reports)
EYE PAIN ( 10 FDA reports)
GLAUCOMA ( 10 FDA reports)
HEPATITIS CHOLESTATIC ( 10 FDA reports)
HYPOVOLAEMIC SHOCK ( 10 FDA reports)
LEG AMPUTATION ( 10 FDA reports)
LOBAR PNEUMONIA ( 10 FDA reports)
MOBILITY DECREASED ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
OESOPHAGITIS ( 10 FDA reports)
ORAL CANDIDIASIS ( 10 FDA reports)
ORTHOPNOEA ( 10 FDA reports)
OVERWEIGHT ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 10 FDA reports)
URETEROSTOMY SITE DISCOMFORT ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
ABDOMINAL HERNIA ( 9 FDA reports)
ACUTE HEPATIC FAILURE ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 9 FDA reports)
ANGIOPATHY ( 9 FDA reports)
AORTIC CALCIFICATION ( 9 FDA reports)
ARTERIAL HAEMORRHAGE ( 9 FDA reports)
ASPHYXIA ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BRAIN OEDEMA ( 9 FDA reports)
CEREBRAL ATROPHY ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
COLITIS ( 9 FDA reports)
COLITIS ISCHAEMIC ( 9 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
DENTAL CARIES ( 9 FDA reports)
DYSPHONIA ( 9 FDA reports)
DYSPNOEA EXERTIONAL ( 9 FDA reports)
ECCHYMOSIS ( 9 FDA reports)
FAECALOMA ( 9 FDA reports)
FAECES DISCOLOURED ( 9 FDA reports)
FLATULENCE ( 9 FDA reports)
GOUT ( 9 FDA reports)
HAEMOLYTIC ANAEMIA ( 9 FDA reports)
HEPATITIS C ( 9 FDA reports)
HEPATOCELLULAR DAMAGE ( 9 FDA reports)
HEPATOMEGALY ( 9 FDA reports)
HYPERLIPIDAEMIA ( 9 FDA reports)
HYPERTENSIVE CRISIS ( 9 FDA reports)
ISCHAEMIC STROKE ( 9 FDA reports)
KAPOSI'S SARCOMA ( 9 FDA reports)
MULTIPLE INJURIES ( 9 FDA reports)
MUSCLE HAEMORRHAGE ( 9 FDA reports)
MUSCULOSKELETAL PAIN ( 9 FDA reports)
NEOPLASM PROGRESSION ( 9 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 9 FDA reports)
POST PROCEDURAL HAEMATOMA ( 9 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 9 FDA reports)
PULMONARY TUBERCULOSIS ( 9 FDA reports)
RECTAL ULCER ( 9 FDA reports)
RENAL INJURY ( 9 FDA reports)
RHEUMATOID NODULE ( 9 FDA reports)
RIGHT VENTRICULAR FAILURE ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
AGEUSIA ( 8 FDA reports)
AKATHISIA ( 8 FDA reports)
ANGINA UNSTABLE ( 8 FDA reports)
APNOEA ( 8 FDA reports)
ASPERGILLOSIS ( 8 FDA reports)
ASPIRATION ( 8 FDA reports)
BACTERAEMIA ( 8 FDA reports)
BLOOD ALBUMIN DECREASED ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BRONCHITIS CHRONIC ( 8 FDA reports)
CARDIAC VALVE VEGETATION ( 8 FDA reports)
DECUBITUS ULCER ( 8 FDA reports)
DRUG LEVEL DECREASED ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
DYSPNOEA AT REST ( 8 FDA reports)
FAMILY STRESS ( 8 FDA reports)
FUNGAL SEPSIS ( 8 FDA reports)
GRAFT LOSS ( 8 FDA reports)
GRANULOCYTOPENIA ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 8 FDA reports)
INTESTINAL PERFORATION ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 8 FDA reports)
LETHARGY ( 8 FDA reports)
LIVER TRANSPLANT REJECTION ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
MIDDLE EAR INFLAMMATION ( 8 FDA reports)
MITRAL VALVE DISEASE ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
NEUTROPHIL COUNT INCREASED ( 8 FDA reports)
OCULAR HYPERAEMIA ( 8 FDA reports)
PORTAL VEIN THROMBOSIS ( 8 FDA reports)
PULMONARY HAEMORRHAGE ( 8 FDA reports)
RASH GENERALISED ( 8 FDA reports)
RASH PUSTULAR ( 8 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 8 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SHOCK HAEMORRHAGIC ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SOCIAL PROBLEM ( 8 FDA reports)
SPINA BIFIDA ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 8 FDA reports)
TUMOUR LYSIS SYNDROME ( 8 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
ABASIA ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ABSCESS ( 7 FDA reports)
ACUTE ABDOMEN ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 7 FDA reports)
AREFLEXIA ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 7 FDA reports)
BILE DUCT STENOSIS ( 7 FDA reports)
BLOOD LACTIC ACID INCREASED ( 7 FDA reports)
CARDIAC MURMUR ( 7 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 7 FDA reports)
CLAUSTROPHOBIA ( 7 FDA reports)
CLOSTRIDIUM COLITIS ( 7 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 7 FDA reports)
DECREASED INTEREST ( 7 FDA reports)
DRUG DISPENSING ERROR ( 7 FDA reports)
DRY EYE ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
EAR DISCOMFORT ( 7 FDA reports)
ECZEMA ( 7 FDA reports)
ERYSIPELAS ( 7 FDA reports)
EXERCISE TOLERANCE DECREASED ( 7 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 7 FDA reports)
FLUID RETENTION ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HAEMODYNAMIC INSTABILITY ( 7 FDA reports)
HAEMORRHAGIC DIATHESIS ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATITIS ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 7 FDA reports)
HYPERURICAEMIA ( 7 FDA reports)
INCISIONAL HERNIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 7 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 7 FDA reports)
ISCHAEMIA ( 7 FDA reports)
METASTASES TO LUNG ( 7 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
OLIGURIA ( 7 FDA reports)
ORAL INTAKE REDUCED ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 7 FDA reports)
PURPURA ( 7 FDA reports)
RASH MACULAR ( 7 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 7 FDA reports)
RENAL TUBULAR NECROSIS ( 7 FDA reports)
RESPIRATORY MONILIASIS ( 7 FDA reports)
RHINORRHOEA ( 7 FDA reports)
SKIN DISORDER ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
SPINAL FRACTURE ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
TENDON RUPTURE ( 7 FDA reports)
THINKING ABNORMAL ( 7 FDA reports)
THROAT IRRITATION ( 7 FDA reports)
TINNITUS ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
ADDISON'S DISEASE ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
AORTIC STENOSIS ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK ( 6 FDA reports)
AUTOIMMUNE DISORDER ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 6 FDA reports)
BODY TEMPERATURE DECREASED ( 6 FDA reports)
BREATH SOUNDS ABNORMAL ( 6 FDA reports)
CARDIAC ASTHMA ( 6 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
DISABILITY ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
DYSAESTHESIA ( 6 FDA reports)
ECZEMA ASTEATOTIC ( 6 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 6 FDA reports)
HALLUCINATION, VISUAL ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HERPES VIRUS INFECTION ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HYPERVOLAEMIA ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
HYPOKINESIA ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LIP EROSION ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
MYDRIASIS ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 6 FDA reports)
NIGHTMARE ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PARKINSON'S DISEASE ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
RALES ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
SENSATION OF HEAVINESS ( 6 FDA reports)
SEROMA ( 6 FDA reports)
SHOULDER PAIN ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SPINAL OSTEOARTHRITIS ( 6 FDA reports)
SUDDEN CARDIAC DEATH ( 6 FDA reports)
TOOTH INFECTION ( 6 FDA reports)
TOOTHACHE ( 6 FDA reports)
TUMOUR HAEMORRHAGE ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
ABDOMINAL SEPSIS ( 5 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ACUTE PULMONARY OEDEMA ( 5 FDA reports)
AEROMONA INFECTION ( 5 FDA reports)
AMNESIA ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 5 FDA reports)
APHONIA ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 5 FDA reports)
ATAXIA ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BRAIN HERNIATION ( 5 FDA reports)
BREATH ODOUR ( 5 FDA reports)
BURNOUT SYNDROME ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC PACEMAKER INSERTION ( 5 FDA reports)
CAROTID ARTERY STENOSIS ( 5 FDA reports)
CHOLECYSTITIS ( 5 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
DEAFNESS NEUROSENSORY ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
DERMATITIS ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DEVICE DISLOCATION ( 5 FDA reports)
DIABETIC GASTROPATHY ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GANGRENE ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
GINGIVITIS ( 5 FDA reports)
HEAD DISCOMFORT ( 5 FDA reports)
HEPATIC ARTERY STENOSIS ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HYPERCALCAEMIA ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INCISIONAL DRAINAGE ( 5 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 5 FDA reports)
INTESTINAL GANGRENE ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RECTAL CANCER ( 5 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 5 FDA reports)
RESPIRATORY ACIDOSIS ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
SCAR ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SKIN LACERATION ( 5 FDA reports)
SNEEZING ( 5 FDA reports)
SPLENIC INFARCTION ( 5 FDA reports)
SPUTUM DISCOLOURED ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
STILLBIRTH ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
SUPERINFECTION ( 5 FDA reports)
SURGICAL PROCEDURE REPEATED ( 5 FDA reports)
SWELLING ( 5 FDA reports)
TENSION ( 5 FDA reports)
TUMOUR NECROSIS ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
VENTRICULAR DYSFUNCTION ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
ABDOMINAL HERNIA REPAIR ( 4 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 4 FDA reports)
AORTIC ANEURYSM REPAIR ( 4 FDA reports)
AORTIC THROMBOSIS ( 4 FDA reports)
AORTIC VALVE STENOSIS ( 4 FDA reports)
ARTERIAL BYPASS OPERATION ( 4 FDA reports)
BACK INJURY ( 4 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BRAIN STEM STROKE ( 4 FDA reports)
BRONCHIECTASIS ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CEREBELLAR ATROPHY ( 4 FDA reports)
CEREBRAL CALCIFICATION ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COGNITIVE DETERIORATION ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COORDINATION ABNORMAL ( 4 FDA reports)
CYST ( 4 FDA reports)
CYSTITIS ( 4 FDA reports)
CYTOMEGALOVIRUS TEST ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DYSPHORIA ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
FLUID INTAKE REDUCED ( 4 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
FORMICATION ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HYPERACUSIS ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
INTERVERTEBRAL DISCITIS ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
JOINT EFFUSION ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LUNG TRANSPLANT ( 4 FDA reports)
LYMPHANGITIS ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MOUTH HAEMORRHAGE ( 4 FDA reports)
MUSCLE CONTRACTURE ( 4 FDA reports)
MUSCLE RIGIDITY ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEURODEGENERATIVE DISORDER ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
NIEMANN-PICK DISEASE ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
NOCTURNAL DYSPNOEA ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PANCREATIC INSUFFICIENCY ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PLEURAL FIBROSIS ( 4 FDA reports)
POISONING DELIBERATE ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
POLYP ( 4 FDA reports)
PRESYNCOPE ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
PSYCHOSOMATIC DISEASE ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
QRS AXIS ABNORMAL ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
SCRATCH ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SLOW RESPONSE TO STIMULI ( 4 FDA reports)
SLUGGISHNESS ( 4 FDA reports)
SPUTUM INCREASED ( 4 FDA reports)
STEREOTYPY ( 4 FDA reports)
STUPOR ( 4 FDA reports)
SURGERY ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
THIRST ( 4 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
URETERIC STENOSIS ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ADRENAL CARCINOMA ( 3 FDA reports)
ALLERGY TEST ( 3 FDA reports)
ANASTOMOTIC STENOSIS ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC VALVE DISEASE ( 3 FDA reports)
AORTIC VALVE REPLACEMENT ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 3 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BRONCHIOLITIS ( 3 FDA reports)
BRONCHOSTENOSIS ( 3 FDA reports)
BUDD-CHIARI SYNDROME ( 3 FDA reports)
CAPILLARY FRAGILITY ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC OPERATION ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
CONDUCTIVE DEAFNESS ( 3 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DERMATOPHYTOSIS ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DISINHIBITION ( 3 FDA reports)
DISSEMINATED TUBERCULOSIS ( 3 FDA reports)
DIVERTICULUM INTESTINAL ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
DYSPNOEA EXACERBATED ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GAS GANGRENE ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC ISCHAEMIA ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HEPATITIS E ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOCOAGULABLE STATE ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCISION SITE COMPLICATION ( 3 FDA reports)
INCISION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTENTIONAL MISUSE ( 3 FDA reports)
INTESTINAL DILATATION ( 3 FDA reports)
INTESTINAL INFARCTION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
INTESTINAL PROLAPSE ( 3 FDA reports)
IRREGULAR SLEEP PHASE ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LARYNGEAL INJURY ( 3 FDA reports)
LARYNGITIS BACTERIAL ( 3 FDA reports)
LARYNGITIS FUNGAL ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NASAL ODOUR ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OBSTRUCTION GASTRIC ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PITTING OEDEMA ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PROCTITIS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY MASS ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PYLORIC STENOSIS ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL CORTICAL NECROSIS ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL HYPERTENSION ( 3 FDA reports)
RESPIRATION ABNORMAL ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SINUS POLYP ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
TENOSYNOVITIS ( 3 FDA reports)
THALAMIC INFARCTION ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
THYROXINE FREE DECREASED ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
TRISOMY 21 ( 3 FDA reports)
TWIN PREGNANCY ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 3 FDA reports)
VENOUS INSUFFICIENCY ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WOUND ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS NECK ( 2 FDA reports)
ACQUIRED MACROGLOSSIA ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL ABUSE ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANION GAP INCREASED ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
AORTIC DISORDER ( 2 FDA reports)
APATHY ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTERIAL STENOSIS ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BILIARY ISCHAEMIA ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLIGHTED OVUM ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BORRELIA TEST POSITIVE ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN INJURY ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BREAST CANCER MALE ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHIAL SECRETION RETENTION ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOMYOPATHY NEONATAL ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPLICATION OF PREGNANCY ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONGENITAL MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEBRIDEMENT ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISEASE COMPLICATION ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 2 FDA reports)
EPIDERMOLYSIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FOETAL DEATH ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
GALLBLADDER NECROSIS ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL TOXICITY ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC SIDEROSIS ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IDIOPATHIC URTICARIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INCREASED TENDENCY TO BRUISE ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
INNER EAR INFLAMMATION ( 2 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LARYNGEAL STENOSIS ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE 0 ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEUROPATHIC ULCER ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NO ADVERSE REACTION ( 2 FDA reports)
NODAL ARRHYTHMIA ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL DISORDER ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PELVIC ABSCESS ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 2 FDA reports)
POISONING ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST-TRAUMATIC PAIN ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSEUDOMONAL SEPSIS ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TENDON PAIN ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
URINOMA ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERTIGO POSITIONAL ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WALKING DISABILITY ( 2 FDA reports)
WOUND EVISCERATION ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENAL MASS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL RUPTURE ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY ANASTOMOSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NECROSIS ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLEPHAROPLASTY ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD INSULIN ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIABETIC ULCER ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSMORPHOPHOBIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROCARDIAC SYNDROME ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GENITAL EROSION ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIAPRAXIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHARYNGEAL CANCER ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL DISORDER ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM SKIN ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODULE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL FISTULA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY THERAPY ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER DEPRESSIVE TYPE ( 1 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 1 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTOPLASTY ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS POLYP DEGENERATION ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN OPERATION ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL FISTULA REPAIR ( 1 FDA reports)
TRACHEAL OPERATION ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEILLONELLA INFECTION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use