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

DIARRHOEA ( 613 FDA reports)
HEPATIC FAILURE ( 378 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 342 FDA reports)
HEPATIC ENCEPHALOPATHY ( 320 FDA reports)
FATIGUE ( 300 FDA reports)
RASH ( 276 FDA reports)
ASCITES ( 253 FDA reports)
ABDOMINAL PAIN ( 237 FDA reports)
DECREASED APPETITE ( 226 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 198 FDA reports)
PYREXIA ( 191 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 179 FDA reports)
NAUSEA ( 165 FDA reports)
HYPERTENSION ( 160 FDA reports)
ASTHENIA ( 154 FDA reports)
DEHYDRATION ( 140 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 133 FDA reports)
CONFUSIONAL STATE ( 131 FDA reports)
DYSPNOEA ( 131 FDA reports)
HYPOKALAEMIA ( 125 FDA reports)
ALOPECIA ( 124 FDA reports)
VOMITING ( 118 FDA reports)
CONSTIPATION ( 115 FDA reports)
INTERSTITIAL LUNG DISEASE ( 114 FDA reports)
DEATH ( 113 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 113 FDA reports)
ENDOCARDITIS ( 112 FDA reports)
ARTHRALGIA ( 111 FDA reports)
STOMATITIS ( 111 FDA reports)
ABDOMINAL PAIN UPPER ( 110 FDA reports)
JAUNDICE ( 108 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 106 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 106 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 103 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 103 FDA reports)
LIVER CARCINOMA RUPTURED ( 101 FDA reports)
OEDEMA PERIPHERAL ( 97 FDA reports)
PLEURAL EFFUSION ( 97 FDA reports)
ENTEROBACTER INFECTION ( 96 FDA reports)
PNEUMONIA BACTERIAL ( 96 FDA reports)
STAPHYLOCOCCAL INFECTION ( 96 FDA reports)
MYOPATHY ( 95 FDA reports)
DRY MOUTH ( 94 FDA reports)
PAIN IN EXTREMITY ( 93 FDA reports)
ANXIETY ( 90 FDA reports)
MALAISE ( 89 FDA reports)
PULMONARY EMBOLISM ( 85 FDA reports)
ANAEMIA ( 84 FDA reports)
PLATELET COUNT DECREASED ( 81 FDA reports)
BACK PAIN ( 79 FDA reports)
PRURITUS ( 78 FDA reports)
SEPSIS ( 78 FDA reports)
DUODENAL ULCER ( 77 FDA reports)
HYPOGLYCAEMIA ( 76 FDA reports)
MIGRAINE ( 76 FDA reports)
MITRAL VALVE INCOMPETENCE ( 76 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 74 FDA reports)
BLOOD PRESSURE INCREASED ( 73 FDA reports)
VARICES OESOPHAGEAL ( 73 FDA reports)
HEADACHE ( 72 FDA reports)
RETINAL VEIN OCCLUSION ( 72 FDA reports)
ABASIA ( 69 FDA reports)
RENAL FAILURE ACUTE ( 69 FDA reports)
DEEP VEIN THROMBOSIS ( 67 FDA reports)
WEIGHT DECREASED ( 67 FDA reports)
DIZZINESS ( 65 FDA reports)
ERYTHEMA ( 65 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 64 FDA reports)
CONVULSION ( 63 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 62 FDA reports)
DYSPHONIA ( 62 FDA reports)
CEREBRAL HAEMORRHAGE ( 60 FDA reports)
APHAGIA ( 58 FDA reports)
COLITIS ( 58 FDA reports)
PNEUMONIA ( 57 FDA reports)
GASTRIC ULCER ( 56 FDA reports)
HYPONATRAEMIA ( 55 FDA reports)
HAEMOGLOBIN DECREASED ( 53 FDA reports)
LUNG DISORDER ( 52 FDA reports)
RESPIRATORY FAILURE ( 52 FDA reports)
CEREBRAL ISCHAEMIA ( 49 FDA reports)
PARAESTHESIA ( 49 FDA reports)
BLOOD BILIRUBIN INCREASED ( 48 FDA reports)
GAIT DISTURBANCE ( 48 FDA reports)
THYROID CANCER METASTATIC ( 44 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 43 FDA reports)
BLISTER ( 41 FDA reports)
PERICARDIAL EFFUSION ( 41 FDA reports)
THROMBOCYTOPENIA ( 41 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 40 FDA reports)
CHILLS ( 40 FDA reports)
FEBRILE NEUTROPENIA ( 40 FDA reports)
HALLUCINATION ( 40 FDA reports)
AMMONIA INCREASED ( 39 FDA reports)
SKIN ULCER ( 39 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 38 FDA reports)
HYPOALBUMINAEMIA ( 38 FDA reports)
PAIN ( 38 FDA reports)
BLOOD PRESSURE DECREASED ( 37 FDA reports)
FALL ( 37 FDA reports)
HYPOCALCAEMIA ( 37 FDA reports)
POLLAKIURIA ( 37 FDA reports)
SKIN EXFOLIATION ( 37 FDA reports)
CARDIAC ARREST ( 36 FDA reports)
INSOMNIA ( 36 FDA reports)
HYPOAESTHESIA ( 35 FDA reports)
INFECTIOUS PERITONITIS ( 35 FDA reports)
MYOCARDIAL INFARCTION ( 35 FDA reports)
LIPASE INCREASED ( 34 FDA reports)
RENAL FAILURE ( 34 FDA reports)
RETINAL VASCULAR DISORDER ( 34 FDA reports)
HYPERGLYCAEMIA ( 33 FDA reports)
HYPERKALAEMIA ( 33 FDA reports)
HAEMOPTYSIS ( 31 FDA reports)
ATRIAL FIBRILLATION ( 30 FDA reports)
FAECAL INCONTINENCE ( 30 FDA reports)
GENERALISED OEDEMA ( 30 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 30 FDA reports)
CELLULITIS ( 29 FDA reports)
CHEST PAIN ( 29 FDA reports)
SOMNOLENCE ( 29 FDA reports)
HYPERBILIRUBINAEMIA ( 28 FDA reports)
HYPOTENSION ( 28 FDA reports)
MUSCLE SPASMS ( 28 FDA reports)
ABDOMINAL DISTENSION ( 27 FDA reports)
VISION BLURRED ( 27 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 27 FDA reports)
BLOOD ALBUMIN DECREASED ( 26 FDA reports)
HEPATIC PAIN ( 26 FDA reports)
BLOOD SODIUM DECREASED ( 25 FDA reports)
BLOOD URIC ACID INCREASED ( 25 FDA reports)
COMA ( 25 FDA reports)
COUGH ( 25 FDA reports)
DYSURIA ( 25 FDA reports)
PANCYTOPENIA ( 25 FDA reports)
RASH GENERALISED ( 25 FDA reports)
ACUTE ABDOMEN ( 24 FDA reports)
CEREBROVASCULAR ACCIDENT ( 24 FDA reports)
EOSINOPHIL COUNT INCREASED ( 24 FDA reports)
CEREBRAL INFARCTION ( 23 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 23 FDA reports)
HYPOMAGNESAEMIA ( 23 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 23 FDA reports)
RETINAL VEIN THROMBOSIS ( 23 FDA reports)
BLOOD CREATININE INCREASED ( 22 FDA reports)
HYPOPHOSPHATAEMIA ( 22 FDA reports)
INFECTION ( 22 FDA reports)
LETHARGY ( 22 FDA reports)
NEUTROPENIA ( 22 FDA reports)
ORAL PAIN ( 22 FDA reports)
RENAL IMPAIRMENT ( 22 FDA reports)
TUMOUR LYSIS SYNDROME ( 22 FDA reports)
HAEMATEMESIS ( 21 FDA reports)
LIVER ABSCESS ( 21 FDA reports)
SKIN TOXICITY ( 21 FDA reports)
TONGUE BLISTERING ( 21 FDA reports)
HYPOPHAGIA ( 20 FDA reports)
MENTAL IMPAIRMENT ( 20 FDA reports)
NEPHROTIC SYNDROME ( 20 FDA reports)
NERVOUSNESS ( 20 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 20 FDA reports)
ADRENAL INSUFFICIENCY ( 19 FDA reports)
BLOOD AMYLASE INCREASED ( 19 FDA reports)
COMA HEPATIC ( 19 FDA reports)
DRY SKIN ( 19 FDA reports)
DYSPEPSIA ( 19 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 19 FDA reports)
OEDEMA ( 19 FDA reports)
CEREBRAL ATROPHY ( 18 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 18 FDA reports)
DIABETIC FOOT INFECTION ( 18 FDA reports)
DIVERTICULITIS ( 18 FDA reports)
ECZEMA ( 18 FDA reports)
HEART RATE INCREASED ( 18 FDA reports)
HYPERTENSIVE CRISIS ( 18 FDA reports)
MEDICAL DEVICE COMPLICATION ( 18 FDA reports)
MYALGIA ( 18 FDA reports)
NECK PAIN ( 18 FDA reports)
NEUROMYOPATHY ( 18 FDA reports)
OSTEOMYELITIS ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 17 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 17 FDA reports)
GASTROINTESTINAL DISORDER ( 17 FDA reports)
HAEMATOCHEZIA ( 17 FDA reports)
HYPOTHYROIDISM ( 17 FDA reports)
NEOPLASM PROGRESSION ( 17 FDA reports)
OLIGURIA ( 17 FDA reports)
OROPHARYNGEAL PAIN ( 17 FDA reports)
TRANSAMINASES INCREASED ( 17 FDA reports)
DYSGEUSIA ( 16 FDA reports)
EPILEPSY ( 16 FDA reports)
FAECES DISCOLOURED ( 16 FDA reports)
FEAR ( 16 FDA reports)
HYPERSOMNIA ( 16 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 16 FDA reports)
KLEBSIELLA SEPSIS ( 16 FDA reports)
LUNG INFECTION ( 16 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 16 FDA reports)
METASTASES TO ADRENALS ( 16 FDA reports)
METASTASES TO LUNG ( 16 FDA reports)
MULTI-ORGAN FAILURE ( 16 FDA reports)
MUSCULAR WEAKNESS ( 16 FDA reports)
MYOCARDIAL ISCHAEMIA ( 16 FDA reports)
PAIN OF SKIN ( 16 FDA reports)
PANCREATIC CARCINOMA ( 16 FDA reports)
PANIC REACTION ( 16 FDA reports)
SPINAL FRACTURE ( 16 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 16 FDA reports)
TACHYCARDIA ( 16 FDA reports)
ACNE ( 15 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 15 FDA reports)
DISORIENTATION ( 15 FDA reports)
ELECTROLYTE DEPLETION ( 15 FDA reports)
ENCEPHALOPATHY ( 15 FDA reports)
HERPES ZOSTER ( 15 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 15 FDA reports)
KERATOACANTHOMA ( 15 FDA reports)
MUSCULOSKELETAL PAIN ( 15 FDA reports)
SKIN BURNING SENSATION ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 15 FDA reports)
TREMOR ( 15 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 15 FDA reports)
ACUTE HEPATIC FAILURE ( 14 FDA reports)
BONE ABSCESS ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
MUSCLE STRAIN ( 14 FDA reports)
NASOPHARYNGITIS ( 14 FDA reports)
PORTAL VEIN THROMBOSIS ( 14 FDA reports)
RASH ERYTHEMATOUS ( 14 FDA reports)
RENAL CELL CARCINOMA ( 14 FDA reports)
CARDIO-RESPIRATORY ARREST ( 13 FDA reports)
CATHETER SITE CELLULITIS ( 13 FDA reports)
FACE OEDEMA ( 13 FDA reports)
MUCOSAL INFLAMMATION ( 13 FDA reports)
PULMONARY CAVITATION ( 13 FDA reports)
TETANY ( 13 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 12 FDA reports)
AMENORRHOEA ( 12 FDA reports)
ANORECTAL DISORDER ( 12 FDA reports)
APPENDICITIS PERFORATED ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLADDER DISORDER ( 12 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 12 FDA reports)
BLOOD POTASSIUM INCREASED ( 12 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
CIRCULATORY COLLAPSE ( 12 FDA reports)
DYSAESTHESIA ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
HEPATIC CIRRHOSIS ( 12 FDA reports)
HEPATIC INFARCTION ( 12 FDA reports)
HEPATIC NECROSIS ( 12 FDA reports)
LABORATORY TEST ABNORMAL ( 12 FDA reports)
LACERATION ( 12 FDA reports)
NEOPLASM MALIGNANT ( 12 FDA reports)
RECTAL HAEMORRHAGE ( 12 FDA reports)
RESPIRATORY DISORDER ( 12 FDA reports)
THROMBOSIS ( 12 FDA reports)
WOUND ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
BURNING SENSATION ( 11 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 11 FDA reports)
DYSPHAGIA ( 11 FDA reports)
GASTRIC HAEMORRHAGE ( 11 FDA reports)
LOCAL SWELLING ( 11 FDA reports)
OXYGEN SATURATION DECREASED ( 11 FDA reports)
RASH PRURITIC ( 11 FDA reports)
ASTERIXIS ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
BLOOD COUNT ABNORMAL ( 10 FDA reports)
CELLULITIS STREPTOCOCCAL ( 10 FDA reports)
DECUBITUS ULCER ( 10 FDA reports)
ERYSIPELAS ( 10 FDA reports)
FLUID RETENTION ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
HEMIPARESIS ( 10 FDA reports)
HOSPITALISATION ( 10 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 10 FDA reports)
IMPAIRED HEALING ( 10 FDA reports)
INTESTINAL FISTULA ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MENTAL STATUS CHANGES ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
NEUROPATHY PERIPHERAL ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PNEUMOTHORAX ( 10 FDA reports)
SKIN DISORDER ( 10 FDA reports)
SPEECH DISORDER ( 10 FDA reports)
ANAL EROSION ( 9 FDA reports)
BLADDER NEOPLASM ( 9 FDA reports)
BLOOD PRESSURE ABNORMAL ( 9 FDA reports)
BONE PAIN ( 9 FDA reports)
BUNION ( 9 FDA reports)
CHOLELITHIASIS ( 9 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 9 FDA reports)
COAGULOPATHY ( 9 FDA reports)
CONVULSIONS LOCAL ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HYPERLIPASAEMIA ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
LYMPHOPENIA ( 9 FDA reports)
PARALYSIS ( 9 FDA reports)
PRODUCTIVE COUGH ( 9 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 9 FDA reports)
PROTHROMBIN TIME PROLONGED ( 9 FDA reports)
RENAL PAIN ( 9 FDA reports)
SENSORY DISTURBANCE ( 9 FDA reports)
SINUS CONGESTION ( 9 FDA reports)
SKIN NECROSIS ( 9 FDA reports)
SWELLING ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
THROMBOCYTOSIS ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 8 FDA reports)
BRAIN STEM HAEMORRHAGE ( 8 FDA reports)
DELIRIUM ( 8 FDA reports)
DEVICE BREAKAGE ( 8 FDA reports)
DUODENITIS ( 8 FDA reports)
EATING DISORDER ( 8 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HYPERAMMONAEMIA ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
NIPPLE SWELLING ( 8 FDA reports)
OROPHARYNGEAL BLISTERING ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
ABDOMINAL ABSCESS ( 7 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BODY TEMPERATURE INCREASED ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
EXCORIATION ( 7 FDA reports)
HYPERURICAEMIA ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 7 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 7 FDA reports)
MUCOSAL INFECTION ( 7 FDA reports)
MUSCLE ENZYME INCREASED ( 7 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER ( 7 FDA reports)
OBSTRUCTION GASTRIC ( 7 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 7 FDA reports)
PNEUMATOSIS INTESTINALIS ( 7 FDA reports)
RECTAL ULCER ( 7 FDA reports)
RETCHING ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
SKIN IRRITATION ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ABSCESS RUPTURE ( 6 FDA reports)
ANGIODYSPLASIA ( 6 FDA reports)
ATAXIA ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
CHROMATURIA ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
DYSENTERY ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
ENZYME ABNORMALITY ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
FEMORAL ARTERY OCCLUSION ( 6 FDA reports)
GASTRIC PERFORATION ( 6 FDA reports)
GOUTY ARTHRITIS ( 6 FDA reports)
HEPATIC ENZYME ABNORMAL ( 6 FDA reports)
HICCUPS ( 6 FDA reports)
HYPERCREATINAEMIA ( 6 FDA reports)
HYPERKERATOSIS ( 6 FDA reports)
HYPOAESTHESIA ORAL ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
ILEUS ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
LARGE INTESTINE CARCINOMA ( 6 FDA reports)
LIVER INJURY ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MUSCLE NECROSIS ( 6 FDA reports)
PANIC DISORDER ( 6 FDA reports)
PARAESTHESIA ORAL ( 6 FDA reports)
PROSTATITIS ( 6 FDA reports)
RASH MORBILLIFORM ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
THERMOHYPOAESTHESIA ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
APHASIA ( 5 FDA reports)
APNOEA ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
DEPRESSION SUICIDAL ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
FAILURE TO THRIVE ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GASTROINTESTINAL FISTULA ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GENITAL RASH ( 5 FDA reports)
GOUT ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
INCOHERENT ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
ORAL DISCOMFORT ( 5 FDA reports)
POLYMENORRHOEA ( 5 FDA reports)
PRURITUS GENERALISED ( 5 FDA reports)
PULMONARY THROMBOSIS ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
SCROTAL PAIN ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SKIN INDURATION ( 5 FDA reports)
VENA CAVA THROMBOSIS ( 5 FDA reports)
AGEUSIA ( 4 FDA reports)
ANXIETY DISORDER ( 4 FDA reports)
AORTIC BYPASS ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BLOOD URINE PRESENT ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
CRANIOCEREBRAL INJURY ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DEVICE OCCLUSION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEPATIC MASS ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
JAUNDICE CHOLESTATIC ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
NODULE ( 4 FDA reports)
ORTHOPNOEA ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 4 FDA reports)
PERICARDIAL HAEMORRHAGE ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RENAL ABSCESS ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TROPONIN I INCREASED ( 4 FDA reports)
TUMOUR NECROSIS ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ANGIOSARCOMA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 3 FDA reports)
BREAST CANCER METASTATIC ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GASTROINTESTINAL INJURY ( 3 FDA reports)
HEPATIC NEOPLASM ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
INFECTED DERMAL CYST ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
JUGULAR VEIN THROMBOSIS ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERITONEAL HAEMORRHAGE ( 3 FDA reports)
PIGMENTATION DISORDER ( 3 FDA reports)
PNEUMONIA KLEBSIELLA ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
SARCOMA ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
TACHYARRHYTHMIA ( 3 FDA reports)
TONGUE ULCERATION ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINE ODOUR ABNORMAL ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VERTEBRAL WEDGING ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ABSCESS LIMB ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMMONIA ABNORMAL ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANORECTAL DISCOMFORT ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST DISCHARGE ( 2 FDA reports)
BREAST SWELLING ( 2 FDA reports)
BURNS THIRD DEGREE ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHLORACNE ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DEVICE LEAKAGE ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DUODENAL OBSTRUCTION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROENTERITIS RADIATION ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLIOMA ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
INTERTRIGO CANDIDA ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MACULE ( 2 FDA reports)
MASS ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
METASTASES TO ABDOMINAL WALL ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PENILE BLISTER ( 2 FDA reports)
PERITONEAL TUBERCULOSIS ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHARYNGEAL INJURY ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PORTAL HYPERTENSIVE ENTEROPATHY ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY MICROEMBOLI ( 2 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SPLENIC VARICES ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER EXTREMITY MASS ( 2 FDA reports)
URINE FLOW DECREASED ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIRAL SINUSITIS ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC HYDROTHORAX ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)