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

PNEUMONIA ( 518 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 411 FDA reports)
INTERSTITIAL LUNG DISEASE ( 348 FDA reports)
ARTHRALGIA ( 343 FDA reports)
ANAEMIA ( 342 FDA reports)
CELLULITIS ( 336 FDA reports)
DIARRHOEA ( 317 FDA reports)
NASOPHARYNGITIS ( 288 FDA reports)
HYPERTENSION ( 287 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 273 FDA reports)
RHEUMATOID ARTHRITIS ( 264 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 258 FDA reports)
NAUSEA ( 248 FDA reports)
BRONCHITIS ( 245 FDA reports)
RASH ( 227 FDA reports)
PRURITUS ( 220 FDA reports)
DEATH ( 216 FDA reports)
PYREXIA ( 214 FDA reports)
DYSPNOEA ( 211 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 208 FDA reports)
HEADACHE ( 208 FDA reports)
CARDIAC FAILURE ( 203 FDA reports)
OEDEMA PERIPHERAL ( 181 FDA reports)
PAIN ( 181 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 178 FDA reports)
DRUG INEFFECTIVE ( 176 FDA reports)
INFLUENZA ( 176 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 174 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 169 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 168 FDA reports)
PLATELET COUNT DECREASED ( 163 FDA reports)
SEPSIS ( 163 FDA reports)
PAIN IN EXTREMITY ( 162 FDA reports)
VOMITING ( 161 FDA reports)
JUVENILE ARTHRITIS ( 158 FDA reports)
MALAISE ( 158 FDA reports)
CHEST PAIN ( 156 FDA reports)
DIZZINESS ( 152 FDA reports)
MYOCARDIAL INFARCTION ( 149 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 146 FDA reports)
SEPTIC SHOCK ( 144 FDA reports)
JOINT SWELLING ( 141 FDA reports)
ABDOMINAL PAIN UPPER ( 139 FDA reports)
CEREBRAL INFARCTION ( 135 FDA reports)
HYPERCHOLESTEROLAEMIA ( 135 FDA reports)
ARTHRITIS ( 132 FDA reports)
SKIN ULCER ( 127 FDA reports)
ABDOMINAL PAIN ( 122 FDA reports)
OROPHARYNGEAL PAIN ( 119 FDA reports)
PLEURAL EFFUSION ( 119 FDA reports)
URINARY TRACT INFECTION ( 118 FDA reports)
FALL ( 117 FDA reports)
SUBCUTANEOUS ABSCESS ( 117 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 117 FDA reports)
HYPERSENSITIVITY ( 115 FDA reports)
HYPOTENSION ( 115 FDA reports)
ILEUS ( 115 FDA reports)
HYPERLIPIDAEMIA ( 114 FDA reports)
DEEP VEIN THROMBOSIS ( 113 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 112 FDA reports)
CHOLELITHIASIS ( 111 FDA reports)
INFUSION RELATED REACTION ( 110 FDA reports)
STOMATITIS ( 108 FDA reports)
INFECTION ( 106 FDA reports)
LIVER DISORDER ( 106 FDA reports)
PERICARDIAL EFFUSION ( 106 FDA reports)
ATRIAL FIBRILLATION ( 103 FDA reports)
HODGKIN'S DISEASE ( 102 FDA reports)
ANGINA PECTORIS ( 101 FDA reports)
PLEURISY ( 99 FDA reports)
IMPAIRED HEALING ( 98 FDA reports)
DEPRESSION ( 97 FDA reports)
THROMBOCYTOPENIA ( 97 FDA reports)
DIVERTICULITIS ( 96 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 95 FDA reports)
FATIGUE ( 93 FDA reports)
HERPES ZOSTER ( 92 FDA reports)
PROTEIN URINE PRESENT ( 92 FDA reports)
PULMONARY EMBOLISM ( 92 FDA reports)
WHEEZING ( 89 FDA reports)
BACTERAEMIA ( 88 FDA reports)
CEREBRAL HAEMORRHAGE ( 87 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 86 FDA reports)
PORTAL VEIN THROMBOSIS ( 86 FDA reports)
UROSEPSIS ( 82 FDA reports)
OXYGEN SATURATION DECREASED ( 80 FDA reports)
DIABETES MELLITUS ( 79 FDA reports)
BILE DUCT STONE ( 78 FDA reports)
CHOLANGITIS ACUTE ( 78 FDA reports)
INFECTIOUS PERITONITIS ( 78 FDA reports)
CARDIAC ARREST ( 77 FDA reports)
CHOLANGITIS SUPPURATIVE ( 76 FDA reports)
SWELLING ( 75 FDA reports)
BACK PAIN ( 74 FDA reports)
ERYTHEMA ( 74 FDA reports)
URTICARIA ( 74 FDA reports)
LARGE INTESTINAL ULCER ( 73 FDA reports)
KNEE ARTHROPLASTY ( 72 FDA reports)
PANCREATITIS ACUTE ( 72 FDA reports)
CEREBROVASCULAR ACCIDENT ( 70 FDA reports)
HEPATORENAL FAILURE ( 70 FDA reports)
IVTH NERVE PARALYSIS ( 70 FDA reports)
COUGH ( 69 FDA reports)
NEUTROPENIA ( 69 FDA reports)
PANCYTOPENIA ( 69 FDA reports)
TACHYCARDIA ( 69 FDA reports)
ANAL CANCER ( 68 FDA reports)
PNEUMOTHORAX ( 68 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 67 FDA reports)
DEHYDRATION ( 67 FDA reports)
RESPIRATORY FAILURE ( 67 FDA reports)
GASTRITIS ( 66 FDA reports)
ASTHENIA ( 64 FDA reports)
LARGE INTESTINE PERFORATION ( 64 FDA reports)
LUMBAR SPINAL STENOSIS ( 64 FDA reports)
WEIGHT INCREASED ( 64 FDA reports)
NEUTROPHIL COUNT DECREASED ( 63 FDA reports)
RENAL FAILURE ( 63 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 61 FDA reports)
CHEST DISCOMFORT ( 60 FDA reports)
CORONARY ARTERY OCCLUSION ( 60 FDA reports)
RENAL IMPAIRMENT ( 60 FDA reports)
LUNG NEOPLASM MALIGNANT ( 59 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 59 FDA reports)
LYMPHADENITIS ( 58 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 57 FDA reports)
ANAL FISSURE ( 56 FDA reports)
ACUTE RESPIRATORY FAILURE ( 55 FDA reports)
ANAPHYLACTIC REACTION ( 55 FDA reports)
AZOTAEMIA ( 55 FDA reports)
CARDIO-RESPIRATORY ARREST ( 55 FDA reports)
GASTRIC CANCER ( 55 FDA reports)
ASTHMA ( 54 FDA reports)
BLOOD PRESSURE INCREASED ( 54 FDA reports)
SINUSITIS ( 54 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 54 FDA reports)
CHEST X-RAY ABNORMAL ( 53 FDA reports)
INSOMNIA ( 53 FDA reports)
LEUKOPENIA ( 53 FDA reports)
NEPHROLITHIASIS ( 53 FDA reports)
THROMBOSIS ( 53 FDA reports)
IMMUNODEFICIENCY ( 52 FDA reports)
PUSTULAR PSORIASIS ( 52 FDA reports)
BLOOD PRESSURE DECREASED ( 51 FDA reports)
WEIGHT DECREASED ( 51 FDA reports)
FEMORAL NECK FRACTURE ( 50 FDA reports)
GASTROENTERITIS ( 50 FDA reports)
HYPERHIDROSIS ( 50 FDA reports)
CARDIAC FAILURE ACUTE ( 49 FDA reports)
PARAESTHESIA ( 49 FDA reports)
LOWER LIMB FRACTURE ( 48 FDA reports)
PERITONITIS ( 48 FDA reports)
RHEUMATOID VASCULITIS ( 48 FDA reports)
ALOPECIA ( 47 FDA reports)
ANAL ULCER HAEMORRHAGE ( 47 FDA reports)
ARTHROPATHY ( 47 FDA reports)
DECREASED APPETITE ( 47 FDA reports)
DEVICE RELATED INFECTION ( 47 FDA reports)
STAPHYLOCOCCAL INFECTION ( 47 FDA reports)
CHILLS ( 46 FDA reports)
HYPOAESTHESIA ( 46 FDA reports)
PNEUMONIA ASPIRATION ( 46 FDA reports)
PULMONARY OEDEMA ( 46 FDA reports)
HAEMATURIA ( 45 FDA reports)
RENAL FAILURE CHRONIC ( 45 FDA reports)
BLISTER ( 44 FDA reports)
CONJUNCTIVITIS ( 44 FDA reports)
GAIT DISTURBANCE ( 44 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 44 FDA reports)
JOINT DISLOCATION ( 44 FDA reports)
SHOCK ( 44 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 44 FDA reports)
BREAST CANCER ( 43 FDA reports)
CANDIDIASIS ( 43 FDA reports)
MUSCULOSKELETAL PAIN ( 43 FDA reports)
NECROTISING FASCIITIS ( 43 FDA reports)
ANKLE FRACTURE ( 42 FDA reports)
HEPATIC ENZYME INCREASED ( 42 FDA reports)
LYMPHOMA ( 42 FDA reports)
OSTEOARTHRITIS ( 42 FDA reports)
VASCULITIS ( 42 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 41 FDA reports)
COLITIS ( 41 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 41 FDA reports)
DIVERTICULAR PERFORATION ( 40 FDA reports)
HEPATIC STEATOSIS ( 40 FDA reports)
LOSS OF CONSCIOUSNESS ( 40 FDA reports)
LUNG DISORDER ( 40 FDA reports)
LYMPHOPENIA ( 40 FDA reports)
OSTEOMYELITIS ( 40 FDA reports)
RIB FRACTURE ( 40 FDA reports)
TOOTH INFECTION ( 40 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 39 FDA reports)
SMALL INTESTINE ULCER ( 39 FDA reports)
TONSILLITIS ( 39 FDA reports)
AORTIC VALVE STENOSIS ( 38 FDA reports)
CONVULSION ( 38 FDA reports)
PULMONARY HYPERTENSION ( 38 FDA reports)
VIITH NERVE PARALYSIS ( 38 FDA reports)
ABSCESS LIMB ( 37 FDA reports)
ANAPHYLACTIC SHOCK ( 37 FDA reports)
BLOOD UREA INCREASED ( 37 FDA reports)
DERMAL CYST ( 37 FDA reports)
DISLOCATION OF VERTEBRA ( 37 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 36 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 36 FDA reports)
CONTUSION ( 36 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 36 FDA reports)
HEPATITIS ( 36 FDA reports)
INJURY ( 36 FDA reports)
PROTEIN TOTAL DECREASED ( 36 FDA reports)
CARDIAC DISORDER ( 35 FDA reports)
COLON CANCER STAGE II ( 35 FDA reports)
COMA ( 35 FDA reports)
GASTROINTESTINAL PERFORATION ( 35 FDA reports)
MIGRAINE ( 35 FDA reports)
ORAL HERPES ( 35 FDA reports)
RHEUMATOID FACTOR INCREASED ( 35 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 35 FDA reports)
ABDOMINAL DISCOMFORT ( 34 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 34 FDA reports)
OEDEMA ( 34 FDA reports)
PRIMARY CEREBELLAR DEGENERATION ( 34 FDA reports)
RECTAL CANCER ( 34 FDA reports)
SKIN CANCER ( 34 FDA reports)
SUDDEN DEATH ( 34 FDA reports)
ARTHRITIS BACTERIAL ( 33 FDA reports)
BLEPHARITIS ( 33 FDA reports)
LUNG ADENOCARCINOMA ( 33 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 33 FDA reports)
SPINAL OSTEOARTHRITIS ( 33 FDA reports)
SQUAMOUS CELL CARCINOMA ( 33 FDA reports)
AORTIC ANEURYSM ( 32 FDA reports)
AORTIC DISSECTION ( 32 FDA reports)
ASCITES ( 32 FDA reports)
BACTERIAL INFECTION ( 32 FDA reports)
BLOOD BILIRUBIN INCREASED ( 32 FDA reports)
CORONARY ARTERY STENOSIS ( 32 FDA reports)
FRACTURE ( 32 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 32 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 32 FDA reports)
NASAL CONGESTION ( 32 FDA reports)
PROSTATE CANCER ( 32 FDA reports)
PURPURA ( 32 FDA reports)
RECTAL PROLAPSE ( 32 FDA reports)
VENOUS THROMBOSIS LIMB ( 32 FDA reports)
CHOLANGITIS ( 31 FDA reports)
HAEMOPTYSIS ( 31 FDA reports)
LYMPHADENOPATHY ( 31 FDA reports)
THROMBOCYTOPENIC PURPURA ( 31 FDA reports)
ULCERATIVE KERATITIS ( 31 FDA reports)
DEVICE DISLOCATION ( 30 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 30 FDA reports)
MEMORY IMPAIRMENT ( 30 FDA reports)
PALLOR ( 30 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 29 FDA reports)
ECZEMA ( 29 FDA reports)
HAEMATOMA ( 29 FDA reports)
SMALL INTESTINAL PERFORATION ( 29 FDA reports)
TENDON RUPTURE ( 29 FDA reports)
AORTIC ANEURYSM RUPTURE ( 28 FDA reports)
ARRHYTHMIA ( 28 FDA reports)
COMPRESSION FRACTURE ( 28 FDA reports)
CONSTIPATION ( 28 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 28 FDA reports)
EAR INFECTION ( 28 FDA reports)
FRACTURED ISCHIUM ( 28 FDA reports)
HAEMATOCRIT DECREASED ( 28 FDA reports)
ISCHAEMIC STROKE ( 28 FDA reports)
JOINT SURGERY ( 28 FDA reports)
LEUKOCYTOSIS ( 28 FDA reports)
MENINGIOMA ( 28 FDA reports)
MOUTH ULCERATION ( 28 FDA reports)
PETECHIAE ( 28 FDA reports)
PUBIS FRACTURE ( 28 FDA reports)
RASH MACULAR ( 28 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 28 FDA reports)
ABSCESS STERILE ( 27 FDA reports)
APNOEA ( 27 FDA reports)
COLON CANCER ( 27 FDA reports)
DRY SKIN ( 27 FDA reports)
HAEMOGLOBIN DECREASED ( 27 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 27 FDA reports)
NERVOUSNESS ( 27 FDA reports)
PULMONARY TUBERCULOSIS ( 27 FDA reports)
CELL MARKER INCREASED ( 26 FDA reports)
COLITIS ULCERATIVE ( 26 FDA reports)
ERYSIPELAS ( 26 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 26 FDA reports)
RENAL FAILURE ACUTE ( 26 FDA reports)
STRESS CARDIOMYOPATHY ( 26 FDA reports)
TREMOR ( 26 FDA reports)
VERTIGO ( 26 FDA reports)
ABSCESS ( 25 FDA reports)
CARDIOMEGALY ( 25 FDA reports)
DRUG ERUPTION ( 25 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 25 FDA reports)
IRON DEFICIENCY ANAEMIA ( 25 FDA reports)
LUNG NEOPLASM ( 25 FDA reports)
PAROTITIS ( 25 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 25 FDA reports)
PHARYNGITIS ( 25 FDA reports)
PYODERMA GANGRENOSUM ( 25 FDA reports)
SKIN DISCOLOURATION ( 25 FDA reports)
SYNCOPE ( 25 FDA reports)
THROMBOPHLEBITIS ( 25 FDA reports)
BRONCHOPNEUMONIA ( 24 FDA reports)
COLON NEOPLASM ( 24 FDA reports)
DECUBITUS ULCER ( 24 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 24 FDA reports)
HYDRONEPHROSIS ( 24 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 24 FDA reports)
NEUROPATHY PERIPHERAL ( 24 FDA reports)
PALPITATIONS ( 24 FDA reports)
PSORIASIS ( 24 FDA reports)
SOMNOLENCE ( 24 FDA reports)
ABASIA ( 23 FDA reports)
BACTERIAL SEPSIS ( 23 FDA reports)
CONDITION AGGRAVATED ( 23 FDA reports)
ENTERITIS INFECTIOUS ( 23 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 23 FDA reports)
FLUID RETENTION ( 23 FDA reports)
FOOT AMPUTATION ( 23 FDA reports)
PANCREATITIS ( 23 FDA reports)
PERIARTHRITIS ( 23 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 23 FDA reports)
BLOOD GLUCOSE INCREASED ( 22 FDA reports)
CATARACT ( 22 FDA reports)
EPISTAXIS ( 22 FDA reports)
ERYTHEMA MULTIFORME ( 22 FDA reports)
GASTROINTESTINAL DISORDER ( 22 FDA reports)
HYPOXIA ( 22 FDA reports)
LARGE INTESTINE CARCINOMA ( 22 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 22 FDA reports)
MULTI-ORGAN FAILURE ( 22 FDA reports)
OESOPHAGEAL CARCINOMA ( 22 FDA reports)
POLYARTERITIS NODOSA ( 22 FDA reports)
PREGNANCY ( 22 FDA reports)
PYELONEPHRITIS ( 22 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 22 FDA reports)
WOUND ( 22 FDA reports)
ANXIETY ( 21 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 21 FDA reports)
INTESTINAL OBSTRUCTION ( 21 FDA reports)
PHLEBITIS ( 21 FDA reports)
POLLAKIURIA ( 21 FDA reports)
RECTAL POLYP ( 21 FDA reports)
SEASONAL ALLERGY ( 21 FDA reports)
SKIN NECROSIS ( 21 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 21 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 20 FDA reports)
CALCULUS URINARY ( 20 FDA reports)
DEMYELINATION ( 20 FDA reports)
DRUG INTERACTION ( 20 FDA reports)
DYSPEPSIA ( 20 FDA reports)
ENDOCARDITIS ( 20 FDA reports)
FEELING HOT ( 20 FDA reports)
FLUSHING ( 20 FDA reports)
INJECTION SITE SWELLING ( 20 FDA reports)
MYALGIA ( 20 FDA reports)
NEURALGIA ( 20 FDA reports)
PULMONARY FIBROSIS ( 20 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 20 FDA reports)
SKIN INFECTION ( 20 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 20 FDA reports)
CARDIOMYOPATHY ( 19 FDA reports)
CYTOLYTIC HEPATITIS ( 19 FDA reports)
DUODENAL ULCER ( 19 FDA reports)
DYSKINESIA ( 19 FDA reports)
DYSLIPIDAEMIA ( 19 FDA reports)
EOSINOPHILIA ( 19 FDA reports)
HIP ARTHROPLASTY ( 19 FDA reports)
HYPOGLYCAEMIA ( 19 FDA reports)
ILL-DEFINED DISORDER ( 19 FDA reports)
JOINT EFFUSION ( 19 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 19 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 19 FDA reports)
NEPHROGENIC ANAEMIA ( 19 FDA reports)
OVARIAN NEOPLASM ( 19 FDA reports)
PHARYNGEAL OEDEMA ( 19 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 19 FDA reports)
POSTOPERATIVE ILEUS ( 19 FDA reports)
SPINAL COMPRESSION FRACTURE ( 19 FDA reports)
THYROID CANCER ( 19 FDA reports)
ACUTE CORONARY SYNDROME ( 18 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 18 FDA reports)
BODY MASS INDEX INCREASED ( 18 FDA reports)
BONE MARROW FAILURE ( 18 FDA reports)
EYE DISORDER ( 18 FDA reports)
FISTULA ( 18 FDA reports)
GASTRIC BANDING ( 18 FDA reports)
INFUSION SITE ERYTHEMA ( 18 FDA reports)
INFUSION SITE PRURITUS ( 18 FDA reports)
JAUNDICE ( 18 FDA reports)
JOINT INJURY ( 18 FDA reports)
MEDICAL DEVICE COMPLICATION ( 18 FDA reports)
PARONYCHIA ( 18 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 18 FDA reports)
ROAD TRAFFIC ACCIDENT ( 18 FDA reports)
VOCAL CORD PARALYSIS ( 18 FDA reports)
ABDOMINAL ABSCESS ( 17 FDA reports)
ABORTION SPONTANEOUS ( 17 FDA reports)
ANAEMIA MACROCYTIC ( 17 FDA reports)
ANASTOMOTIC STENOSIS ( 17 FDA reports)
ANASTOMOTIC ULCER ( 17 FDA reports)
ANKLE ARTHROPLASTY ( 17 FDA reports)
CHOLECYSTITIS ACUTE ( 17 FDA reports)
COLITIS ISCHAEMIC ( 17 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 17 FDA reports)
DERMATITIS ( 17 FDA reports)
FEELING OF DESPAIR ( 17 FDA reports)
GASTRIC ULCER ( 17 FDA reports)
HAEMATOCHEZIA ( 17 FDA reports)
ILEAL ULCER ( 17 FDA reports)
INFLAMMATION ( 17 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 17 FDA reports)
MALIGNANT ASCITES ( 17 FDA reports)
MYOCARDITIS ( 17 FDA reports)
PULMONARY HAEMORRHAGE ( 17 FDA reports)
THERMAL BURN ( 17 FDA reports)
WOUND INFECTION ( 17 FDA reports)
AMYLOIDOSIS ( 16 FDA reports)
ARTHRITIS INFECTIVE ( 16 FDA reports)
BREAST DISORDER ( 16 FDA reports)
BRONCHIOLITIS ( 16 FDA reports)
CHOLECYSTITIS ( 16 FDA reports)
CYST ( 16 FDA reports)
DISEASE PROGRESSION ( 16 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 16 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 16 FDA reports)
EMBOLISM ARTERIAL ( 16 FDA reports)
EPIGASTRIC DISCOMFORT ( 16 FDA reports)
GENERALISED OEDEMA ( 16 FDA reports)
HAEMOTHORAX ( 16 FDA reports)
HAND DEFORMITY ( 16 FDA reports)
HIP FRACTURE ( 16 FDA reports)
HORMONE LEVEL ABNORMAL ( 16 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 16 FDA reports)
HYPERURICAEMIA ( 16 FDA reports)
INJECTION SITE WARMTH ( 16 FDA reports)
JOINT ARTHROPLASTY ( 16 FDA reports)
JOINT WARMTH ( 16 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 16 FDA reports)
NASAL SEPTUM PERFORATION ( 16 FDA reports)
OCULAR HYPERAEMIA ( 16 FDA reports)
PANNICULITIS ( 16 FDA reports)
RECTAL HAEMORRHAGE ( 16 FDA reports)
REFLUX OESOPHAGITIS ( 16 FDA reports)
RENAL INFARCT ( 16 FDA reports)
SEROMA ( 16 FDA reports)
SKIN ATROPHY ( 16 FDA reports)
THALAMUS HAEMORRHAGE ( 16 FDA reports)
UPPER LIMB FRACTURE ( 16 FDA reports)
VARICOSE VEIN RUPTURED ( 16 FDA reports)
VENOUS THROMBOSIS ( 16 FDA reports)
VISUAL ACUITY REDUCED ( 16 FDA reports)
ARTHRODESIS ( 15 FDA reports)
BURNING SENSATION ( 15 FDA reports)
BURSITIS ( 15 FDA reports)
CARDIOGENIC SHOCK ( 15 FDA reports)
DIALYSIS ( 15 FDA reports)
ENTEROCOLITIS ( 15 FDA reports)
EYE INFECTION FUNGAL ( 15 FDA reports)
FASCIITIS ( 15 FDA reports)
FIBULA FRACTURE ( 15 FDA reports)
HYPERGLYCAEMIA ( 15 FDA reports)
HYPERTHERMIA ( 15 FDA reports)
INJECTION SITE PAIN ( 15 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 15 FDA reports)
MUSCULAR WEAKNESS ( 15 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 15 FDA reports)
NEOPLASM MALIGNANT ( 15 FDA reports)
SHOCK HAEMORRHAGIC ( 15 FDA reports)
SPINAL CORD INJURY ( 15 FDA reports)
TUBERCULIN TEST POSITIVE ( 15 FDA reports)
TUBERCULOSIS ( 15 FDA reports)
ULCER ( 15 FDA reports)
VIRAL INFECTION ( 15 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
AMNESIA ( 14 FDA reports)
BASEDOW'S DISEASE ( 14 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 14 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 14 FDA reports)
CALCIPHYLAXIS ( 14 FDA reports)
ERYTHEMA NODOSUM ( 14 FDA reports)
GASTRITIS EROSIVE ( 14 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 14 FDA reports)
HEPATIC CIRRHOSIS ( 14 FDA reports)
HYPERKALAEMIA ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 14 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 14 FDA reports)
NEOPLASM OF ORBIT ( 14 FDA reports)
ONYCHOMADESIS ( 14 FDA reports)
OPTIC NEURITIS ( 14 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
OVERDOSE ( 14 FDA reports)
PERINEPHRIC ABSCESS ( 14 FDA reports)
SINUSITIS FUNGAL ( 14 FDA reports)
STREPTOCOCCAL INFECTION ( 14 FDA reports)
SYNOVIAL CYST ( 14 FDA reports)
UNEVALUABLE EVENT ( 14 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 13 FDA reports)
CONFUSIONAL STATE ( 13 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
CYSTITIS ( 13 FDA reports)
DENTAL CARIES ( 13 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 13 FDA reports)
EPILEPSY ( 13 FDA reports)
FEMUR FRACTURE ( 13 FDA reports)
GANGRENE ( 13 FDA reports)
HAEMORRHOIDS ( 13 FDA reports)
HYPOKINESIA ( 13 FDA reports)
HYPOVITAMINOSIS ( 13 FDA reports)
LUNG INFECTION ( 13 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 13 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 13 FDA reports)
NAIL INFECTION ( 13 FDA reports)
NIGHT SWEATS ( 13 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 13 FDA reports)
OLIGURIA ( 13 FDA reports)
ORAL CANDIDIASIS ( 13 FDA reports)
ORGANISING PNEUMONIA ( 13 FDA reports)
OSTEONECROSIS ( 13 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 13 FDA reports)
PREMATURE BABY ( 13 FDA reports)
PRURITUS GENERALISED ( 13 FDA reports)
RADIUS FRACTURE ( 13 FDA reports)
RESPIRATORY DISTRESS ( 13 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 13 FDA reports)
SURGERY ( 13 FDA reports)
SWELLING FACE ( 13 FDA reports)
THROAT IRRITATION ( 13 FDA reports)
TRANSAMINASES INCREASED ( 13 FDA reports)
VAGINAL HAEMORRHAGE ( 13 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 12 FDA reports)
BLADDER CANCER ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
BLOOD URIC ACID INCREASED ( 12 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 12 FDA reports)
CEREBROVASCULAR DISORDER ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
DRUG INTOLERANCE ( 12 FDA reports)
ERUCTATION ( 12 FDA reports)
GRIP STRENGTH DECREASED ( 12 FDA reports)
HAEMORRHAGE ( 12 FDA reports)
HYPOKALAEMIA ( 12 FDA reports)
INFECTED SKIN ULCER ( 12 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 12 FDA reports)
INFLUENZA LIKE ILLNESS ( 12 FDA reports)
JOINT STIFFNESS ( 12 FDA reports)
KLEBSIELLA INFECTION ( 12 FDA reports)
MATRIX METALLOPROTEINASE-3 INCREASED ( 12 FDA reports)
MENINGITIS ( 12 FDA reports)
MYOCARDIAL ISCHAEMIA ( 12 FDA reports)
PSYCHOTIC DISORDER ( 12 FDA reports)
RASH GENERALISED ( 12 FDA reports)
RENAL DISORDER ( 12 FDA reports)
RHEUMATOID NODULE ( 12 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 12 FDA reports)
UVEITIS ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 11 FDA reports)
ANAL ABSCESS ( 11 FDA reports)
BRADYCARDIA ( 11 FDA reports)
CARDIAC FAILURE CHRONIC ( 11 FDA reports)
CARDIOPULMONARY FAILURE ( 11 FDA reports)
CIRCULATORY COLLAPSE ( 11 FDA reports)
DUODENAL PERFORATION ( 11 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 11 FDA reports)
FACE OEDEMA ( 11 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 11 FDA reports)
JOINT DESTRUCTION ( 11 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 11 FDA reports)
NO THERAPEUTIC RESPONSE ( 11 FDA reports)
POLYNEUROPATHY ( 11 FDA reports)
RHINORRHOEA ( 11 FDA reports)
SERUM FERRITIN INCREASED ( 11 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 11 FDA reports)
SUICIDAL IDEATION ( 11 FDA reports)
TENDONITIS ( 11 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 10 FDA reports)
BONE CYST ( 10 FDA reports)
BONE FISTULA ( 10 FDA reports)
CANDIDA PNEUMONIA ( 10 FDA reports)
CASTLEMAN'S DISEASE ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 10 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 10 FDA reports)
DERMATITIS CONTACT ( 10 FDA reports)
DYSGEUSIA ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
EYE IRRITATION ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
FEELING ABNORMAL ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
FUNGAL INFECTION ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
HYPOCHROMIC ANAEMIA ( 10 FDA reports)
ILEUS PARALYTIC ( 10 FDA reports)
LEG AMPUTATION ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
MARASMUS ( 10 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 10 FDA reports)
MEAN CELL VOLUME DECREASED ( 10 FDA reports)
MELAENA ( 10 FDA reports)
MESENTERIC PANNICULITIS ( 10 FDA reports)
METASTATIC NEOPLASM ( 10 FDA reports)
NEOPLASM SKIN ( 10 FDA reports)
NIGHTMARE ( 10 FDA reports)
PACHYMENINGITIS ( 10 FDA reports)
PNEUMONIA BACTERIAL ( 10 FDA reports)
PNEUMONITIS ( 10 FDA reports)
POST PROCEDURAL INFECTION ( 10 FDA reports)
POSTOPERATIVE ABSCESS ( 10 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 10 FDA reports)
RETINAL ARTERY OCCLUSION ( 10 FDA reports)
SCLERODERMA ( 10 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 10 FDA reports)
ANGIOEDEMA ( 9 FDA reports)
APPENDICITIS ( 9 FDA reports)
ASPERGILLOSIS ( 9 FDA reports)
BEHCET'S SYNDROME ( 9 FDA reports)
COMPLETED SUICIDE ( 9 FDA reports)
CUTANEOUS VASCULITIS ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
GASTRIC DISORDER ( 9 FDA reports)
GASTRITIS ATROPHIC ( 9 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 9 FDA reports)
HAND FRACTURE ( 9 FDA reports)
HELICOBACTER INFECTION ( 9 FDA reports)
HEPATOCELLULAR INJURY ( 9 FDA reports)
HUMERUS FRACTURE ( 9 FDA reports)
HYPERCALCAEMIA ( 9 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 9 FDA reports)
INTESTINAL PERFORATION ( 9 FDA reports)
LETHARGY ( 9 FDA reports)
MULTIPLE SCLEROSIS ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
OVARIAN CANCER ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PSOAS ABSCESS ( 9 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
SKIN LESION ( 9 FDA reports)
SPLENOMEGALY ( 9 FDA reports)
TENDON INJURY ( 9 FDA reports)
TYPE 2 DIABETES MELLITUS ( 9 FDA reports)
VASCULITIS CEREBRAL ( 9 FDA reports)
WOUND DEHISCENCE ( 9 FDA reports)
ABDOMINAL PAIN LOWER ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
BONE DISORDER ( 8 FDA reports)
BONE MARROW TOXICITY ( 8 FDA reports)
BONE PAIN ( 8 FDA reports)
BREAST CYST ( 8 FDA reports)
CONCUSSION ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 8 FDA reports)
DERMATITIS ALLERGIC ( 8 FDA reports)
DISCOMFORT ( 8 FDA reports)
DISUSE SYNDROME ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
EXTRADURAL ABSCESS ( 8 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HEART RATE ABNORMAL ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
HERPES SIMPLEX ( 8 FDA reports)
HYPERAESTHESIA ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 8 FDA reports)
INFECTIVE SPONDYLITIS ( 8 FDA reports)
INFUSION SITE EXTRAVASATION ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
JAUNDICE NEONATAL ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LUNG INFILTRATION ( 8 FDA reports)
MENISCUS LESION ( 8 FDA reports)
METASTASES TO LIVER ( 8 FDA reports)
NODULE ( 8 FDA reports)
OCCULT BLOOD POSITIVE ( 8 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PANCREATITIS NECROTISING ( 8 FDA reports)
PAPILLOMA VIRAL INFECTION ( 8 FDA reports)
PARAPARESIS ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PERICARDITIS ( 8 FDA reports)
PERNICIOUS ANAEMIA ( 8 FDA reports)
RETINAL ISCHAEMIA ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SKIN HAEMORRHAGE ( 8 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
ULNA FRACTURE ( 8 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
VASCULAR OCCLUSION ( 8 FDA reports)
VITRITIS ( 8 FDA reports)
ANAPHYLACTOID REACTION ( 7 FDA reports)
APLASTIC ANAEMIA ( 7 FDA reports)
BRONCHITIS CHRONIC ( 7 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 7 FDA reports)
COLONIC OBSTRUCTION ( 7 FDA reports)
DERMATITIS PSORIASIFORM ( 7 FDA reports)
DRUG EFFECT DECREASED ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 7 FDA reports)
EXTRADURAL HAEMATOMA ( 7 FDA reports)
FURUNCLE ( 7 FDA reports)
GENITAL HAEMORRHAGE ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
IMMUNOSUPPRESSION ( 7 FDA reports)
INGUINAL HERNIA ( 7 FDA reports)
INTERVERTEBRAL DISCITIS ( 7 FDA reports)
LEUKOENCEPHALOPATHY ( 7 FDA reports)
LOCALISED INFECTION ( 7 FDA reports)
LUMBAR RADICULOPATHY ( 7 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
PARAESTHESIA ORAL ( 7 FDA reports)
PLEURITIC PAIN ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
PULMONARY HAEMATOMA ( 7 FDA reports)
RESPIRATORY ARREST ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SKIN PAPILLOMA ( 7 FDA reports)
SYNOVITIS ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
ACOUSTIC NEUROMA ( 6 FDA reports)
APHASIA ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
AUTOIMMUNE HEPATITIS ( 6 FDA reports)
AXILLARY PAIN ( 6 FDA reports)
BENIGN OVARIAN TUMOUR ( 6 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 6 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 6 FDA reports)
BLOOD TEST ABNORMAL ( 6 FDA reports)
BRONCHIECTASIS ( 6 FDA reports)
BRONCHOPNEUMOPATHY ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CEREBRAL ISCHAEMIA ( 6 FDA reports)
CHILLBLAINS ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DIASTOLIC DYSFUNCTION ( 6 FDA reports)
DIVERTICULUM INTESTINAL ( 6 FDA reports)
DRY MOUTH ( 6 FDA reports)
DYSAESTHESIA ( 6 FDA reports)
EAR DISORDER ( 6 FDA reports)
ECZEMA VESICULAR ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
FAECES PALE ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HAEMATOMA INFECTION ( 6 FDA reports)
HEPATITIS E ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
HYPOCOAGULABLE STATE ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
LABORATORY TEST ABNORMAL ( 6 FDA reports)
MEDIASTINITIS ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
MUMPS ( 6 FDA reports)
MUSCLE RUPTURE ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
PAPILLOEDEMA ( 6 FDA reports)
PARESIS ( 6 FDA reports)
PHAEOCHROMOCYTOMA ( 6 FDA reports)
POLYARTHRITIS ( 6 FDA reports)
POST PROCEDURAL SWELLING ( 6 FDA reports)
PSEUDARTHROSIS ( 6 FDA reports)
PULMONARY FISTULA ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RHINITIS ( 6 FDA reports)
SAPHO SYNDROME ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SKIN DISORDER ( 6 FDA reports)
SKIN REACTION ( 6 FDA reports)
SOFT TISSUE DISORDER ( 6 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 6 FDA reports)
SPINAL DISORDER ( 6 FDA reports)
SPLENIC INJURY ( 6 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 6 FDA reports)
SYSTEMIC SCLEROSIS ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
TONSILLECTOMY ( 6 FDA reports)
URINARY TRACT INJURY ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VISUAL IMPAIRMENT ( 6 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 5 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 5 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 5 FDA reports)
ARTERITIS INFECTIVE ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
BLOOD BLISTER ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
COLON CANCER METASTATIC ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
EMBOLIC STROKE ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
EYE MOVEMENT DISORDER ( 5 FDA reports)
FLANK PAIN ( 5 FDA reports)
FULL BLOOD COUNT DECREASED ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYPOFIBRINOGENAEMIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
ILEAL PERFORATION ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
IMMINENT ABORTION ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 5 FDA reports)
LARYNGEAL OEDEMA ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 5 FDA reports)
LYMPHADENECTOMY ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NEPHROPATHY ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OSTEITIS ( 5 FDA reports)
PANIC ATTACK ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 5 FDA reports)
PYODERMA ( 5 FDA reports)
RETINAL VASCULITIS ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
THYROID NEOPLASM ( 5 FDA reports)
TOOTH ABSCESS ( 5 FDA reports)
TYPE I HYPERSENSITIVITY ( 5 FDA reports)
UMBILICAL CORD ABNORMALITY ( 5 FDA reports)
ACCIDENT ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ANAL FISTULA ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
AORTITIS ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
ARTHROSCOPY ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BENIGN LUNG NEOPLASM ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BONE ABSCESS ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
CAESAREAN SECTION ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CERVICOBRACHIAL SYNDROME ( 4 FDA reports)
CERVIX CARCINOMA ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
CLAVICLE FRACTURE ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
CRYING ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DRUG ADMINISTRATION ERROR ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
EYELIDS PRURITUS ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FOOT DEFORMITY ( 4 FDA reports)
GASTRIC CANCER STAGE I ( 4 FDA reports)
GASTRIC CANCER STAGE IV ( 4 FDA reports)
GASTROENTERITIS SALMONELLA ( 4 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 4 FDA reports)
GLAUCOMA ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 4 FDA reports)
HAIR DISORDER ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC ATROPHY ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HYPERKERATOSIS ( 4 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
INCOHERENT ( 4 FDA reports)
INFECTED DERMAL CYST ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LENS DISORDER ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
MACULE ( 4 FDA reports)
MANIA ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MONONEUROPATHY MULTIPLEX ( 4 FDA reports)
MOVEMENT DISORDER ( 4 FDA reports)
MUSCULOSKELETAL DISORDER ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PEPTIC ULCER ( 4 FDA reports)
PERIPHERAL COLDNESS ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHARYNGEAL ABSCESS ( 4 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 4 FDA reports)
PHARYNGOTONSILLITIS ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RECTAL TENESMUS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RHEUMATOID LUNG ( 4 FDA reports)
SCLERITIS ( 4 FDA reports)
SERUM SICKNESS ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
STRESS ( 4 FDA reports)
SUBCUTANEOUS NODULE ( 4 FDA reports)
SYNOVIAL RUPTURE ( 4 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
WRIST DEFORMITY ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ALVEOLITIS ALLERGIC ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLADDER INJURY ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BURSITIS INFECTIVE ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
COMPLEMENT FACTOR INCREASED ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EAR LOBE INFECTION ( 3 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 3 FDA reports)
FAT NECROSIS ( 3 FDA reports)
FEELING JITTERY ( 3 FDA reports)
FELTY'S SYNDROME ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEAT ILLNESS ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
IMPLANT SITE EXTRAVASATION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFESTATION ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 3 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 3 FDA reports)
JEJUNITIS ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MESOTHELIOMA MALIGNANT ( 3 FDA reports)
MICROANGIOPATHY ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCLE STRAIN ( 3 FDA reports)
NECK MASS ( 3 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PARAPROTEINAEMIA ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PERICARDITIS CONSTRICTIVE ( 3 FDA reports)
PERICARDITIS RHEUMATIC ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PROTEUS INFECTION ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
RALES ( 3 FDA reports)
RENAL AMYLOIDOSIS ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RETROPERITONEAL ABSCESS ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SJOGREN'S SYNDROME ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYSTOLIC DYSFUNCTION ( 3 FDA reports)
TAKAYASU'S ARTERITIS ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THYROIDITIS ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
TRACHEAL ULCER ( 3 FDA reports)
TRIGEMINAL NEURALGIA ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WOUND DECOMPOSITION ( 3 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANTI-PLATELET ANTIBODY ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APHONIA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOINFLAMMATORY DISEASE ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BIOPSY VAGINA ABNORMAL ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD INSULIN ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BONE DENSITY INCREASED ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BULLOUS IMPETIGO ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
CAPILLARY FRAGILITY ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHEMICAL PERITONITIS ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSPHEMIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FACTOR XIII DEFICIENCY ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FINGER DEFORMITY ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HISTIOCYTIC MEDULLARY RETICULOSIS ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INFECTIVE TENOSYNOVITIS ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LEPROSY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER TENDERNESS ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MECHANICAL ILEUS ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERITONEAL TUBERCULOSIS ( 2 FDA reports)
PLEURAL MESOTHELIOMA ( 2 FDA reports)
PLICATED TONGUE ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
POST PROCEDURAL FISTULA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY GRANULOMA ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RADICULAR PAIN ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEROSITIS ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN CANCER METASTATIC ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 2 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 2 FDA reports)
THYMUS ENLARGEMENT ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRAUMATIC ULCER ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
VARICOSE ULCERATION ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
XANTHOGRANULOMA ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADRENAL ATROPHY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALLERGIC OEDEMA ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL PROLAPSE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANORECTAL VARICES ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIOENTERIC FISTULA ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATROPHIC GLOSSITIS ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACTERIAL TOXAEMIA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICOGENIC HEADACHE ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS AUTOIMMUNE ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEREDITARY SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIP DISARTICULATION ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUMAN CHORIONIC GONADOTROPIN DECREASED ( 1 FDA reports)
HYDROCELE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATITIS INTERSTITIAL ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOSAL NECROSIS ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVE ROOT LESION ( 1 FDA reports)
NERVOUS SYSTEM NEOPLASM BENIGN ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSTRUCTION GASTRIC ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESTRADIOL INCREASED ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONYCHOMALACIA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PALATITIS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERIPHERAL REVASCULARISATION ( 1 FDA reports)
PERIPHLEBITIS ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL INFECTION BACTERIAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SEBACEOUS GLAND INFECTION ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPOROTRICHOSIS ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STARING ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
TESTICULAR NECROSIS ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID CANCER RECURRENT ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UPPER EXTREMITY MASS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VULVAL CANCER ( 1 FDA reports)
VULVECTOMY ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use