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

PYREXIA ( 203 FDA reports)
PNEUMONIA ( 129 FDA reports)
INTERSTITIAL LUNG DISEASE ( 115 FDA reports)
NAUSEA ( 97 FDA reports)
RHEUMATOID ARTHRITIS ( 94 FDA reports)
ARTHRALGIA ( 92 FDA reports)
DIARRHOEA ( 84 FDA reports)
RASH ( 84 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 82 FDA reports)
DYSPNOEA ( 82 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 80 FDA reports)
LIVER DISORDER ( 77 FDA reports)
VOMITING ( 73 FDA reports)
ANAEMIA ( 70 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 69 FDA reports)
DIZZINESS ( 68 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 65 FDA reports)
HEADACHE ( 65 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 64 FDA reports)
PANCYTOPENIA ( 62 FDA reports)
CONDITION AGGRAVATED ( 61 FDA reports)
SEPSIS ( 61 FDA reports)
DRUG ERUPTION ( 60 FDA reports)
DRUG INEFFECTIVE ( 60 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 59 FDA reports)
FATIGUE ( 56 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 56 FDA reports)
HYPERTENSION ( 56 FDA reports)
WEIGHT DECREASED ( 56 FDA reports)
ABDOMINAL PAIN ( 55 FDA reports)
PLEURAL EFFUSION ( 52 FDA reports)
HAEMOGLOBIN DECREASED ( 51 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 49 FDA reports)
PAIN ( 49 FDA reports)
DECREASED APPETITE ( 48 FDA reports)
ERYTHEMA ( 48 FDA reports)
MALAISE ( 48 FDA reports)
MYOCARDIAL INFARCTION ( 46 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 46 FDA reports)
AGRANULOCYTOSIS ( 45 FDA reports)
OEDEMA PERIPHERAL ( 45 FDA reports)
ASTHENIA ( 41 FDA reports)
CHEST PAIN ( 39 FDA reports)
DEHYDRATION ( 39 FDA reports)
LOSS OF CONSCIOUSNESS ( 39 FDA reports)
MULTI-ORGAN FAILURE ( 38 FDA reports)
INFECTION ( 37 FDA reports)
COUGH ( 36 FDA reports)
RESPIRATORY FAILURE ( 35 FDA reports)
STOMATITIS ( 35 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 34 FDA reports)
PARAESTHESIA ( 34 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 33 FDA reports)
CHILLS ( 33 FDA reports)
PAIN IN EXTREMITY ( 33 FDA reports)
PLATELET COUNT DECREASED ( 33 FDA reports)
BACK PAIN ( 32 FDA reports)
CARDIAC FAILURE ( 31 FDA reports)
OEDEMA ( 31 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 31 FDA reports)
RENAL FAILURE ( 31 FDA reports)
CELLULITIS ( 30 FDA reports)
CEREBRAL INFARCTION ( 29 FDA reports)
CHEST DISCOMFORT ( 29 FDA reports)
FALL ( 29 FDA reports)
HYPERSENSITIVITY ( 29 FDA reports)
DEATH ( 28 FDA reports)
PALPITATIONS ( 28 FDA reports)
THROMBOCYTOPENIA ( 28 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 28 FDA reports)
ANXIETY ( 27 FDA reports)
LYMPHADENOPATHY ( 27 FDA reports)
DEPRESSION ( 26 FDA reports)
HYPOAESTHESIA ( 26 FDA reports)
INFUSION RELATED REACTION ( 26 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 26 FDA reports)
PRURITUS ( 26 FDA reports)
BLOOD PRESSURE DECREASED ( 25 FDA reports)
CONSTIPATION ( 25 FDA reports)
CONVULSION ( 25 FDA reports)
DRUG HYPERSENSITIVITY ( 25 FDA reports)
LYMPHOMA ( 25 FDA reports)
OROPHARYNGEAL PAIN ( 25 FDA reports)
DEEP VEIN THROMBOSIS ( 24 FDA reports)
JOINT SWELLING ( 24 FDA reports)
ANOREXIA ( 23 FDA reports)
ASTHMA ( 23 FDA reports)
BLOOD ALBUMIN DECREASED ( 23 FDA reports)
CARDIOMEGALY ( 23 FDA reports)
PERICARDIAL EFFUSION ( 23 FDA reports)
ABDOMINAL PAIN UPPER ( 22 FDA reports)
ARRHYTHMIA ( 22 FDA reports)
HERPES ZOSTER ( 22 FDA reports)
ANAPHYLACTIC SHOCK ( 21 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 21 FDA reports)
HYPOTHYROIDISM ( 21 FDA reports)
LEUKOPENIA ( 21 FDA reports)
NASOPHARYNGITIS ( 21 FDA reports)
BLOOD UREA INCREASED ( 20 FDA reports)
FEELING ABNORMAL ( 20 FDA reports)
GENERALISED ERYTHEMA ( 20 FDA reports)
INFLUENZA ( 20 FDA reports)
URINARY TRACT INFECTION ( 20 FDA reports)
BRONCHITIS ( 19 FDA reports)
JAUNDICE ( 19 FDA reports)
PNEUMONIA BACTERIAL ( 19 FDA reports)
SEPTIC SHOCK ( 19 FDA reports)
ABDOMINAL DISCOMFORT ( 18 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 18 FDA reports)
ENTEROCOLITIS ( 18 FDA reports)
GASTRIC ULCER ( 18 FDA reports)
GRANULOCYTOPENIA ( 18 FDA reports)
HAEMATOCRIT DECREASED ( 18 FDA reports)
MUSCULAR WEAKNESS ( 18 FDA reports)
RENAL IMPAIRMENT ( 18 FDA reports)
STRESS ( 18 FDA reports)
ASCITES ( 17 FDA reports)
BLOOD PRESSURE INCREASED ( 17 FDA reports)
DYSGEUSIA ( 17 FDA reports)
FACE OEDEMA ( 17 FDA reports)
HEART RATE INCREASED ( 17 FDA reports)
HYPERHIDROSIS ( 17 FDA reports)
MUSCLE SPASMS ( 17 FDA reports)
PROTEIN TOTAL DECREASED ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
SURGERY ( 17 FDA reports)
COLITIS ULCERATIVE ( 16 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 16 FDA reports)
INJECTION SITE PAIN ( 16 FDA reports)
MYELODYSPLASTIC SYNDROME ( 16 FDA reports)
PLEURISY ( 16 FDA reports)
SOMNOLENCE ( 16 FDA reports)
TUBERCULOUS PLEURISY ( 16 FDA reports)
ATRIAL FIBRILLATION ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
DRUG INTERACTION ( 15 FDA reports)
MUSCULOSKELETAL PAIN ( 15 FDA reports)
MYALGIA ( 15 FDA reports)
PERICARDITIS ( 15 FDA reports)
PULMONARY EMBOLISM ( 15 FDA reports)
PYELONEPHRITIS ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 15 FDA reports)
TOXIC SKIN ERUPTION ( 15 FDA reports)
TUBERCULOSIS ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
BONE MARROW FAILURE ( 14 FDA reports)
BREAST CANCER ( 14 FDA reports)
CHEST X-RAY ABNORMAL ( 14 FDA reports)
CROHN'S DISEASE ( 14 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 14 FDA reports)
HAEMATOCHEZIA ( 14 FDA reports)
INFLAMMATION ( 14 FDA reports)
NEUTROPENIA ( 14 FDA reports)
SWELLING FACE ( 14 FDA reports)
BRADYCARDIA ( 13 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 13 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 13 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 13 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 13 FDA reports)
HEPATIC ENZYME INCREASED ( 13 FDA reports)
HYPERGLYCAEMIA ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
ILEUS ( 13 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 13 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 13 FDA reports)
NECK PAIN ( 13 FDA reports)
OSTEOMYELITIS ( 13 FDA reports)
PNEUMONIA ASPIRATION ( 13 FDA reports)
PSORIATIC ARTHROPATHY ( 13 FDA reports)
RASH GENERALISED ( 13 FDA reports)
RENAL DISORDER ( 13 FDA reports)
RIB FRACTURE ( 13 FDA reports)
SINUSITIS ( 13 FDA reports)
URTICARIA ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
WEIGHT INCREASED ( 13 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
COAGULOPATHY ( 12 FDA reports)
CORONARY ARTERY DISEASE ( 12 FDA reports)
DISSEMINATED TUBERCULOSIS ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
FLUSHING ( 12 FDA reports)
INSOMNIA ( 12 FDA reports)
NEPHROTIC SYNDROME ( 12 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 12 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 12 FDA reports)
SKIN ULCER ( 12 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ARTHRITIS ( 11 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 11 FDA reports)
DRUG EFFECT DECREASED ( 11 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 11 FDA reports)
DRY MOUTH ( 11 FDA reports)
EOSINOPHILIC PNEUMONIA ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
GASTRITIS ( 11 FDA reports)
GASTROENTERITIS ( 11 FDA reports)
HERPES OESOPHAGITIS ( 11 FDA reports)
HIATUS HERNIA ( 11 FDA reports)
INJECTION SITE REACTION ( 11 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 11 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 11 FDA reports)
NEUROPATHY PERIPHERAL ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
ORGANISING PNEUMONIA ( 11 FDA reports)
POST PROCEDURAL COMPLICATION ( 11 FDA reports)
PULMONARY TUBERCULOSIS ( 11 FDA reports)
TINNITUS ( 11 FDA reports)
TREMOR ( 11 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 10 FDA reports)
APLASTIC ANAEMIA ( 10 FDA reports)
ATELECTASIS ( 10 FDA reports)
BRONCHIOLITIS ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 10 FDA reports)
ILL-DEFINED DISORDER ( 10 FDA reports)
INFLUENZA LIKE ILLNESS ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
LUNG NEOPLASM MALIGNANT ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 10 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 10 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PERITONITIS ( 10 FDA reports)
PLATELET COUNT INCREASED ( 10 FDA reports)
RESPIRATORY TRACT INFECTION ( 10 FDA reports)
SINUS DISORDER ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
STAPHYLOCOCCAL INFECTION ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
URINE OUTPUT DECREASED ( 10 FDA reports)
VASCULITIS ( 10 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 10 FDA reports)
VIRAL INFECTION ( 10 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
BLADDER CANCER ( 9 FDA reports)
BLISTER ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
BURNING SENSATION ( 9 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
DECUBITUS ULCER ( 9 FDA reports)
DERMATITIS EXFOLIATIVE ( 9 FDA reports)
DIVERTICULITIS ( 9 FDA reports)
EOSINOPHIL COUNT INCREASED ( 9 FDA reports)
GASTROINTESTINAL DISORDER ( 9 FDA reports)
HEPATIC STEATOSIS ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
HYPOPHAGIA ( 9 FDA reports)
INJECTION SITE HAEMATOMA ( 9 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 9 FDA reports)
NOCTURIA ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
PERITONEAL TUBERCULOSIS ( 9 FDA reports)
PNEUMOTHORAX ( 9 FDA reports)
PRURITUS GENERALISED ( 9 FDA reports)
PSORIASIS ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
PURPURA ( 9 FDA reports)
SKIN EXFOLIATION ( 9 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
URINARY INCONTINENCE ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ACUTE TONSILLITIS ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
ARTHROPATHY ( 8 FDA reports)
BILOMA ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
DUODENAL ULCER ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
FEMUR FRACTURE ( 8 FDA reports)
FLUID RETENTION ( 8 FDA reports)
GASTROINTESTINAL PAIN ( 8 FDA reports)
GROIN PAIN ( 8 FDA reports)
HAEMOLYTIC ANAEMIA ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
IMMUNOSUPPRESSION ( 8 FDA reports)
IMPAIRED HEALING ( 8 FDA reports)
INADEQUATE ANALGESIA ( 8 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 8 FDA reports)
INTESTINAL OBSTRUCTION ( 8 FDA reports)
IRON DEFICIENCY ANAEMIA ( 8 FDA reports)
LUNG INFILTRATION ( 8 FDA reports)
MELAENA ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
NASAL DRYNESS ( 8 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
POLLAKIURIA ( 8 FDA reports)
PRODUCTIVE COUGH ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SPLENOMEGALY ( 8 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
VENTRICULAR FIBRILLATION ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
WHEEZING ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
AFFECT LABILITY ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CHOKING ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DIALYSIS ( 7 FDA reports)
DIFFICULTY IN WALKING ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DRUG DEPENDENCE ( 7 FDA reports)
EJACULATION DISORDER ( 7 FDA reports)
EMPHYSEMA ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FIBROMYALGIA ( 7 FDA reports)
FLAT AFFECT ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 7 FDA reports)
HAEMATOMA ( 7 FDA reports)
HAEMATURIA ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HEPATITIS B ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
HYPOALBUMINAEMIA ( 7 FDA reports)
INGUINAL HERNIA ( 7 FDA reports)
INJURY ( 7 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 7 FDA reports)
LENTIGO ( 7 FDA reports)
LUNG ABSCESS ( 7 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 7 FDA reports)
MALNUTRITION ( 7 FDA reports)
MENTAL DISORDER ( 7 FDA reports)
MOVEMENT DISORDER ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PARANOIA ( 7 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 7 FDA reports)
PROSTATE CANCER ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
RESPIRATORY DISORDER ( 7 FDA reports)
RHEUMATOID LUNG ( 7 FDA reports)
RHINITIS SEASONAL ( 7 FDA reports)
SKIN NODULE ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
STEVENS-JOHNSON SYNDROME ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
URINARY HESITATION ( 7 FDA reports)
ABDOMINAL ABSCESS ( 6 FDA reports)
ABSCESS ( 6 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ANOSMIA ( 6 FDA reports)
ANURIA ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 6 FDA reports)
APPETITE DISORDER ( 6 FDA reports)
ASPERGILLOSIS ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
CALCIUM DEFICIENCY ( 6 FDA reports)
CALCULUS URINARY ( 6 FDA reports)
CATARACT ( 6 FDA reports)
COLITIS ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 6 FDA reports)
GENERALISED OEDEMA ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HAEMORRHOIDS ( 6 FDA reports)
HELICOBACTER INFECTION ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
INCREASED TENDENCY TO BRUISE ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 6 FDA reports)
JOINT ANKYLOSIS ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
NERVOUS SYSTEM DISORDER ( 6 FDA reports)
PANCREATIC PSEUDOCYST ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PUBIS FRACTURE ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
SHOCK ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SWELLING ( 6 FDA reports)
SYNOVITIS ( 6 FDA reports)
TONIC CONVULSION ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
UVEITIS ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
ABDOMINAL NEOPLASM ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ABORTION SPONTANEOUS ( 5 FDA reports)
ABSCESS LIMB ( 5 FDA reports)
AGEUSIA ( 5 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
ATHEROSCLEROSIS ( 5 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BODY HEIGHT DECREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
BREAST CANCER METASTATIC ( 5 FDA reports)
BRONCHIECTASIS ( 5 FDA reports)
BURNS SECOND DEGREE ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
CERVICAL SPINAL STENOSIS ( 5 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 5 FDA reports)
CHOLANGITIS ACUTE ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
DERMATITIS BULLOUS ( 5 FDA reports)
DIZZINESS POSTURAL ( 5 FDA reports)
DRY THROAT ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 5 FDA reports)
GALLBLADDER DISORDER ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HILAR LYMPHADENOPATHY ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
JOINT EFFUSION ( 5 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
MASS ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MICROANGIOPATHY ( 5 FDA reports)
MOTOR NEURONE DISEASE ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
NASAL CONGESTION ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
NIGHTMARE ( 5 FDA reports)
OCULAR HYPERAEMIA ( 5 FDA reports)
OESOPHAGEAL CARCINOMA ( 5 FDA reports)
OESOPHAGEAL ULCER ( 5 FDA reports)
ORAL PAIN ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SMALL INTESTINE CARCINOMA ( 5 FDA reports)
SPUTUM CULTURE POSITIVE ( 5 FDA reports)
TESTICULAR NEOPLASM ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TORSADE DE POINTES ( 5 FDA reports)
TUMOUR LYSIS SYNDROME ( 5 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
URINE ANALYSIS ABNORMAL ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ABORTION MISSED ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANKLE FRACTURE ( 4 FDA reports)
ANKLE OPERATION ( 4 FDA reports)
AORTIC ANEURYSM RUPTURE ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
BREAST CYST ( 4 FDA reports)
BURNS THIRD DEGREE ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CERVICAL MYELOPATHY ( 4 FDA reports)
CHROMATURIA ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
COMPRESSION FRACTURE ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 4 FDA reports)
DEMYELINATION ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DYSPLASIA ( 4 FDA reports)
DYSSTASIA ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
ENTERITIS ( 4 FDA reports)
ENTEROCOLITIS VIRAL ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
EXOSTOSIS ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GASTRITIS HAEMORRHAGIC ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 4 FDA reports)
HYPERTROPHY ( 4 FDA reports)
HYPOCHROMASIA ( 4 FDA reports)
ILEAL PERFORATION ( 4 FDA reports)
ILEAL STENOSIS ( 4 FDA reports)
ILEAL ULCER ( 4 FDA reports)
IMMUNOGLOBULINS DECREASED ( 4 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INJECTION SITE PHLEBITIS ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIMB INJURY ( 4 FDA reports)
LISTLESS ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MICROCYTOSIS ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MULTIPLE SCLEROSIS ( 4 FDA reports)
MUSCLE HAEMORRHAGE ( 4 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
OESOPHAGEAL IRRITATION ( 4 FDA reports)
OESOPHAGEAL PAIN ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
ORAL MUCOSA EROSION ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PAIN IN JAW ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PATHOLOGICAL FRACTURE ( 4 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PIGMENTATION DISORDER ( 4 FDA reports)
PNEUMOMEDIASTINUM ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYMYALGIA RHEUMATICA ( 4 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 4 FDA reports)
PRINZMETAL ANGINA ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH MACULAR ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 4 FDA reports)
RENAL CYST ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RETROPERITONEAL ABSCESS ( 4 FDA reports)
RHINITIS ALLERGIC ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
STRESS ULCER ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC VALVE CALCIFICATION ( 3 FDA reports)
AORTIC VALVE STENOSIS ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ASPERGILLOSIS ORAL ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BONE FRAGMENTATION ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CALCULUS BLADDER ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHOLECYSTITIS INFECTIVE ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CRYPTOCOCCOSIS ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FEAR ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOOD INTOLERANCE ( 3 FDA reports)
FOREIGN BODY ( 3 FDA reports)
FRACTURE NONUNION ( 3 FDA reports)
GASTRIC CANCER STAGE IV ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HAIR DISORDER ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOACUSIS ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
ILEAL OPERATION ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LARYNGITIS ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIMB ASYMMETRY ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
LYMPHADENITIS ( 3 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
MYCOSIS FUNGOIDES ( 3 FDA reports)
NAIL DISORDER ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 3 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 3 FDA reports)
PANCREATITIS CHRONIC ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POST HERPETIC NEURALGIA ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PULMONARY GRANULOMA ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
PYELONEPHRITIS ACUTE ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
RENAL HAEMORRHAGE ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SOFT TISSUE NEOPLASM ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUBCUTANEOUS NODULE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
SYNOVIAL CYST ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THIRST ( 3 FDA reports)
THYROIDITIS SUBACUTE ( 3 FDA reports)
TOE DEFORMITY ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
TYPE 2 DIABETES MELLITUS ( 3 FDA reports)
ULCER ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
WRIST FRACTURE ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ABSCESS SWEAT GLAND ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADRENAL NEOPLASM ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ALPHA 1 FOETOPROTEIN DECREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL EROSION ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTIC RUPTURE ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRADYKINESIA ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CERVICAL GLAND TUBERCULOSIS ( 2 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COMA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS BACTERIAL ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DEATH OF SPOUSE ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DIABETIC DERMOPATHY ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOSCOPY ABNORMAL ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FOREARM FRACTURE ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 2 FDA reports)
GANGLIONEUROMA ( 2 FDA reports)
GASTRIC CANCER RECURRENT ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL EROSION ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTES MATURATION ARREST ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HAEMOSTASIS ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HUMAN EHRLICHIOSIS ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTIVE ANEURYSM ( 2 FDA reports)
INFECTIVE SPONDYLITIS ( 2 FDA reports)
INFERTILITY MALE ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE FIBROSIS ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MANIA ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MATRIX METALLOPROTEINASE-3 INCREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
MYOCARDITIS RHEUMATIC ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NODULE ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PAPILLOMA VIRAL INFECTION ( 2 FDA reports)
PARATHYROID TUMOUR BENIGN ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PAROTID GLAND ENLARGEMENT ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHARYNGEAL EROSION ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PROCEDURAL DIZZINESS ( 2 FDA reports)
PROCEDURAL HYPOTENSION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
SACROILIITIS ( 2 FDA reports)
SALIVARY GLAND PAIN ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCLERITIS ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SEBORRHOEIC KERATOSIS ( 2 FDA reports)
SENSITIVITY OF TEETH ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPINAL PAIN ( 2 FDA reports)
SPLENIC CYST ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TERATOMA OF TESTIS ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE GEOGRAPHIC ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UTERINE DILATION AND EVACUATION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VOMITING PROJECTILE ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALPHA 1 GLOBULIN ABNORMAL ( 1 FDA reports)
ALPHA 2 GLOBULIN ABNORMAL ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRITIS ENTEROPATHIC ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
ASTHENOSPERMIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AURA ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BANDAEMIA ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BETA GLOBULIN ABNORMAL ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHONDROPATHY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELDERLY ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCEPHALOPATHY ALLERGIC ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXPOSURE TO ALLERGEN ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) STAGE II ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FOREIGN TRAVEL ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHARYNGEAL CANCER STAGE III ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONONUCLEOSIS SYNDROME ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGODENDROGLIOMA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OSTEOSYNTHESIS ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PERIODONTAL DISEASE ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PITYRIASIS ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLASMACYTOSIS ( 1 FDA reports)
PLATELET DISTRIBUTION WIDTH ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYP ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESENILE DEMENTIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT SYNOVITIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCLEROMALACIA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPERMATOZOA MORPHOLOGY ABNORMAL ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SULPHAEMOGLOBINAEMIA ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENOTOMY ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUBERCULOSIS OF PERIPHERAL LYMPH NODES ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VIIITH NERVE INJURY ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use